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Effective photosensitized, electrosensitized, and mechanosensitized luminescence of lanthanide complexes


The 4f–4f emission of Tb(III), Eu(III), and Sm(III) complexes plays an important role in the design of monochromatic green, red, and deep-red luminescent materials for displays, lighting, and sensing devices. The 4f–4f emission of Yb(III), Nd(III), and Er(III) complexes is observed in the near-infrared (IR) region for bioimaging and security applications. However, their absorption coefficients are extremely small (ε < 10 L mol−1 cm−1). In this review, photosensitized luminescent lanthanide(III) complexes containing organic chromophores (ligands) with large absorption coefficients (ε > 10,000 L mol−1 cm−1) are introduced. Organic molecular design elements, including (1) the control of the excited triplet (T1) state, (2) the effects on the charge-transfer (CT) band, and (3) the energy transfer from metal ions for effective photosensitized luminescence, are explained. The characteristic electrosensitized luminescence (electroluminescence) and mechanoluminescence (triboluminescence) of lanthanide(III) complexes are also explained. Lanthanide(III) complexes with well-designed organic molecules are expected to open avenues of research among the fields of chemistry, physics, electronics, and material science.


Lanthanides comprise a family of highly electropositive period 6 metals. According to the previous literature, lanthanides are defined as lanthanum (La) and 14 other elements (Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu)1. A general lanthanide is represented by the symbol Ln. Lanthanides in the stable (III) oxidation state are simply characterized by an incompletely filled 4f shell. The 4f orbital is shielded from the surroundings by the filled 5s2 and 5p2 orbitals (an image of the 4f radial distribution function: Fig. 1a). In a configurational coordinate diagram, these levels appear as parallel parabolas (a small offset case: Fig. 1b) because the 4f electrons are well shielded from their surroundings. Therefore, emission transitions yield sharp lines (full-width at half-maximum, FWHM <10 nm) in different spectra, which is a much different result from that seen for semiconductors, transition materials, and organic molecules, as shown in Fig. 1c (in a large-stokes-shift case: FWHM >50 nm)2,3. The emission of light radiation for lanthanide(III) ions comes mainly from electric dipole transitions. Transitions formed in the 4fi inner shell of free ions are forbidden because they do not correspond to a change in parity. However, the transitions that are forbidden by odd-parity states become partially allowed by the mixing of the 4f and 5d orbitals through the ligand field. Since the parity does not change dramatically in such a transition, the lifetime of the excited state is long (τ > ms).

Fig. 1

a Image of the radial distribution function of the 4f, 5s, 5p, 5d, and 6s orbitals. b Emission process of the 4f–4f transition in lanthanide(III) ions. c Emission process of organic molecules and transition metal complexes

Lanthanide complexes with attached organic ligands are regarded as attractive luminescent materials because of their characteristic narrow emission bands and long emission lifetimes over a wide range of wavelengths (ultraviolet/visible/near-infrared (UV/vis/near-IR)). The 4f–4f emissions from Tb(III), Eu(III), and Sm(III) complexes play an important role in the design of monochromatic green, red, and deep-red luminescent materials for displays, lighting, and sensing devices, respectively (Fig. 2a, b)3,4,5,6,7,8. The near-IR 4f–4f luminescence of Nd(III), Er(III), and Yb(III) complexes with long emission lifetimes is useful in bioimaging applications (Fig. 2c)8. Effective wavelength converters using lanthanide complexes for silicon solar cells have also been reported (Fig. 2d)9,10.

Fig. 2

a Emission processes in the energy diagrams of lanthanide(III) ions. b Luminescent plastics using Tb(III) and Eu(III) complexes and polymethylmethacrylate. c Bioimaging using a Eu(III) complex. Reprinted with permission from Bünzli et al8. Copyright 2010 Royal Society of Chemistry. d Luminescent EVA film containing Eu(III) complexes on a silicon solar cell. Reprinted with permission from Hasegawa et al9. Copyright 2015 SPST

Here, we introduce the history of lanthanide complex studies. The 1930s and early 1940s witnessed the first spectroscopic studies of lanthanide ions in solution. Freed and co-workers11 found that the relative intensities of the absorption bands of Eu(III) were different in different solvents, and Weissman12 observed that complexes of Eu(III) with certain UV absorbing ligands were highly luminescent when excited with UV light. Since Eu(III) itself shows only a few very weak absorption bands, the solution of this ion does not offer very bright luminescence. Obviously, certain organic ligands can photosensitize the luminescence of lanthanide ions. It was also found that lanthanide ions quench the fluorescence of organic ligands13. Such studies can be considered as the starting points for the research and development of luminescent lanthanide complexes. It took, however, approximately 20 years for photochemists and coordination chemists to take a serious interest in these materials. At the beginning of the 1980s, the field received a new impulse when it became clear that lanthanide complexes could find widespread use in medical diagnostics14. In the past 40 years, lanthanide ions also started to receive the attention of the growing number of organic and supramolecular chemists. At the present stage, many types of luminescent lanthanide complexes have been reported15,16.

The focus of this review is photosensitized and electrosensitized luminescence of lanthanide complexes with effective organic ligands. The absorption coefficients of 4f–4f transitions in Ln(III) ions are extremely small (4f–4f transition bands: ε < 10 L mol−1 cm−1). The photosensitized and electrosensitized energy transfer from an organic ligand to a lanthanide(III) ion is a key point for achieving effective luminescence of lanthanide(III) complexes. Various types of organic chromophores (ligands) have been developed to photosensitize the luminescence of lanthanide(III) ions. Luminescent lanthanide(III) complexes with large absorption coefficients (π–π* transition band: ε > 10,000 L mol−1 cm−1) have been promising molecules as luminescent materials in the fields of optoelectronics, analytical chemistry, photophysical, and biomedical science.

Organic molecular designs that include (1) the control of the excited triplet (T1) state, (2) the effect on the charge-transfer (CT) band, and (3) the energy transfer from metal ions for effective photosensitized luminescence are explained in the next chapter. The transition bands provide effective photosensitized luminescence of lanthanide complexes. We also summarize the electroluminescence (EL) and mechanoluminescence of lanthanide(III) complexes as energy transfer from the electroexcitation of the organic ligand. The EL of lanthanide(III) complexes has been studied for the development of display devices. The historical reports and recent progress of EL using lanthanide complexes are introduced in this review.

The mechanoluminescence of lanthanide(III) complexes has also been studied over the past several decades. Mechanoluminescence is also called triboluminescence, which is the emission of light from bulk solid materials that originates from mechanical stress. While there have been extensive discussions on the origin of triboluminescence in molecular crystals, some studies have indicated a contribution from the piezoelectric effect upon breaking non-centrosymmetric bulk crystals. Their EL and mechanoluminescence are dependent on the energy transfer process from the ligands in lanthanide complexes.

The molecular design and the strategies for the development of strong luminescent lanthanide(III) complexes are reviewed to illustrate novel developments in the fields of molecular science, photophysics, electronics, and material science.

Photosensitized luminescence from an organic ligand

Control of the T 1 state

First, we introduce the photosensitized energy transfer from organic ligands to lanthanide ions for the development of a strong luminescent lanthanide(III) complex. Effective photosensitized energy transfer is achieved by excitation at the π–π* bands of organic ligands. The π–π* bands of organic ligands can transition and have large absorption coefficients (ε > 10,000 L mol−1 cm−1). In the case of a lanthanide(III) complex, the S1 state of the organic ligand irradiated at the π–π* band rapidly changes to a T1 state because of the heavy metal effect of the lanthanide(III) ions. For this reason, energy transfer efficiency between the T1 state and lanthanide(III) ion is key for effective photosensitization.

Here, the photosensitized energy transfer process is explained by using a simple schematic diagram (Fig. 3). First, the organic ligand in the lanthanide(III) complex is excited by photoirradiation at the π–π* transition band, and then, a T1 state of the ligand is formed. The energy transfer process between the T1 and 4f–4f transition bands of the lanthanide ion (4f–4f′) is generally explained by the Förster and Dexter mechanisms15,16. Effective energy transfer (forward energy transfer) between the T1 (donor) and 4f–4f′ (acceptor) leads to the formation of an excited Ln(III) complex. However, a small energy gap between the T1 state and emitting level of the Ln(III) ion promotes energy back transfer from the 4f–4f′ emitting level (donor) to the T1 state (acceptor), resulting in the prevention of effective forward energy transfer. Thus, effective energy transfer is dependent on the energy gap between the T1 state and the emitting level in lanthanide(III) complexes.

Fig. 3

Photosensitized emission process of a lanthanide(III) complex attached with π-conjugated organic ligands

In Eu(III) complexes with β-diketonate, pyridyl, and carboxylate ligands, the ideal energy gaps between the T1 state and the emitting level (Tb(III): 7F6-5D4, Eu(III): 7F0-5D0) for the suppression of energy back transfer are estimated to be more than 2400 and 2500 cm−1, respectively17,18,19,20,21,22,23,24, although effective energy transfer with a small energy gap between the T1 state and emitting level (7F0-5D0) has also been reported22,23. The effective energy transfer between an organic ligand and lanthanide(III) ion is dependent on the ligand moiety.

Generally, the expansion of the π-conjugated system in a ligand leads to a decrease in the T1 level. However, the emitting level of lanthanide(III) ion is not changed by the surrounding media, such as an organic ligand and solvent. The emitting levels of the Eu(III), Tb(III), Sm(III), Yb(III), Nd(III) and Er(III) ions have been estimated to be 17,293, 20,500, 17,900, 10,260, 11,100, and 6535 cm−1, respectively3. When the energy level of the T1 state is lower than that of the emitting level, the lanthanide complex does not emit photons. Typical π-conjugate systems and their T1 energy levels are summarized in Fig. 425,26,27. When the energy gap between the T1 and the emitting levels is also <2500 cm−1, energy back transfer from Ln(III) to the ligand is observed. From the photophysical findings, the expansive limitation of the π-conjugate structure in an organic ligand should be required for effective energy forward transfer from the T1 state of an organic ligand to the emitting level of a lanthanide(III) ion.

Fig. 4

Chemical structures and triplet (T1) energy levels of π-conjugated benzene, naphthalene, anthracene, tetracene, phenanthorene, and pyrene

The overall emission quantum yield of an Ln(III) complex excited at the π–π* band of an organic ligand, Φπ–π*, is calculated as follows:

$${\mathrm{\Phi }}_{\pi - \pi ^\ast } = {\mathrm{\Phi }}_{\mathrm{f - f}} \times \eta _{\mathrm{sens}} = \frac{{k_{\mathrm{r}}}}{{k_{\mathrm{r}} + k_{\mathrm{nr}}}} \times \eta _{\mathrm{sens}},$$

where Φf–f, ηsens, kr, and knr are the lanthanide(III)-centered emission quantum yield, efficiency of the sensitization process, and radiative and non-radiative rate constants, respectively. Knag et al.28 reported the photosensitized luminescence of Nd(III), Yb(III), and Er(III) complexes with anthracene-attached diketonate ligands. The ηsens values of the Nd(III) and Er(III) complexes were estimated to be 0.89% and 0.086%, respectively (Fig. 5a). Reddy and co-workers29 described efficient photosensitized energy transfer of Nd(III) complexes with pyrene-attached diketonate ligands (ηsens of Nd(III) complex: 44%) (Fig. 5b). He also showed highly efficient photosensitized energy transfer of Eu(III) complexes with phenanthrene-attached diketonate (Fig. 5c)30. In another case, the photosensitized luminescence of Eu(III) and Tb(III) ions with triphenylene in calix [4] arene systems has been reported (Fig. 5d);31 however, the expansion of π-conjugated systems in aromatic ligands leads to a decrease in the energy level of the T1 state, resulting in energy back transfer from the excited Ln(III) ions to the T1 state of the aromatic ligands.

Fig. 5

Chemical structures of lanthanide(III) complexes attached with π-conjugated organic ligands

We have suggested a novel molecular strategy for the expansion of π-conjugated systems for the effective photosensitization of a lanthanide(III) complex using a helical-shaped helicene unit (Fig. 5e)32,33. We here explain the concept of molecular design for the effective photosensitization of a lanthanide(III) complex. The equation for the T1(−S0) level of the molecules is as follows:

$$E\left( {{\mathrm{T}}_1} \right) = E_f - E_i - J_{ij},$$

where E is the orbital energy and J is a coulombic integral that represents the electrostatic repulsion between the orbital charge distributions. The subscripts i and f are the occupied and unoccupied orbitals related to the T1 states, respectively. The Jif value tends to decrease with the increasing delocalization of the electronic orbital density, when the π-conjugated system is extended. Herein, we consider a simple molecular design for maintaining the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels for extended π-conjugated systems using the fragment molecular orbital (FMO) method and DFT calculations (Gaussian 03, B3LYP/6-31G(d))34,35.

As a standard for π-conjugated molecules, we used naphthalene, which has a higher energy of the excited state (21,250 cm−1) than those of the emitting levels of Eu(III), Tb(III), and Sm(III) ions. Extending the π-conjugation by coupling naphthalene and butadiene results in anthracene or phenanthrene molecules. For phenanthrene, the HOMOs (5.79 and 6.19 eV) and LUMOs (0.96 and 0.82 eV) are electronically coupled, resulting in nearly unchanged HOMO (5.73 eV) and LUMO (0.99 eV) energies relative to those of naphthalene. Therefore, the T1 level of phenanthrene is almost unchanged (21,740 cm−1). Based on this conceptual design, an extended π-conjugated structure by coupling phenanthrene and butadiene provides [4]-helicene (T1 = 19,980 cm1). By using the molecular design based on the FMO and DFT, we successfully synthesized a phosphine oxide ligand containing a helical [5]-helicene unit (HPO ligand, T1 = 18,410 cm−1)32. For an Eu(III) complex with an HPO ligand, [Eu(hfa)3(HPO)2] (hfa: hexafluoroacetylacetonate), the longer wavelength excitation (λex = 430 nm) of the HPO ligands induces the photosensitized luminescence of the Eu(III) complex (ηsens = 10%) (Fig. 5e)32,33.

We also reported the effective photosensitized luminescence of Eu(III) and Tb(III) nonanuclear clusters with 16 salicylate derivative ligands (Fig. 5f)36,37. The Tb(III) clusters showed large absorption coefficients (ε > 55,000 M−1 cm−1). The photosensitized energy transfer efficiency is dependent on the T1 state of the aromatic ligands. The emission quantum yield of Tb-4-methylsalycylate (R1=H, R2=CH3: Φπ−π* = 31%) was found to be 13 times larger than that of Tb-5-methylsalycylate (R1= CH3, R2=H: Φπ−π* = 2.4%). The photophysical characterization and DFT calculations revealed the effect of the methyl group on the electronic structure of the methyl salicylate ligand.

Photosensitized luminescence of lanthanide(III) complexes with π-conjugated radical ligands has also been reported (Fig. 5g)38,39,40. The π-conjugated radial ligands show large absorption coefficients; however, the absorption bands of radical ligands are generally lying in the vis region (wavelength >700 nm). The absorption bands in the vis region prevent the photosensitized luminescence of Eu(III) and Sm(III) complexes38. Near-IR luminescence of Nd(III), Tm(III), and Yb(III) complexes with radical ligands has been reported39,40. The control and consideration of the energy level of the lowest excited state in an organic chromophore are the most important aspects for developing strong luminescent lanthanide(III) complexes.

Effect on CT band

The photosensitized luminescence of lanthanide complexes is influenced by a specific band, for example, the CT band in a lanthanide complex. The CT band located in the vis region affects the effective energy transfer from the ligand to the lanthanide(III) ion. The CT transition is categorized into three types: (1) intra-ligand CT (intra-LCT), (2) inter-ligand CT (inter-LCT), and (3) ligand-to-metal CT (LMCT). The CT bands affect the intersystem crossing process or the energy transfer process between the ligand and the lanthanide(III) ion (Fig. 6).

Fig. 6

Photosensitized emission process of a lanthanide(III) complex assisted with charge-transfer (CT) bands

According to the photosensitized luminescence of lanthanide(III) complexes accelerated by intra-LCT, Eu(III), Yb(III), Nd(III), and Er(III) complexes with donor amine-attached diketonate ligands have been reported (Φπ−π*: Nd = 0.0078%, Yb = 0.04%, Fig. 7a)41,42. The effective luminescence of lanthanide(III) complexes with donor pyridine-attached ligands has been reported (Φπ−π*: Eu = 43%, Nd = 0.22%, Yb = 0.59%, Fig. 7b)43. Lanthanide(III) complexes with donor pyridine-attached ligands also show solvatochromic properties, which are dependent on the organic solvent as a sounding medium.

Fig. 7

Chemical structures of lanthanide(III) complexes with photosensitized luminescence accelerated with CT bands

The first example of photosensitized energy transfer from inter-LCT was presented using Eu(III) and Tb(III) complexes with hfa ligands in a solid44. The emission quantum yield and energy transfer efficiency of the Eu(III) complex were estimated to be 58% and 81%, respectively. The effective formation of an inter-LCT state using an Eu(III) complex with phenanthroline ligands was later observed45. The inter-LCT-supported near-IR luminescence of Yb(III), Nd(III), and Er(III) complexes using crown-type ligands was also reported (Fig. 7c)46.

Generally, effective photosensitized luminescence accelerated by intra- and inter-LCT bands is observed in the solid state. Eliseeva et al.44 recently reported that the formation of low-lying inter-LCT states contributes to the improvement of the ligand-to-metal energy transfer efficiency. Characteristic intra-LCT and inter-LCT bands are formed in the tightly packed crystals. The tightly packed crystals can be built as a polymeric structural design with a large strain in the π-conjugated ligands. The wavelength of the inter-LCT transition band of the strained ligand in solid media is longer than that of corresponding π–π* transition bands of a normal ligand in liquid media. We observed an effective inter-LCT band using Eu(III) coordination polymers (Fig. 7d)47. The coordination polymers were composed of luminescent Eu(hfa)3 parts and joint organic ligands, bipypo (bipypo: 3,3′-bis(diphenylphosphoryl)-2,2′-bipyridine). The effective inter-LCT band of the diketonate ligands was observed at approximately 400 nm in the solid state. The quantum efficiency accelerated by the inter-LCT in the solid state, Φπ–π*, was found to be 61%. We also consider that luminescent lanthanide(III) coordination polymers with a characteristic inter-LCT band can be constructed by a zig-zag chained polymer. The tightly packed zig-zag structure of the Eu(III) coordination polymers was prepared using zig-zag-shaped joint ligands, dpt (2,5-bis(diphenylphosphoryl)thiophene), to enhance the photosensitized luminescence supported by the inter-LCT (Fig. 7e)48. They exhibit a high intrinsic emission quantum yield (75%) due to their asymmetrical and low-vibrational coordination structures around the Eu(III) ions. The characteristic alternative zig-zag orientation of the substituents also contributes to the dramatically high energy transfer efficiencies supported by the inter-LCT of up to 80% in the solid state. The high ηsens might be due to the formation of inter-LCT states induced by the densely packed zig-zag orientation. We estimated the dipole moment D of the bridging ligands by DFT calculations (B3LYP/6-31G (d)) based on the CIF data of their X-ray single-crystal analysis data. Compared to the linear-type Eu(III) coordination polymer [Eu(hfa)3(dpbp)]n (Fig. 7f, dpbp: 4,4'-bis(diphenylphosphoryl)-1,1'-biphenyl, D = 0.0005), the zig-zag-type Eu(III) coordination polymers show large D values (1.1664 for [Eu(hfa)3(dpt)]n and 4.2992 for [Eu(hfa)3(dpedot)]n (dpedot: 2,5-bis(diphenylphosphoryl)ethylenedioxythiophene). The polar character of the bridging ligands resulted in a characteristic alternative orientation of the inter-polymer or intra-polymer chains.

We also reported the strong photosensitized luminescence of a three-dimensional Eu(III) coordination polymer with an attached triangular spacer ligand, tppb (1,3,5-tris(4-diphenylphosphorylphenyl)benzene). The intrinsic and photosensitized emission quantum yields, Φf–f and Φπ–π*, were calculated to be 82%, and 64%, respectively. The energy transfer efficiency, ηsens, was calculated to be 78%, which is similar to that of the zig-zag-shaped Eu(III) coordination polymers (Fig. 7g)49.

The LMCT bands of some Eu(III) complexes are observed at approximately 400 nm. The LMCT band in a lanthanide(III) complex does not generate effective energy transfer. In Eu(III) complexes, the LMCT band from the S0 state of the ligand to the Eu(III) ion leads to effective quenching of the excited Eu(III) complex50,51,52,53,54,55. The results of the detailed analysis of quenching by the LMCT band using a dinuclear Eu(III) complex have been reported56,57. Studies on photosensitized luminescence assisted by the LMCT band of lanthanide(III) complexes are limited; however, the photosensitized luminescence of some Eu(III) and Sm(III) complexes assisted by the LMCT bands have been reported as specific examples (Fig. 7h)58,59,60.

Generally, the standard electrode reduction potential of Eu(III) in water is estimated to be −0.35 V, which is smoothly transformed to meta-stable Eu(II) ions. For this reason, the excitation of the LMCT band in an Eu(III) complex promotes the intramolecular photoreduction of the Eu(III) ion and the formation of the Eu(II) ion61,62. Using the photoreduction technique, we also observed the decomposition of Eu(III) complexes and the formation of Eu(II) compounds (EuO and EuS nanoparticles) under the condition of LMCT band excitation63,64,65. Decomposition processes using gas-phase and laser-assisted MOCVD techniques have also been reported66,67.

The effective photosensitized luminescence of lanthanide(III) complexes is assisted by the presence of (1) an intra-LCT band formed by the introduction of donor parts in the organic ligands and (2) an inter-LCT band formed by the steric strain in the organic ligands in the crystals. The design of intra-LCT and inter-LCT is a promising strategy for developing a strong luminescent lanthanide(III) complex.

Photosensitized luminescence from a metal complex

Light and transition metal complexes

The photosensitized luminescence of lanthanide(III) complexes attached with metal complexes has been widely reported. There are three species of metal complexes for photosensitization: (1) light metal complexes, (2) transition metal complexes, and (3) lanthanide(III) complexes.

First, the photosensitized luminescence of lanthanide(III) complexes excited at the transition bands in light metal complexes are explained. Xu et al.68 reported the photosensitized luminescence of polynuclear Eu(III), Nd(III), and Yb(III) hfa complexes attached with three Al(III) quinolinate complexes (Fig. 8a). Aluminum (Al) is an element in family 13 (IIIA) in the periodic table. Al(III) quinolinate complexes are well known as green luminescent chromophores for EL devices69. The emission quantum yield of Eu(III) complexes with photosensitized Al(III) parts was estimated to be 6.1%. Furthermore, Smith et al.70 reported the photosensitized luminescence of Eu(III) complexes with monodentate and bidentate boron complexes in diketonate ligands (Fig. 8b). Boron complexes with three aryl groups, triarylborons, are transformed by the presence of fluorine ions, resulting in the formation of a B–F bond in the triarylboron unit. The formation of a B–F compound in the triarylboron unit accelerates the photosensitized luminescence of the Eu(III) complex. Eu(III) complexes with monodentate and bidentate triarylboron units are sensitive to fluorine ions in liquid media.

Fig. 8

Chemical structures of lanthanide(III) complexes with Al, B, Zn, Ir, and Ru complexes

Next, the photosensitized luminescence of lanthanide(III) complexes with transition metal complexes are introduced. Various types of transition metal complexes for the photosensitization of lanthanide(III) complexes have been reported. Among them, luminescent Zn(II), Ir(III), and Ru(II) complexes are generally used for the photosensitized luminescence of lanthanide(III) complexes.

The metal-to-ligand CT (MLCT) bands in Zn(II) complexes are observed in the UV region. The energy levels of their MLCT bands are higher than those of the emitting levels of Tb(III) and Eu(III) ions. The MLCT bands promote effective photosensitized energy transfer in Zn(II)–Ln(III) hybrid complexes. Dinuclear Zn(II)–Ln(III) complexes with Schiff base ligands show effective photosensitized luminescence (Fig. 8c)71,72,73,74. Luminescent polynuclear Zn(II)–Ln(III) complexes with Zn(II) quinolinate, terpyridine, phenanthroline, and a Schiff base have also been reported (Fig. 8d)75,76,77,78,79,80. We synthesized an Eu(III) coordination polymer cross-linked with a Zn(II) complex as a joint ligand (Fig. 8e)81. The intrinsic emission quantum yield (Φf–f) was estimated to be 59%.

Various types of lanthanide(III) complexes attached with Ir(III) complexes have also been reported (Fig. 8f)82,83,84,85. Generally, Ir(III) complexes show blue, green, and red luminescence at room temperature based on the MLCT transition bands. The MLCT transition of an Ir(III) complex leads to efficient luminescence with a high-emission quantum yield86. The emission color of an Ir(III) complex is dependent on the energy level of the organic ligands. Blue and green luminescent Ir(III) complexes are used for the photosensitized luminescence of lanthanide(III) complexes. The effective photosensitization of a polynuclear Ir(III)–Eu(III) complex has been reported. The emission quantum yield excited at the MLCT band is estimated to be 44% (Fig. 8g)84. Bian and Ward reported the photosensitized luminescence of red luminescent Ir(III)–Eu(III) and green luminescent Ir(III)–Tb(III) systems (Fig. 8h)87,88,89,90.

The Ru(II)–Ln(III) complex is also a popular system for the photosensitized luminescence of a lanthanide (III) complex. Generally, the emission band of an Ru(II) complex is observed at approximately 600 nm. The red luminescence of an Ru(II) complex is effective for the photosensitization of near-IR luminescence of Yb(III) and Nd(III) complexes. Gunnlaugsson, Charbonnière, and Faulkner91,92 reported the near-IR luminescence of Ru(II)–Ln(III) (Ln = Nd(III) and Yb(III)) complexes in water media. Rigaut and co-workers93 reported Yb(III) complexes with a carbon-rich ruthenium antenna (Fig. 8i). Sun made a molecular architecture composed of Ru(II) bipyridyl complexes and Ln(III) acetates94. Furthermore, organometallic ruthenocene [Ru(C5H5)2] exhibits a white color, and the MLCT band is located in the UV region. We reported luminescent Eu(III) complexes attached with ruthenocene units (Fig. 8j)95. Ward96 reviewed the energy transfer of Ru(II)–Ln(III) complexes.

Photosensitized luminescence using Re–Ln(III)92,97, Pt–Ln(III)98,99,100, Au–Ln(III)99,101, Ag–Ln(III)99,102, Cd–Ln(III)103,104, and Os–Ln(III)96 systems has also been reported. In general, their CT (MLCT, LMCT, metal-metal-to-ligand CT, etc.) bands of Re, Au, Ag, Cd, and Os complexes show emission in the vis region. From these photophysical findings, the near-IR luminescence of Nd(III) and Yb(III) complexes with Re, Au, Ag, Cd, and Os complexes has been described.

Active use of energy transfer in lanthanide complexes

The energy transfer between the Ln(III) ions in polynuclear lanthanide(III) complexes and the clusters leads to characteristic emission properties, energy migration, temperature-dependent luminescence, multi-color component emission (triple luminescence), and upconversion luminescence. In this section, characteristic luminescence related to energy transfer between Ln(III) ions is described.

We reported the effective energy migration of a Tb(III) cluster composed of 9 Tb(III) ions and 16 salicylate ligands (Fig. 5f)105. The energy migration in a Tb(III) nonanuclear cluster leads to a decrease in the energy back transfer from the excited Tb(III) ions to the T1 state of the ligands, resulting in thermal relaxation and a decrease in the emission quantum yield. The kinetics analysis of the temperature dependence of emission lifetimes using Tb(III)/Gd(III) mixed nonanuclear clusters showed that the energy transfer between Tb(III) ions competes with the energy back transfer. The results provide a new molecular design strategy to improve the efficiency of the luminescence of lanthanide(III) complexes.

We also reported the temperature-dependent luminescence of lanthanide coordination polymers composed of Tb(III) and Eu(III) complexes, [Tb,Eu(hfa)3(dpbp)]n (Tb(III)/Eu(III) = 99), for temperature sensing between 200 and 500 K (Fig. 9)106. The remarkable thermosensitive properties of [Tb0.99Eu0.01(hfa)3(dpbp)]n are influenced by the energy transfer efficiency between the Tb(III) and Eu(III) ions in the coordination polymer matrix. The energy transfer efficiency between the Tb(III) and Eu(III) ions is estimated by

$$\eta _{\mathrm{Tb - Eu}} = 1 - \left( {\tau _{\mathrm{obs}}/\tau _{\mathrm{Tb}}} \right),$$
Fig. 9

Temperature-dependent color changing properties of a Tb(III)/Eu(III) mixed coordination polymer [Tb,Eu(hfa)3(dpbp)]n. Color pictures of [Tb0.99Eu0.01(hfa)3(dpbp)]n under UV (365 nm) irradiation, which show brilliant green, yellow, orange, and red emission. Reprinted with permission from Iki et al106 Copyright 2013 Wiley-VCH Verlag GmbH & Co

where τobs and τTb are the emission lifetimes of [Tb,Eu(hfa)3(dpbp)]n and [Tb(hfa)3(dpbp)]n, respectively. Using this equation, the values of ηTb-Eu at 200, 250, 275, and 300 K are estimated to be 1%, 19%, 26%, and 38%, respectively. The value of ηTb-Eu increases with the increase in temperature. We observed the temperature-dependent energy transfer efficiency of a [Tb,Eu(hfa)3(dpbp)]n crystal. Previously, the energy transfer from Tb(III) ions to Eu(III) ions was studied by using mononuclear and dinuclear lanthanide complexes in homogeneous organic and aqueous media. We consider that the energy transfer mechanism of [Tb,Eu(hfa)3(dpbp)]n is different from those in previously reported homogeneous systems in solution. Regarding the energy transfer mechanism of [Tb,Eu(hfa)3(dpbp)]n, Hatanaka et al.107 and Hatanaka and Morokuma108 first reported the presence of the activation energy on organic joint ligands determined by quantum calculations. A collaborative study using quantum calculations as additional experiments is expected to open up a new field of photophysical theory of the energy transfer process. The development of thermosensitive luminophores using the energy transfer in Ln(III) polynuclear complexes, coordination polymers and clusters has also been explored109,110,111,112,113,114,115,116,117,118.

The multi-color component emission (triple luminescence) of a photosensitized lanthanide(III) system using Eu(III)/Tb(III)/Gd(III) MOF (metal–organic framework) systems119,120,121 cross-linked with aromatic joint parts containing pyridyl, sulfonyl, and/or carbonyl groups has been reported. The multi-color emission is composed of a red luminescent Eu(III) complex, a green luminescent Tb(III) complex, and a blue luminescent ligand (phosphorescence) in the Gd(III) parts (the emitting level of the Gd(III) ion is higher than the T1 state of the organic ligands). The triple component emission of the Eu(III)/Tb(III)/Gd(III) MOF system plays a role in precise color tuning for the naked eye and the creation of white lighting. Eu(III)/Tb(III)/La, Eu(III)/Tb(III)/Gd(III)/Zn(II), and Eu(III)/Tb(III)/ligand MOF systems have also been reported122,123,124.

In the field of inorganic material science and engineering, the upconversion luminescence of lanthanide compounds is well known as a wavelength conversion phenomenon from lower to higher photon energy. The upconversion luminescence is based on the energy transfer between metal and lanthanide ions125. In 2011, Piguet and co-workers126 reported the first example of the upconversion luminescence of an Er(III) helical complex with two Cr(III) units (Fig. 10a). The result of detailed analysis of the Er(III) helical complex with two Cr(III) units has also been reported127. Charbonnière and co-workers128,129 reported the upconversion luminescence of a dinuclear Er(III) complex (Fig 10b) and a polynuclear Tb(III)/Yb(III) complex. Faulkner and co-workers130 reported the upconversion luminescence of a mononuclear Tm(III) complex in solution. A hybrid system composed of Yb(III)/Tm2O3 interfacial coordination nanoparticles was also reported (Fig. 10c)131. Lanthanide coordination compounds are expected to play an important role in the molecular-level analysis of upconversion luminescence.

Fig. 10

Chemical structures and upconversion energy diagram of lanthanide(III) complexes with upconversion luminescence

The photosensitized luminescence from neighboring lanthanide(III) ions in a coordination system promotes not only the enhancement of the emission intensity but also the characteristic energy migration luminescence, temperature-dependent luminescence, multi-color component emission (triple luminescence), and upconversion luminescence. The photosensitized luminescence from activated lanthanide ions is a key phenomenon for the creation of new advanced luminescent materials in the future.

Electrosensitized luminescence

Lanthanide(III) complexes on glass electrodes or semiconductor crystals are expected to be useful for applications in display devices, such as organo-EL or electrochemically luminescent devices, light-emitting diode (LED) tip devices, and photovoltaic polymer memories. Kido et al.132 was first to report the EL of a Tb(III) acetylacetonate complex in EL devices (Fig. 11a). We also reported the near-IR EL of an Nd(III) complex (Fig. 11b)133. Kido and Okamoto5, de Bettencourt-Dias6 and Xu et al.134 have written reviews of lanthanide complex-based emitting materials in the field of LEDs. Wang et al.135 also reported the EL of Eu(III) complexes with hfa and phosphine monodentate oxide ligands. The EL luminance was estimated to be >90 cd m−2.

Fig. 11

Chemical structures of electroluminescent lanthanide(III) complexes

The performance of EL devices depends on the molecular structure of the lanthanide(III) coordination compounds. Recently, thermo-stable polymer materials attached with lanthanide complexes have been synthesized (Fig. 11c)136. The glass transition temperature and EL luminance were estimated to be 220 °C and 149 cd m−2, respectively. We also reported Eu(III) coordination nanoparticles on glass electrodes for EL devices137. The thermostability of a luminescent lanthanide complex is one of important factors for the fabrication of EL devices.

The characteristic EL performance has been reported. White EL using an Eu(III) coordination polymer has also been reported (Fig. 11d)138. Bari and co-workers139 showed effective circularly polarized EL using a chiral Eu(III) complex (Fig. 11e). Zhang and co-workers140 reported high-performance EL combined with an Ir(III) complex, a Tb(III) complex and a Gd(III) complex in devices (145,071 cd m−2).

Various types of organic EL devices using organic molecules and transition metal complexes have been extensively studied. Highly efficient Ir(III) complexes and the characteristic TADF (thermally activated delayed fluorescence) of organic dyes have been studied for the fabrication of bright luminescent EL devices141,142,143,144. The EL properties of lanthanide(III) complexes are greatly different from those of organic molecules and transition metal complexes. The 4f–4f emissions of lanthanide(III) complexes play an important role in the design of monochromatic luminescent materials for display devices (narrow emission band: FWHM <10 nm)145, although EL devices using organic dye and transition metal complexes show broad emission spectra (FWHM >50 nm). At present, the luminance of EL devices using lanthanide complexes is smaller than that of EL devices using organic molecules and transition metal complexes. However, lanthanide(III) complexes with characteristic EL are expected to be key materials for future displays.

Mechanosensitized luminescence

The luminescence generated upon grinding solid materials is called triboluminescence (tribo-sensitized luminescence). In the seventeenth century, it was first noted by Francis Bacon who mentioned that “It is well known that all sugar, whether candied or plain, if it be hard, will sparkle when broken or scraped in the dark.” Triboluminescent materials, unlike well-known photoluminescence materials, have the advantage of emission without requiring a light source146,147,148. The fracture-induced luminescent properties of triboluminescent materials make them attractive for applications as structural damage sensors and pressure sensors and for advanced security marking techniques149,150,151,152.

Different types of materials that exhibit triboluminescence, such as organic crystals, polymers, and metal complexes, have been studied. The first example of triboluminescence using a lanthanide(III) complex was reported in 1966 (Fig. 12a)153. In 1987, Sweeting and Rheingold154 showed the importance of charge separation and recombination in solid state lanthanide(III) complexes. Some triboluminescence phenomena of lanthanide(III) complexes in crystals and polymer matrices have also been reported (Fig. 12b, c)155,156,157,158,159,160,161,162,163,164,165,166. Chen et al.167 suggested that strongly luminescent lanthanide coordination polymer crystals with non-centrosymmetric structures are expected to show efficient triboluminescence because of the generation of opposite electric charges on opposing faces of cracks perpendicular to their polar axes. Charge recombination on the crystal faces produces triboluminescence. From this point, triboluminescence is regarded as electrosensitized luminescence.

Fig. 12

Chemical structures of mechanoluminescent lanthanide(III) complexes

Eliseeva et al.168 reported triboluminescence from a lanthanide coordination polymer composed of lanthanide(III) hfa complexes and 1,4-dimethylterephthalate joint ligands (Fig. 12d). We also reported strong triboluminescence from an Eu(III) coordination polymer with phosphine oxide joint ligands, [Eu(hfa)3bipypo]n (Fig. 7d)47. The Eu(III) coordination polymer with a specific coordination structure of low-vibrational frequency and coordination networks exhibits intense triboluminescence upon breaking, which is clearly observed even at ambient temperatures in daylight (Fig. 13). The triboluminescence of a supramolecular lanthanide(III) coordination system has also been reported (Fig. 12e)169.

Fig. 13

ah Observed sequential images of triboluminescence from [Eu(hfa)3(bipypo)]n powder upon pushing with a black stick at ambient temperature and in daylight. Reprinted with permission from Hasegawa and co-workers47. Copyright 2011 Wiley-VCH Verlag GmbH & Co

Triboluminescence-active compounds are known to show photoluminescence as well. Triboluminescence and photoluminescence occur from distinct stimuli, namely, grinding and photoirradiation, respectively; however, their spectra usually exhibit similar profiles. The relationship between triboluminescence and photoluminescence is still being discussed from a scientific point of view.

Reddy and co-workers156 recently demonstrated bright red triboluminescence and photoluminescence of [Eu(DPPF)3(DDXPO)] (DPPF = 1-(4-(diphenylphosphino)phenyl)-4,4,5,5,5-pentafluoropentane-1,3-dione, DDXPO = 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene oxide). They also reported a slight decrease in the triboluminescence intensity when dispersed in PMMA films compared with that in the solid state. Teotonio et al.170 and Mikhalyova et al.171 suggested the possibility of triboluminescent energy transfer using lanthanide(III) complexes. Based on the difference between photoluminescence and triboluminescence properties, we discussed the spectral difference using a polar furan-linked Tb(III)/Eu(III) mixed coordination polymer with strong triboluminscence, [Tb/Eu(hfa)3dpf]]n (dpf: 2,5-bis(diphenylphosphoryl)furan) (Fig. 12f)172. The Tb and Eu units in [Tb/Eu(hfa)3(dpf)]n show strong photosensitized luminescence. The intrinsic emission quantum yield and energy transfer efficiency of the Eu(III) unit [Eu(hfa)3(dpf)]n are estimated to be 73% and 88%, respectively. The intrinsic emission quantum yield and energy transfer efficiency of the Tb(III) units [Tb(hfa)3(dpf)]n is also calculated to be 88% and 45%, respectively. By using a Tb(III)/Eu(III) mixed coordination polymer [Tb/Eu(hfa)3(dpf)]n, we successfully observed a drastic spectral difference between the triboluminescence and photoluminescence. Based on the results, we consider the triboluminescence of the lanthanide(III) coordination compounds to be responsible for both the ligand excitation and direct Ln(III) excitation, unlike the selective excitation with specific wavelengths (for example, λex = 380 nm) in photoluminescence. We also assume that the Tb(III)-to-Eu(III) energy transfer occurs in both triboluminescence and photoluminescence with the same efficiency and that it is not responsible for the drastic color difference between the triboluminescence and photoluminescence.

Quantitative estimation of the triboluminescence efficiency is important to clarify the mechanism of triboluminescence and to develop strong triboluminescent materials. Generally, the drop-tower method is used to estimate the triboluminescence efficiency173,174,175. However, it is difficult to use the drop-tower method as a quantitative estimation (for calculations of the radiative and non-radiative rate constants). The development of a quantitative estimation method is needed to advance the field of triboluminescent material science. We developed a method to quantitatively estimate the triboluminescence using shockwave laser irradiation. The value of knr for triboluminescence is four times larger than that for photoluminescence in [Eu3(hfa)9(tppb)2]n crystals (tppb = tris(4-diphenylphosphorylphenyl)benzene) (Fig. 7g)49. These results indicate that the mechanical crushing of molecular crystals leads to an enhanced non-radiative transition in the quantum process. The shockwave irradiation is considered to promote the effective mechanical crushing of organic crystals and the formation of an excited state of the ligands.

A highly photosensitized luminescence efficiency in Eu(III) coordination compounds should be the key to observing triboluminescence. The effective molecular design and a suitable experimental analysis method for triboluminescent lanthanide(III) coordination compounds are expected to open a research pathway between coordination chemistry, materials chemistry, and photophysical chemistry.


The photo and electrosensitized luminescence of lanthanide(III) complexes can be manipulated by the ligand design. The luminescence of lanthanide(III) complexes can be realized and enhanced by designing ligands that coordinate to the lanthanide(III) ions.

In the section on photosensitized luminescence, the importance of two factors, (1) the control of the T1 state of the ligand and (2) the presence of intra-LCT and inter-LCT, was explained. These ligand designs lead to the development of a strong luminescent lanthanide(III) complex. The energy transfer processes from neighboring light metal, transition metal, and lanthanide(III) complexes were also described. The characteristic energy migration, temperature-dependent luminescence, multi-color luminescence, and upconversion luminescence for polynuclear lanthanide(III) complexes, clusters, coordination polymers and nanoparticles are expected to lead to the development of new molecular materials for photonic and opto-electronic devices.

We then described electrosensitized luminescence (EL) and mechanosensitized luminescence (triboluminescence) as electric field sensitization phenomena. EL using lanthanide(III) complexes can provide highly pure green and red luminescence with a narrow FWHM, which is fundamental toward the fabrication of full-color display devices. Invisible near-IR EL can also be achieved by a lanthanide(III) complex for industrial security applications. These characteristic EL properties of lanthanide(III) complexes are greatly different from those of corresponding organic and transition metal complexes. The construction of novel lanthanide complexes with efficient carrier injection is required for the development of EL materials. The study of the triboluminescence of molecular crystals started in the seventeenth century; however, the mechanism of triboluminescence has still not been clarified. Determination of the excited state concentrations is required to gain a more complete understanding of the triboluminescence mechanism. The study of the triboluminescence of lanthanide(III) complexes is expected to open up a new research avenue in the field of material science.

In this review, we introduced different molecular designs for the enhancement of the photosensitized luminescence properties of lanthanide(III) complexes. The emission quantum efficiency of a lanthanide(III) complex is also dependent on its coordination geometry and vibrational structure. We reported the importance of the radiative kr constant depending on the lanthanide(III) coordination geometry176,177,178,179,180,181,182,183,184,185 and the non-radiative knr constant depending on the vibrational structure of the organic ligands186,187,188,189,190,191,192,193,194,195,196,197. Control of the kr and knr constants in an excited lanthanide(III) complex is also important for the development of a strong luminescent lanthanide(III) complex.

Luminescent materials that include lanthanide(III) complexes are desirable for applications in novel organic lanthanide(III) devices, such as organic lasers, luminescent plastics, optical fibers, lasers, displays, lighting, wavelength converters for solar cells, and physical and biomedical sensors. The study of the photosensitized luminescence of lanthanide(III) complexes is expected to open research avenues among the fields of chemistry, physics, electronics, and materials science.


  1. 1.

    Shriver, D. F. & Atkins, P. W. Inorganic Chemistry 3rd edn, 320 (Oxford Univ., Oxford, 1999).

    Google Scholar 

  2. 2.

    Hasegawa, Y., Wada, Y. & Yanagida, S. Strategies for the design of luminescent lanthanide(III) complexes and their photonic applications. J. Photochem. Photobiol. C 5, 183–202 (2004).

    Article  CAS  Google Scholar 

  3. 3.

    Hasegawa, Y. Photofunctional lanthanoid complexes, coordination polymers, and nanocrystals for future photonic applications. Bull. Chem. Soc. Jpn. 87, 1029–1057 (2014).

    Article  CAS  Google Scholar 

  4. 4.

    Oyamada, T., Kawamura, Y., Koyama, T., Sasabe, H. & Adachi, C. Formation of europium chelate complexes by vacuum co-deposition and their application in organic light-emitting diodes. Adv. Mater. 16, 1082–1086 (2004).

    Article  CAS  Google Scholar 

  5. 5.

    Kido, J. & Okamoto, Y. Organo lanthanide metal complexes for electroluminescent materials. Chem. Rev. 102, 2357–2368 (2002).

    Article  CAS  Google Scholar 

  6. 6.

    Bettencourt-Dias, A. Lanthanide-based emitting materials in light-emitting diodes. Dalton Trans. 2229–2241 (2007).

  7. 7.

    Hasegawa, Y. & Nakanishi, T. Luminescent lanthanide coordination polymers for photonic applications. RSC Adv. 5, 338–353 (2015).

    Article  CAS  Google Scholar 

  8. 8.

    Eliseeva, S. V. & Bünzli, J.-C. G. Lanthanide luminescence for functional materials and bio-sciences. Chem. Soc. Rev. 39, 189–227 (2010).

    Article  CAS  Google Scholar 

  9. 9.

    Kataoka, H., Omagari, S., Nakanishi, T. & Hasegawa, Y. Photo-degradation analysis of luminescent polymers with lanthanide complexes. J. Photopolym. Sci. Technol. 28, 247–254 (2015).

    Article  CAS  Google Scholar 

  10. 10.

    Kataoka, H. et al. Drastically improved durability and efficiency of silicon solar cells using hyper-stable lanthanide coordination polymer beads. Bull. Chem. Soc. Jpn. 89, 103–109 (2016).

    Article  CAS  Google Scholar 

  11. 11.

    Freed, S., Weissman, S. I., Fortress, F. E. & Jacobson, H. F. Ions of europium distributed between different configurations in homogeneous solutions. J. Chem. Phys. 7, 824–828 (1939).

    Article  CAS  Google Scholar 

  12. 12.

    Weissman, S. I. Intramolecular energy transfer the fluorescence of complexes of europium. J. Chem. Phys. 10, 214–217 (1942).

    Article  CAS  Google Scholar 

  13. 13.

    Yuster, P. & Weissman, S. I. Effects of perturbations on phosphorescence: Luminescence of metal organic complexes. J. Chem. Phys. 17, 1182–1188 (1949).

    Article  CAS  Google Scholar 

  14. 14.

    Hemmila, I. Luminescent lanthanide chelates—a way to more sensitive diagnostic methods. J. Alloy Compd. 225, 480–485 (1995).

    Article  CAS  Google Scholar 

  15. 15.

    Bünzli, J.-C. G. On the design of highly luminescent lanthanide complexes. Coord. Chem. Rev. 293–294, 19–47 (2015).

    Article  CAS  Google Scholar 

  16. 16.

    De Sá, G. F. et al. Spectroscopic properties and design of highly luminescent lanthanide coordination complexes. Coord. Chem. Rev. 196, 165–195 (2000).

    Article  Google Scholar 

  17. 17.

    Sato, S. & Wada, M. Relations between intramolecular energy transfer efficiencies and triplet state energies in rare earth beta-diketone chelates. Bull. Chem. Soc. Jpn. 43, 1955–1962 (1970).

    Article  CAS  Google Scholar 

  18. 18.

    Latva, M. et al. Correlation between the lowest triplet state energy level of the ligand and lanthanide(III) luminescence quantum yield. J. Lumin. 75, 149–169 (1997).

    Article  CAS  Google Scholar 

  19. 19.

    Shavaleev, N. M., Eliseeva, S. V., Scopelliti, R. & Bünzli, J.-C. G. N-aryl chromophore ligands for bright europium luminescence. Inorg. Chem. 49, 3927–3936 (2010).

    Article  CAS  Google Scholar 

  20. 20.

    Shavaleev, N. M., Eliseeva, S. V., Scopelliti, R. & Bünzli, J.-C. G. Designing simple tridentate ligands for highly luminescent europium complexes. Chem. Eur. J. 15, 10790–10802 (2009).

    Article  CAS  Google Scholar 

  21. 21.

    Shavaleev, N. M., Gumy, F., Scopelliti, R. & Bünzli, J.-C. G. Highly luminescent homoleptic europium chelates. Inorg. Chem. 48, 5611–5613 (2009).

    Article  CAS  Google Scholar 

  22. 22.

    Archer, R. D., Chen, H. & Thomson, L. C. Synthesis, characterization, and luminescence of europium(III) schiff-base complexes. Inorg. Chem. 37, 2089–2095 (1998).

    Article  CAS  Google Scholar 

  23. 23.

    Bünzli, J.-C. G. & Eliseeva, S. V. In Lanthanide Luminescence: Photophysical, Analytical and Biological Aspects, Hänninen, P. & Härmä, H., Eds., Vol. 7, 1–45 (Springer, Berlin, 2010).

    Chapter  Google Scholar 

  24. 24.

    Samuel, A. P. S., Xu, J. D. & Raymond, K. N. Predicting efficient antenna ligands for Tb(III) emission. Inorg. Chem. 48, 687–698 (2009).

    Article  CAS  Google Scholar 

  25. 25.

    Nijegorodov, N., Ramachandran, V. & Winkoun, D. P. The dependence of the absorption and fluorescence parameters, the intersystem crossing and internal conversion rate constants on the number of rings in polyacene molecules. Spectrochim. Acta Part A 53, 1813–1824 (1997).

    Article  Google Scholar 

  26. 26.

    Morgan, D. D., Warshawsky, D. & Atkinson, T. The relationship between carcinogenic activities of polycyclic aromatic hydrocarbons and their singlet, triplet, and singlet-triplet splitting energies of phosphorescence lifetimes. Photochem. Photobiol. 25, 31–38 (1977).

    Article  CAS  Google Scholar 

  27. 27.

    Palewska, K. & Chojnacki, H. Electronic spectra and luminescence properties of helicenes in crystalline matrices at 4.2K. Mol. Cryst. Liq. Cryst. 229, 31–36 (1993).

    Article  CAS  Google Scholar 

  28. 28.

    Kang, J.-S. et al. Neighbour-sensitized near-infrared emission of new Nd(iii) and Er(iii) complexes with 1-(anthracene-2-yl)-4,4,4-trifluoro-1,3-butanedione. N. J. Chem. 40, 9702–9710 (2016).

    Article  CAS  Google Scholar 

  29. 29.

    George, T. M., Varughese, S. & Reddy, M. L. P. Near-infrared luminescence of Nd3+ and Yb3+ complexes using a polyfluorinated pyrene-based β-diketonate ligand. RSC Adv. 6, 69509–69520 (2016).

    Article  CAS  Google Scholar 

  30. 30.

    Divya, V. & Reddy, M. L. P. Visible-light excited red emitting luminescent nanocomposites derived from Eu3+-phenathrene-based fluorinated β-diketonate complexes and multi-walled carbon nanotubes. J. Mater. Chem. C 1, 160–170 (2013).

    Article  CAS  Google Scholar 

  31. 31.

    Steemers, F. J., Verboom, W., Reinhoudt, D. N., van der Tol, E. B. & Verhoeven, J. W. New sensitizer-modified calix[4]arenes enabling near-UV excitation of complexed luminescent lanthanide ions. J. Am. Chem. Soc. 117, 9408–9414 (1995).

    Article  CAS  Google Scholar 

  32. 32.

    Kitagawa, Y., Ohno, R., Nakanishi, T., Fushimi, K. & Hasegawa, Y. Visible luminescent lanthanide ions and large π-conjugated ligand system shake hands. Phys. Chem. Chem. Phys. 18, 31012–31016 (2016).

    Article  CAS  Google Scholar 

  33. 33.

    Kitagawa, Y., Ohno, R., Nakanishi, T., Fushimi, K. & Hasegawa, Y. Solvent-dependent dual-luminescence properties of europium complex with helical π-conjugated ligands. Photochem. Photobiol. Sci. 5, 683–689 (2017).

    Article  Google Scholar 

  34. 34.

    Lee, C. T., Yang, W. T. & Parr, R. G. Development of the colle-salvetti correlation-energy formula into a functional of the electron-density. Phys. Rev. B 37, 785–789 (1988).

    Article  CAS  Google Scholar 

  35. 35.

    Becke, A. D. Density-functional thermochemistry. III. The role of exact exchange. J. Chem. Phys. 98, 5648–5652 (1993).

    Article  CAS  Google Scholar 

  36. 36.

    Zhang, B. et al. Systematic study of the luminescent europium-based nonanuclear clusters with modified 2-hydroxybenzophenone ligands. Inorg. Chem. 52, 13332–13340 (2013).

    Article  CAS  Google Scholar 

  37. 37.

    Omagari, S. et al. Effective photosensitized energy transfer of nonanuclear terbium cluster using methyl salicylate derivatives. J. Phys. Chem. A 119, 1943–1947 (2015).

    Article  CAS  Google Scholar 

  38. 38.

    Lescop, C., Luneau, D., Bussière, G., Triest, H. & Reber, C. Ligand-centered near-infrared luminescence from lanthanide complexes with chelating nitronyl nitroxide free radicals. Inorg. Chem. 39, 3740–1947 (2000).

    Article  CAS  Google Scholar 

  39. 39.

    Kaizaki, S., Shirotani, D., Tsukahara, Y. & Nakata, H. First observation of NIR 4f–4f luminescence through the energy transfer from the SOMO π* doublet in nitronyl nitroxide radical lanthanide(III) complexes. Eur. J. Inorg. Chem. 2005, 3503–3505 (2005).

    Article  CAS  Google Scholar 

  40. 40.

    Kaizaki, S. Coordination effects of nitroxide radicals in transition metal and lanthanide complexes. Coord. Chem. Rev. 250, 1804–1818 (2006).

    Article  CAS  Google Scholar 

  41. 41.

    Nie, D. et al. Energy transfer pathways in the carbazole functionalized β-diketonate europium complex. N. J. Chem. 31, 1639–1646 (2007).

    Article  CAS  Google Scholar 

  42. 42.

    Shavaleev, N. M., Scopelliti, R., Gumy, F. & Bünzli, J.-C. G. Visible-light excitation of infrared lanthanide luminescence via intra-ligand charge-transfer state in 1,3-diketonates containing push-pull chromophores. Eur. J. Inorg. Chem. 2008, 1523–1529 (2008).

    Article  CAS  Google Scholar 

  43. 43.

    D’Aleo, A. et al. Efficient sensitization of europium, ytterbium, and neodymium functionalized tris-dipicolinate lanthanide complexes through tunable charge-transfer excited states. Inorg. Chem. 47, 10258–10268 (2008).

    Article  CAS  Google Scholar 

  44. 44.

    Eliseeva, S. V. et al. Role of the ancillary ligand N,N-dimethylaminoethanol in the sensitization of EuIII and TbIII luminescence in dimeric β-diketonates. J. Phys. Chem. A 112, 3614–3626 (2008).

    Article  CAS  Google Scholar 

  45. 45.

    Puntus, L. N., Lyssenko, K. A., Antipin, M. Y. & Bünzli, J.-C. Role of inner- and outer-sphere bonding in the sensitization of Eu-luminescence deciphered by combined analysis of experimental electron density distribution function and photophysical data. Inorg. Chem. 47, 11095–11107 (2008).

    Article  CAS  Google Scholar 

  46. 46.

    Trivedi, E. R. et al. Highly emitting near-infrared lanthanide “encapsulated sandwich” metallacrown complexes with excitation shifted toward lower energy. J. Am. Chem. Soc. 136, 1526–1534 (2014).

    Article  CAS  Google Scholar 

  47. 47.

    Hasegawa, Y., Hieda, R., Miyata, K., Nakagawa, T. & Kawai, T. Brilliant triboluminescence of a lanthanide coordination polymer with low-vibrational-frequency and non-centrosymmetric structural networks. Eur. J. Inorg. Chem. 2011, 4978–4984 (2011).

    Article  CAS  Google Scholar 

  48. 48.

    Hirai, Y. et al. Luminescent europium(III) coordination zippers linked with thiophene-based bridges. Angew. Chem. Int. Ed. 55, 12059–12062 (2016).

    Article  CAS  Google Scholar 

  49. 49.

    Hasegawa, Y. et al. Effective photo- and triboluminescent Eu(III) coordination polymers with rigid triangular spacer ligands. Chem. Eur. J. 23, 2666–2672 (2017).

    Article  CAS  Google Scholar 

  50. 50.

    Napier, G. D. R., Neilson, J. D. & Shepherd, T. M. Charge-transfer excited state in tris(acetylacetonato) europium(III). Chem. Phys. Lett. 31, 328–330 (1975).

    Article  CAS  Google Scholar 

  51. 51.

    Faustino, W. M., Malta, O. L. & de Sá, G. F. Theoretical modeling of thermally activated luminescence quenching through charge transfer states in lanthanide complexes. Chem. Phys. Lett. 429, 595–599 (2006).

    Article  CAS  Google Scholar 

  52. 52.

    Costa, S. M., de, B., Queimado, M. M. & Frausto da Silva, J. J. R. Energy transfer in complexes between a crown ether and various lanthanide salts. J. Photochem. 12, 31–39 (1980).

    Article  CAS  Google Scholar 

  53. 53.

    Tsaryuk, V., Zolin, V. & Legendziewicz, J. The structures of ligands and effects of the europium luminescence excitation. J. Lumin. 102–103, 744–750 (2003).

    Article  CAS  Google Scholar 

  54. 54.

    Faustino, W. M. et al. Photoluminescence of europium(III) dithiocarbamate complexes: Electronic structure, charge transfer and energy transfer. J. Phys. Chem. A 110, 2510–2516 (2006).

    Article  CAS  Google Scholar 

  55. 55.

    Regulacio, M. D. et al. Luminescence of Ln(III) dithiocarbamate complexes (Ln = La, Pr, Sm, Eu, Gd, Tb, Dy). Inorg. Chem. 47, 1512–1523 (2008).

    Article  CAS  Google Scholar 

  56. 56.

    Miranda, Y. C. et al. The role of the ligand-to-metal charge-transfer state in the dipivaloylmethanate-lanthanide intramolecular energy transfer process. Eur. J. Inorg. Chem. 18, 3019–3027 (2015).

    Article  CAS  Google Scholar 

  57. 57.

    An, Y., Schramm, G. E. & Berry, M. T. Ligand-to-metal charge-transfer quenching of the Eu3+(5D1) state in europium-doped tris(2,2,6,6-tetramethyl-3,5-heptanedionato)gadolinium (III). J. Lumin. 97, 7–12 (2002).

    Article  CAS  Google Scholar 

  58. 58.

    Yang, C. et al. A highly luminescent europium complex showing visible-light-sensitized red emission: Direct observation of the singlet pathway. Angew. Chem. Int. Ed. 43, 5010–5013 (2004).

    Article  CAS  Google Scholar 

  59. 59.

    Fu, L.-M. et al. Role of ligand-to-metal charge transfer state in nontriplet photosensitization of luminescent europium complex. J. Phys. Chem. A 114, 4494–4500 (2010).

    Article  CAS  Google Scholar 

  60. 60.

    Lo, W.-S., Zhang, J., Wong, W.-T. & Law, G.-L. Highly luminescent SmIII complexes with intraligand charge-transfer sensitization and the effect of solvent polarity on their luminescent properties. Inorg. Chem. 54, 3725–3727 (2015).

    Article  CAS  Google Scholar 

  61. 61.

    Jorgensen, C. K. & Brinen, J. S. Far ultra-violet absorption spectra of cerium(III) and europium(III) aqua ions. Mol. Phys. 6, 629–631 (1963).

    Article  Google Scholar 

  62. 62.

    Kusaba, M., Nakashima, N., Izawa, Y., Kawamura, W. & Yamanaka, C. Higher yield of photoreduction of Eu3+ to Eu2+ with shorter wavelength irradiation. Chem. Phys. Lett. 197, 136–140 (1992).

    Article  CAS  Google Scholar 

  63. 63.

    Hasegawa, Y. et al. Enhanced luminescence and photomagnetic properties of surface-modified EuO nanocrystals. Angew. Chem. Int. Ed. 41, 2073–2075 (2002).

    Article  CAS  Google Scholar 

  64. 64.

    Hasegawa, Y. et al. EuO nanocrystal formation under ArF laser irradiation. Chem. Lett. 32, 708–709 (2003).

    Article  CAS  Google Scholar 

  65. 65.

    Hasegawa, Y., Afzaal, M., O’Brien, P., Wada, Y. & Yanagida, S. A novel method for synthesizing EuS nanocrystals from a single-source precursor under white LED irradiation. Chem. Commun. 242–243 (2005).

  66. 66.

    Meng, Q. et al. Thin film deposition and photodissociation mechanisms for lanthanide oxide production from tris(2,2,6,6-tetramethyl-3,5-heptanedionato)Ln(III) in laser-assisted MOCVD. Chem. Mater. 22, 6056–6064 (2010).

    Article  CAS  Google Scholar 

  67. 67.

    Ow, F. P., Berry, M. T., May, P. S. & Zink, J. I. Wavelength and metal dependence in the photofragmentation of a gas-phase lanthanide β-diketonate complex. J. Phys. Chem. A 111, 4144–4149 (2007).

    Article  CAS  Google Scholar 

  68. 68.

    Xu H.-B., Chen X.-M., Zhang Q.-S., Zhang L.-Y. & Chen Z.-N. Fluoride-enhanced lanthanide luminescence and white-light emitting in multifunctional Al3Ln2 (Ln = Nd, Eu, Yb) heteropentanuclear complexes. Chem. Commun. 7318–7320 (2009).

  69. 69.

    Tang, C. W. & Vanslyke, S. A. Organic electroluminescent diodes. Appl. Phys. Lett. 51, 913–915 (1987).

    Article  CAS  Google Scholar 

  70. 70.

    Smith, L. F., Blight, B. A., Park, H.-J. & Wang, S. Sensitizing Tb(III) and Eu(III) emission with triarylboron functionalized 1,3-diketonato ligands. Inorg. Chem. 53, 8036–8044 (2014).

    Article  CAS  Google Scholar 

  71. 71.

    Pasatoiu, T. D., Madalan, A. M., Kumke, M. U., Tiseanu, C. & Andruh, M. Temperature switch of LMCT role: from quenching to sensitization of europium emission in a ZnII–EuIII binuclear complex. Inorg. Chem. 49, 2310–2315 (2010).

    Article  CAS  Google Scholar 

  72. 72.

    Wei, T. et al. Co-existence of heterometallic Zn2Er and ZnEr arrayed chromophores for the sensitization of near-infrared (NIR) luminescence. Inorg. Chem. Commun. 12, 1216–1219 (2009).

    Article  CAS  Google Scholar 

  73. 73.

    Abtab, S. M. T. et al. Tetranuclear homo- (ZnII 4 and CdII 4) and hetero-metal (ZnII 2TbIII 2 and CdII 2TbIII 2) complexes with a pair of carboxylate ligands in a rare η224-bridging mode: syntheses, structures and emission properties. Dalton Trans. 42, 1848–1861 (2013).

    Article  CAS  Google Scholar 

  74. 74.

    Pasatoiu, T. D. et al. Study of the luminescent and magnetic properties of a series of heterodinuclear [ZnIILnIII] complexes. Inorg. Chem. 50, 5879–5889 (2011).

    Article  CAS  Google Scholar 

  75. 75.

    Xu, H.-B., Zhong, Y.-T., Zhang, W.-X., Chen, Z.-N. & Chen, X.-M. Syntheses, structures and photophysical properties of heterotrinuclear Zn2Ln clusters (Ln = Nd, Eu, Tb, Er, Yb). Dalton Trans. 39, 5676–5682 (2010).

    Article  CAS  Google Scholar 

  76. 76.

    Chi, Y.-X., Niu, S.-Y., Wang, R., Jin, J. & Zhang, G.-N. Syntheses, structures and photophysical properties of heteronuclear Zn–Ln coordination complexes. J. Lumin. 131, 1707–1713 (2011).

    Article  CAS  Google Scholar 

  77. 77.

    Li, Z. Q., Hou, Z. H., Ha, D. H. & Li, H. R. A ratiometric luminescent thermometer co-doped with lanthanide and transition metals. Chem. Asian J. 10, 2719–2723 (2015).

    Google Scholar 

  78. 78.

    Akine, S., Utsuno, F., Taniguchi, T. & Nabeshima, T. Dinuclear complexes of the N2O2 oxime chelate ligand with zinc(II)–lanthanide(III) as a selective sensitization system for Sm3+. Eur. J. Inorg. Chem. 2010, 3143–3152 (2010).

    Article  CAS  Google Scholar 

  79. 79.

    Swinburne, A. N., Paterson, M. J., Beeby, A. & Steed, J. W. Fluorescent twist-on sensing by induced-fit anion stabilisation of a planar chromophore. Chem. Eur. J. 16, 2714–2718 (2010).

    Article  CAS  Google Scholar 

  80. 80.

    Zhao, S. et al. Effective enhancement of near-infrared emission by carbazole modification in the Zn–Nd bimetallic Schiff-base complexes. Inorg. Chem. Commun. 20, 41–45 (2012).

    Article  CAS  Google Scholar 

  81. 81.

    Yamamoto, M., Nakanishi, T., Kitagawa, Y., Fushimi, K. & Hasegawa, Y. Luminescent Eu(III) coordination polymer cross-linked with Zn(II) complexes. Mater. Lett. 167, 183–187 (2016).

    Article  CAS  Google Scholar 

  82. 82.

    Sykes, D. et al. d–f energy transfer in a series of IrIII/EuIII dyads: energy-transfer mechanisms and white-light emission. Inorg. Chem. 50, 11323–11339 (2011).

    Article  CAS  Google Scholar 

  83. 83.

    Jones, J. E., Jenkins, R. L., Hicks, R. S., Hallett, A. J. & Pope, S. J. A. Water-soluble, luminescent iridium(III)–ytterbium(III) complexes using dipyrido[3,2-a:2′,3′-c]phenazine derivatives as bridging units. Dalton Trans. 41, 10372–10381 (2012).

    Article  CAS  Google Scholar 

  84. 84.

    Jiang, W. et al. A green-emitting iridium complex used for sensitizing europium ion with high quantum yield. Inorg. Chim. Acta 459, 124–130 (2017).

    Article  CAS  Google Scholar 

  85. 85.

    Tart, N. M., Sykes, D., Sazanovich, I., Tidmarsh, I. S. & Ward, M. D. Iridium(III) luminophores as energy donors for sensitised emission from lanthanides in the visible and near-infrared regions. Photochem. Photobiol. Sci. 9, 886–889 (2010).

    Article  CAS  Google Scholar 

  86. 86.

    Tamayo, A. B. et al. Synthesis and characterization of facial and meridional tris-cyclometalated Iridium(III) complexes. J. Am. Chem. Soc. 125, 7377–7387 (2003).

    Article  CAS  Google Scholar 

  87. 87.

    Lian, P., Wei, H., Zheng, C., Nie, Y., Bian, J., Bian, Z. & Huang, C. Synthesis, characteristics and photoluminescent properties of novel Ir–Eu heteronuclear complexes containing 2-carboxyl-pyrimidine as a bridging ligand. Dalton Trans. 40, 5476–5482 (2011).

    Article  CAS  Google Scholar 

  88. 88.

    Jiang, W., Lou, B., Wang, J., Lv, H., Bian, Z., & Huang, C. The influence of triplet energy levels of bridging ligands on energy transfer processes in Ir(III)/Eu(III) dyads. Dalton Trans. 40, 11410–11418 (2011).

    Article  CAS  Google Scholar 

  89. 89.

    Sykes, D. & Ward, M. D. Visible-light sensitisation of Tb(III) luminescence using a blue-emitting Ir(III) complex as energy-donor. Chem. Commun. 47, 2279–2281 (2011).

    Article  CAS  Google Scholar 

  90. 90.

    Edkins, R. M., Sykes, D., Beeby, A. & Ward, M. D. Combined two-photon excitation and d–f energy-transfer in Ir/lanthanide dyads with time-gated selection from a two-component emission spectrum. Chem. Commun. 48, 9977–9979 (2012).

    Article  CAS  Google Scholar 

  91. 91.

    Nonat, A. M., Allain, C., Faulkner, S. & Gunnlaugsson, T. Mixed d−f3 coordination complexes possessing improved near-infrared (NIR) lanthanide luminescent properties in aqueous solution. Inorg. Chem. 49, 8449–8456 (2010).

    Article  CAS  Google Scholar 

  92. 92.

    Charbonnière, L. J. et al. Ln2M complexes (M = Ru, Re) derived from a bismacrocyclic ligand containing a 4,4′-dimethyl-2,2′-bipyridyl bridging unit. Dalton Trans. 42, 3667–3681 (2013).

    Article  CAS  Google Scholar 

  93. 93.

    Di Piazza, E. et al. d–f Heterobimetallic association between ytterbium and ruthenium carbon-rich complexes: Redox commutation of near-IR luminescence. J. Am. Chem. Soc. 133, 6174–6176 (2011).

    Article  CAS  Google Scholar 

  94. 94.

    Wang, L., Xie, Z., Dang, S. & Sun, Z. Self-assembly of tunable heterometallic Ln–Ru coordination polymers with near-infrared luminescence and magnetocaloric effect. Chem. Eur. J. 23, 2852–2857 (2017).

    Article  CAS  Google Scholar 

  95. 95.

    Hasegawa, Y. et al. Enhanced electric dipole transition in lanthanide complex with organometallic ruthenocene units. J. Phys. Chem. A 119, 4825–4833 (2015).

    Article  CAS  Google Scholar 

  96. 96.

    Ward, M. D. Mechanisms of sensitization of lanthanide(III)-based luminescence in transition metal/lanthanide and anthracene/lanthanide dyads. Coord. Chem. Rev. 254, 2634–2642 (2010).

    Article  CAS  Google Scholar 

  97. 97.

    Tropiano, M. et al. Synthesis and Spectroscopic study of d–f hybrid lanthanide complexes derived from triazolylDO3A. Organometallics 31, 5673–5676 (2012).

    Article  CAS  Google Scholar 

  98. 98.

    Xu, H. B., Zhang, L. Y., Chen, X. M., Li, X. L. & Chen, Z. N. Modulation of Pt→Ln energy transfer in PtLn2 (Ln = Nd, Er, Yb) complexes with 2,2′-bipyridyl/2,2′:6′2″-terpyridyl ethynyl ligands. Cryst. Growth Des. 9, 569–576 (2009).

    Article  CAS  Google Scholar 

  99. 99.

    Li, J., Wang, J.-Y. & Chen, Z.-N. Sensitized EuIII luminescence through energy transfer from PtM2 (M = Ag or Au) alkynyl chromophores in PtM2Eu2 heteropentanuclear complexes. J. Mater. Chem. C 1, 3661–3668 (2013).

    Article  CAS  Google Scholar 

  100. 100.

    Maynard, B. A. et al. Emission enhancement through dual donor sensitization: modulation of structural and spectroscopic properties in a series of europium tetracyanoplatinates. Inorg. Chem. 48, 6425–6435 (2009).

    Article  CAS  Google Scholar 

  101. 101.

    Li, X. L., Zhang, K. J., Li, J. J., Cheng, X. X. & Chen, Z. N. Dual luminescent dinuclear gold(I) complexes of terpyridyl-functionalized alkyne ligands and their efficient sensitization of Eu-III and Yb-III luminescence. Eur. J. Inorg. Chem. 2010, 3449–3457 (2010).

    Article  CAS  Google Scholar 

  102. 102.

    Iki, N., Hiro-oka, S., Tanaka, T., Kabuto, C. & Hoshino, H. Highly efficient near-infrared-emitting lanthanide(III) complexes formed by heterogeneous self-assembly of AgI, LnIII, and thiacalix[4]arene-p-tetrasulfonate in Aqueous Solution (LnIII = NdIII, YbIII). Inorg. Chem. 51, 1648–1656 (2012).

    Article  CAS  Google Scholar 

  103. 103.

    Yang, X., Schipper, D., Jones, R. A., Lytwak, L. A. & Holliday, B. J. et al Anion-dependent self-assembly of near-infrared luminescent 24- and 32-metal Cd–Ln complexes with drum-like architectures. J. Am. Chem. Soc. 135, 8468–8471 (2014).

    Article  CAS  Google Scholar 

  104. 104.

    Song, X. Q., Cheng, G. Q. & Liu, Y. A. Enhanced Tb(III) luminescence by d10 transition metal coordination. Inorg. Chim. Acta 450, 386–394 (2016).

    Article  CAS  Google Scholar 

  105. 105.

    Omagari, S. et al. Critical role of energy transfer between terbium ions for suppression of back energy transfer in nonanuclear terbium clusters. Sci. Rep. 6, 37008 (2016).

    Article  CAS  Google Scholar 

  106. 106.

    Miyata, K. et al. Chameleon luminophore for sensing temperatures: control of metal-to-metal and energy back transfer in lanthanide coordination polymers. Angew. Chem. Int. Ed. 52, 6413–6416 (2013).

    Article  CAS  Google Scholar 

  107. 107.

    Hatanaka, M. et al. Organic linkers control the thermosensitivity of the emission intensities from Tb(III) and Eu(III) in a chameleon polymer. Chem. Sci. 8, 423–429 (2017).

    Article  CAS  Google Scholar 

  108. 108.

    Hatanaka, M. & Morokuma, K. Exploring the reaction coordinates for f–f emission and quenching of lanthanide complexes—thermosensitivity of terbium(III) luminescence. J. Chem. Theory Comput. 10, 4184–4188 (2014).

    Article  CAS  Google Scholar 

  109. 109.

    Hirai, Y., Nakanishi, T., Miyata, K., Fushimi, K. & Hasegawa, Y. Thermo-sensitive luminescent materials composed of Tb(III) and Eu(III) complexes. Mater. Lett. 130, 91–93 (2014).

    Article  CAS  Google Scholar 

  110. 110.

    Irfanullah, M., Iftikhar & Inorg, K. New hetero-dilanthanide complexes containing Ln1(fod)3 and Ln2(fod)3 fragments (Ln=Pr–Nd; Nd–Sm; Eu–Tb and Ho–Er) linked by bis-diimine bridging ligand. Inorg. Chem. Commun. 13, 694–698 (2010).

    Article  CAS  Google Scholar 

  111. 111.

    Hirai, Y. et al. Glass transition properties and temperature-sensitive luminescence of lanthanide coordination glasses linked by thienyl, naphthyl, and phenyl bridges with ethynyl group. Bull. Chem. Soc. Jpn. 90, 322–326 (2017).

    Article  CAS  Google Scholar 

  112. 112.

    Wang, H., Zhao, D., Cui, Y., Yang, Y. & Qian, G. A Eu/Tb-mixed MOF for luminescent high-temperature sensing. J. Sol. State Chem. 246, 341–345 (2017).

    Article  CAS  Google Scholar 

  113. 113.

    Wei, Y., Sa, R., Li, Q. & Wu, K. Highly stable and sensitive LnMOF ratiometric thermometers constructed with mixed ligands. Dalton Trans. 44, 3067–3074 (2015).

    Article  CAS  Google Scholar 

  114. 114.

    Nakajima, A., Nakanishi, T., Kitagawa, Y., Fushimi, K. & Hasegawa, Y. Thermosensitive luminescent lanthanide complex with two photosensitized ligands. Sens. Mater. 28, 845–850 (2016).

    CAS  Google Scholar 

  115. 115.

    Zhou, Y., Yan, B. & Lei, F. Postsynthetic lanthanide functionalization of nanosized metal–organic frameworks for highly sensitive ratiometric luminescent thermometry. Chem. Commun. 50, 15235–15238 (2014).

    Article  CAS  Google Scholar 

  116. 116.

    Rocha, J., Brites, C. D. S. & Carlos, L. D. Lanthanide organic framework luminescent thermometers. Chem. Eur. J. 22, 14782–14795 (2016).

    Article  CAS  Google Scholar 

  117. 117.

    Cui, Y. J., Chen, B. L. & Qian, G. D. Lanthanide metal–organic frameworks for luminescent sensing and light-emitting applications. Coord. Chem. Rev. 273–274, 76–86 (2014).

    Article  CAS  Google Scholar 

  118. 118.

    Yi, F.-Y., Chen, D., Wu, M.-K., Han, L. & Jiang, H.-L. Chemical sensors based on metal–organic frameworks. ChemPlusChem 81, 675–690 (2016).

    Article  CAS  Google Scholar 

  119. 119.

    D’Vries, R. F. et al. Multimetal rare earth MOFs for lighting and thermometry: tailoring color and optimal temperature range through enhanced disulfobenzoic triplet phosphorescence. J. Mater. Chem. C 1, 6316–6324 (2013).

    Article  CAS  Google Scholar 

  120. 120.

    Matthes, P. R. et al. Luminescence tuning of MOFs via ligand to metal and metal to metal energy transfer by co-doping of 2 [Gd2Cl6(bipy)3]·2bipy with europium and terbium. J. Mater. Chem. 22, 10179–10187 (2012).

    Article  CAS  Google Scholar 

  121. 121.

    Zhang, H. B. et al. A highly luminescent chameleon: fine-tuned emission trajectory and controllable energy transfer. J. Mater. Chem. C 2, 1367–1371 (2014).

    Article  CAS  Google Scholar 

  122. 122.

    Liu, L., Zhang, X., Fu, G., Lü, X. & Wong, W.-K. et al Singe-component Zn2+-Eu3+-Tb3+-containing and Zn2+-Eu3+-Tb3+-Gd3+-containing metallopolymer-type materials with ultra-high color rendering index white-light. Dyes Pigm 141, 137–147 (2017).

    Article  CAS  Google Scholar 

  123. 123.

    Tang, Q. et al. Color tuning and white light emission via in situ doping of luminescent lanthanide metal–organic frameworks. Inorg. Chem. 53, 289–293 (2014).

    Article  CAS  Google Scholar 

  124. 124.

    Ye, J.-W. et al. Mixed-lanthanide porous coordination polymers showing range-tunable ratiometric luminescence for O2 sensing. Inorg. Chem. 56, 4238–4243 (2017).

    Article  CAS  Google Scholar 

  125. 125.

    Auzel, F. Upconversion and anti-stokes processes with F and D ions in solids. Chem. Rev. 104, 139–174 (2004).

    Article  CAS  Google Scholar 

  126. 126.

    Aboshyan-Sorgho, L. et al. Near-infrared→visible light upconversion in a molecular trinuclear d–f–d complex. Angew. Chem. Int. Ed. 50, 4108–4112 (2011).

    Article  CAS  Google Scholar 

  127. 127.

    Suffren, Y. et al. Taming lanthanide-centered upconversion at the molecular level. Inorg. Chem. 55, 9964–9972 (2016).

    Article  CAS  Google Scholar 

  128. 128.

    Nonat, A. et al. Room temperature molecular up conversion in solution. Nat. Commun. 7, 11978 (2016).

    Article  CAS  Google Scholar 

  129. 129.

    Souri, N. et al. Upconverted photosensitization of Tb visible emission by NIR Yb excitation in discrete supramolecular heteropolynuclear complexes. J. Am. Chem. Soc. 139, 1456–1459 (2017).

    Article  CAS  Google Scholar 

  130. 130.

    Blackburn, O. A. et al. Luminescence and upconversion from thulium(III) species in solution. Phys. Chem. Chem. Phys. 14, 13378–13384 (2012).

    Article  CAS  Google Scholar 

  131. 131.

    Ishii, A. & Hasegawa, M. Solar-pumping upconversion of interfacial coordination nanoparticles. Sci. Rep. 7, 41446 (2017).

    Article  CAS  Google Scholar 

  132. 132.

    Kido, J., Nagai, K. & Ohashi, Y. Electroluminescence in a terbium complex. Chem. Lett. 19, 657–660 (1990).

    Article  Google Scholar 

  133. 133.

    Kawamura, Y. et al. Observation of neodymium electroluminescence. Appl. Phys. Lett. 74, 3245–3247 (1999).

    Article  CAS  Google Scholar 

  134. 134.

    Xu, H., Sun, Q., An, Z., Wei, Y. & Liu, X. Electroluminescence from europium(III) complexes. Coord. Chem. Rev. 293–294, 228–249 (2015).

    Article  CAS  Google Scholar 

  135. 135.

    Wang, J. Z. et al. Solution-processible brilliantly luminescent EuIII complexes with host-featured phosphine oxide ligands for monochromic red-light-emitting diodes. Chem. Eur. J. 20, 11137–11148 (2014).

    Article  CAS  Google Scholar 

  136. 136.

    Xu, H., Zhu, R., Zhao, P. & Huang, W. Monochromic red-emitting nonconjugated copolymers containing double-carrier-trapping phosphine oxide Eu3+ segments: toward bright and efficient electroluminescence. J. Phys. Chem. C 115, 15627–15638 (2011).

    Article  CAS  Google Scholar 

  137. 137.

    Hasegawa, Y. et al. Luminescent thin films composed of nanosized europium coordination polymers on glass electrodes. ChemPlusChem 81, 187–193 (2016).

    Article  CAS  Google Scholar 

  138. 138.

    Xu, H. et al. A unique white electroluminescent one-dimensional europium(iii) coordination polymer. J. Mater. Chem. C 3, 1893–1903 (2015).

    Article  CAS  Google Scholar 

  139. 139.

    Zinna, F., Giovanella, U. & Bari, L. D. Highly circularly polarized electroluminescence from a chiral europium complex. Adv. Mater. 27, 1791–1795 (2015).

    Article  CAS  Google Scholar 

  140. 140.

    Cui, R. et al. High performance red phosphorescent organic electroluminescent devices with characteristic mechanisms by utilizing terbium or gadolinium complexes as sensitizers. J. Mater. Chem. C 5, 2066–2073 (2017).

    Article  CAS  Google Scholar 

  141. 141.

    Adachi, C., Baldo, M. A., Thompson, M. E. & Forrest, S. R. Nearly 100% internal phosphorescence efficiency in an organic light-emitting device. J. Appl. Phys. 90, 5048–5051 (2001).

    Article  CAS  Google Scholar 

  142. 142.

    Uoyama, H., Goushi, K., Shizu, K., Nomura, H. & Adachi, C. Highly efficient organic light-emitting diodes from delayed fluorescence. Nature 492, 234–238 (2012).

    Article  CAS  Google Scholar 

  143. 143.

    Lee, S. Y., Yasuda, T., Komiyama, H., Lee, J. & Adachi, C. Thermally activated delayed fluorescence polymers for efficient solution-processed organic light-emitting diodes. Adv. Mater. 28, 4019–4024 (2016).

    Article  CAS  Google Scholar 

  144. 144.

    Lee, S. Y., Adachi, C. & Yasuda, T. High-efficiency blue organic light-emitting diodes based on thermally activated delayed fluorescence from phenoxaphosphine and phenoxathiin derivatives. Adv. Mater. 28, 4626–4631 (2016).

    Article  CAS  Google Scholar 

  145. 145.

    Hasegawa, Y., Tsuruoka, S., Yoshida, T., Kawai, H. & Kawai, T. Enhanced deep-red luminescence of tris(hexafluoroacetylacetonato)samarium(III) complex with phenanthroline in solution by control of ligand coordination. J. Phys. Chem. A 112, 803–807 (2008).

    Article  CAS  Google Scholar 

  146. 146.

    Wiedemann, E. & Schmidt, G. C. Thermoluminescence induced by electron beams in alkali halides. Ann. Phys. Chem. 54, 604–625 (1895).

    Google Scholar 

  147. 147.

    Walton, A. J. Triboluminescence. Adv. Phys. 26, 887–948 (1977).

    Article  CAS  Google Scholar 

  148. 148.

    Zink, J. I. Triboluminescence. Acc. Chem. Res. 11, 289–295 (1978).

    Article  CAS  Google Scholar 

  149. 149.

    Olawale, D. O. et al. Progress in triboluminescence-based smart optical sensor system. J. Lumin. 131, 1407–1418 (2011).

    Article  CAS  Google Scholar 

  150. 150.

    Wang, X. D. et al. Dynamic pressure mapping of personalized handwriting by a flexible sensor matrix based on the mechanoluminescence process. Adv. Mater. 27, 2324–2331 (2015).

    Article  CAS  Google Scholar 

  151. 151.

    Olawale, D. O. et al. Real time failure detection in unreinforced cementitious composites with triboluminescent sensor. J. Lumin. 147, 235–241 (2014).

    Article  CAS  Google Scholar 

  152. 152.

    Fontenot, R. S., Hollerman, W. A., Bhat, K. N., Aggarwal, M. D. & Penn, B. G. Incorporating strongly triboluminescent europium dibenzoylmethide triethylammonium into simple polymers. Polym. J. 46, 111–116 (2014).

    Article  CAS  Google Scholar 

  153. 153.

    Hurt, C. R., McAvoy, N., Bjorklund, S. & Filipescu, N. High intensity triboluminescence in europium tetrakis (dibenzoylmethide)-triethylammonium. Nature 212, 179–180 (1966).

    Article  CAS  Google Scholar 

  154. 154.

    Sweeting, L. M. & Rheingold, A. L. Crystal disorder and triboluminescence: triethylammonium tetrakis(dibenzoylmethanato)europate. J. Am. Chem. Soc. 109, 2652–2658 (1987).

    Article  CAS  Google Scholar 

  155. 155.

    Takada, N., Sugiyama, J., Katoh, R., Minami, N. & Hieda, S. Mechanoluminescent properties of europium complexes. Synth. Met. 91, 351–354 (1997).

    Article  CAS  Google Scholar 

  156. 156.

    George, T. M., Sajan, M. J., Gopakumar, N. & Reddy, M. L. P. Bright red luminescence and triboluminescence from PMMA-doped polymer film materials supported by Eu3+-triphenylphosphine based beta-diketonate and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene oxide. J. Photochem. Photobiol. A 317, 88–99 (2016).

    Article  CAS  Google Scholar 

  157. 157.

    Cotton, F. A., Daniels, L. M. & Huang, P. Refutation of an alleged example of a disordered but centrosymmetric triboluminescent crystal. Inorg. Chem. Commun. 4, 319–321 (2001).

    Article  Google Scholar 

  158. 158.

    Zhang, S. et al. Eu-MOFs with 2-(4-carboxyphenyl)imidazo[4,5-f]-1,10-phenanthroline and ditopic carboxylates as coligands: synthesis, structure, high thermostability, and luminescence properties. Inorg. Chem. 53, 10952–10963 (2014).

    Article  CAS  Google Scholar 

  159. 159.

    Bukvetskii, B. V., Mirochnik, A. G., Zhikhareva, P. A. & Karasev, V. E. Crystal structure and triboluminescence of the [Eu(TTA)2(NO3)(TPPO)2] complex. J. Struct. Chem. 47, 575–580 (2006).

    Article  CAS  Google Scholar 

  160. 160.

    Bukvetskii, B. V., Shishov, A. S. & Mirochnik, A. G. Triboluminescence and crystal structure of the centrosymmetric complex [Tb(NO3)2(Acac)(Phen)2]·H2O. Luminescence 31, 1329–1334 (2016).

    Article  CAS  Google Scholar 

  161. 161.

    Li, X.-L., Zheng, Y., Zuo, J.-L., Song, Y. & You, X.-Z. Synthesis, crystal structures and triboluminescence of a pair of Eu(III)-based enantiomers. Polyhedron 26, 5257–5262 (2007).

    Article  CAS  Google Scholar 

  162. 162.

    Li, D.-P. et al. Synthesis and physical properties of two chiral terpyridyl europium(III) complexes with distinct crystal polarity. Eur. J. Inorg. Chem. 2009, 4844–4849 (2009).

    Article  CAS  Google Scholar 

  163. 163.

    Fontenot, R. S., Hollerman, W. A., Bhat, K. N. & Aggarwal, M. D. Synthesis and characterization of highly triboluminescent doped europium tetrakis compounds. J. Lumin. 132, 1812–1818 (2012).

    Article  CAS  Google Scholar 

  164. 164.

    Chen, X.-F. et al. Crystal structures and triboluminescent activities of samarium(III) complexes. J. Coord. Chem. 52, 97–110 (2000).

    Article  CAS  Google Scholar 

  165. 165.

    Akerboom, S., Meijer, M. S., Siegler, M. A., Fu, W. T. & Bouwman, E. Structure, photo- and triboluminescence of the lanthanoid dibenzoylmethanates: HNEt3[Ln(dbm)4]. J. Lumin. 145, 278–282 (2014).

    Article  CAS  Google Scholar 

  166. 166.

    Biju, S. et al. Brilliant photoluminescence and triboluminescence from ternary complexes of DyIII and TbIII with 3-phenyl-4-propanoyl-5-isoxazolonate and a bidentate phosphine oxide coligand. Inorg. Chem. 52, 8750–8758 (2013).

    Article  CAS  Google Scholar 

  167. 167.

    Chen, X.-F. et al. Triboluminescence and crystal structures of non-ionic europium complexes. J. Mater. Chem. 9, 2919–2922 (1999).

    Article  CAS  Google Scholar 

  168. 168.

    Eliseeva, S. V. et al. Highly luminescent and triboluminescent coordination polymers assembled from lanthanide β-diketonates and aromatic bidentate O-donor ligands. Inorg. Chem. 49, 9300–9311 (2010).

    Article  CAS  Google Scholar 

  169. 169.

    Mikhalyova, E. A. et al. Manifestation of π–π Stacking Interactions in luminescence properties and energy transfer in aromatically-derived Tb, Eu and Gd tris(pyrazolyl)borate complexes. Inorg. Chem. 54, 3125–3133 (2015).

    Article  CAS  Google Scholar 

  170. 170.

    Teotonio, E. E. S. et al. Evaluation of intramolecular energy transfer process in the lanthanide(III) bis- and tris-(TTA) complexes: photoluminescent and triboluminescent behavior. J. Lumin. 128, 190–198 (2008).

    Article  CAS  Google Scholar 

  171. 171.

    Mikhalyova, E. A. et al. Crystal structures and intense luminescence of tris(3-(2′-pyridyl)-pyrazolyl)borate Tb3+ and Eu3+ complexes with carboxylate co-ligands. Dalton Trans. 46, 3457–3469 (2017).

    Article  CAS  Google Scholar 

  172. 172.

    Hirai, Y. et al. Triboluminescence of lanthanide coordination polymers with face-to-face arranged substituents. Angew. Chem. Int. Ed. 56, 7171–7175 (2017).

    Article  CAS  Google Scholar 

  173. 173.

    Fontenot, R. S., Hollermana, W. A., Aggarwal, M. D., Bhat, K. N. & Goedekea, S. M. A versatile low-cost laboratory apparatus for testing triboluminescent materials. Measurement 45, 431–436 (2012).

    Article  Google Scholar 

  174. 174.

    Wong, H.-Y., Lo, W.-S., Chan, W. T. K. & Law, G. L. Mechanistic investigation of inducing triboluminescence in lanthanide(III) β-diketonate complexes. Inorg. Chem. 56, 5135–5140 (2017).

    Article  CAS  Google Scholar 

  175. 175.

    İncel, A., Emirdag-Eanes, M., McMillen, C. D. & Demir, M. M. Integration of triboluminescent EuD4TEA crystals to transparent polymers: impact sensor application. ACS Appl. Mater. Interfaces 9, 6488–6496 (2017).

    Google Scholar 

  176. 176.

    Hasegawa, Y. et al. Luminescent polymer containing the Eu(III) complex having fast radiation rate and high wmission quantum efficiency. J. Phys. Chem. A 107, 1697–1702 (2003).

    Article  CAS  Google Scholar 

  177. 177.

    Nakamura, K. et al. Enhanced lasing properties of dissymmetric Eu(III) complex with bidentate phosphine ligands. J. Phys. Chem. A. 111, 3029–3037 (2007).

    Article  CAS  Google Scholar 

  178. 178.

    Miyata, K. et al. Remarkable luminescence properties of lanthanide complexes with asymmetric dodecahedron structures. Chem. Eur. J. 17, 521–528 (2011).

    Article  CAS  Google Scholar 

  179. 179.

    Hasegawa, Y. et al. Effect of ligand polarization on asymmetric structural formation for strongly luminescent lanthanide complexes. Eur. J. Inorg. Chem. 2013, 5913–5918 (2013).

    Article  CAS  Google Scholar 

  180. 180.

    Yanagisawa, K. et al. Seven-coordinate luminophores: brilliant luminescence of lanthanide complexes with C3v geometrical structures. Eur. J. Inorg. Chem. 2015, 4769–4774 (2015).

    Article  CAS  Google Scholar 

  181. 181.

    Yanagisawa, K., et al. Enhanced luminescence of asymmetrical seven-coordinate EuIII complexes including LMCT perturbation. Eur. J. Inorg. Chem. 2017, in press.

  182. 182.

    Iwamuro, M. et al. Luminescence of Nd3+ complexes with some asymmetric ligands in organic solutions. J. Lumin. 79, 29–38 (1998).

    Article  CAS  Google Scholar 

  183. 183.

    Nakamura, K., Hasegawa, Y., Wada, Y. & Yanagida, S. Novel luminescent Eu(III) complex with remarkably narrow emission band. Chem. Phys. Lett. 398, 500–504 (2004).

    Article  CAS  Google Scholar 

  184. 184.

    Hasegawa, Y. et al. Enhanced emission of deuterated tris(hexafluoroacetylacetonato) neodymium(III) complex in solution by suppression of radiationless transition via vibrational excitation. J. Phys. Chem. 100, 10201–10205 (1996).

    Article  CAS  Google Scholar 

  185. 185.

    Nakamura, K. et al. High lasing oscillation efficiency of Eu(III) complexes having remarkably sharp emission band. J. Alloy Compd. 408, 771–775 (2006).

    Article  CAS  Google Scholar 

  186. 186.

    Hasegawa, Y. et al. Enhancement of luminescence of Nd3+ complexes with deuterated hexafluoroacetylacetonato ligands in organic solvent. Chem. Phys. Lett. 248, 8–12 (1996).

    Article  CAS  Google Scholar 

  187. 187.

    Hasegawa, Y. et al. Characteristic emission of β-diketonato Nd3+ complexes dressed with perfluoroalkyl groups in DMSO-d6. Chem. Phys. Lett. 260, 173–177 (1996). S..

    Article  CAS  Google Scholar 

  188. 188.

    Hasegawa, Y. et al. Enhanced emission of Nd3+ in liquid systems: formation of symmetrical rigid shells of tightly solvated DMSO molecules and weakly coordinated low-vibrational β-diketonato ligands. Bull. Chem. Soc. Jpn. 71, 2573–2581 (1998).

    Article  CAS  Google Scholar 

  189. 189.

    Yanagida, S. et al. Strategies for enhancing photoluminescence of Nd3+ in liquid media. Coord. Chem. Rev. 171, 461–480 (1998).

    Article  CAS  Google Scholar 

  190. 190.

    Hasegawa, Y. et al. Enhanced luminescence of lanthanide(III) complexes in polymer matrices. Chem. Lett. 1, 35–36 (1999).

    Article  Google Scholar 

  191. 191.

    Wada, Y. et al. High efficiency near-IR emission of Nd(III) based on low-vibrational environment in cages of nanosized zeolites. J. Am. Chem. Soc. 122, 8583–8584 (2000).

    Article  CAS  Google Scholar 

  192. 192.

    Yanagida, S., Hasegawa, Y. & Wada, Y. Remarkable luminescence of novel Nd(III) complexes with low-vibrational hexafluoroacetylacetone and DMSO-d 6 molecule. J. Lumin. 87, 995–998 (2000).

    Article  Google Scholar 

  193. 193.

    Hasegawa, H. et al. Luminescence of novel neodymium sulfonylaminate complexes in organic media. Angew. Chem. Int. Ed. 39, 357–360 (2000).

    Article  CAS  Google Scholar 

  194. 194.

    Ryo, M. et al. Spectroscopic study on strongly luminescent Nd(III) exchanged zeolite: TMA+-containing FAU type zeolite as a suitable host for ship-in-bottle synthesis. J. Mater. Chem. 12, 1748–1753 (2002).

    Article  CAS  Google Scholar 

  195. 195.

    Ryo, M., Wada, Y., Okubo, T., Hasegawa, Y. & Yanagida, S. Intrazeolite nanostructure of Nd(III) complex giving strong near-infrared luminescence. J. Phys. Chem. B 107, 11302–11306 (2003).

    Article  CAS  Google Scholar 

  196. 196.

    Hasegawa, Y., Sogabe, K., Wada, Y. & Yanagida, S. Low-vibrational luminescent polymers including tris(bis-perfluoromethane and ethanesulfonylaminate)neodymium(III) with 8 coordinated DMSO-d 6. J. Lumin. 101, 235–242 (2003).

    Article  CAS  Google Scholar 

  197. 197.

    Hasegawa, Y. et al. Molecular design of luminescent Eu(III) complexes as lanthanide lasing material and their optical properties. J. Alloy Compd. 408, 669–674 (2006).

    Article  CAS  Google Scholar 

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The author is very grateful to Prof. emeritus S. Yanagida (Osaka University), Prof. Y. Wada (Tokyo Institute of Technology), Prof. T. Kawai, Prof. T. Nakashima, (Nara Institute of Science and Technology), Dr. J. Yuasa (Tokyo University of Science), Prof. N. Nakashima (Osaka City University), Prof. T. Yamanaka (Osaka University), Prof. K. Murakoshi, Prof. M. Kato, Prof. H. Ito, Prof. Y. Hinatsu, Prof. H. Koizumi, Dr. A. Kobayashi, Dr. T. Seki, Dr. Y. Doi (Hokkaido University), Prof. K. Tanaka, Prof. K. Fujita (Kyoto University), Prof. P. O'Brien (University of Manchester), Prof. T. Asahi (Ehime University), Dr. K. Nakamura (Chiba University), Dr. T. Nakagawa (Yokohama National University), Dr. Y. Kuramochi (Tokyo Institute of Technology), Dr. T. Harada (Shimane University), Prof. K. Fushimi (Hokkaido University) for their collaboration, measurements, and helpful comments. I would also like to thank the members of the Laboratory of Molecular Process Engineering at Osaka University, the Laboratory for Photonic Molecular Science at Nara Institute of Science and Technology, and the Laboratory of Advanced Materials Chemistry at Hokkaido University. This work was supported in part by Grants-in-Aid for Scientific Research on Innovative Areas of “New Polymeric Materials Based on Element-Blocks (No. 2401)” (24102012) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan.

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Hasegawa, Y., Kitagawa, Y. & Nakanishi, T. Effective photosensitized, electrosensitized, and mechanosensitized luminescence of lanthanide complexes. NPG Asia Mater 10, 52–70 (2018).

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