Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Evolution of cooperativity in the spin transition of an iron(II) complex on a graphite surface

This article has been updated


Cooperative effects determine the spin-state bistability of spin-crossover molecules (SCMs). Herein, the ultimate scale limit at which cooperative spin switching becomes effective is investigated in a complex [Fe(H2B(pz)2)2(bipy)] deposited on a highly oriented pyrolytic graphite surface, using x-ray absorption spectroscopy. This system exhibits a complete thermal- and light-induced spin transition at thicknesses ranging from submonolayers to multilayers. On increasing the coverage from 0.35(4) to 10(1) monolayers, the width of the temperature-induced spin transition curve narrows significantly, evidencing the buildup of cooperative effects. While the molecules at the submonolayers exhibit an apparent anticooperative behavior, the multilayers starting from a double-layer exhibit a distinctly cooperative spin switching, with a free-molecule-like behavior indicated at around a monolayer. These observations will serve as useful guidelines in designing SCM-based devices.


Spin-crossover molecules (SCMs) offer a tantalizing route towards the realization of molecular spintronics1,2,3 and other nanoscale devices4,5,6,7 due to their bistability in the spin state, which can be manipulated or switched reversibly with external stimuli like temperature, light, pressure, electric field, magnetic field, or x rays8,9,10,11,12. The spin-crossover phenomenon in SCMs stems from the competition between the mean spin-pairing energy (Δ), which favors the high-spin (HS, paramagnetic) state and the ligand field—quantified by the ligand-field parameter 10Dq—which favors the low-spin (LS, diamagnetic or less paramagnetic than HS) state. Recent experiments with single molecules, thin films, and nanoparticles of SCMs revealed a rich and interesting interplay between the transport properties and the molecular spin states: high conductance in the HS state and low conductance in the LS state11,13,14,15, accompanied by the generation of spin-polarized current depending upon the spin state of the molecule and the electrodes16, and memory effects in the room-temperature regime17,18,19.

To put things into perspective, besides SCMs, the family of bistable molecules with a comparable promise of technological spin-offs are single-molecule magnets (SMMs)20,21,22. SCMs, however, offer one distinct advantage over SMMs: whereas SMMs exhibit bistability only at low temperatures23, room-temperature regimes can be reached for SCMs24,25,26,27. Nevertheless, reports of SCMs on surfaces are relatively scarce. This can be traced back to two main reasons: the paucity of SCMs that are vacuum-evaporable, with only a few cases reported so far27,28,29,30,31,32,33,34,35,36,37,38, and the coexistence of the two spin states or the loss of spin-crossover behavior altogether on contact with surfaces. It appears to be rather the norm that SCMs in contact with a surface invariably lead to the co-existence of the HS and the LS states at all temperatures36,39,40,41,42,43,44, though a few exceptions exist33,45.

In a study of [Fe(phen)2(NCS)2] on a Cu surface, spin-state coexistence in a series of submonolayer coverages has been reported, while molecules decoupled from the substrate (bilayer) exhibit a dominant spin state39. In the same system, electrically induced spin switching has been reported with the introduction of a thin insulating spacer layer of CuN between the molecules and the substrate13. In our previous studies, we have shown that for the SCMs [Fe(H2B(pz)2)2(phen)]40 and [Fe(H2B(pz)2)2(phen-me4)]36 (an analog of the former) in contact with a Au surface, the molecules undergo fragmentation, while only in the second layer, the molecules’ integrity, as well as the spin-crossover are preserved. However, on a Bi surface, even though the molecules’ integrity is preserved already in the first layer, about half of the molecules are locked in the HS state36. In a bilayer of [Fe(H2B(pz)2)2(bipy)] (hereafter referred to as Fe(bpz)-bipy) on Au probed with temperature-dependent scanning tunneling microscopy (STM), spin-state coexistence has been reported while the composition of the spin states was independent from temperature46. This led to the speculation of the spin-state coexistence to be an intrinsic property of SCMs in ultrathin films46. In a recent STM-based study of a monolayer of [FeII((3,5-(CH3)2Pz)3BH)2] on a Au surface, the authors reported a collective behavior in the light-induced HS→LS transition at 4.6 K, albeit with both spin-states coexisting43. Owing to the observed long-range order of alternating HS and LS states43, it is likely that the molecules undergo an antagonistic or anticooperative spin transition.

The absence or presence of cooperativity in the spin transition of SCMs and their characteristics is one of the most important issues for research, since it is responsible for the bistability in the spin states of SCMs. SCMs in the bulk generally exhibit cooperativity while undergoing the spin transition, which is ascribed to elastic interactions arising from the volume difference between the HS state (larger volume) and the LS state (smaller volume)47,48. The strength of the cooperative effects can be inferred from the degree of steepness of the temperature-induced spin transition curve. The interactions that favor “like-spin” pairings (HS–HS or LS–LS) are termed cooperative (ferromagnetic-like), while those that favor “unlike-spin” pairings (HS–LS) are termed anticooperative (antiferromagnetic-like). Determining the ultimate scale limit at which cooperativity becomes effective is of major interest when aiming at applications at reduced size or dimensionality. Future devices will likely involve integrating multi-functional molecules like SCMs with 2D materials exhibiting novel properties. In this regard, graphene is among the material of choice due to its robust optical, electrical and mechanical properties49. Understanding the behavior of SCMs on a highly oriented pyrolytic graphite (HOPG) surface will be an ideal platform towards integrating it with graphene.

Herein, we report on the complete and efficient thermal- and light-induced spin-crossover of Fe(bpz)-bipy on an HOPG surface with coverages ranging from 0.35(4) to 10(1) ML (monolayers) investigated by x-ray absorption spectroscopy, while addressing two main traits: the nature of the spin-crossover behavior for molecules in direct contact with the surface as well as upon increasing the coverage of the molecular layers, and the metastability of the HS state on the surface after it is switched from the LS state by illumination with a green LED (light emitting diode, λ = 520 nm) at low temperatures. Our results reveal the evolution of cooperativity in the spin-crossover of ultrathin molecular layers of SCMs adsorbed on a solid surface, which is evident from an increased steepness in the thermal spin-crossover curves. (The degree of steepness or the transition-width (ΔT) is defined as the temperature difference at which 80% of the molecules are in the HS and LS states, respectively45.) The interaction strength, deduced from fits to the phenomenological Slichter and Drickamer mean-field model50, increases monotonically with the coverage, reaching about 60% of the bulk value at a coverage of 10(1) ML. On the other hand, the HS→LS relaxation measurements of submonolayer coverages at 8, 20, 30, and 40 K show a stretched exponential behavior of the amount of HS molecules as a function of time, which may be explained by assuming anticooperativity at submonolayer coverages.


Temperature- and light-induced spin-crossover

To probe the spin state of the molecules, x-ray absorption spectroscopy (XAS) is used. XAS is very well suited for studying SCMs on surfaces due to its element selectivity and high sensitivity in tracing a subtle electronic or chemical change51. More specifically, the Fe L2,3 (2p63d6→2p53d7) or the Fe L3 \(\left( {2{\mathrm{p}}_{{\mathrm{3/2}}}^{\mathrm{4}}3{\mathrm{d}}^6 \to 2{\mathrm{p}}_{{\mathrm{3/2}}}^{\mathrm{3}}3{\mathrm{d}}^7} \right)\) edge spectral line shape is a fingerprint of the magnetic state of the molecule52. Schematic representations of the 3d-orbital electronic distributions of Fe(bpz)-bipy (Fig. 1a) in the HS and the LS states, and transitions from the \(2{\mathrm{p}}_{{\mathrm{3/2}}}^{\mathrm{4}}\) core level causing the Fe L3 absorption edge are shown in Fig. 1b, c, respectively. It should be noted as a word of caution that the x-ray beam can induce LS→HS or HS→LS transitions at low temperatures, a process termed as soft x-ray-induced excited spin state trapping (SOXIESST)12, and reverse-SOXIESST53, respectively. The x-ray-induced effects on the spin states can be largely mitigated by maintaining the photon flux in the range of ~109 photons s−1 mm−2 53 (cf. Methods).

Fig. 1
figure 1

High-spin and low-spin states of spin-crossover molecules as revealed by x-ray absorption spectroscopy. a Chemical structure of Fe(bpz)-bipy; b The size of the ligand field splitting of the Fe 3d6 orbital into eg and t2g (10Dq) relative to the mean spin-pairing energy (Δ) leads to the HS or LS state; c Interaction of x rays with \(2{\mathrm{p}}_{{\mathrm{3/2}}}^{\mathrm{4}}\) electrons and their excitation to the 3d orbital (Fe L3 edge); d RT Fe L3 absorption spectra of 10(1) ML and 0.35(4) ML of Fe(bpz)-bipy on HOPG (black and magenta lines, respectively), and e at 72 K and 62 K before illumination (black and magenta lines, respectively), and after illumination with a green LED (blue and dark-yellow lines, respectively) at 5 K. The absorption intensities of the 0.35(4)-ML sample have been scaled to that of the 10(1)-ML sample

Figure 1d, e shows the Fe L3 spectra of 0.35(4) and 10(1) ML at RT (room temperature) and at LT (low temperature) before and after illumination with a green LED. The RT and LT spectra before illumination have sharply contrasting Fe L3 line shapes: the RT spectrum is characterized by two main peaks at 708.1 and 708.9 eV and the LT spectrum by a single main peak at 709.4 eV before illumination with light. These spectral line shapes have been established as characteristic of the HS and the LS states, respectively33,45,52. The spectrum at any other intermediate temperature is a linear combination of the two (cf. Supplementary Figure 1), as has also been shown elsewhere33,45. Upon illumination with the green LED at 5 K, the RT spectral line shape is recovered albeit with higher XA intensity (LS→HS transition). The molecules are thus again in the HS state, which is termed light-induced excited spin-state trapping (LIESST)9. The bulk Fe L3 spectra recorded at RT and at LT also yielded correspondingly similar line shapes to the ones described above (cf. Supplementary Figure 1). While SOXIESST is saturated at about 60% HS with an x-ray photon flux of about ~1 × 109 photons s−1 mm−2 53, the final states in LIESST are assumed to be 100% HS following ref.45, where the spectral profiles can be reproduced by spin-multiplet calculations. On warming up to 70–90 K, the samples can be converted back to the LS state. To test the reversibility in the spin switching during the cooling and heating cycles, systematic measurements to track the change in Fe L3 spectra (and hence the change in the spin state) have been carried out between 5 and 96 K under continuous illumination, for the 0.69(8)-ML sample as proof of concept. This is shown in Supplementary Figure 2: the sample exhibits a near-complete reversible spin transition from HS to LS state during ramp-up and LS to HS state during ramp-down in the aforementioned temperature range.

The fraction of HS molecules (γHS) at any given temperature is estimated by fitting the corresponding spectrum to that of a linear combination of the RT Fe L3 XA spectrum (HS state) and the LT spectrum (LS state) recorded at low temperature before the onset of LIESST or SOXIESST. The low-temperature HS and LS spectra across all the coverages have similar line shapes upon scaling, though the HS spectra at RT show some minor variations which appeared as about 3% change in the spin-state compositions (c.f. Supplementary Figure 1). For uniformity, the RT spectrum of 10(1) ML is taken as the reference HS state for all the coverages, with its γHS assumed to be 0.91 in conformity with that reported for the bulk molecule54; this number is also reproduced by using the LT spectrum after LIESST (100% HS) as the reference HS state. The presence of a certain quantity of LS molecules at RT in thin films of Fe(bpz)-bipy – similar to the bulk – has also been reported elsewhere31. The temperature-dependent measurements of γHS are carried out by cooling the sample at the rate of 4 K min−1 while simultaneously recording the spectra. The result is shown in Fig. 2a, and is characterized by a gradual to a relatively steeper spin transition when going from submonolayer to multilayer coverages, indicating an increase in cooperativity in the molecular spin switching processes.

Fig. 2
figure 2

Temperature-dependent spin-crossover curves as signatures of cooperative effects. a Temperature-dependent spin-crossover of different coverages of Fe(bpz)-bipy on HOPG along with that of the bulk data; the dots represent experimental data while the solid lines are fits obtained from the Slichter–Drickamer model. b Dependence of the interaction parameter Γ (left-axis) and the transition width ΔT (right-axis) upon the coverage indicating the inverse relation between the two. The bulk data are taken from Moliner et al.54

Traditionally, elastic interactions between the molecules have been invoked to rationalize the occurrence of cooperativity: The spin transition is concomitantly accompanied by a change in volume (expansion and contraction in the HS and LS states, respectively), which induces elastic strain, resulting in both short- and long-range interactions between the molecules47,55. However, a recent wave-function ab initio calculation suggests the cooperativity to arise mainly from electrostatic contributions as a result of the simultaneous electronic relocalization within the molecules and fluctuations in the Madelung field during the spin transition56,57. Herein, we choose to treat the interaction between the molecules in contact with the HOPG surface and at higher coverages by the classical thermodynamic model of Slichter and Drickamer (S−D model)50. In this model, a term Γ(1 − γHS)γHS is introduced in the expression of Gibb’s free energy, where Γ is a phenomenological interaction parameter. The macroscopic S−D model is similar to the microscopic two-level Ising-like model in the mean-field approach58. A model based on interacting HS and LS domains (as opposed to HS and LS states) still yields a Gibb’s free energy similar to the S–D model59. Wavefunction ab initio calculations also reproduced the S–D model57, which has been used recently to explore the possibility of an enhanced cooperativity in surface-supported 2D metal-organic frameworks60. At equilibrium, the S−D model leads to the implicit equation:

$${\mathrm{ln}}\left( {\frac{{1 - \gamma _{\mathrm{HS}}}}{{\gamma _{\mathrm{HS}}}}} \right) = \frac{{{\mathrm{\Delta }}H + \Gamma (1 - 2\gamma _{\mathrm{HS}})}}{{RT}} - \frac{{{\mathrm{\Delta }}S}}{R}{\kern 1pt} $$

where ΔH and ΔS are the differences in enthalpy and entropy, respectively, between the HS and LS states; R is the universal gas constant. The experimental input in Equation (1) is the HS fraction γHS. Of the three fitting parameters, namely, Γ, ΔH and ΔS; ΔH and ΔS are related by the transition temperature T1/2 (defined as the temperature where the population of the HS and the LS species are equal), as ΔH = T1/2ΔS. If Γ = 0, then Equation (1) reduces to the van’t Hoff’s model – a non-interacting molecular system.

The results obtained by a fit of the experimental data by the S–D model using the method of least-square deviation are presented in Table 1 together with bulk data taken from Moliner et al.54. It yields a gradual evolution in cooperative spin transition in going from submonolayers to multilayers: negative interaction parameters at 0.35(4) (Γ = −0.44(0.23) kJ mol−1) and 0.69(8) ML (Γ = −0.1(2) kJ mol−1), positive at 2.0(3) ML (Γ = 0.3(1) kJ mol−1), and further increase with increasing coverage. In contrast, the entropy change ΔS and the enthalpy change ΔH across all coverages yield roughly constant values. The result for Γ is plotted in Fig. 2b as a function of coverage (blue data points, left axis). The interaction parameter Γ and the transition width ΔT, also shown in Fig. 2b, show an inverse relation. The similar values of ΔT obtained from the experimental data and the S−D model fit across all coverages (Fig. 2b right axis, magenta and black dots) are an indication of the suitability of the model in tracing the evolution of cooperativity in the spin-transition processes in ultrathin films. The details of the S–D model fits are given in Supplementary Figures 35 and Supplementary Table 1.

Table 1 Thermodynamic parameters

The time-dependent population of the HS state upon illumination with a green LED for all the coverages at 5 K is shown in Fig. 3b. The process, known as LIESST, has been rationalized in terms of intersystem crossing48 (the scheme is shown in Fig. 3a) and has been probed in detail with ultrafast optical and x-ray spectroscopies61. Because the light-induced LS→HS transition is quite fast, the kinetics of this effect cannot be measured by taking complete absorption spectra. Instead, it was determined by recording the time dependence of the absorption signal with the x-ray energy fixed at 708.1 eV (the intensity of the Fe L3 spectrum at this energy above the background is proportional to the HS content), while keeping the illumination on. The complete Fe L3 XA spectra recorded before and after such a timescan are used to ascertain the conversion of the spin states (cf. Supplementary Figure 6).

Fig. 3
figure 3

Light-induced LS→HS state transition and the eventual HS→LS state decay at low temperatures. a Schematic representation of the light-induced LS→HS state transition—the excitation of electrons from the LS state to the MLCT (metal-to-ligand charge transfer) states, and subsequent relaxation to the HS state via intermediate states—and the eventual decay of HS to the LS state; b light-induced LS → HS state transition at 5 K for the different coverages, and c the HS→LS relaxation of 0.35(4) ML at 8, 20, 30, and 40 K (dots). The solid lines are the result of a simultaneous fits to Equation (2) together with the SOXIESST rates. The step-like features at the data points are due to the SOXIESST (soft-x-ray-induced excited spin-state trapping) terms

The HS fraction as a function of illumination time is obtained by normalization of the recorded timescan signal between 0 (the LS state) and 1 (the HS state). Fitting the LS→HS transition with a single exponential function yields rate constants of 0.065(1), 0.0501(1), 0.0583(2), and 0.0823(1) s−1 for 0.35(4), 2.0(3), 3.9(5), and 10(1) ML, respectively. However, these rate constants consist of LIESST, as well as SOXIESST components; the latter arising from the x-ray exposure during the timescan. In order to separate the two, one can use the x-ray-induced LS→HS (SOXIESST) and HS→LS (reverse-SOXIESST) transition rate constants reported in the same system (0.8 ML of Fe-(bpz)bipy on HOPG) at the same temperature (5 K), which are 3.50(3) × 10−4 s−1 and 2.3(1) × 10−4 s−1, respectively53. The rate constants solely from LIESST are then estimated as 0.0369(1), 0.0505(1), 0.0589(2), and 0.0827(1) s−1 for 0.35(4), 2.0(3), 3.9(5), and 10(1) ML, respectively. With the green LED photon flux density of 4.2(8) × 1014 photons s−1 mm−2 (c.f. Methods), the corresponding effective cross sections are estimated as 0.009(2), 0.012(2), 0.014(3), and 0.019(4) Å2, respectively. Since each of the curves can be fitted by a mono-exponential function albeit with different rate constants, it is concluded that the light-induced LS→HS transition arises from an individual molecule–photon interactions without any role of cooperative effects. This result is in agreement with LIESST in bulk SCMs, where it is also found to be a single–molecule phenomenon48. The observed efficient switching of the spin states with light in these SCMs in contact with an HOPG surface can be exploited for applications in optical memory and display elements4.

Stability of light-induced HS state at low temperatures

Figure 3c shows the results of HS→LS relaxation measurements of 0.35(4) ML at 8, 20, 30, and 40 K. The measurements are done by firstly switching the sample to the HS state by green-LED illumination. With the illumination off, the subsequent spin relaxation is traced from Fe L3 spectra recorded as a function of time. The low-temperature HS→LS relaxation process is characterized by an initial fast relaxation and then slows down with time, leading to a stretched exponential. This is in sharp contrast to the bulk, where the HS state is rather stable in the temperature range considered here, and only in the thermally activated regime (>40 K), the spin relaxation becomes pronounced and exhibits sigmoidal characteristics54. The HS → LS relaxation observed on the surface can be modeled with a phenomenological equation involving a negative interaction parameter α:

$$\frac{{\partial \gamma _{\mathrm{HS}}}}{{\partial t}} = - k_{hl}{\kern 1pt} \gamma _{\mathrm{HS}}\,{\mathrm{exp}}\left[ {\alpha \left( {1 - \gamma _{\mathrm{HS}}} \right)} \right]$$

where khl denotes the HS → LS relaxation rate constant. Equation (2) is similar to the phenomenological model introduced by Hauser to explain the HS → LS relaxation in the bulk SCMs, but with α replaced by α/T in the thermally activated regime so as to account for the sigmoidal-type HS → LS relaxation behavior62. For an accurate modeling of the HS→LS relaxation, the x-ray-induced spin transitions occuring during the data acquisition, namely, k1 · (1 − γHS) for LS→HS and k2·γHS for HS→LS transitions have to be included in Equation (2)53. A simultaneous fit of Equation (2) to the spin relaxation measurements at all temperatures including the SOXIESST terms yields the value of the interaction parameter α to be −6.3(3). The relaxation measurements of 0.69(8) ML show a behavior similar to that of 0.35(4) ML (cf. Supplementary Figure 7). A comparison of ln(khl(T)) for both coverages is also given in Supplementary Figure 7. In comparison to the 0.69(8)-ML sample, the metastable HS state of the 0.35(4)-ML sample decays much more rapidly to the ground state (LS state) in the temperature range between 8 and 30 K (cf. Supplementary Figure 7). However, at 40 K, the relaxation rates become similar: 0.025(5) and 0.021(7) s−1 for the 0.35(4) and 0.69(8)-ML sample, respectively. In the bulk relaxation data provided in ref.54, the relaxation rate at 42 K is about three orders of magnitude lower than that of the submonolayer samples at 40 K. These differences in the decay rates might arise either from enhanced tunneling rates or a reduction in the energy barriers between the HS and LS wells; or a combination of both, in the submonolayer samples as compared to the bulk (the quantum tunneling rate is related to the characteristic vibrational frequency of the [FeN6] core62).


For SCMs in the bulk, the interaction parameters α and Γ are related by a constant, α = pΓ62. The constant p is inversely proportional to the characteristic vibrational frequency of the [FeN6] core and has a weaker dependence upon the vertical displacement as well as the horizontal displacement of the LS and HS wells through the reduced energy and the Huang-Rhys factor, respectively, which enter logarithmically62. The horizontal displacement is proportional to the Fe–N bond-length difference between the HS and LS states while the reduced energy is the ratio of the vertical displacement (ΔEhl, Fig. 3(a), the zero-point energy difference between the HS and LS wells) to the characteristic vibrational quanta of the [FeN6] core. Using the values of the parameters given in ref.54, p is estimated to be 1.3 × 10−3 J−1 mol for Fe(bpz)-bipy in the bulk. For the 0.35(4)-ML sample and assuming that the same relation still holds (given the negative values of both α and Γ), a value of p = 1.4(9) × 10−2 J−1 mol is obtained. The higher value of p by about an order of magnitude in the 0.35(4)-ML sample as compared to the bulk might be attributed to a reduced characteristic vibrational frequency of the [FeN6] core in the former, possibly due to molecule–substrate interactions. Alternatively, a distribution in the energy barriers between HS and LS states – arising from disorder or conformational flexibility of the ligand – can also result in a stretched exponential HS→LS relaxation, as reported in the case of some bulk SCMs exhibiting strong cooperativity in the temperature-induced spin transition, but nevertheless displaying a stretched-exponential spin relaxation due to such factors63,64. It is therefore not clear whether the stretched exponential decay results exclusively from an antagonistic (or anticooperative) spin transition. Regardless of the mechanism, it should be mentioned that this is the first report on the HS→LS relaxation of SCMs on a surface exhibiting a stretched exponential decay.

The buildup of cooperativity in molecular layers of only a few monolayers thickness indicates the presence of intermolecular interactions across the molecular layers. While a two-dimensional arrangement such as submonolayer islands exhibits an apparent antagonistic behavior arising either from interactions that favor unlike-spin states or from a distribution in the energy barriers between the two spin states, clear signs of cooperative spin switching are observed starting already from the second layer. The further increase in the degree of cooperativity with increasing thickness could be related to the higher coordination of molecules in the inner layers compared to the surface layers, the reduction in the relative amount of surface or interface molecules, and/or the reduced importance of molecules in direct contact with the substrate. It is interesting to compare the results presented here with spin-crossover nanoparticles, although the direct external environments of SCMs on the surface and those of nanoparticles are different in that the nanoparticles are always coated with a stabilizer which acts as a rigid matrix. Nevertheless, spin-crossover nanoparticles are also found to exhibit a gradual temperature-dependent spin-transition like the one observed here in the case of ultrathin films, but with the transition temperatures being proportional to the particles’ sizes. However, at particle sizes of less than 10 nm, hysteretic behavior (memory effects) appears – which have been attributed to an increase in the lattice stiffness leading to greater cooperative effects65. The presence (or absence) of hysteretic behavior in these ultrathin films of Fe(bpz)-bipy is not known, as the spin-state change in the opposite direction, i.e., temperature ramp-up from low- to room-temperature, has not been measured. It is worth noting that a small hysteresis of about 4 K has been reported in a relatively thick vacuum-deposited film (355 nm) of Fe(bpz)-bipy31, despite the absence of such a behavior in the bulk54,66. To the best of our knowledge, however, for vacuum-deposited films with thickness in the range of our samples – maximum thickness of about 12 nm – the presence of hysteresis has never been reported.

In summary, we have shown the complete thermal- and (highly efficient) light-induced spin-crossover of Fe(bpz)-bipy on the HOPG surface of coverages ranging from 0.35(4) ML to 10(1) ML. While a free-molecule-like spin-crossover around a monolayer is indicated, cooperativity is clearly evident in the double layer and at higher coverages as revealed by the transition width of the thermal-induced spin-crossover curves. The light-induced LS→HS state switching, on the other hand, is independent of cooperative effects. These findings are relevant for nanoscale applications relying on spin-state bistability.


Sample preparation

The SCM Fe(bpz)-bipy is synthesized according to the procedure reported by Real et al.66. The molecular powder is evaporated from a tantalum Knudsen cell at 160 °C at a pressure of ~2 × 10−9 mbar, and deposited onto the HOPG substrate held at room-temperature. The evaporation rate is controlled from the frequency change of a quartz crystal attached to the Knudsen cell. The HOPG substrate (ZYA) of dimension 12 × 12 × 2 mm3 and mosaic spread angle of 0.4(1)° is purchased from Structure Probe. The cleaving of the HOPG substrate with a carbon tape is performed (so as to obtain a clean surface) in a loadlock chamber maintained at ~10−7 mbar connected to the sample preparation chamber. The molecular coverage is estimated from integrated peak intensity of the Fe L3 spectrum and frequency shifts of the quartz crystal which is integrated with the evaporator. The details of the coverage estimation procedure are provided in Supplementary Figure 8 and Supplementary Notes 1.

X-ray absorption spectroscopy

The XAS measurements are performed in-situ at the high-field diffractometer of the beamline UE46-PGM1 and at the VEKMAG end-station of the beamline PM2 of BESSY II at a pressure of about 5 × 10−11 mbar and 1.5 × 10−10 mbar, respectively. The photon flux at the UE46-PGM1 beamline is reduced by a factor of about 15 by damping the beam with an Al-foil of thickness ~3 μm, such that the estimated photon flux is ~1 × 10photons s−1 mm−2; this is done in order to mitigate the soft-x-ray-induced excited spin state trapping (SOXIESST) at low temperatures53. At the PM2 beamline, the photon flux is estimated to be ~1.6 × 109 photons s−1 mm−2. The data shown in Figs. 1e, 2, 3b originates from the high-field diffractometer end-station, while the data shown in Fig. 3c was measured at the VEKMAG end-station. All spectra are recorded by means of total electron yield, where the sample drain current is recorded as a function of the x-ray photon energy and normalized to the photocurrent of a Au grid (a Pt grid in PM2-VEKMAG67) upstream to the experiment, and to the background signal from a clean HOPG substrate. The Fe L3 spectra are recorded at the magic angle 54.7° between the surface and the k vector of the linearly p-polarized x rays. At this angle, the XA resonance intensities are independent of the orientations of the molecular orbitals. The measurements involving light-induced effects at low temperatures were performed with a green LED of λ = 520 nm with a spectral width (fwhm) of 30 nm. The flux density at the sample position is estimated as 4.2(8) × 1014 photons s−1 mm−2. The details of the optical setup have been described elsewhere45.

Atomic force microscopy

In order to ascertain the efficacy in the deposition of the Fe(bpz)-bipy on the HOPG surface, atomic force microscopy (AFM) images of a series of submonolayer coverages have been recorded ex situ at room temperature. One such image is shown in Supplementary Figure 9; under ambient conditions, the molecules form nanoporous islands, quite similar to the structure of a submonolayer of [Fe(H2B(pz)2)2(phen)] on the same surface45. The line profile reveals an island height in the range of 1.0 nm, which is consistent with the height of a molecule. This is true for all the submonolayer coverages recorded. Although the morphology of the molecular islands in vacuum may be different, one can conclude that no 3D crystallites are formed and that all the molecules are in contact with the surface. The AFM (Nanotec Cervantes) measurements are carried out ex situ in ambient conditions in tapping mode using a Si cantilever of stiffness 2.7 N/m with a resonance frequency of 75 kHz.

Data Availability

All the relevant data can be obtained from the authors on reasonable request.

Change history

  • 08 August 2018

    The original HTML version of this Article was updated shortly after publication to add links the Transparent Peer Review file.


  1. Fert, A. Nobel lecture: Origin, development, and future of spintronics. Rev. Mod. Phys. 80, 1517–1530 (2008).

    ADS  Article  CAS  Google Scholar 

  2. Moth-Poulsen, K. & Bjornholm, T. Molecular electronics with single molecules in solid-state devices. Nat. Nanotechnol. 4, 551–556 (2009).

    ADS  Article  PubMed  CAS  Google Scholar 

  3. Song, H., Reed, M. A. & Lee, T. Single molecule electronic devices. Adv. Mater. 23, 1583–1608 (2011).

    Article  PubMed  CAS  Google Scholar 

  4. Kahn, O. & Martinez, C. J. Spin-transition polymers: from molecular materials toward memory devices. Science 279, 44–48 (1998).

    ADS  Article  CAS  Google Scholar 

  5. Salmon, L. et al. A novel approach for fluorescent thermometry and thermal imaging purposes using spin crossover nanoparticles. J. Mater. Chem. 20, 5499–5503 (2010).

    Article  CAS  Google Scholar 

  6. Shepherd, H. J. et al. Molecular actuators driven by cooperative spin-state switching. Nat. Commun. 4, 2607 (2013).

    Article  PubMed  CAS  Google Scholar 

  7. Linares, J., Codjovi, E. & Garcia, Y. Pressure and temperature spin crossover sensors with optical detection. Sensors 12, 4479–4492 (2012).

    Article  PubMed  CAS  Google Scholar 

  8. Cambi, L. & Szegö, L. Über die magnetische Susceptibilität der komplexen Verbindungen. Ber. Dtsch. Chem. Ges. 64, 2591–2598 (1931).

    Article  Google Scholar 

  9. Decurtins, S., Gütlich, P., Köhler, C., Spiering, H. & Hauser, A. Light-induced excited spin state trapping in a transition-metal complex: The hexa-1-propyltetrazole-iron (II) tetrafluoroborate spin-crossover system. Chem. Phys. Lett. 105, 1–4 (1984).

    ADS  Article  CAS  Google Scholar 

  10. Halcrow, M. A. (ed.). Spin-Crossover Materials: Properties and Applications. (John Wiley & Sons, Ltd., New York, 2013).

    Google Scholar 

  11. Gopakumar, T. G. et al. Electron-induced spin crossover of single molecules in a bilayer on gold. Angew. Chem. Int. Ed. 51, 6262–6266 (2012).

    Article  CAS  Google Scholar 

  12. Collison, D. et al. Soft x-ray induced excited spin state trapping and soft x-ray photochemistry at the Iron L2,3 edge in [Fe(phen)2(NCS)2] and [Fe(phen)2(NCSe)2] (phen=1, 10-phenanthroline). J. Chem. Soc., Dalton Trans. 0, 4371–4376 (1997).

    Article  CAS  Google Scholar 

  13. Miyamachi, T. et al. Robust spin crossover and memristance across a single molecule. Nat. Commun. 3, 938 (2012).

    Article  PubMed  CAS  Google Scholar 

  14. Frisenda, R. et al. Stretching-induced conductance increase in a spin-crossover molecule. Nano Lett. 16, 4733 (2016).

    ADS  Article  PubMed  CAS  Google Scholar 

  15. Lefter, C. et al. Current switching coupled to molecular spin-states in large-area junctions. Adv. Mater. 28, 7508–7514 (2016).

    Article  PubMed  CAS  Google Scholar 

  16. Aragonés, A. C. et al. Large conductance switching in a single-molecule device through room temperature spin-dependent transport. Nano Lett. 16, 218–226 (2016).

    ADS  Article  PubMed  CAS  Google Scholar 

  17. Coronado, E., Galán-Mascarós, J., Monrabal-Capilla, M., García-Martínez, J. & Pardo-Ibáñez, P. Bistable spin-crossover nanoparticles showing magnetic thermal hysteresis near room temperature. Adv. Mater. 19, 1359–1361 (2007).

    Article  CAS  Google Scholar 

  18. Prins, F., Monrabal-Capilla, M., Osorio, E. A., Coronado, E. & van der Zant, H. S. J. Room-temperature electrical addressing of a bistable spin-crossover molecular system. Adv. Mater. 23, 1545–1549 (2011).

    Article  PubMed  CAS  Google Scholar 

  19. Holovchenko, A. et al. Near room-temperature memory devices based on hybrid spin-crossover@SiO2 nanoparticles coupled to single-layer graphene nanoelectrodes. Adv. Mater. 28, 7228–7233 (2016).

    Article  PubMed  CAS  Google Scholar 

  20. Sessoli, R., Gatteschi, D., Caneschi, A. & Novak, M. A. Magnetic bistability in a metal-ion cluster. Nature 365, 141–143 (1993).

    ADS  Article  CAS  Google Scholar 

  21. Cornia, A., Mannini, M., Sainctavit, P. & Sessoli, R. Chemical strategies and characterization tools for the organization of single molecule magnets on surfaces. Coord. Chem. Rev. 40, 3076–3091 (2011).

    CAS  Google Scholar 

  22. Holmberg, R. J. & Murugesu, M. Adhering magnetic molecules to surfaces. J. Mater. Chem. C 3, 11986–11998 (2015).

    Article  CAS  Google Scholar 

  23. Sessoli, R. Materials science: Magnetic molecules back in the race. Nature 548, 400–401 (2017).

    ADS  Article  PubMed  CAS  Google Scholar 

  24. Venkataramani, S. et al. Magnetic bistability of molecules in homogeneous solution at room temperature. Science 331, 445–448 (2011).

    ADS  Article  PubMed  CAS  Google Scholar 

  25. Milek, M., Heinemann, F. W. & Khusniyarov, M. M. Spin crossover meets diarylethenes: efficient photoswitching of magnetic properties in solution at room temperature. Inorg. Chem. 52, 11585–11592 (2013).

    Article  PubMed  CAS  Google Scholar 

  26. Rösner, B. et al. Reversible photoswitching of a spin-crossover molecular complex in the solid state at room temperature. Angew. Chem. Int. Ed. 54, 12976–12980 (2015).

    Article  CAS  Google Scholar 

  27. Shalabaeva, V. et al. Vacuum deposition of high-quality thin films displaying spin transition near room temperature. J. Mater. Chem. C 5, 4419–4425 (2017).

    Article  CAS  Google Scholar 

  28. Naggert, H. et al. First observation of light-induced spin change in vacuum deposited thin films of iron spin crossover complexes. Dalton. Trans. 40, 6364 (2011).

    Article  PubMed  CAS  Google Scholar 

  29. Shi, S. et al. Study of molecular spin-crossover complex Fe(phen)2(NCS)2 thin films. Appl. Phys. Lett. 95, 043303 (2009).

    ADS  Article  CAS  Google Scholar 

  30. Mahfoud, T. et al. Electrical properties and non-volatile memory effect of the [Fe(HB(pz)3)2] spin crossover complex integrated in a microelectrode device. Appl. Phys. Lett. 99, 053307 (2011).

    ADS  Article  CAS  Google Scholar 

  31. Palamarciuc, T. et al. Spin crossover materials evaporated under clean high vacuum and ultra-high vacuum conditions: from thin films to single molecules. J. Mater. Chem. 22, 9690–9695 (2012).

    Article  CAS  Google Scholar 

  32. Ellingsworth, E. C., Turner, B. & Szulczewski, G. Thermal conversion of [Fe(phen)3](SCN)2 thin films into the spin crossover complex Fe(phen)2(NCS)2. RSC Adv. 3, 3745 (2013).

    Article  CAS  Google Scholar 

  33. Bernien, M. et al. Spin crossover in a vacuum-deposited submonolayer of a molecular Fe(II) complex. J. Phys. Chem. Lett. 3, 3431–3434 (2012).

    Article  PubMed  CAS  Google Scholar 

  34. Naggert, H. et al. Vacuum-evaporable spin-crossover complexes: physicochemical properties in the crystalline bulk and in thin films deposited from the gas phase. J. Mater. Chem. C 3, 7870–7877 (2015).

    Article  CAS  Google Scholar 

  35. Davesne, V. et al. Hysteresis and change of transition temperature in thin films of Fe[Me2Pyrz]3BH2, a new sublimable spin-crossover molecule. J. Chem. Phys. 142, 194702 (2015).

    ADS  Article  PubMed  CAS  Google Scholar 

  36. Ossinger, S. et al. Vacuum-evaporable spin-crossover complexes in direct contact with a solid surface: Bismuth versus gold. J. Mater. Chem. C 121, 1210–1219 (2017).

    CAS  Google Scholar 

  37. Jasper-Tönnies, T. et al. Deposition of a cationic FeIII spin-crossover complex on Au(111): impact of the counter ion. J. Phys. Chem. Lett. 8, 1569–1573 (2017).

    Article  PubMed  CAS  Google Scholar 

  38. Iasco, O. et al. The disentangling of hysteretic spin transition, polymorphism and metastability in bistable thin films formed by sublimation of bis(scorpionate) Fe(II) molecules. J. Mater. Chem. C 5, 11067–11075 (2017).

    Article  CAS  Google Scholar 

  39. Gruber, M. et al. Spin state of spin-crossover complexes: from single molecules to ultrathin films. Phys. Rev. B 89, 195415 (2014).

    ADS  Article  CAS  Google Scholar 

  40. Gopakumar, T. G. et al. Spin-crossover complex on Au(111): structural and electronic differences between mono- and multilayers. Chem. Eur. J. 19, 15702–15709 (2013).

    Article  PubMed  CAS  Google Scholar 

  41. Warner, B. et al. Temperature- and light-induced spin crossover observed by x-ray spectroscopy on isolated Fe(II) complexes on gold. J. Phys. Chem. Lett. 4, 1546–1552 (2013).

    Article  PubMed  CAS  Google Scholar 

  42. Alam, M. S. et al. Spin-state patterns in surface-grafted beads of iron(II) complexes. Angew. Chem. Int. Ed. 49, 1159–1163 (2010).

    Article  CAS  Google Scholar 

  43. Bairagi, K. et al. Molecular-scale dynamics of light-induced spin cross-over in a two-dimensional layer. Nat. Commun. 7, 12212 (2016).

    ADS  Article  PubMed  PubMed Central  CAS  Google Scholar 

  44. Beniwal, S. et al. Surface-induced spin state locking of the [Fe(H2B(pz)2)2(bipy)] spin crossover complex. J. Phys. Condens. Matter 28, 206002 (2016).

    ADS  Article  PubMed  CAS  Google Scholar 

  45. Bernien, M. et al. Highly efficient thermal and light-induced spin-state switching of an Fe(II) complex in direct contact with a solid surface. ACS Nano 9, 8960–8966 (2015).

    Article  PubMed  CAS  Google Scholar 

  46. Pronschinske, A. et al. Modification of molecular spin crossover in ultrathin films. Nano Lett. 13, 1429–1434 (2013).

    ADS  Article  PubMed  CAS  Google Scholar 

  47. Spiering, H. Topics in Current Chemistry Vol. 235 (Springer Berlin Heidelberg, 2004).

  48. Gütlich, P., Hauser, A. & Spiering, H. Thermal and optical switching of iron(II) complexes. Angew. Chem. Int. Ed. 33, 2024–2054 (1994).

    Article  Google Scholar 

  49. Geim, A. K. & Novoselov, K. S. The rise of graphene. Nat. Mater. 6, 183 (2007).

    ADS  Article  PubMed  CAS  Google Scholar 

  50. Slichter, C. & Drickamer, H. Pressure induced electronic changes in compounds of Iron. J. Chem. Phys. 56, 2142–2160 (1972).

    ADS  Article  CAS  Google Scholar 

  51. Stöhr, J. (ed.). NEXAFS Spectroscopy Vol. 25 (Springer-Verlag: Berlin, Heidelberg, 1992).

    Google Scholar 

  52. Cartier dit Moulin,  C., Rudolf, P., Flank, A. M. & Chen, C. T. Spin transition evidenced by soft x-ray absorption spectroscopy. J. Phys. Chem. 96, 6196–6198 (1992).

    Article  Google Scholar 

  53. Kipgen, L. et al. Soft-x-ray-induced spin-state switching of an adsorbed Fe(II) spin-crossover complex. J. Phys. Condens. Matter 29, 394003 (2017).

    Article  PubMed  Google Scholar 

  54. Moliner, N. et al. Thermal and optical switching of molecular spin states in the [FeL[H2B(pz)2]2] spin-crossover system (L = bpy, phen). J. Phys. Chem. B 106, 4276 (2002).

    Article  CAS  Google Scholar 

  55. Bousseksou, A., Molnár, G., Salmon, L. & Nicolazzi, W. Molecular spin crossover phenomenon: recent achievements and prospects. Coord. Chem. Rev. 40, 3313–3335 (2011).

    CAS  Google Scholar 

  56. Kepenekian, M., Le Guennic, B. & Robert, V. Primary role of the electrostatic contributions in a rational growth of hysteresis loop in spin-crossover Fe(II) complexes. J. Am. Chem. Soc. 131, 11498–11502 (2009).

    Article  PubMed  CAS  Google Scholar 

  57. Kepenekian, M., Le Guennic, B. & Robert, V. Magnetic bistability: From microscopic to macroscopic understandings of hysteretic behavior using ab initio calculations. Phys. Rev. B 79, 094428 (2009).

    ADS  Article  CAS  Google Scholar 

  58. Zimmermann, R. & König, E. A model for high-spin/low-spin transitions in solids including the effect of lattice vibrations. J. Phys. Chem. Solids 38, 779–788 (1977).

    ADS  Article  CAS  Google Scholar 

  59. Cantin, C., Kliava, J., Marbeuf, A. & Mikaïlitchenko, D. Cooperativity in a spin transition ferrous polymer: Interacting domain model, thermodynamic, optical and EPR study. Eur. Phys. J. B 12, 525–540 (1999).

    ADS  Article  CAS  Google Scholar 

  60. Groizard, T., Papior, N., Le Guennic, B., Robert, V. & Kepenekian, M. Enhanced cooperativity in supported spin-crossover metalorganic frameworks. J. Phys. Chem. Lett. 8, 3415–3420 (2017).

    Article  PubMed  CAS  Google Scholar 

  61. Zhang, W. et al. Tracking excited-state charge and spin dynamics in iron coordination complexes. Nature 509, 345–348 (2014).

    ADS  Article  PubMed  PubMed Central  CAS  Google Scholar 

  62. Hauser, A., Jeftić, J., Romstedt, H., Hinek, R. & Spiering, H. Cooperative phenomena and light-induced bistability in iron(II) spin-crossover compounds. Coord. Chem. Rev. 190–192, 471–491 (1999).

    Article  Google Scholar 

  63. Mishra, V. et al. Temperature-dependent interactions and disorder in the spin-transition compound [FeII(L)2][ClO4]2C7H8 through structural, calorimetric, magnetic, photomagnetic, and diffuse reflectance investigations. Inorg. Chem. 47, 7577–7587 (2008).

    Article  PubMed  CAS  Google Scholar 

  64. Enachescu, C. et al. Nonexponential relaxation of the metastable state of the spin-crossover system [Fe(L)2](ClO4)2H2O [L = 2,6-Bis(pyrazol-1-ylmethyl)pyridine]. Inorg. Chem. 43, 4880–4888 (2004).

    Article  PubMed  CAS  Google Scholar 

  65. Mikolasek, M. et al. Finite size effects in molecular spin crossover materials. New J. Chem. 38, 1834–1839 (2014).

    Article  CAS  Google Scholar 

  66. Real, J. A., Muñoz, M. C., Faus, J. & Solans, X. Spin crossover in novel dihydrobis(1-pyrazolyl)borate [H2B(pz)2]-containing Fe(II) complexes. Synthesis, x-ray structure, and magnetic properties of [FeL(H2B(pz)2)2] (L = 1,10-Phenanthroline and 2,2-Bipyridine). Inorg. Chem. 36, 3008 (1997).

    Article  PubMed  CAS  Google Scholar 

  67. Noll, T. & Radu, F. in: Proc. MEDSI2016, Barcelona, Spain, September 11–16, 2016, 9 (ed. Schaa, V. R. W.) 370–373 (JACoW, Geneva, Switzerland, 2017).

Download references


Financial support by the DFG through SFB 658, SFB 677, and SFB/TRR 227 is gratefully acknowledged. L.M.A. acknowledges funding from CAPES (No. 9469/13-3). The x-ray absorption measurements were carried out at the high-field diffractometer and at the VEKMAG end-stations of the UE46-PGM1 and PM2-VEKMAG beamlines, respectively, of BESSY II, Helmholtz-Zentrum Berlin (HZB). We thank the HZB for the allocation of synchrotron radiation beamtime. Financial support for developing and building the PM2-VEKMAG beamline and VEKMAG end-station was provided by HZB and BMBF (05K10PC2, 05K10WR1, 05K10KE1), respectively. Steffen Rudorff is acknowledged for technical support.

Author information

Authors and Affiliations



S.O. and H.N. synthesized the molecules. The XAS experiments were conceived by M.B., L.K., F.N., E.S, E.W. and performed by M.B., L.K, F.N., A.J.B., L.M.A. under the supervision of E.S, E.W., C.Lu., H.R., and F.R. The analyses is done by L.K. and M.B. L.K. performed and analyzed the AFM measurements and is supervised by C.Lo. The results were interpreted by L.K., M.B., F.T. and W.K. The project is supervised by F.T. and W.K. L.K. and W.K. co-wrote the manuscript. All authors discussed the results and contributed to the manuscript.

Corresponding authors

Correspondence to Lalminthang Kipgen or Wolfgang Kuch.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Kipgen, L., Bernien, M., Ossinger, S. et al. Evolution of cooperativity in the spin transition of an iron(II) complex on a graphite surface. Nat Commun 9, 2984 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing