The applications of lanthanide-doped upconversion nanomaterials are limited by unsatisfactory brightness currently. Herein, a general strategy is proposed for boosting the upconversion efficiency in Er3+ ions, based on combined use of a core−shell nanostructured host and an integrated optical waveguide circuit excitation platform. A NaErF4@NaYF4 core−shell nanoparticle is constructed to host the upconversion process for minimizing non-radiative dissipation of excitation energy by surface quenchers. Furthermore, an integrated optical microring resonator is designed to promote absorption of excitation light by the nanoparticles, which alleviates quenching of excited states due to cross-relaxation and phonon-assisted energy transfer. As a result, multiphoton upconversion emission with a large anti-Stokes shift (greater than 1150 nm) and a high energy conversion efficiency (over 5.0%) is achieved under excitation at 1550 nm. These advances in controlling photon upconversion offer exciting opportunities for important photonics applications.
Lanthanide-doped upconversion nanoparticles that convert low energy excitation into higher-energy emissions are important for applications in diverse fields ranging from life science to information technology. By integrating upconversion nanoparticles into various systems, localized visible and ultraviolet (UV) emissions can be generated upon near-infrared (NIR) excitation. The effect has enabled precise and remote control of biochemical reactions as well as the creation of full-color 3D displays1,2,3,4,5,6,7. Nevertheless, despite of the unique optical properties, wider application of upconversion processes has been hindered by limited emission intensity due to low concentration of optical centers (or dopants) in most nanoparticles. When dopant concentration increases, interactions of optical centers become significant as a result of reduced inter-dopant distance, causing depopulation of excited states and thus attenuation in the upconversion emission (Fig. 1).
Attempts have been made to alleviate concentration quenching so that unusually high dopant concentrations can be used to boost upconversion emission intensity. By promoting the excitation process through the use of high excitation irradiance (~106 W cm−2) and dye sensitization, depopulations of excited states are compensated and lead to elevated quenching concentrations of Tm3+, Er3+, and Nd3+ activators8,9,10. Core−shell nanostructural engineering has also been exploited to mitigating concentration quenching by eliminating dissipation of energy to lattice and surface defects. Using this method, concentration quenching in both sensitizer (Yb3+) and activator (Er3+) ions is greatly suppressed11,12,13,14,15,16,17. Despite these research efforts, photon upconversion at a high concentration of activators is usually dominated by low-order processes featuring emission in the spectral region of long wavelengths. Challenges remain for achieving highly efficient multiphoton upconversion with emissions in the short-wavelength regime by using low power excitation. Particularly, there are no known effective approaches to achieve efficient UV emission under excitation in the wavelength range for optical communication, where many inexpensive and high-performance lasers and optical components can be readily acquired from the mature telecommunications industry.
Here, we present rational control of concentration quenching in a stoichiometric Er3+ compound by combined use of a core−shell nanostructured host and an integrated optical waveguide circuit excitation platform. We show an experimental validation of enhancing multiphoton UV upconversion under excitation at 1550 nm, corresponding to an anti-Stokes shift of over 1150 nm, through collective control of intra-particle energy transfer and excitation method. By taking advantage of the efficient 1550 nm-to-UV upconversion, we further demonstrate a novel technique for precise formation of polymer waveguides and periodic patterns with the upconverted UV emission.
Synthesis and characterization
We first investigated the behaviors of concentration quenching in different energy states of Er3+, which has not been clearly delineated18. To this end, we conduct a comparative investigation of a series of NaYF4:Er (2−100%) nanoparticles with and without a protection layer of NaYF4. The inert NaYF4 shell is able to selectively suppress energy loss to lattice defects and surface quenching sites that arises from energy migration through the dopant sublattice19. Assessment of the core−shell nanoparticles thereby allows us to probe the quenching mechanism. The nanoparticles were synthesized by a layer-by-layer epitaxial growth protocol (Supplementary Fig. 1)20. Figure 2a shows transmission electron microscopy (TEM) images of the nanoparticles comprising different concentration of Er3+, revealing highly uniform size and shape across the whole concentration series. High-angle annular dark-field (HAADF) scanning TEM image of a representative sample shows distinguished Z-contrast between the NaErF4 and NaYF4 layers (Fig. 2b), clearly revealing the core−shell nature of the nanoparticles. The X-ray powder diffraction (XRD) and high-resolution TEM (Supplementary Figs. 1 and 2) measurements further confirm high crystallinity of the nanoparticles with a single hexagonal phase. The consistent structural feature qualifies these nanoparticles as model platforms for investigating the effects of dopant concentration on upconversion properties.
Concentration quenching effect
We studied the lifetimes of several energy states of Er3+, which are all involved in the upconversion process and may be subject to concentration quenching (Fig. 2c and Supplementary Fig. 3). Because the decay curves were found to display an appreciable dependence on excitation power density due to intra-particle energy transfer (Supplementary Fig. 4), the dopant concentration-induced changes in lifetimes were examined under the same excitation power density. Figure 2d shows the lifetimes for the major excited states of Er3+ as a function of dopant concentration in the core nanoparticles (see Supplementary Fig. 5 for the decay curves). In accord with concentration-induced quenching, the lifetimes for the excited states under study all drop quickly with increasing Er3+ concentration, which is consistent with the steady-state spectral measurement of the core nanoparticles. By contrast, the NaYF4-coated core−shell counterparts showed much longer lifetimes especially when Er3+ concentrations are high (Fig. 2e), indicating largely alleviated quenching processes.
It is noted that the dependence of lifetime on Er3+ concentration is not uniform for different excited states (Fig. 2e). Therefore, concentration quenching of individual excited state is dominated by different processes (Fig. 3a). Lifetimes of the 4I11/2 and 4I13/2 states are mostly preserved as Er3+ concentration increases, revealing a major role of energy migration to quenching centers in depopulating these two states. Core−shell nanostructures confine energy migration and prevent energy trapping by quenching centers21,22. In comparison, decay rates of the 4S3/2, 4F9/2, and 4I9/2 states are appreciably accelerated by elevating Er3+ concentrations. The lifetime gradient was unlikely to level off by enhancing surface protection through the use of thicker shells (Supplementary Figs. 6−8). Thus, these three states largely suffered from depopulation by cross-relaxation and phonon-assisted energy transfer, which are localized processes and remain active in nanostructured hosts.
The steady-state spectra agree with the time decay studies that not all the excited states were equally protected in the core−shell nanoparticles (Fig. 3b and Supplementary Fig. 8b). In line with effective suppression of depopulation in the 4I11/2 and 4I13/2 states, the emission originating from the 4F9/2 state (658 nm) was considerably enhanced at high Er3+ concentrations. By contrast, emissions at short wavelengths are only marginally intensified, resulting in decreased relative intensity ratio of green to red emissions at elevated Er3+ concentrations. The observations are ascribed to quenching of the 4S3/2, 4F9/2, and 4I9/2 states by cross-relaxation and phonon-assisted energy transfer (Fig. 3a). As these intermediate states are critical for establishing the population in the higher-lying 2H9/2 and 4G11/2 states, the blue and violet emissions are extremely weak relative to the red emission. Concentration quenching of the emitting states (2H9/2 and 4G11/2) also accounts for the weak emissions at the short-wavelength end (Supplementary Fig. 9).
To shed more light on the concentration quenching effect, we calculated the relative oscillator strength (ROS) of each excited state as a function of Er3+ concentration on the overall core−shell model23. In general, the ROS grows near-linearly as Er3+ concentration increases to 50% (Fig. 3c), which is ascribed to increasing number of optical centers in the nanoparticles. With further increase of Er3+ concentration to 75%, abnormal increases of the ROSs were noted for the 4F9/2, 4I9/2, 4I11/2, and 4I13/2 states. The leap of the ROS corroborates de-excitation of the higher-lying excited states due to concentration quenching, which accounts for the elevated population in the low-lying ones. The drop of ROSs for the 4I11/2 and 4I13/2 states at a substantially high Er3+ concentration (100%) is attributed to the enhancement of energy transfer upconversion that depletes these two states (Supplementary Fig. 10)13.
The mechanistic investigation reveals that the use of core−shell nanostructure alone is unable to alleviate concentration quenching in all the energy states of Er3+. In order to achieve efficient multiphoton upconversion luminescence, joint use of high excitation power is also crucial to counteract the depopulation of the high-lying intermediate states. In an upconversion process, an intermediate state is depopulated by being excited to a higher-lying state in addition to linear decay to lower-lying states. The excitation process is pump power dependent and thus upconversion emission dominates over luminescence quenching under high excitation powers24.
Microring resonator-assisted excitation of upconversion
In view of the small absorption cross-section of the lanthanide ions (~10−21 cm2)25, conventional approaches for enhancing the upconversion rates are focused on increasing the excitation intensity and/or localizing the illumination field. Attempts have been made to modulate excitation field around upconversion nanoparticles by surface-plasmon coupling and photonic-crystal engineering26,27. However, these methods need tedious processing of upconversion nanoparticles and the amplification of optical field may prove to be limited. Here we propose a more effective approach to enhance the upconversion by using an optical microring resonator excitation platform (Fig. 4a). The integrated waveguide circuit increases the interaction length between the excitation photons with the nanoparticles. When it is on resonance, the excitation light circulates in the microring resonator by a number of times proportional to its Q-factor. As the circulating light cumulates, the optical field in the microring resonator can also be enhanced by orders of magnitude28. Thus, the chance for the photon to be absorbed by the nanoparticles will be markedly increased.
The microring resonator used in this work is composed of high-index doped silica glass that is semi-buried within a SiO229. In this application, the surface of the chip is polished flat with the surface of the core waveguide exposed (Supplementary Fig. 11). Upconversion nanoparticles are applied on the surface of the substrate and excited by evanescent fields of the waveguides. A narrow linewidth tunable continuous-wave laser is used to tune the input excitation on/off resonance of the resonator. While on resonance, the input signal circulates within the resonator in phase, thereby affording a much stronger electric field relative to that in the straight waveguide (Fig. 4b). Importantly, due to high wavelength-selectivity of the ring resonator (Supplementary Fig. 12), circulation of incident light can be disabled by subtle detuning of wavelength (<0.01 nm), which permits in situ examination of the enhancement effect28,29,30,31,32,33,34,35.
Figure 4c depicts upconversion property of NaErF4@NaYF4 core−shell nanoparticles sitting on the waveguide structure. At a constant input power of 20 mW, the microring resonator provided a largely amplified excitation density with respect to the straight bus waveguide (2300 versus 133 kW cm−2) (Supplementary Fig. 13). Accordingly, upconversion luminescence, especially emission in the short-wavelength region, was appreciably enhanced when the resonance status was changed by tuning the wavelength of incident light from 1550.00 nm (off-resonance) to 1549.47 nm (on-resonance). Correspondingly, we recorded an increase of energy conversion efficiency from 1.1 to 5.0% (Supplementary Fig. 14). The results clearly support reduced quenching in the intermediate states at a high excitation power density. It is worth noting that the actual energy conversion efficiency offered by the ring resonator is underestimated by the current experimental setup, which inevitably suffers from interference of the less efficient upconversion processes occurring at the long bus waveguide (inset of Fig. 4c). Due to effective alleviation of concentration quenching, UV lasing was achieved from NaErF4@NaYF4 nanoparticles incorporated into a microdisk laser cavity (Supplementary Fig. 15)36.
The microring resonator circuit is versatile for providing amplified excitation to upconversion particles, without the need for controlling their assembly on the waveguide (Supplementary Fig. 16). However, the magnitude of upconversion enhancement was found to depend on nanoparticle composition and input power (Supplementary Fig. 17). In general, the enhancement effect weakens with increasing excitation power and Er3+ concentration due to saturation of upconversion emissions in the high-power regime (Supplementary Fig. 17b). However, the use of highly Er3+-doped nanoparticles is essential for achieving bright multiphoton upconversion in the short-wavelength regime. As Er3+ concentration decreases, both UV emission intensity and UV-to-visible intensity ratio decrease rapidly at the same excitation power (Fig. 4d, e). The observations are ascribed to a reduction in density of optical carriers, which diminish the absorption of surplus excitation light. A low Er3+ content also disfavors interionic interaction and thus inhibits the efficient energy transfer upconversion process.
Micropatterning through upconversion
The availability of intense UV emission from the surface of the waveguide structures offers a great opportunity for microfabrication of fine structures and patterns on them to modify their optical responses or to form advanced devices when incorporated with functional polymers37,38,39,40,41,42,43,44. As a proof of concept, we demonstrate the precise fabrication of an SU-8 polymer waveguide on top of the microring resonator (Fig. 5a). The procedure involves sequential deposition of upconversion nanoparticles and SU-8 on the resonator substrate by drop-casting and spin-coating, respectively (Supplementary Fig. 18). Selective exposure of the SU-8 film is achieved by the locally upconverted UV light in the region of the ring resonator under on-resonance excitation (Fig. 5b). Our study shows that curing of a 2 μm thick SU-8 waveguide can be accomplished in <10 min by excitation of only 20 μW near 1550 nm. After developing, the SU-8 copies the ring structure well on the substrate with a perfect alignment and a smooth surface (Fig. 5d and Supplementary Fig. 19). Notably, this approach is simple and fast for controllable curing of photoresists without the need for a photomask or control of laser scanning, which provides a powerful addition to existing techniques for photopatterning of polymers45,46.
The same methodology can be adopted to fabricate periodic structures on waveguides utilizing their own interference patterns. By using a simple channel waveguide with core index (n = 1.60) that is slightly higher than the SU-8 index (n = 1.57) (Supplementary Fig. 20), strong intensity patterns from the coupling between its odd and even modes were created and modulated the solidification of the SU-8 (Fig. 5d–f). The observed period at an SU-8 thickness of 0.5 μm is around 25 μm (Fig. 5f), which is in consistence with the calculated beat period (Λ) by the FEM method (Fig. 5g–i). In agreement with the beating between the odd and even modes of the waveguide, we further achieved tuning of the pattern period by controlling the thickness of the SU-8 coating (Supplementary Fig. 21). These findings demonstrate one promising approach for rapid fabrication of periodic structures through photolithography.
The investigation of photon upconversion in a core−shell nanostructured NaErF4 crystal under an integrated optical waveguide circuit excitation platform enables improved understanding and control of concentration quenching. The ability to mitigate complex concentration quenching in a multitude of lanthanide excited states consolidates the position of using high dopant concentration as a versatile approach for enhancing multiphoton upconversion. On a separate note, the realization of efficient UV emission by excitation in the wavelength range for optical communications would largely promote photonic applications of upconversion nanomaterials.
The oscillator strengths were derived from calculated electric-dipole transitions by time-dependent density functional theory (TD-DFT). To perform the excited state calculations, we chose the two-electron based Tamm-Dancoff approximation imported from self-consistently corrected ground state wavefunctions23. β-NaREF4 comprising different amount of Er3+ dopants (12.5–100%) were examined by a series of TD-DFT calculations. The electrical field in the microring resonator was simulated by three-dimensional finite-difference time domain (3D-FDTD) method. Finite element method (FEM) was used to calculate the modal propagation constants and field profiles of E-field.
TEM and HAADF scanning TEM were carried out on a JEM-2100F transmission electron microscope at an acceleration voltage of 200 kV. The upconversion emission spectra were recorded with a Hitachi F-4600 spectrophotometer. The decay curves were measured by an Edinburgh FLSP920 spectrometer. Optical micrographs were recorded with an advanced research microscope (ECLIPSE Ni-U, Nikon). All measurements were performed at room temperature.
The data that support the findings of this study are available from the corresponding author upon request.
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This work was supported by the National Natural Science Foundation of China (Nos. 21573185, 21773200 and 51332008) and the Research Grants Council of Hong Kong (CityU 11208215 and CityU 11204717). The authors thank Prof. X. Xie for help with HAADF scanning TEM measurement.
The authors declare no competing interests.
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Sun, T., Li, Y., Ho, W.L. et al. Integrating temporal and spatial control of electronic transitions for bright multiphoton upconversion. Nat Commun 10, 1811 (2019). https://doi.org/10.1038/s41467-019-09850-2
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