Upconversion Luminescence Intensity Research Articles

Equal Rights for Activators – Ytterbium to Terbium Cooperative Sensitization in Molecular Upconversion

Equal Rights for Activators – Ytterbium to Terbium Cooperative Sensitization in Molecular Upconversion

Behavior of Microstrain in Nd3+-Sensitized Near-Infrared Upconverting Core-Shell Nanocrystals for Defect-Induced Tailoring of Luminescence Intensity.

In an attempt to optimize the upconversion luminescence (UCL) output of a Nd3+-sensitized near-infrared (808 nm) upconverting core-shell (CS) nanocrystal through deliberate incorporation of lattice defects, a comprehensive analysis of microstrain both at the CS interface and within the core layer was performed using integral breadth calculation of high-energy synchrotron X-ray (λ = 0.568551 Å) diffraction. An atomic level interpretation of such microstrain was performed using pair distribution function analysis of the high-energy total scattering. The core NC developed compressive microstrain, which gradually transformed into tensile microstrain with the growth of the epitaxial shell. Such a reversal was rationalized in terms of a consistent negative lattice mismatch. Upon introduction of lattice defects into the CS systems upon incorporation of Li+, the corresponding UCL intensity was maximized at some specific Li+ incorporation, where the tensile microstrain of CS, compressive microstrain of the core, and atomic level disorders exhibited their respective extreme values irrespective of the activator ions.

Enhancement of Upconversion Luminescence through Three-Dimensional Design of Plasma Ti3O5-Coupled Structural Domain-Limiting Effects.

Upconversion luminescence plays a crucial role in various technological applications, and among the various valence states of lanthanide elements, Ln3+ has the highest stability. The 4f orbitals of these elements are in a fully empty, semifull, or full state. This special 4f electron configuration allows them to exhibit rich discrete energy levels. However, the 4f-4f transition of Ln3+ rare earth ions itself is prohibited, resulting in a lower luminescence efficiency. This limitation greatly hinders the practical application of upconversion luminescence. In this study, we report nanostructured luminescence-enhanced substrate platforms with both semiconductive local surface plasmons and spatially confined domain effects on a single defect semiconductor substrate. By coupling NaYF4:Yb-Er nanoparticle emitters to the surface of Ti3O5 NC-arrays plasmonic nanostructures, an ultrabright luminescence with a 32-fold increase in green emission and a 40-fold increase in red emission was achieved. Furthermore, the fluorescence resonance energy transfer characteristics observed in the R6G/NaYF4/Ti3O5 NC-array composite film enable accurate detection of fluorescent molecules. The results provide an innovative and intelligent approach to enhance the upconversion luminescence intensity of rare-doped nanoparticles and develop highly sensitive molecular detection systems based on the above luminescence enhancement.

Novel CeF3:Tm3+, Er3+ nanoparticles: NIR up-down conversion luminescence properties based on energy transfer of Tm3+ and Ce3+

A novel CeF3:Tm3+, Er3+ NIR up-down conversion luminescent nanoparticles with highly efficient visible and near-infrared second window (NIR-II) emission were synthesized by direct precipitation and hydrothermal methods. The two different emission modes of visible-NIR II light of Er3+were realized through the energy transfer of Tm3+ and Ce3+at the excitation wavelength of 808 nm. Which successfully combined the narrow emission peaks of visible light and the deep tissue penetration advantage of NIR-II. First, the effects of preparation conditions on the structure, morphology, stability and luminescence properties of CeF3:Tm3+, Er3+ nanoparticles were analyzed by XRD, SEM, TEM and PL. The results showed that the crystallinity, morphology and luminescence intensity of CeF3:Tm3+,Er3+ nanoparticles produced by hydrothermal method (reaction time of 10 h) were optimal compared with that of direct precipitation method. CeF3: Tm3+,Er3+ nanoparticles has better thermal stability, and fluorescence lifetime of 5D0→7F2 (525 nm), 4I15/2→4I11/2 (1066 nm) and 4I15/2→4I13/2 (1386 nm) for Er3+ are 15.51 ns, 48.78 us and 57.06 us, separately. At the same time, the surface of CeF3:Tm3+, Er3+ nanoparticles was modified by PEG and Lys. And then the effects of the surface modification on the hydration size, zeta potential and up-down conversion luminescent properties (visible and NIR-II light emission) were investigated. The results show that the modification of PEG effectively slows down the agglomeration of CeF3:Tm3+, Er3+ nanoparticles and improves their stability and dispersion under the same conditions. More importantly, the modification of PEG effectively increases the up-conversion luminescence intensity of CeF3:Tm3+, Er3+ nanoparticles under 808 nm excitation. Moreover, the CeF3:Tm3+, Er3+-PEG nanoparticles with 20–40 nm showed stronger NIR up-down conversion emission intensity in aqueous solutions (pH = 5,6,7) and better thermal stability. Furthermore, the CeF3:Tm3+, Er3+-PEG nanoparticles has low cytotoxicity and good biocompatibility. This study provides a theoretical basis for the development of high-performance rare-earth NIR up-down conversion luminescence materials.

Ultrasensitive upconverting nanoprobes for in situ imaging of drug-induced liver injury using miR-122 as the biomarker

Drug-induced liver injury (DILI) is a frequent adverse drug reaction. The current clinical diagnostic methods are inadequate for accurate and early detection of DILI due to the lack of effective diagnostic biomarkers. Hepatocyte-specific miR-122 is released from injured hepatocytes promptly and its efflux is significantly correlated with the progression of DILI. Therefore, achieving precise in situ detection of miR-122 with high sensitivity is vital for early visualization of DILI. Herein, a new nanoprobe, consisting of miR-122 aptamer, upconversion nanoparticles (UCNPs) and Prussian blue nanoparticles (PBNPs) was introduced for the early and sensitive detection of DILI in situ. As the nanoprobes reached in the liver, miR-122 aptamer-based entropy-driven strand displacement (ESDR) signal amplification reaction was triggered and luminescence resonance energy transfer (LRET) between UCNPs and PBNPs was responded to achieve the high-fidelity detection of DILI. A negative correlation was observed between the intensity of upconversion luminescence (UCL) and the concentration of miR-122. UCL imaging conducted both in vivo and ex vivo indicated that a reduction in miR-122 concentration led to an increase in UCL intensity, revealing a precise state of DILI. The detection technique demonstrated a positive correlation between signal intensity and severity, offering a more straightforward and intuitive method of visualizing DILI.

Effect of vacuum annealing on the upconversion luminescence of β-Ba2ScAlO5: Yb3+, Ho3+ phosphor

Upconversion luminescence (UCL) materials with narrow emission peaks, long fluorescence lifetime, and large anti-Stokes shift have attracted considerable attention in biomedical, display, anti-counterfeiting, and solid-state lasers. This study presents a new synthesis method, combining air sintering and vacuum annealing, to obtain intense green UCL emission β-Ba2ScAlO5: 0.15 Yb3+, 0.005Ho3+ phosphor. After vacuum annealing, the green, red, and near-infrared emissions of Ho3+ are enhanced by factors of 40, 133, and 37, respectively. The diffuse reflectance spectra demonstrate that there is a defect energy band ranging from 330 to 860 nm in the air-treated samples, and it is reduced dramatically after vacuum annealing. This defect band covers the three wavelengths of Ho3+ emissions in the visible range and results in the reabsorption of UCL by the host lattice. X-ray Rietveld refinements and EPR spectra reveal the difference in the oxygen defects of the air-synthesized and vacuum-annealed phosphors and reflect that the absorption band is related to the oxygen defects. This research provides a new approach to obtain intense UCL emission of β-Ba2ScAlO5 hosted phosphors and offers an excellent green phosphor for application in anti-counterfeiting or displays.

Highly efficient upconversion luminescence in narrow-bandgap Y2Mo4O15.

Lanthanide-doped upconversion (UC) materials have been extensively investigated for their unique capability to convert low-energy excitation into high-energy emission. Contrary to previous reports suggesting that efficient UC luminescence (UCL) is exclusively observed in materials with a wide bandgap, we have discovered in this study that Y2Mo4O15:Yb3+/Tm3+ microcrystals, a narrowband material, exhibit highly efficient UC emission. Remarkably, these microcrystals do not display any four- or five-photon UC emission bands. This particular optical phenomenon is independent of the variation in doping ion concentration, temperature, phonon energy, and excitation power density. Combining theoretical calculations and experimental results, we attribute the vanishing emission bands to the strong interaction between the bandgap of the Y2Mo4O15 host matrix (3.37 eV) and the high-energy levels (1I6 and 1D2) of Tm3+ ions. This interaction can effectively catalyze the UC emission process of Tm3+ ions, which leads to Y2Mo4O15:Yb3+/Tm3+ microcrystals possessing very strong UCL intensity. The brightness of these microcrystals outshines commercial UC NaYF4:Yb3+,Er3+ green phosphors by a factor of 10 and is 1.4 times greater than that of UC NaYF4:Yb3+,Tm3+ blue phosphors. Ultimately, Y2Mo4O15:Yb3+/Tm3+ microcrystals, with their distinctive optical characteristics, are being tailored for sophisticated anti-counterfeiting and information encryption applications.

Luminescence enhancement of Y2O3 thin films based on LSPR effect of Ag nanolayers

Based on the local surface plasmon resonance effect of Ag nanolayer, the luminescence enhancement in the visible light range of multilayer thin film has been investigated combined with metal/spacer molecule/photoluminescence material structure. The luminescence enhancement effect of multilayer thin films can be improved by adjusting the spin-coating number of Ag nanolayer and SiO2 spacer in the multilayer structure. At the same time, the mechanism of enhanced luminescence has been analyzed according to the change in fluorescence lifetime. The effect of the coupling between Ag nanolayer and luminescence layer on the radiative transition rate and fluorescence quantum yield have been discussed. The up-conversion luminescence intensity of the noble metal-modified multilayer thin film can be further improved by combining the multilayer structure with sensitized layer.

Thermal Enhancement of Upconversion in Sub‐10 nm Yb3+/Er3+/Na+ Tridoped Cs2ZrF6 Nanocrystals for Ratiometric Temperature Sensing

AbstractAlkaline zirconium fluorides (AxZryFx+y, A = Li, Na, and K), featuring unique crystallographic structures, have recently emerged as a class of attractive hosts for fabricating lanthanide (Ln3+)‐doped upconversion nanocrystals (UCNCs) that exhibited distinct morphology, upconversion luminescence (UCL) performance, and physicochemical property. In this paper, for the first time the controlled preparation of Yb3+/Er3+‐doped UCNCs is reported based on the trigonal Cs2ZrF6 host, leading to tunable morphology and size of the resulting UCNCs by varying the reaction temperature and time. By further incorporating Na+ ions into the Cs2ZrF6 crystal lattice, sub‐10 nm Yb3+/Er3+/Na+ tridoped UCNCs with highly improved crystallinity and thus greatly enhanced UCL intensity are obtained. Moreover, these resulting UCNCs display abnormal thermal enhancement of UCL over a temperature range from 333 to 493 K, enabling the fabrication of supersensitive luminescent nanothermometers for temperature sensing. Based on the luminescence intensity ratio of two nonthermally coupled levels (i.e., 4F9/2 and 2H11/2) of Er3+, the as‐prepared Cs2ZrF6:Yb/Er/Na UCNCs exhibit an extremely large absolute sensitivity of 177.3% K−1 and a considerably high relative sensitivity of 1.52% K−1 at 333 K. These results unambiguously demonstrate that Cs2ZrF6 is a suitable host material for preparing small‐sized Ln3+‐doped UCNCs as nanothermometer for high‐performance ratiometric temperature sensing.

Laser-induced changes on the upconversion luminescence properties of BiF3:Yb,Er nanoparticles

BiF3 nanoparticles doped with Yb3+ and Er3+ ions in varying ratios were prepared by co-precipitation method and its upconversion luminescence (UCL) properties were investigated in detail before and after high-intensity laser treatment. Green-to-red ratio (GRR) of luminescence from cubic-BiF3:Yb,Er nanoparticles is found to increase with an increase in laser power for as prepared sample. Unlike this, for conventional Yb,Er doped upconversion nanoparticles (UCNPs) such as cubic NaYF4:Yb,Er and hexagonal-NaYF4:Yb,Er, a decrease in GRR values is observed with an increase in laser power. This has been explained based on the reduced extent of Er3+-Er3+ interaction in BiF3:Yb,Er nanoparticles compared to that existing in cubic and hexagonal forms of NaYF4:Yb,Er, nanoparticles. Reduced interaction is brought about by higher lattice parameter of BiF3 host compared to the NaYF4 host which leads to a lesser extent of cross-relaxation in the former host thereby favoring the population of 4S3/2 and 2H11/2 levels of Er3+. Effect of high-intensity laser (180W/cm2) irradiation on BiF3:Yb,Er nanoparticles resulted in an irreversible five-fold increase in upconversion luminescence intensity and this is attributed to combined effect of partial conversion of BiF3 to cubic Bi2O3 and removal of adsorbed water molecules. These inferences are confirmed by XRD and TEM measurements carried out on laser-treated sample. Improved luminescence intensity from the laser-treated sample is also confirmed by the high-contrast clear images obtained from impressions made using high-intensity laser irradiation on BiF3:Yb,Er nanoparticles. BiF3:Yb,Er nanoparticles showed an excellent thermal sensitivity of 0.3% K−1 at room temperature and the value is comparable with that of conventional β-NaYF4:Yb,Er nanoparticles.

Systematic study on the intensified upconversion performance of LaVO4:Yb3+/Er3+ nanocrystals through Ti4+ ions doping by combining experiments and DFT calculations

The inherent low-efficiency for upconversion fluorescence materials constricts their further applications in many research domains. Over the last decades, considerable efforts have been paid to the fluorides, less works concering LaVO4 are reported. Based on series of impurity content-dependent experiments, Ti4+ ions doped LaVO4:Yb3+/Er3+ crystals are hydrothermally fabricated. The products are characterized by XRD, ICP, TEM and luminescence spectroscopy. Through modulating the Ti4+ ions doping concentration, the UCL intensity of 533 nm and 664 nm emissions are greatly intensified. The reasons are analyzed on the basis of three major factors. Meanwhile, extra DFT calculations are performed to support the experimental result. This report paves a new way for enhancing upconversion luminescence intensity of LaVO4 nanocrystals based on impurity doping.

Phase-separation enhanced upconversion luminescence with regulated pure-red emission in manganese fluorosilicate glass

In this work, rare earth ions (REs) including Yb3+/Er3+, Yb3+/Ho3+ and Yb3+/Tm3+ co-doped manganese oxyfluoride glasses were fabricated using melt quenching method. By fully utilizing the upconversion luminescence (UCL) of REs and regulating energy transfer between the different energy levels of RE ions and the 4T1 level of Mn2+, the output of UCL was regulated and even pure-red light can be achieved. Moreover, owing to the selective partitioning caused by phase-separation network structure in the oxyfluoride glass, the UCL intensity of glasses annealed for 72 h is significantly enhanced 58 times compared to the rapidly quenched samples.

Upconversion luminescence and temperature sensing performance of Zn2+-doped Ba2GdAlO5: Yb3+, Er3+ phosphors

Although upconversion luminescence (UCL) materials have attracted considerable attention in biomedical, lighting, anti-counterfeiting, and solar cells due to their excellent fluorescence properties, reports of the dibarium gadolinium aluminum oxide (Ba2GdAlO5) are scarce. Herein, we synthesized the single-phase Ba2GdAlO5 material with non-stoichiometric Ba2Gd1.06Al0.94O5 (denoted as BGAO, hereafter). The X-ray Rietveld refinement reveals that the substitution of Gd for Al accounts for the non-stoichiometry. Notably, the UCL properties of BGAO are realized by doping with Yb3+ and Er3+ ion pair, and it can be further enhanced significantly by co-doping with appropriate Zn2+ ions. The SEM images show that the particle size increases as the concentration of Zn2+ ions increases. The X-ray Rietveld refinement results of the Zn-doped BGAO: 0.1 Yb3+, 0.03Er3+ phosphor indicate the substitution of Zn2+ for Ba2+ and Al3+ ions simultaneously. Grain growth and lattice distortion account for the improvement of UCL properties after Zn2+ ions doping. In addition, the temperature sensing performance of the Zn2+-doped sample has been researched based on the fluorescence intensity ratio (FIR) technique, and the maximum absolute and relative sensitivities (SA-max and SR-max) are obtained to be 4.8 × 10−3 K−1 at 498 K and 1.1% K−1 at 298 K, respectively. This work provides a candidate with high UCL intensity for potential applications in optical temperature sensors.

Effect of microwave heat-treatment on up-conversion luminescence of Er3+/Yb3+ co-doped NaYF4 oxy-fluoride glass-ceramics

The microscopic properties of fluoride grains are known to play critical roles in the up-conversion luminescence properties of phosphors carrying rare-earth-based luminescence centers. To study the effect of different heating methods during preparation on the microstructure and up-conversion luminescence performance of oxy-fluoride glass-ceramics, we synthesized Er3+/Yb3+ co-doped NaYF4 nanocrystals containing transparent glass-ceramics by microwave heat-treatment and the normally heating methods. We characterized the internal structure of glass-ceramics by X-ray diffraction, transmission electron microscopy, mid-infrared spectroscopy, and Raman spectroscopy. While glass-ceramics samples prepared by both methods have extremely high optical transmittance similar to that of a glass, the microwave heat-treatment promoted faster grain growth rate, the glass-ceramics sample had better crystallinity and much improved up-conversion luminescence intensity compared to the sample obtained by the normally heating method.

Optical and Electrical properties of KNN-SBN:Ho/xYb Transmittance Luminescent Ferroelectric Ceramics

Transparent luminescent ceramics 0.94(K0.5Na0.5)NbO3-0.06Sr(Bi0.5Nb0.5)O3: 0.1Ho2O3/xYb2O3 (KNN-SBN:Ho/xYb, x=0.5, 1.0, 1.5, 2.0) have been synthesized using a solid-state reaction method.All the ceramic materials exhibit a pseudo-cubic structure without heterogeneous phases at room temperature. In addition, the microstructure of KNN-SBN:Ho/xYb transparent luminescent ceramics is very dense, and at the same time, good optical transparency is obtained, with a transmittance of 70.19% when x is 0.5. KNN-SBN:Ho/xYb transparent luminescent ceramics exhibit upconversion luminescence properties, and the best upconversion luminescence intensity is obtained when x is 1.5. The KNN-SBN:Ho/xYb transparent luminescent ceramics are ferroelectrics with good ferroelectric properties under an applied electric field of 120 kV·cm−1, and the maximum polarization intensity is the highest when x is 0.5, which is 21.32 μC·cm−2.

High quenching concentration of the CaLuAlO4:Er3+ upconversion phosphor with short-range energy migration

Low activator concentration in upconversion phosphors has been a hindrance in improving luminescence performance. Herein, we report an Er3+ doping concentration as high as 30 at. % in the CaLuAlO4 upconversion host. The CaLuAlO4:Er3+ phosphors were prepared by the traditional high-temperature solid-state method. Under the excitation of a 980 nm laser, the optimal concentration of Er3+ approaches 30% according to the total integrated intensity of red and green upconversion luminescence. This quenching concentration is one order of magnitude higher than that in the traditional Er3+ doped upconversion polycrystals. The results obtained from first-principles calculations suggest that there are no in-plane or chain rare-earth ions in the cell. This increases the difficulty of propagating excitation energy to quench centers and is advantageous for high doping concentration. Our work can spark people's interest in the research and application of highly doped upconversion phosphors.

Molten Salt Synthesized CaTa4O11:Er3+/Yb3+ with Superior Upconversion Luminescence.

Low phonon tantalate-based phosphors with a layer structure are considered to have excellent upconversion luminescence (UCL) intensity, which could be reduced due to the existence of impure phase defects and inappropriate doped rare earth ions. To improve their UCL performance, we have prepared single-phase CaTa4O11:Er3+/Yb3+ samples by a molten salt synthesis (MSS) using KCl as the reaction medium and compared its UCL properties with counterparts made by a conventional solid-state reaction (SSR) in this study. We have demonstrated that the MSS samples have a much higher UCL intensity under 980 nm laser excitation than the SSR ones due to accurate replacement of Ca2+ sites by Er3+/Yb3+ in high-purity single-phase MSS samples. We have further enhanced the green UCL intensity of the MSS samples by 1.57 times via acid picking (AP). Under 980 nm laser excitation at a high powder density of 61.3 W/cm2, the green UCL intensity of the MSS-AP samples can reach 3.72 times that of the SSR-AP samples. For potential luminescence thermometry applications, the maximum absolute sensitivity (SA) of the MSS-AP samples reaches 0.01316 K-1 at 501 K based on the luminescence intensity ratio. This study shows that CaTa4O11:Er3+/Yb3+ phosphors prepared by the MSS method are single-phase samples with excellent pure green UCL as a suitable temperature sensing material.

Preparation and strong green upconversion luminescence of Ca9Y(VO4)7: Yb3+/Er3+ phosphor

Exploring novel oxysalt compounds remains significant due to their affordability and versatile applications, such as serving as laser crystals, piezoelectric crystals, frequency-doubling crystals, and luminescent materials. Specifically, this study introduces a new near-single green upconversion luminescent Ca9(VO4)7: Yb3+/Er3+ material, synthesized through high-temperature solid-phase methods. When subjected to 980 nm near-infrared laser irradiation, the Ca9(VO4)7: 0.3 Yb3+, 0.02 Er3+ phosphor demonstrates robust green luminescence at 531 nm (2H11/2 → 4I15/2) and 558 nm (4S3/2 → 4I15/2), accompanied by faint red luminescence at 665 nm (4F9/2 → 4I15/2). The optimal doping concentrations for Yb3+ and Er3+ ions, yielding the highest upconversion luminescence intensity, are determined to be 0.3 and 0.02, respectively. The investigation elucidates the upconversion luminescence mechanism through the downward shift spectrum in photoluminescence and the pumping power dependence of upconversion green-red luminescence. The primary excitation pathway identified for the upconversion process in Ca9Y(VO4)7: 0.3 Yb3+, 0.02 Er3+ involves Yb3+ (2F5/2) + Er3+ (4I11/2) → Yb3+ (2F7/2) + Er3+ (4F7/2). This research contributes to the exploration of new materials, injecting vitality into modern industries and production processes.

Enhancement of NaYF<sub>4</sub>:Yb<sup>3+</sup>/Er<sup>3+</sup> up-conversion luminescence based on anodized alumina template

Up-conversion nanoparticle (UCNP) can collect near-infrared (NIR) light and convert it into visible light. Therefore, UCNP has potential applications in fields such as biomedicine, anti-counterfeiting, and solar cells. However, the efficiency of traditional UCNP in the above-mentioned fields is relatively low, greatly limiting its use in related fields. Therefore, enhancing the up-conversion luminescence intensity of up-conversion nanoparticles is particularly important and urgently needed. In this work, anodic alumina templates are used to enhance the luminescence intensity of up-conversion nanocrystals. NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>with a diameter of 35 nm is prepared by using co-precipitation method. Single pass AAO templates with pore size and pore spacing of 88 nm and 100 nm are prepared by using two-step anodization method. Finally, NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>/AAO composite structures are formed by using spin coating method. The red green light emission intensity of NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>/AAO sample can increase 4.4 and 9.0 times that of NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>/Al reference sample, respectively. The enhancement mechanism is explored by using the finite difference time domain method, and the results show that the primary source of enhancement is the localized surface plasmon resonance effect of the pores in the anodic alumina template. At the same time, the relationship between the up-conversion luminescence intensity of NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>/AAO sample and the incident angle is investigated. The experimental results show that as the incident angle increases, the luminescence intensity of the red and green light of NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>/AAO samples first decrease and then increase. Due to the coupling of the local surface plasmon resonance with the excitation wavelength and emission wavelength, the up-conversion luminescence intensity of the sample can be affected. The relationship of AAO channel enhancement factor with incident angle at excitation wavelength and emission wavelength is studied by using the finite difference time domain method. The results indicate that as the incident angle increases, the enhancement factor at the excitation wavelength decreases, while the enhancement factor at the emission wavelength increases after being illuminated at an incident angle of 15°. Therefore, when the incident angle is less than 20°, the electric field intensity at 980 nm dominates, but when it is greater than 20°, the electric field intensity at 540 nm and 650 nm takes precedence. The above results provide a reference for putting them into practical applications in the fields of anti-counterfeiting and solar cells.

Strong green upconversion emission from submicron spindle-shaped SrMoO4:Yb3+,Er3.

Upconversion luminescence (UCL) is a fluorescence process where two or more lower-energy photons convert into a higher-energy photon. Lanthanide (Ln3+)-doped UCL materials often suffer from weak luminescence, especially when directly synthesized by a hydrothermal (HT) process due to the existing hydroxyl group and undesirable arrangement of dopants within host lattices which quench luminescence and limit energy transfer. Therefore, additional heat treatment processes are required to enhance their UCL emission, even though direct hydrothermal synthesis without further heat treatment has the advantages of low energy consumption, fast synthesis, and wide applicability to generate UCL materials. In this study, via a HT process without annealing, we have produced Yb3+ and Er3+ co-doped SrMoO4 submicron spindles with a strong green UCL emission which can be seen with the naked eye, which HT produced oxide-based UCL materials often fail to demonstrate. We have investigated different HT synthesis conditions, such as temperature, time, pH and dopant composition, which control the nucleation, growth, lattice structure arrangement, and ultimately their UCL properties through XRD, SEM, EDS and UCL measurements. The bright green UCL from the SrMoO4:Yb,Er submicron spindles is further enhanced by post-synthesis annealing within a molten NaNO3/KNO3 system to prevent particle size growth. The green UCL intensity from the annealed SrMoO4:Yb,Er submicron spindles surpasses samples produced by the solid-state method and is comparable to that from the commercial NaYF4:Yb,Er sample. We have further studied the temperature-dependent luminescence of both the HT-prepared and molten-salt annealed SrMoO4:Yb,Er submicron spindle samples. The strong UCL from our SrMoO4:Yb,Er submicron spindles could warrant their candidacy for bioimaging and anticounterfeiting applications.