Upconversion Luminescence Properties Research Articles

Simultaneous evolutions in composition, structure, morphology, and upconversion luminescence of BiOxFy:Yb/Er microcrystals and their application for ratiometric temperature sensing

Lanthanide upconversion luminescent materials featuring multi-peak and tunable emissions allow for ratiometric luminescence thermometry in a remote detection manner. However, wide explorations are still required to develop relevant materials for efficient thermometric performances. Herein, Yb3+/Er3+ co-doped non-stoichiometric analogues of bismuth oxyfluoride were obtained by simply tuning the F−/(Bi3+ + Ln3+) molar ratio of the reactants in a solid-state reaction method, for the first time. We achieved simultaneous regulations in composition, structure, morphology, and upconversion luminescence properties of BiOxFy:Yb/Er (2/1 mol%) microcrystals. Compositional analysis revealed not only the predictable increase of fluorine content, but also the constant O/(Bi + Ln) atomic ratios in all nominal BiOxFy:Yb/Er. Experimental results showed the structure and morphology evolutions from hexagonal-phase micro-flowers, to tetragonal-phase microplates, and further to orthorhombic-phase irregular microcrystals. Benefiting from adjustable composition, structure and morphology, up-conversion luminescence with adjustable intensity and color was obtained. Temperature dependent upconversion properties and ratiometric thermometric performances based on the thermally coupled levels, 2H11/2 and 4S3/2 of Er3+, were explored. BiOF:Yb/Er, BiO0.67F1.66:Yb/Er, and BiF3:Yb/Er microcrystals were found as suitable temperature sensing candidates with operating temperature range as wide as 298−673/723 K, high relative sensitivity up to 1.24% K-1, and minimum temperature uncertainty of 0.15 K. These results benefit not only further explorations for high-performance lanthanide-based luminescence thermometers, but also the chemistry of fluorides made from the solid-state reaction method.

The single near-infrared upconversion luminescence of a novel KYb (MoO4)2: Er3+ phosphor for the temperature sensing

The rare earth doping upconversion luminescence (UCL) materials exhibit multimodal emission, which has huge potential applications. However, it is still a difficult problem to obtain a single emission by modulating UCL, especially the modulation of single red light and single near-infrared light. In this work, we report a novel UCL KYb (MoO4)2: Er3+ phosphor, which can achieve a single near-infrared emission (804 nm) under rare earth Er3+ doping. Its pure phase was successfully prepared by high-temperature solid-state method, and its optimal Er3+ doping concentration was found to be 0.1 %. Excited at 980 nm laser, KYb (MoO4)2: Er3+ exhibit a single near-infrared UCL attributed to the 4I9/2 → 4I15/2 transition of Er3+ ions. To further explain its UCL mechanism, the power dependence, ultraviolet-visible-near-infrared absorption spectrum, excitation spectrum and emission spectrum of KYb (MoO4)2: Er3+ was measured. Due to the excellent near-infrared emission, the temperature-dependent UCL properties of the KYb (MoO4)2: Er3+ material is investigated in the temperature range from 298 K to 673 K. The linear relationship between the UCL and the temperature, And the sensitivity of KYb (MoO4)2: Er3+ phosphor reaches the maximum value at 673 K, which is 0.0078 K−1. The single near-infrared luminescence with good penetrability and large sensitivity makes KYb (MoO4)2: Er3+ have a promising application prospect in the fields of non-contact temperature sensing and bioimaging.

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.

Exploring energy mechanisms involved in the luminescence reduction due to Ce3+ doping via core-multishell upconversion nanoparticles highly doped with Ho3+ and Yb3+

Upconversion nanoparticles (UCNPs), particularly those that are highly doped, possess outstanding properties and have demonstrated tremendous application potential. However, novel fine-tuning strategies are urgently required to enhance the upconversion luminescence (UCL) performance of UCNPs. In this study, a series of core–multishell UCNPs highly doped with Ho3+ and Yb3+ ions were synthesized via the oleate route. The X-ray diffraction (XRD), transmission electron microscopy (TEM), and UCL spectra and decay times, and pump power dependency of the synthesized UCNPs were used to examine their morphology, size, and the UCL properties. Ce3+ ions were introduced to enhance Ho3+-based red UCL, and their doping strategy was also optimized based on summarized UCL trends and detailed UCL mechanism analysis. NaHoF4:Gd3+@NaGdF4:Yb3+,Ce3+@NaGdF4:Yb3+ UCNPs that had 10 mol% Ce3+ dopants in their middle shells exhibited better UCL properties than the larger traditional NaGdF4:Yb3+,Ce3+,Ho3+ UCNPs, probably because of the combined influence of the energy interactions between the Ce3+ ions and surface groups, sensitizing energy enhancement by active shells, and the positive cooperation between the Ce3+ ions and highly-doped core–shell structures. In this study, the phenomenon of UCL decrease resulting from Ce3+ ion doping was explored. Using unique core–multishell structures with highly-doped activators and sensitizers placed within and outside the structures, respectively, the UCL decrease due to Ce3+ ion doping was attributed to a competition for photons. Doping the UCNPs with Ce3+ ions near the UCNP surfaces favors Ho3+-based red UCL. Our study findings can deepen the understanding of the Ho3+-based UCL mechanisms and increase the potential uses of NaHoF4 materials in photo-induced therapy.

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.

High-efficiency upconversion luminescence in UCNPs/CsPbBr3 nanocomposites enhanced by silver nanoparticles.

Upconversion nanocomposites with multiple light-emitting centers have attracted great attention as functional materials, but their low efficiency limits their further applications. Herein, a novel, to the best of our knowledge, system for nanocomposites consisting of upconversion nanoparticles (UCNPs) and perovskite quantum dots (PeQDs) assembled with Ag nanoparticles (NPs) is proposed. Upconversion luminescence (UCL) operation from PeQDs is triggered by near-infrared (NIR) sensitization through Förster resonance energy transfer (FRET) and photon reabsorption (PR). Especially, the photoluminescence (PL) emission efficiency is found to be significantly enhanced due to the increased energy transfer efficiency and radiative decay rate in the UCNPs/CsPbBr3 nanocomposites. The results offer new opportunities to improve the UCL properties of perovskites and open new development in the fields of LED lighting, solar cells, biomedicine, and so on.

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.

Upconversion Luminescence Properties of Ho3+/Tm3+/Yb3+ Co-doped NaGd(MO4)2 Prepared by Hydrothermal Method

In this paper, Ho$$^{3+}$$/Tm$$^{3+}$$/Yb$$^{3+}$$-doped NaGd(MO$$_{4})_{2}$$ phosphors were prepared using the hydrothermal method and the effect of Yb$$^{3+}$$ doping amount on the luminescence properties of these phosphor materials was investigated. NaGd(MO$$_{4})_{2}$$ was characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), and spectral analysis. The results showed that Ho$$^{3+}$$/Tm$$^{3+}$$/Yb$$^{3+}$$-doped NaGd(MO$$_{4})_{2}$$ has tetragonal phase structures, and doping with rare-earth ions decreases the cell parameters of NaGd(MO$$_{4})_{2}$$. NaGd(MO$$_{4})_{2}$$:Ho$$^{3}$$/Tm$$^{3+}$$/Yb$$^{3+}$$ generates blue, green, and red lights at 477, 545, and 659 nm, respectively, under an excitation of 980 nm. The emission of these three lights is called a three-photon process. As the doping ratio of Yb$$^{3+}$$ increases, the colour coordinates of samples gradually approach the white region from the red region, enabling NaGd(MO$$_{4})_{2}$$:0.1Ho/1Tm/20Yb to exhibit white emission. Doping with Yb$$^{3 + }$$ increases the energy transfer and quantum efficiencies of NaGd(MO$$_{4})_{2}$$. When the concentration of Yb$$^{3+}$$ reached 30%, the quantum efficiency of NaGd(MO$$_{4})_{2}$$ reached the maximum value of 188.37%. Overall, NaGd(MO$$_{4})_{2}$$:Ho/Tm/Yb has broad application prospects in the field of white lighting.

NaYF4:Yb3+/Ho3+ up-conversion luminescence and its low temperature sensing characteristics

Pure hexagonal [Formula: see text]-NaYF4 micron crystals were synthesized by the hydrothermal method with the up-conversion luminescence properties studied by doping Yb[Formula: see text]/Ho[Formula: see text]. The up-conversion fluorescence spectra and fluorescence lifetime of [Formula: see text]-NaYF4 micron crystals were determined by FLS-980 transient fluorescence spectrometer. By changing the doping concentration of Yb[Formula: see text]/Ho[Formula: see text], the optimal doping concentration was confirmed to be 20%Yb[Formula: see text]/2%Ho[Formula: see text]. The fluorescence spectrum was obtained by changing pump power, the relationship between power and intensity was analyzed, and the [Formula: see text]-NaYF4 micron crystal green and red emission up-conversion process was obtained into a two-photon process. The 5F[Formula: see text]I8 and 5S[Formula: see text]I8 of the sample were thermally coupled to obtain a large absolute sensitivity (Sa) of low temperature. The maximum absolute sensitivity within the range of 64–194[Formula: see text]K is 0.0097[Formula: see text]K[Formula: see text] at 144[Formula: see text]K, while maximum absolute sensitivity at 333[Formula: see text]K is 0.00335[Formula: see text]K[Formula: see text] in the range of 293–493[Formula: see text]K. The experimental results show that the sensing characteristics of [Formula: see text]-NaYF4:Yb[Formula: see text]/Ho[Formula: see text] at low temperature are better than those at high temperature, and it has the potential to be used in the field of temperature sensing.

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.

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.

Recent progress of UCNPs-MoS2 nanocomposites as a platform for biological applications.

Composite materials can take advantages of the functional benefits of multiple pure nanomaterials to a greater degree than single nanomaterials alone. The UCNPs-MoS2 composite is a nano-application platform that combines upconversion luminescence and photothermal properties. Upconversion nanoparticles (UCNPs) are inorganic nanomaterials with long-wavelength excitation and short-wavelength tunable emission capabilities, and are able to effectively convert near-infrared (NIR) light into visible light for increased photostability. However, UCNPs have a low capacity for absorbing visible light, whereas MoS2 shows better absorption in the ultraviolet and visible regions. By integrating the benefits of UCNPs and MoS2, UCNPs-MoS2 nanocomposites can convert NIR light with a higher depth of detection into visible light for application with MoS2 through fluorescence resonance energy transfer (FRET), which compensates for the issues of MoS2's low tissue penetration light-absorbing wavelengths and expands its potential biological applications. Therefore, starting from the construction of UCNPs-MoS2 nanoplatforms, herein, we review the research progress in biological applications, including biosensing, phototherapy, bioimaging, and targeted drug delivery. Additionally, the current challenges and future development trends of UCNPs-MoS2 nanocomposites for biological applications are also discussed.

Anti-thermal quenching of luminescence in Y2W3O12:Yb3+/RE3+ (RE = Er/Ho/Tm) and its temperature sensing application.

Herein, a series of Y2W3O12:10%Yb3+/x%RE3+ (RE = Er/Ho/Tm) phosphors is prepared via a solid-state reaction. The upconversion and downshift luminescence properties of the phosphors were investigated under an excitation of 980 nm. The bright blue light emission from Tm3+ ion and the green and red light emissions from Ho3+(Er3+) ions were observed. The near-infrared light intensity of NIR-I (Tm3+, ∼850 nm), NIR-II (Er3+: ∼1550 nm; Tm3+: ∼1783 nm) and NIR-III (Ho3+: ∼2050 nm) were analyzed. In particular, the dramatic thermal enhancement phenomenon in visible and NIR regions was exhibited by the Y2W3O12:10%Yb3+/x%RE3+ (RE = Er/Ho/Tm) phosphors. Among them, the green light intensity of Er3+ ions increased 26.77 times, from 303 to 573 K. The NIR-II emission band (∼1783 nm) intensity of Tm3+ ions at 533 K increased 168.7 times compared to that at 313 K. The possible thermal enhancement mechanism is illustrated by the negative thermal expansion (NTE) and Frenkel defect of the Y2W3O12 host. Finally, the optical temperature sensing performances of Y2W3O12:10%Yb3+/x%RE3+ (RE = Er/Ho/Tm) samples are investigated according to the luminescence intensity dependence relationship on temperature. The maximum value of SR reached 4.24% K-1 at 353 K for Y2W3O12:10%Yb3+/0.6%Ho3+ phosphor. The results indicate that the Y2W3O12:10%Yb3+/x%RE3+ (RE = Er/Ho/Tm) phosphors possess anti-thermal quenching properties and are suitable for developing optical temperature sensors.

Regulating the upconversion luminescence properties of Tm3+/Yb3+-codoped ZrScW2PO12 microparticles with a negative thermal expansion effect through thermal stimulation for optical thermometry.

Tm3+/Yb3+-codoped ZrScW2PO12 microparticles were prepared in order to solve the problems of the severe thermal quenching and unsatisfactory thermometric properties of most luminescent materials. The synthesized materials exhibit a rarely observed negative thermal expansion (NTE) effect, which was verified by in situ X-ray diffraction experiments, performed under high temperature conditions. Upon excitation with a 980 nm laser, bright blue upconversion (UC) emissions originating from Tm3+ were observed. Moreover, owing to the promoted energy transfer, cross-relaxation and non-radiative decay processes at high temperatures triggered by the NTE effect, the observed UC emissions arising from 1G4 and 3F2,3 levels show non-monotonic responses to temperature. By analysing the temperature-dependent luminescence intensity ratio of these UC emissions originating from the non-thermally coupled levels of Tm3+ (1G4 and 3F2,3), the thermometric properties of the prepared microparticles were investigated in detail. Interestingly, the maximum absolute and relative sensitivities of the synthesized compounds are 0.09 and 1.45% K-1, respectively, which are independent of Yb3+ content, but they can be manipulated by employing different sensing modes. Our results manifest that the exploitation of the NTE effect is an efficient way to control the UC luminescence features of rare earth ions and to realize high performance optical thermometry.

Investigating the effect of synthesis parameters on the structure and upconversion luminescent properties of NaYF4:Tm,Yb for anticounterfeiting printing ink

Introduction: In this study, NaYF4:Tm,Yb upconversion microparticles were prepared by a hydrothermal method. Methods: The effects of fabrication parameters such as rare earth concentration, reaction temperature and reaction time on the structure and luminescence properties of the materials were studied by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and photoluminescence spectroscopy (PL). Depending on the reaction temperature and time, the morphology of NaYF4:Tm,Yb is either a nanoparticle or a branched structure. Results: The crystallite size is approximately 70 nm and remains almost unchanged with increasing reaction temperature and time. These NaYF4:Tm,Yb powders strongly emit at 450 nm and 798 nm. In addition, the surface of the UCMPs was also modified with maleic anhydride to improve their dispersibility in solvents and binding to biological molecules. Conclusion: Printing ink based on UCMPs modified with maleic anhydride and polyamide for screen printing was prepared. The printed patterns on paper and polymer substrates glow blue light under LED excitation at 980 nm, and they are completely transparent in daylight.

Thermal sensitivity of Ho3+ fluorescence in oxyfluoride nanocrystals and derivative embedded fibers

(Y1-x-yHoxYby)OF/polyacrylonitrile (YOF-HuYv/PAN) composite fibers prepared by electrostatic spinning have been demonstrated to possess effective upconversion (UC) luminescence and sensitive temperature feedback properties for laser display and real-time temperature monitoring in complex environments. When the excitation power density is increased to 73 mW/mm2, the total luminous flux reaches 3.35 mlm, demonstrating that the Ho3+/Yb3+ co-doped YOF nanocrystals embedded in the composite fibers are efficient luminous materials. The quantum yields (QYs) of green and red emissions from Ho3+ are derived to be 2.97 × 10−5 and 1.40 × 10−5 respectively when the pump power density arrives at 73 mW/mm2 under 977 nm laser, and the high photon generation efficiency ensures sufficient fluorescence intensity for tracing temperature feedback. The maximum relative sensitivities appear at 303 K, while the absolute sensitivity (SA) and relative sensitivity (SR) of the nanofibers retain 13.77% K−1 and 0.34% K−1 at 433 K respectively, demonstrating that the nanofibers have superior optical temperature sensing properties. The composite fibers with effective luminescence and high temperature sensitivity as luminescent materials provide a potential option for the field of laser display and temperature sensing.

Excitation wavelength and pumping power dependent temperature sensing property of Nd3+/Yb3+/Er3+ triply-doped LaNbO4 phosphor

Optical thermometry based on the fluorescence intensity ratio technology between the thermally coupled energy levels of Er3+ has become a research hotspot, but it is often limited by excitation conditions, which reduces its universality and reliability. In this work, Nd3+/Yb3+/Er3+ triply-doped LaNbO4 phosphor with excellent up-conversion (UC) luminescence characteristic and reliable temperature sensing sensitivity has been prepared by solid-state reaction method. Intense green and weak red UC emissions were gained under 808 nm and 980 nm excitations. The temperature dependent UC luminescence property and temperature sensing behavior of the sample has been investigated. The results demonstrated that the intensity ratio of the two green emissions was insensitive to the excitation wavelength and pumping power of the lasers, and the maximum absolute sensitivity was derived to be 0.91 % K−1 at 481 K. This work provides a new material with reliable and high temperature sensing sensitivity for optical thermometers.

Magnetic-responsive upconversion luminescence resonance energy transfer (LRET) biosensor for ultrasensitive detection of SARS-CoV-2 spike protein

Upconversion nanoparticles (UCNPs) are ideal donors for luminescence resonance energy transfer (LRET)-based biosensors due to their excellent upconversion luminescence properties. However, the relatively large size of antibodies and proteins limits the application of UCNPs-based LRET biosensors in protein detection because the large steric hindrance of proteins leads to low energy transfer efficiency between UCNPs and receptors. Herein, we developed a magnetic responsive UCNPs-based LRET biosensor to control the coupling distance between antibody-functionalized UCNPs (Ab-UCNPs) as donors and antibody-PEG linker-magnetic gold nanoparticles (Ab-PEG-MGNs) as acceptors for ultrasensitive and highly selective detection of SARS-CoV-2 spike proteins. Our results showed that this platform reversibly shortened the coupling distance between UCNPs and MGNs and enhanced the LRET signal with a 10-fold increase in the limit of detection (LOD) from 20.6 pg/mL without magnetic modulation to 2.1 pg/mL with magnetic modulation within 1 h. The finite-difference time-domain (FDTD) simulation with cyclic distance change confirmed the distance-dependent LRET efficiency under magnetic modulation, which supported the experimental results. Moreover, the applications of this magnetic-responsive UCNP-based LRET biosensor could be extended to other large-size biomolecule detection.

Synthesis and up-conversion luminescence properties of Ho3+-Yb3+ co-doped glass ceramics with perovskite structure

By using melt solidification crystallization method, Ho3+-Yb3+ co-doped transparent glass ceramics (GCs) containing LaTiO3 microcrystal were successfully prepared. The structure of the GCs was characterized by X-ray diffraction (XRD), which proved that LaTiO3 microcrystal was precipitated in the precursor glass (PG). The structures of PG and GCs were studied by infrared spectrum, which showed that a new absorption peak appeared in the GCs, which was attributed to the stretching vibration of the Ti-O bond in the [TiO6] octahedral group, and it further demonstrated the precipitation of the LaTiO3 microcrystal. By studying the up-conversion luminescence (UCL) properties, it is found that there were three emission peaks at 546, 652 and 484 nm, which are attributed to the 5F4/5S2 → 5I8, 5F5 → 5I8 and 5F3 → 5I8 transitions of Ho3+, respectively, and the optimal doping concentrations of Ho3+ and Yb3+ were determined. The chrominance coordinate of Ho3+-Yb3+ co-doped glass ceramic (GC) is situated in the green light area and the color purity is as high as 98.03 %. The researches above show that Ho3+-Yb3+ co-doped GCs with LaTiO3 microcrystal have a wide application prospect in green luminescence.