Er3+单掺与Er3+/Yb3+共掺Y2SiO5的上转换发光

报道了一种新的上转换发光材料X2型Y2SiO5:Er, Yb并研究了Yb3 浓度和泵浦功率对样品的上转换发光特性的影响:(1)随着Yb3 浓度的增加,绿、红光发射均呈先增强后减弱的变化,但相对于绿光发射,红光发射受Yb3 浓度的影响更剧烈,并且当12%(摩尔分数)Yb3 时,可以得到很纯的红光发射;(2)上转换发光强度与泵浦功率的关系表明,双光子吸收贡献样品的上转换发射.此外,讨论了可能的上转换机制.认为随着Yb3 浓度增加,Er3 的激发态吸收、Yb3 到Er3 的能量传递和Er3 的交叉弛豫对上转换发光的作用依次逐渐加强.     

Infrared to visible upconversion luminescence in Er/Yb co-doped CeO2 inverse opal

Infrared to visible upconversion luminescence has been investigated in Er³⁺/Yb³⁺ co-doped CeO₂ inverse opal. Under the excitation of 980 nm diode lasers, visible emissions centered at 525, 547, 561, 660 and 680 nm are observed, which are assigned to the Er³⁺ transitions of ²H_11/2 → ⁴I_15/2 (525 nm), ⁴S_3/2 → ⁴I_15/2 (547, 561 nm), ⁴F_9/2 → ⁴I_15/2 (660 and 680 nm), respectively. The effect of photonic band gap on the upconversion luminescence intensity was also obtained. Additionally, the upconversion luminescence mechanism was studied. The dependence of Er³⁺ upconversion emission intensity on pump power reveals that it is a two-photon excitation process.     

Strong upconversion luminescence in LiYMo2O8:Er,Yb towards efficiency enhancement of dye-sensitized solar cells

Strong green upconversion (UC) emissions induced by a 940 nm laser have been observed in a series of Er³⁺, Yb³⁺ co-doped LiYMo₂O₈ samples. The diffuse reflectance absorption spectra show that the co-doped samples can absorb the photons in the range of 900–1050 nm efficiently, demonstrating the excellent sensitization effect of Yb³⁺ ions. Based on power switched UC luminescence, UC mechanisms are discussed, and the emission spectra excited by 490 nm are also measured to give additional evidence. The results reveal that application of these phosphors may improve the conversion efficiency of DSSCs.     

Flame synthesis and effects of host materials on Yb/Er co-doped upconversion nanophosphors

The upconversion nanophosphors (UCNPs) of Yb³⁺/Er³⁺ co-doped into Y₂O₃, La₂O₃, and Gd₂O₃ were synthesized via the combustion method and characterized by powder X-ray diffractometer (XRD), scanning electron microscopy (SEM) and upconversion fluorescence spectroscopy. The characterization results showed that at the same flame temperature (2705 K) and precursor concentration (0.1 M), pure monoclinic and cubic-phase phosphors were achieved on Gd₂O₃ and Y₂O₃ hosted UCNPs, respectively; while the mixed phases were observed on La₂O₃ hosted UCNPs. Further annealing process at 850 °C produced pure cubic-phase La₂O₃:Yb³⁺,Er³⁺ UCNPs; while there was no phase transition observed on Gd₂O₃:Yb³⁺,Er³⁺ UCNPs. The dependence of upconversion luminescence on precursor concentrations and host materials was then examined. The La₂O₃ and Gd₂O₃ hosts were shown to be the promising alternates for the commonly used Y₂O₃ hosts for rare-earth doped phosphors.     

Yb3+ concentration dependence of upconversion luminescence in Y2Sn2O7:Yb3+/Er3+ nanophosphors

Pyrochlore Y₂Sn₂O₇ nanophosphors codoped with Er³⁺ (fixed 2 at.%) and Yb³⁺ ions (2–16 at.%) were synthesized via hydrothermal process followed by heat treatment. We investigate the infrared-to-visible upconversion (UC) luminescence properties of Er–Yb codoped Y₂Sn₂O₇. Upon 980 nm excitation at room temperature, green (at ~522 and 544 nm) and red (at ~661 nm) UC emissions were observed, which are ascribed to the (²H_11/2, ⁴S_3/2) → ⁴I_15/2 and ⁴F_9/2 → ⁴I_15/2 transitions, respectively. It has been found that the Yb³⁺-doping concentrations have greatly influenced on the UC luminescence intensity and the emission ratio of the red and green in Y₂Sn₂O₇:Yb³⁺/Er³⁺ nanophosphors. The tunable emission is due to the energy back transfer from Er³⁺ to Yb³⁺ and the cross relaxation between the two neighboring Er³⁺ ions. It is expected that the achieved single and intense red emission band may have potential application for in vivo bioimaging.     

Synthesis of LaF3: Yb3+ ,Ln3+ nanoparticles with improved upconversion luminescence

Yb³⁺/Er³⁺ and Yb³⁺/Tm³⁺ co-doped LaF₃ nanoparticles with upconversion luminescence properties were prepared via the co-precipitation method, followed by heat treatment at different temperatures in the range of 180°C to 600°C. We investigated the influence of heat treatment temperatures on the size, morphology, and upconversion luminescence intensity of the nanoparticles. Significant increases of the particle size and upconversion luminescence intensity of the nanoparticles were observed with increasing heat treatment temperature. The upconversion mechanism of the LaF₃:Yb³⁺,Er³⁺ and LaF₃:Yb³⁺,Tm³⁺ nanoparticles was also discussed.     

Up-conversion luminescence properties of Y2O2S:Yb3+,Er3+ nanophosphors

Up-converting yttrium oxysulfide nanomaterials doped with ytterbium and erbium (Y₂O₂S:Yb³⁺,Er³⁺) were prepared with the flux method. The precursor oxide materials were prepared using the combustion synthesis. The morphology of the oxysulfides was characterized with transmission electron microscopy (TEM). The particle size distribution was 10–110 nm, depending on the heating temperature. According to the X-ray powder diffraction (XPD), the crystal structure was found hexagonal and the particle sizes estimated with the Scherrer equation agreeded with the TEM images. Upon the 970 nm infrared (IR) laser excitation, the materials yield moderate green ((²H_11/2, ⁴S_3/2) → ⁴I_15/2 transition) and strong red (⁴F_9/2 → ⁴I_15/2) luminescence. The green luminescence was enhanced with respect to the red one by an increase in both the crystallite size and erbium concentration due to the cross-relaxation (CR) processes. The most intense up-conversion luminescence was achieved with x_Yb and x_Er equal to 0.10 and 0.005, respectively. Above these concentrations, concentration quenching occurred.     

Polyol-mediated synthesis of water-soluble LaF3:Yb,Er upconversion fluorescent nanocrystals

Well-crystallized LaF₃:Yb,Er nanoparticles were prepared by the polyol method and three kinds of polyols (glycol, diethylene glycol and glycerol) were chosen as the reaction medium respectively. All of the obtained LaF₃:Yb,Er nanoparticles have roughly spherical shapes, and the average sizes of these nanoparticles ranged from 5 to 7 nm. These nanoparticles could be well dispersed in water or ethanol to form colloidal solutions. When these nanoparticles were excited by the 980 nm laser, several upconversion emissions were observed.     

Anti-stokes luminescence of Y2O3:Er

Diffuse reflectance and spontaneous photoluminescence excitation spectra of the Y₂O₃:Er (10 at % Er) compound have been studied under varied optical pumping conditions. The results demonstrate that the anti-Stokes luminescence of erbium-doped yttrium oxide has high intensity when two different photon energies are used for infrared illumination. The resonance wavelengths of IR photons for two-photon excitation of visible emission in the Y₂O₃:Er phosphor have been determined, and the corresponding electron transitions in erbium-related emission centers have been identified for the Stokes and anti-Stokes luminescence.     

Yb3+ and Er3+ co-doped Y2Ce2O7 nanoparticles: synthesis and spectroscopic properties

Yb³⁺ and Er³⁺co-doped Y₂Ce₂O₇ nanoparticles sintered at different temperatures were prepared by homogeneous co-precipitation method. The products were characterized by X-ray powder diffraction (XRD), energy-dispersive spectroscopy (EDS) and transmission electron microscopy (TEM). The results indicated that the particle sizes and morphologies of the samples were heavily influenced by the sintering temperature. As temperature increased, the particle sizes became gradually larger and more agglomerate. The emissions including green and red upconversion emissions were investigated under 980 nm excitation. The emission intensities of the samples also depended on the sintering temperature. Two photon processes were mainly responsible for green and red upconversion emissions.     

络合沉淀法合成纳米Y2O3:Yb,Er及其上转换发光性能

以EDTA为螯合剂,采用络合沉淀法合成了纳米级Yb、Er共掺杂的Y2O3上转换发光粉.通过X射线衍射(XRD)、透射电子显微镜(TEM)、光致发光(PL)光谱和红外(IR)光谱对微晶进行了表征.结果表明,经980℃焙烧后的粒子为单一的立方晶相,其颗粒基本为球形,并且其粒径约为30nm.PL谱和IR谱分析结果表明:纳米粒子的表面效应使得表面原子更易吸附空气中的水和二氧化碳,从而增强了4S3/2→4F9/2的无辐射弛豫过程,使得样品所发红光与体材料相比具有更高的荧光分支比.另外,本文还对样品的发光性能作了详细的讨论.     

2种方法制备的Y2O3:Yb,Er前驱体对Y2O2S:Yb,Er性能的影响

利用溶胶-凝胶燃烧合成法和共沉淀法成功地制备出单一均相的Y2O3:Yb,Er前驱体,采用传统的硫熔法制备了单一均相的Y2O2S:Yb,Er粉体,同时对传统硫熔法的后处理过程进行了改进.分别采用XRD、FTIR、SEM和EDS对合成的粉体进行了物相分析、化学键分析、形貌表征和元素组成分析,并对粉体进行了发光性能测试,在980nm激发下,共沉淀法制备的前驱体硫化后得到的Y2O2S;Yb,Er发光强度比溶胶-凝胶燃烧合成法制备的前驱体硫化后得到的Y2O2S:Yb,Er发光强度高得多.     

Li doping effects on the upconversion luminescence of Yb3+/Er3+-doped ABO4 (A = Ca,Sr; B = W,Mo) phosphors

ABO₄ (A = Ca, Sr; B = W, Mo):Er³⁺/Yb³⁺/Li⁺ phosphors tri-doped with different concentrations of Li⁺ ion ranging from 0 to 22.5 mol% were prepared by using a solid-state reaction method. And their upconversion (UC) luminescence properties were in estimated under a 975 nm laser-diode excitation. The four kinds of phosphors (CaWO₄, CaMoO₄, SrWO₄, and SrMoO₄) tri-doped with Er³⁺, Yb³⁺ and Li⁺ ions showed strong green UC emission peaks at 530 nm and 550 nm and weak red UC emission. The intensity of green UC emission of Li⁺ doped samples was several higher than that of Li⁺ un-doped samples due to the reduction of lattice constant and the local crystal field distortion around rare-earth ions. The optimum doping concentration of Li⁺ ions was investigated and the effects of Li⁺ concentration for UC emission intensity were studied in detail.     

Up-conversion luminescence and optical temperature sensing behaviour of Yb3+/Er3+ codoped CaWO4 material

Present article report on structural and optical properties of Er³⁺/Yb³⁺ codoped CaWO₄ phosphors. Structural properties are explored using XRD and Raman technologies. The upconversion emission has been investigated with 980 nm excitation. The upconversion emission intensity is dependent on the concentrations of Yb³⁺ ions and reaches a maximum at 7%. Logarithmic plots of power dependencies reveal that the green and red emissions originate from a two-photon upconversion process. Based on the photon energy and the emission spectra, the possible upconversion processes and emission mechanisms are discussed. Finally, the optical temperature sensing properties has been performed using the fluorescence intensity ratio technique based on green upconversion emissions. Its temperature sensitivity is found to be above 0.0025 K^-1 in the whole temperature range of 300–540 K, revealing this phosphor to be a promising optical temperature sensing material.     

Enhanced luminescence of silica thin films co-doped with Er and Yb

Er³⁺- and Yb³⁺- ions-co-doped silica thin films were prepared by RF magnetron sputtering. Enhanced photoluminescence centered at 1.534 μm was detected at room temperature when excited by a Nd–YAG laser line at 1.064 μm. The photoluminescence intensity increases with Yb-atom doped concentration and tends to saturate at the Yb-atom concentration of 3.0%, indicating that the enhanced photoluminescence results from the energy transfer from Yb³⁺ to Er³⁺.     

Preparation and upconversion luminescence of Y2SiO5:Yb3+, Ho3+ nanophosphors

X1 type monoclinic Y2SiO5:Yb3+, Ho3+ nanophosphors with fixed (varied) Ho3+ and varied (fixed) Yb3+ concentrations were synthesized by sol-gel method. The nanophosphors presented lacunaris shape with an average size of about 47 nm measured by transmission electron microscopy and scanning electron microscopy. Up-conversion emissions have been observed at 550 nm corresponding to (5F4, 5S2)-5I8 transition and 661 nm due to 5F5-5I8 transition of Ho3+ upon 980 nm excitation at room temperature. The results indicate that both green and red luminescences are based on the two-photon process through the energy transfer from Yb3+. However, the intensity of green emission is weaker than that of the red, because the 5I7 level of Ho3+ can be effectively populated. The integrated upconversion emission intensity on the Yb3+ and Ho3+ concentrations were also studied.     

Size-dependent luminescence of spherical Y2O3:Er nanoparticles

Spherical nanocrystalline Y₂O₃:Er particles differing in composition and size, with a scatter in the range 10–15%, have been prepared through the low-temperature thermolysis of an amorphous precursor. We have studied the luminescence, diffuse reflectance, and photoluminescence excitation spectra of Y₂O₃:Er nanoparticles differing in shape. The intensity of the visible luminescence bands of erbium-doped yttria has been shown to depend on sphere diameter. The resonance wavelengths of coupled photons have been determined as functions of Y₂O₃:Er phosphor nanosphere size.     

The influence of Yb doping on the upconversion luminescence of Pr in aluminum oxide based powders prepared by combustion synthesis

The effect of ytterbium (Yb³⁺) doping on the upconversion (UC) emission of praseodymium (Pr³⁺) doped in aluminum oxide based powders prepared by combustion synthesis is reported for near-infrared excitation (λ = 980 nm). Our experimental results show that the crystalline structure and the UC emission changes with the Yb³⁺ concentration. The sample containing only Pr³⁺ (1.0 wt.%) did not show any UC signal and the UC emission profiles of the samples containing Pr³⁺ (1.0 wt.%) and Yb³⁺ (0.5, 2.0 wt.%) are quite different. The sample containing 0.5 wt.% of Yb³⁺ has five emission lines in the visible range associated to Pr³⁺ 4f–4f transitions, ³P₀ → ³H₄ (497 nm), ³P₀ → ³H₅ (525 and 550 nm), ³P₀ → ³H₆ (620 nm) and ³P₀ → ³F₂ (650 nm). We believe that the UC process has its origin in energy transfer from Yb³⁺ ions to Pr³⁺ ions in Pr_0.83Al_11.83O₁₉ phase. The sample containing 2.0 wt.% of Yb³⁺ has only one emission line in the visible range peaked at 507 nm which we believe has its origin in cooperative UC emission due to excited Yb³⁺ pairs in YbAlO₃ phase. The samples containing Yb³⁺ also present UC emission lines in the near-infrared which are assigned to intrinsic lattice defects.     

Sol-gel synthesis and green upconversion luminescence in BaGd2(MoO4)4:Yb,Er phosphors

Yb³⁺/Er³⁺ codoped BaGd₂(MoO₄)₄ phosphor powders were prepared by the Sol-gel method and the upconversion luminescence properties were investigated in detail. Under 980 nm semiconductor laser excitation, BaGd₂(MoO₄)₄:Yb³⁺,Er³⁺ phosphor exhibits green upconversion luminescence with peaks at 530 and 550 nm, which are due to the transitions of Er³⁺ (²H_11/2) → Er³⁺ (⁴I_15/2) and Er³⁺ (⁴S_3/2) → Er³⁺ (⁴I_15/2), respectively. Both of the two green emission lines are produced by populating Er³⁺ ions to the excited state through a two-photon process. By monitoring the intensities of the green upconversion luminescence, the optimum conditions for the Sol-gel synthesis were determined when the molar ratio of citric acid to total chelate metal cations was 2:1 and the sintering temperature was at 1073 K. The concentration quenching effect for Er³⁺ was found at the optimum doping concentration of 6 mol%, and the critical distance for the neighboring Er³⁺ was determined to be about 21.5 Å.