共查询到19条相似文献,搜索用时 78 毫秒
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用熔融急冷法制备了系列Yb3+/Ho3+共掺Ge25Ga5S70硫系玻璃,测试了样品的吸收光谱以及980nm激光泵浦下中红外荧光光谱特性,用Judd–Ofelt理论计算分析了单掺Ho3+在Ge25Ga5S70玻璃中的强度参数Ωi(i=2,4,6)、自发辐射跃迁几率、荧光分支比和辐射寿命等光谱参数。研究了Yb3+/Ho3+共掺样品在980nm激光泵浦下获得的Ho3+:2.9μm中红外荧光光谱性质,表明Yb3+/Ho3+之间存在能量共振转移。当固定Yb3+掺杂浓度为0.5%(质量分数,下同),随着Ho3+掺杂浓度从0增加为0.7%,Yb3+:2F5/2能级寿命明显单调下降,说明Yb3+/Ho3+之间有效的能量传递主要来源于Yb3+:2F5/2能级向Ho3+:5I6能级的共振能量传递。运用Futchbauer-Ladenburg公式计算比较了不同掺杂浓度下Ho3+:5I6→5I7跃迁的受激发射截面。 相似文献
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制备了一系列新型Ga2 S3-Sb2S3-La2S3硫系玻璃,研究了玻璃的热学和光学性能;向优化的玻璃中掺杂Dy3+,研究了玻璃的中红外发光性能;基于优化的玻璃组成,拉制了纤芯/包层结构光纤,评估了其作为中红外激光增益介质的潜力.实验结果表明,Ga2S3-Sb2S3-La2S3玻璃具有宽的红外透过范围(约0.7 ~13.6 μm)和高的线性折射率(约2.655 ~2.707),组成为20Ga2 S3-75Sb2 S3-5La2S3的玻璃具有最佳的抗析晶热稳定性.Dy3+掺杂的玻璃在2.95 μm和4.40 μm具有较高的发光量子效率和较大的受激发射截面.拉制的20Ga2 S3-75Sb2S3-5La2 S3∶0.05wt%Dy3 +/20Ga2 S3-74Sb2 S3-6La2 S3光纤透光范围为2~8 μm,其背景损耗<8 dB/m.在1.32 μm波长激发时,光纤显示出强的中红外发光.这些优异性能表明该玻璃光纤有望成为一种高效的中红外激光增益材料. 相似文献
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Tm3+/Ho3+共掺碲酸盐玻璃中Tm3+交叉弛豫主导的2.0μm发光特性 总被引:1,自引:0,他引:1
研究了不同摩尔分数Tm3 掺杂下Tm3 /Ho3 共掺碲酸盐玻璃在2.0μm处的发光特性.此发光包括两个过程:Tm3 之间的交叉弛豫过程;通过Tm3 与Ho3 之间的能量转移,将能量传递给Ho3 而使Ho3 跃迁至5I7能级上产生布居,当Ho3 跃迁回基态时则发出波长为2.0μm的光.计算了Tm3 的交叉弛豫速率,并根据速率方程分析了Tm3 的交叉弛豫机理.结果表明:随着Tm3 浓度增加,交叉弛豫逐渐增强;2.0μm处发光的强度逐渐增强.证明了在Tm3 /Ho3 共掺情况下,2.0μm处的发光强度取决于Tm3 的交叉弛豫强度. 相似文献
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用熔融急冷法制备了系列Tm3+掺杂浓度的Ge-Ga-Se-CsI硫卤玻璃样品,通过测试的吸收光谱和Judd-Ofelt 理论计算了Tm3+离子的强度参数(Ωi,i=2,4,6)、自发辐射跃迁几率(A)、荧光分支比(β)、以及辐射寿命(Trad)等光谱参数.研究了800 nm激光泵浦下样品红外荧光特性与掺杂浓度之间的关系,计算了常温下Tm3+:3 F4→3 H6(1.8 μm)和3H5→3F4(3.8μm)发射截面以及3F4→3H6(1.8 μm)跃迁的增益截面与波长的函数关系. 相似文献
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通过熔融淬冷法制备了掺杂0.6%(占基质玻璃的质量分数)Er~(3+):65GeS_2-25Ga_2S_3-10CsI(摩尔比)玻璃。通过不同热处理工艺对玻璃样品进行微晶化处理获得了硫卤微晶玻璃。测试了其密度、显微硬度、红外透过光谱、以及中红外荧光光谱。对比研究了基质玻璃与微晶玻璃样品之间性能差异。结果表明:基质玻璃在热处理温度为440℃,热处理时间为14 h后,所获得的微晶玻璃样品的密度和显微硬度明显增加,中远红外透过性能并未有显著的降低,Er~(3+):~4I_(11/2)→~4I_(12/2)跃迁相对应的2.8μm处的中红外荧光光强稍有增强。 相似文献
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实验制备了Dy3+掺杂Ge-Ga-Se系统硫系玻璃样品,测试了玻璃的密度、显微硬度、可见-红外透射光谱、荧光光谱以及荧光寿命.根据玻璃的密度计算了玻璃的摩尔体积以及致密度.讨论了玻璃的这些性能随系统平均配位数<r>的变化关系.实验结果表明该系统中配位数大于2.67的玻璃在1.3 μm具有较好的发光性能,荧光寿命在440~530μs之间,当玻璃组成位于化学门槛即平均配位数为2.73时玻璃的发光强度最强. 相似文献
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Ho3+/Yb3+掺杂铋镓酸盐光学玻璃的上转换发光 总被引:1,自引:0,他引:1
制备了高折射率Ho3 /Yb3 掺杂铋镓酸盐玻璃,用Brewster原理测量玻璃的折射率为2.296.用倒易法计算Yb3 的发射截面面积为2.109×10-20 cm2.在室温,用974nm激光器激发玻璃样品,观察并记录到强烈的双光子上转换荧光.分析认为:铋镓酸盐玻璃中Yb3 直接敏化Ho3 的上转换发光的激发机理是Yb3 到Ho3 的高效能量传递.上转换过程中红光相对强度较强的原因为:玻璃声子能量特性、最大能量声子密度降低和玻璃绿光区强吸收3方面因素增加了5F5能级上的粒子数布居,使5F5→5I8能级的跃迁几率升高,导致红光强度大于绿光强度. 相似文献
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Dy3+‐Doped Selenide Chalcogenide Glasses: Influence of Dy3+ Dopant‐Additive and Containment
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Zhuoqi Tang David Furniss Nigel C. Neate Emma Barney Trevor M. Benson Angela B. Seddon 《Journal of the American Ceramic Society》2016,99(7):2283-2291
This work reports on process‐induced impurities in rare‐earth ion: Dy3+‐doped selenide chalcogenide glasses, which are significant materials for active photonic devices in the mid‐infrared region. In particular, the effect of contamination from the silica glass ampoule containment used in chalcogenide glass synthesis is studied. Heat‐treating Dy‐foil‐only, and DyCl3‐only, separately, within evacuated silica glass ampoules gives direct evidence of silica ampoule corrosion by the rare‐earth additives. The presence of [Ga2Se3] associated with [Dy] on the silica glass ampoule that has been contact with the chalcogenide glass during glass melting, is reported for the first time. Studies of 0–3000 ppmw Dy3+‐doped Ge16.5As9Ga10Se64.5 glasses show that Dy‐foil is better than DyCl3 as the Dy3+ additive in Ge‐As‐Ga‐Se glass in aspects of avoiding bulk crystallization, improving glass surface quality and lowering optical loss. However, some limited Dy/Si/O related contamination is observed on the surfaces of Dy‐foil‐doped chalcogenide glasses, as found for DyCl3‐doped chalcogenide glasses, reported in our previous work. The surface contamination indicates the production of Dy2O3 and/or [≡Si‐O‐Dy=]‐containing particles during chalcogenide glass melting, which are potential light‐scattering centers in chalcogenide bulk glass and heterogeneous nucleation agents for α‐Ga2Se3 crystals. 相似文献
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制备了Tm3+/Yb3+共掺杂的20GaF3-15InF3-17CdF2-15ZnF2-10SnF2-3P2O5-(20-x-y)PbF2-xTmF3-yYbF3(x=0.2~2,y=1~4)系列玻璃。室温下,通过其吸收光谱,运用Judd-Ofelt理论计算了样品的强度参量Ωt(t=2,4,6)、自发辐射几率、荧光分支比和荧光寿命等光谱参数。研究发现,增加Tm3+掺入量对Ω2影响不大,Ω4、Ω6的值有增大的趋势。在980nm激发下的荧光光谱中,观察到5个上转换发射峰,其中发光较强的464nm的蓝光是三光子过程,650nm的红光和800nm的红外光是双光子过程,并讨论了其上转换发光机理和Tm3+、Yb3+掺杂浓度对发光强度的影响。 相似文献
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Transmission electron microscopic and optical spectroscopic studies of Ni2+/Yb3+/Er3+/Tm3+ doped dual‐phase glass‐ceramics
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Zhigang Gao Xiaosong Lu Yindong Zhang Shu Guo Yinyao Liu Shiyu Sun Fei He Piaoping Yang Jing Ren Jun Yang 《Journal of the American Ceramic Society》2018,101(7):2868-2876
Ni2+/Yb3+/Er3+/Tm3+ codoped transparent glass‐ceramics (GCs) containing both hexagonal β‐YF3 and spinel‐like γ‐Ga2O3 dual‐phase nanoparticles (NCs) are synthesized by melt‐quenching and subsequent heating procedures. Two techniques of transmission electron microscopy (TEM) nanoanalytics and optical spectroscopy are conjugated to understand the distribution of the rare‐earth ions (REs) and transition metals (TMs) in the nanostructured GCs. It is found that the REs are located predominantly in β‐YF3, whereas the TMs in γ‐Ga2O3 NCs. As a result, energy transfer (ET) between the REs and TMs is considerably suppressed due to the large spatial separation (> 3 nm), but it is enhanced between the REs partitioned in the β‐YF3 NCs. This has important implications for intended and demanding photoluminescence functions. For example, an ultrabroadband near‐infrared (NIR) emission in the wavelength region of 1000‐2000 nm covering the entire telecommunications window is observed for the first time. Meanwhile, intense upconversion (UC) emissions covering the 3 primary colors and locating in the first biological window can be also recorded under excitation by a single pump source at 980 nm. 相似文献
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De‐Long Zhang Cong‐Xian Qiu Wen‐Zhu Zhang Ping‐Rang Hua Dao‐Yin Yu Edwin Yue‐Bun Pun 《Journal of the American Ceramic Society》2013,96(11):3476-3482
Co‐diffusion characteristics of Er3+ and Tm3+ ions in LiNbO3 crystal have been studied, together with two other properties: doping effect on refractive index of substrate, and Li out‐diffusion. Er3+/Tm3+‐codoped LiNbO3 single‐crystals were prepared by co‐diffusion of stacked Er‐ and Tm‐metal thin films, coated onto parts of the surfaces of X‐ and Z‐cut congruent LiNbO3 crystal plates, at different temperatures and different durations in air. After diffusion, the surface refractive indices of the doped and undoped parts were measured by prism coupling technique, and the surface composition was evaluated from the measured indices. The results show that the dopings have negligible effect on the substrate index and the Li out‐diffusion depends mainly on the diffusion temperature. The Er3+ and Tm3+ profiles were studied using secondary ion mass spectrometry, and a co‐diffusion dynamical model is proposed and verified experimentally. From the measured profiles, the temperature‐dependent Er3+/Tm3+ diffusivity and solubility were obtained together with other relevant parameters, such as diffusion constant, activation energy, solubility constant and heat of solution. The Er3+ and Tm3+ co‐diffusion exhibits similar temperature dependent diffusivity, and the dependence is similar to that of single‐diffusion. In the co‐diffusion case, the total solubility consists of two parts: Er3+ and Tm3+ parts, there is no anisotropy, and the value is equal to that of single‐diffusion case, in which both ions have the similar solubility. The Er3+ and Tm3+ parts of solubility change relatively with the initial metal film thicknesses and hence have different temperature dependences. Nevertheless, their sum, i.e., the co‐diffusion solubility, remains a constant at a given temperature. 相似文献
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