107 resultados para 1995_03161606 TM-7 4500405


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制备了不同Al(PO3)3含量的掺铥系列氟磷玻璃,研究了其结构、热稳定性和光谱性质。随着Al(PO3)3含量的增加,该系列玻璃的密度降低,折射率增加,差热分析表明,转变温度、析晶起始温度、析晶峰温度和熔化温度增加。Al(PO3)3摩尔浓度在7%~9%时析晶稳定性最佳。采用归一化的拉曼光谱分析了材料的结构和声子状况,对于该系列氟磷玻璃,Al(PO3)3含量的增加不会影响声子能量,但使声子密度增大。测试了样品的吸收光谱,Tm^3+的^3H6→^3F4在第三通信窗口的L波段有明显吸收。与在其它玻璃基质中相比,T

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研究了Yb2O3浓度对Tm^3+/Yb^3+共掺氧卤碲酸盐玻璃的上转换发光的影响,分析了上转换发光机理。结果发现,通过980nm的激光二极管激发,在室温下同时观察到强烈的蓝光(475nm)和微弱的红光(649nm),分别是由于Tm^3+离子^1G4→^3H6和^1G4→^3F4跃迁产生的;上转换机理分析表明,上转换蓝光和红光都是由于双光子吸收过程。随Yb2O3浓度增加,Yb^3+离子寿命降低,Yb^3+到Tm^3+的能量转移效率增加,上转换蓝光和红光强度先增加,在Yb2O3摩尔比为3时达到最大,然后降低。

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An efficient near-infrared (NIR) quantum cutting (QC) in GdAl3(BO3)(4):RE3+,Yb3+ (RE=Pr, Tb, and Tm) phosphors has been demonstrated, which involves the conversion of the visible photon into the NIR emission with an optimal quantum efficiency approaching 200%, by exploring the cooperative downconversion mechanism from RE3+ (RE=Pr, Tb, and Tm) excitons to the two activator ions, Yb3+. The development of NIR QC phosphors could open up a new approach in achieving high efficiency silicon-based solar cells by means of downconversion in the visible part of the solar spectrum to similar to 1000 nm photons with a twofold increase in the photon number. (c) 2007 American Institute of Physics.

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稀土掺杂氧氟玻璃是一种优良的上转换发光材料,制备了组分为35SiO2—15AlO1.5-(45-x)PbF2-xCdF2—0.1TmF3—1.5YbF3(x=0,10,20,30)的氧氟硅酸盐玻璃,系统研究了CdF2含量对其热学性能和光学性能的影响。研究表明用CdF2部分替代PbF,可以提高玻璃的热稳定性、使紫外吸收截至边向短波方向移动;随着CdF2含量的增加,开始Tm^3+蓝光和红光上转换发光增强缓慢,而后迅速增强.而近红外上转换发射先显著增强后增强放缓;由于蓝光和近红外发光强度远大于红光发光强度,所以

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2.0 μm spectroscopic properties of Er3+/Tm3+/Ho3+ triply-doped fluorophosphate glasses pumped by 808 nm and the energy transfer mechanisms between the three rare earth ions were investigated. J-O theory was used to calculate the parameters of Ho3+ in fluorophosphate glasses. Absorption and emission cross-sections and the gain coefficients were calculated. The obtained lifetime r and spontaneous transition probability Ar of Ho3+:5I7 level were 10.64 ms and 93.95 s-1 respectively. The calculated maximum emission cross-section of 2.0 μm was 9.26×10-21 cm2. The energy transfer analysis indicated that the cross-relaxation of Tm3+ was important and the resonent energy transfer in Er3+&rarrHo3+, Tm3+&rarrHo3+, Er3+&rarrTm3+&rarrHo3+ process was the main channel. The study revealed that the Er3+/Tm3+/Ho3+ triply-doped fluorophosphate glass would be a potential material for 2.0 μm emission because of the efficient sensitization of Er3+ and Tm3+ to Ho3+.

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Tm3+/Yb3+-codoped heavy metal oxide-halide glasses have been synthesized by conventional melting and quenching method. Structural properties were obtained based on the Raman spectra, indicating that halide ion has an important influence on the phonon density and maximum phonon energy of host glasses. Intense blue and weak red emissions centered at 477 and 650 nm, corresponding to the transitions (1)G(4) -> H-3(6) and (1)G(4) -> H-3(4), respectively, were observed at room temperature. The possible up-conversion mechanisms are discussed and estimated. With increasing halide content, the up-conversion luminescence intensity and blue luminescence lifetimes of Tm3+ ion increase notably. Our results show that with the substitution of halide ion for oxygen ion, the decrease of phonon density and maximum phonon energy of host glasses both contribute to the enhanced up-conversion emissions. (c) 2005 Elsevier B.V. All rights reserved.

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We report on cooperative downconversion in Yb3+-RE3+ (RE = Tm or Pr) codoped lanthanum borogermanate glasses (LBG), which are capable of splitting a visible photon absorbed by Tm3+ or Pr3+ ions into two near-infrared photons. The results indicate that Pr3+-Yb3+ is a more efficient ion couple than Tm3+-Yb3+ in terms of cooperative downconversion. We have obtained a highest quantum yield of 165% and 138% for Pr3+-Yb3+ and Tm3+-Yb3+ codoped LBG glasses under 468 nm excitation, respectively. However, ultraviolet light excitation to the charge transfer band of Yb3+ does not result in quantum splitting as rapid relaxation from the charge transfer band to 4f(13) levels of Yb3+ dominates. (C) 2008 Optical Society of America

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采用提拉法(CZ)生长了质量优异的Tm:YAG晶体.部分晶片在1000℃的空气气氛中退火25h.借助光学显微镜、扫描电子显微镜(SEM),结合化学腐蚀法,对Tm:YAG晶体退火前后(111)面的缺陷特征进行了研究.Tm:YAG晶体(111)面的位错腐蚀坑呈三角形.在偏光显微镜下观察了退火前后Tm:YAG晶体(111)面的应力双折射.同时应用高分辨X射线衍射法测定了晶体的完整性.实验结果表明,长时间空气气氛下高温退火有效降低了晶体中总的位错密度,提高了晶体质量.

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Tm:YAG晶体是性能优异的LD泵浦激光晶体。本文总结了Tm:YAG晶体的生长、光谱性质以及激光性能的研究和发展,并指出了Tm:YAG晶体发展中需要解决的问题。

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By using a pump recycling configuration, the maximum power of 8.1 W in the wavelength range 1.935-1.938 mu m is generated by a 5-mm long Tm:YAlO3 (4 at. %) laser operating at 18 degrees C with a pump power of 24 W. The highest slope efficiency of 42% is attained, and the pump quantum efficiency is up to 100%. The Tm:YAlO3 laser is employed as a pumping source of singly-doped Ho(l%):GdVO4 laser operating at room temperature, in which continuous wave output power of greater than 0.2 W at 2.05 mu m is achieved with a slope efficiency of 9%.

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Absorption spectrum from 400 to 2000 run and upconversion fluorescence spectra under 940 nm pumping of YAG single crystal codoped with 5 at.% Yb3+ and 4 at.% Tm3+ were studied at room temperature. The blue upconversion emission centered at 483 nm corresponds to the transition (1)G(4) -> H-3(6), the emission band around 646 nm corresponds to the transition (1)G(4) -> F-3(4) of Tm3+. Energy transfer from Yb3+ to Tm3+ is mainly nonradiative and the transfer efficiency was experimentally assessed. The line strengths, transition probabilities and radiative lifetimes of (1)G(4) level were calculated by using Judd-Ofelt theory. Gain coefficient calculated from spectra shows that the upconversion corresponding with transitions (1)G(4) -> H-3(6) in YAG doped with Yb3+ and Tm3+ is potentially useful for blue light Output. (c) 2006 Elsevier B.V. All rights reserved.