1000 resultados para 1995_01310720 TM-68 4302812


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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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Er3+, Yb3+ and Tm3+ codoped fluorophosphate glasses emitting blue, green and red upconversion luminescence at 970 nm laser diode excitation were studied. It was shown that Tm3+ behaves as the sensitizer to Er3+ for the green upconversion luminescence through the energy transfer process: Tm 3+:H-3(4) + Er3+:I-4(15/2) -> Er3+:I-4(9/2) + Tm3+:H-3(6), and for the red upconversion luminescence through the energy transfer process: Tm3+:F-3(4) + Er3+:I-4(11/2) -> TM3+:H-3(6) + Er3+:4 F-9/2. Moreover, Er3+ acts as quenching center for the blue upconversion luminescence of TM3+. The sensitization of Tm3+ to Er3+ depends on the concentration of Yb3+. The intensity of blue, green and red emissions can be changed by adjusting the concentrations of the three kinds of rare earth ions. This research may provide useful information for the development of high color and spatial resolution devices and white light simulation. (C) 2006 Elsevier B.V. All rights reserved.

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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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The thermal stability, 2 μm fluorescence properties and energy transfer mechanism in Ho3+ doped fluorophosphate glass sensitized by Yb3+ and Tm3+ were investigated. The characteristic temperatures, absorption spectrum and fluorescence spectrum of the glass sample were measured. ΔT calculated from the characteristic temperatures shows that the thermal stability of fluorophosphate glass is better than fluoride glass. According to the absorption spectrum, several spectroscopic parameters of the glass sample, such as Judd-Ofelt parameters and spontaneous transition probability were calculated and compared with other glass hosts. The largest spontaneous transition probability for Ho3+:5 I7&rarr5I8 transition in fluorophosphate glass which is 78.48 s-1 indicates that fluorophosphate glass is an appropriate base glass to achieve 2 m fluorescence. From the fluorescence spectrum of the glass sample, the extremely strong 2.0 μm fluorescence intensity is observed, which is higher than the intensity of 1.8 μm fluorescence, showing that Ho3+ ions sensitized by Yb3+ and Tm3+ is efficient. Meanwhile, the absorption sections and emission sections of Yb3+, Tm3+ and Ho3+ were calculated and the pumping scheme and energy transfer mechanism among Yb3+, Tm3+ and Ho3+ are discussed. The study indicates that Yb-Tm-Ho tri-doped fluorophosphate glass is a significant sensitization glass system under 980 nm excitation for 2 μm applications.

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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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The near-IR emission spectra of Er3+-Tm3+ codoped 70GeS(2)-20In(2)S(3)-10CsI chalcohalide glasses were studied with an 808 nm laser as an excitation source. A broad emission extending from 1.35 to 1.7 mu m with a FWHM of similar to 160 nm was recorded in a 0.1 mol.% Er2S3, 0.5 mol.% Tm2S3 codoped chalcohalide glass. The fluorescence decay curves of glasses were measured by monitoring the emissions of Tm3+ at 1460 nm and Er3+ at 1540 nm, and the lifetimes were obtained from the first-order exponential fit. The luminescence mechanism and the possible energy-transfer processes are discussed with respect to the energy-level diagram of Er3+ and Tm3+ ions. (C) 2008 Optical Society of America

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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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我们报道了一种以二极管泵浦的 1.94 μm Tm:YAP激光器为泵浦源,常温下在2.1 μm连续运行的Ho:YAG激光器。最大输出功率1.5 W,相应斜率效率为17.9%,二极管到的转换效率为5.6%。

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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.