987 resultados para CR(III)


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This data report contains all the meteorological, hydrological and dynamic data gathered during the VASPI cruises (I : from December 8th to December 13th 1982, II : from March 5th to March 9th 1983, and III : from October 6th to October 10th 1983) carried out along the continental shelf of Ivory Coast by the oceanographic ship "Andre NIZERY". These cruises, which represent a part of a coastal programme, are included in the more general scientific program FOCAL, whose main scientific objective is the study of the thermal context of the intertropical atlantic area.

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Infrared (1.2-1.6 mum) luminescence in a yttrium aluminium garnet (YAG) crystal, co-doped with Yb (10 at.%) and Cr (0.05 at.%) ions, was investigated under CW laser diode pumping (lambda = 940 nm). The Cr4+ emission band was observed with its peak at 1.35 mum and measured to be about 6% with respect to Yb3+ IR luminescence (lambda = 1.03 mum). Analysis of the crystal absorption and luminescence spectra allows one to conclude that Yb3+-Cr4+ energy transfer is a mechanism responsible for the B-3(2)(T-3(2))-B-3(1)((3)A(2)) emission of Cr4+ ions. This crystal is promising as an efficient source of the near infrared emission. (C) 2004 Elsevier B.V. All rights reserved.

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对透光性良好的Cr^3+:Al2O3透明多晶陶瓷的光谱性能进行了研究,其吸收光谱中吸收峰与单晶红宝石相一致,按吸收光谱和Tanabe-Sugano能级图,算出其晶场强度参数Dq及Racah参数B分别为1792cm^-1,689cm^-1,Dq/B=2.6,陶瓷中Cr^3+离子所处格位的晶体场强比单晶弱一些,但Cr^3+:Al2O3透明陶瓷仍属于强场晶体材料;当Cr^3+掺杂浓度到达0.8wt%时,陶瓷的发射谱仍保持较好的R线发射;随Cr^3+掺杂浓度的增大,激发峰位发生“红移”.在Cr^3+:Al2O3透

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The fluorescence emission spectra of Cr:Yb:YAG crystal are measured and the effective stimulated emission cross section of the crystal are obtained from -80 degrees C to +80 degrees C. A linear temperature dependence between -80 degrees C and +80 degrees C is reported for the 1.03 mu m peak stimulated emission cross section of Cr:Yb:YAG crystal. (c) 2004 Elsevier B.V. All rights reserved.

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The fluorescence emission spectra of Cr:Nd:YAG crystal are measured and the effective stimulated emission cross-section of the crystal is obtained from -80 to +80 degrees C. A linear temperature dependence between -80 and +80 degrees C is reported for the 1.064-mu m peak stimulated emission cross-section of Cr:Nd:YAG crystal. (C) 2005 Elsevier Ltd. All rights reserved.

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用光纤耦合激光二极管抽运Cr,Yb:YAG晶体获得了1.03 μm的自调Q激光输出,输出的调Q脉冲非常稳定,抽运阈值功率为680 mW,脉冲宽度为3.3 ns,获得的平均功率为156 mW,斜率效率为18.5%。随着抽运功率的增大,重复频率成线性增长,而脉宽略有减少,单脉冲能量和峰值功率都始终呈增大趋势。光束质量因子M2为1.17。

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用提拉法生长了掺铬、钕的钆镓石榴石(Cr^4+,Nd^3+:GGG)自调Q激光品体。报道了室温下的吸收光谱和荧光光谱特性。分析了Cr离子浓度对光谱性质的影响。比较了Cr^4+:GGG,Nd^3+:GGG和(Cr^4+,Nd^3+):GGG晶体吸收光谱的关系。测量了(Cr^4+,Nd^3+):GGG晶体和Nd^3+:GGG晶体的荧光寿命,它们分别是33μs和250μs。实验表明,(Cr^4+,Nd^3+):GGG晶体是一种非常有潜力的自调Q激光晶体,可以实现大功率激光器的小型化和全固态化。

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用提拉法生长了掺铬、钕的钆镓石榴石(Cr^4+,Nd^3+:GGG)晶体,研究了室温下的吸收光谱和荧光光谱性质,以及晶体中Cr离子浓度对Nd离子光谱性质的影响。应用Judd—ofelt理论计算了强度参数Ωt(t=2,4,6),自发辐射跃迁几率、荧光分支比和辐射辱命等光谱参数。应用McCumber理论计算^4F3/2→^4I11/2能级跃迁的受激发射截面。结果表明:Cr^3+在300~900nm之间较强地增加了吸收截面,尤其是伴随Cr^3+→Nd^3+有效的能量转移。Cr^4+在1.06μm附近的吸收减弱了

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采用传统无压烧结工艺制备出透明性良好的掺Cr3+氧化铝陶瓷;测定了陶瓷的吸收光谱、发射光谱和激发光谱。结果表明,氧化铝陶瓷吸收峰与红宝石单晶一致,吸收截面大小与单晶相近;陶瓷中Cr3+离子所处格位的晶体场强较单晶弱,但其发射谱仍有较好的锐线发射;陶瓷中微量添加剂以及晶界的存在使得Al2O3晶胞发生畸变,造成其发射峰宽化。

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研究了室温下Yb:YAG的上转换荧光光谱,此荧光归因于Yb^3+离子的“合作”发光和Yb抖离子到稀土杂质离子的能量转移。测试了Yb;YAG晶体的X射线荧光,发光峰对应于电荷迁移态到Yb^3+离子的基态、激光态间的跃迁。研究了Cr,Yb:YAG晶体的荧光光谱。讨论了Cr^4+激光输出的可能性。

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采用传统无压烧结工艺制备出透明性良好的掺Cr的Al2O3透明陶瓷;测定了其吸收光谱和荧光光谱,发现在Al2O3六配位的八面体结构中,除了有Cr^3+离子的特征吸收峰外,由于有Mg^2+的电荷补偿作用,也有Cr^4+离子,Cr^4+的荧光发射峰位于1223nm附近,与Cr^4+在四面体中的发光行为一致。但其荧光发射峰较窄,半高宽△λ仅为37nm。

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The Cr(0.1%),Yb(10%):GGG crystals have been grown by the Czochralski method. The chemical composition is: Yb0.33Gd2.47Cr0.005Ga5.2O12. There are no observed Yb3+ ions substituting Ga3+ ions, just like that of Yb:GGG crystals. The defects in Cr,Yb:GGG crystal were also investigated. The absorption and emission spectra of Cr,Yb:GGG crystal at room temperature have been measured. The 02 and H-2 annealing effect of Cr,Yb:GGG crystal have been compared. Cr3+ can greatly weak the visible luminescence of this crystal. The Cr-Yb-codoped crystals may be potential materials for compact, efficient, high stability LD pumped solid state lasers. (C) 2006 Elsevier B.V. All rights reserved.