钬掺杂铌酸锂晶体在550nm激发下紫外至紫光区域上转换发光的研究.docVIP

钬掺杂铌酸锂晶体在550nm激发下紫外至紫光区域上转换发光的研究.doc

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钬掺杂铌酸锂晶体在550nm激发下紫外至紫光区域上转换发光的研究

钬掺杂铌酸锂晶体在550nm激发下紫外至紫光区域上转换发光的研究   【摘要】采用Czochralski法生长出一系列不同Ho3+(0.1,0.3,0.5 mol%)摩尔掺杂浓度的Ho:LiNbO3单晶。X射线衍射结果显示了Ho:LiNbO3晶体的结构特性。在550nm光源的激发下,在样品中检测到了由于3D3→5IJ(J=6和8)和5Gk→5I8(k=3,4,5和6)能级跃迁引起的紫外至紫光区域的上转换发光。交叉弛豫5G4+5I8→5F4/5S2+5I6导致了发光强度随着Ho3+掺杂浓度增加而减弱。晶体的紫外-可见光-进红外吸收光谱表明在Ho3+掺杂浓度为0.3mol%和0.5mol%时,Ho3+占据了LiNbO3晶体的Nb位。   【关键词】Ho:LiNbO3晶体; 上转换; 紫外和紫光   Abstract:Congruent LiNbO3 crystals doped with x mol% Ho3+ ions (x = 0.1, 0.3 and 0.5 mol%) (Ho:LiNbO3) are grown by Czochralski method. The structural properties of the grown crystals are confirmed by the powder X-ray diffraction (XRD) patterns. The ultraviolet and violet upconversion emissions, arising from the transitions of 3D3→5IJ(J=6and8) and 5Gk→5I8(k=3,4,5and6),respectively,were observed in Ho:LiNbO3 crystals under 550 nm excitation.A reduced intensity ratio of UC emission at 380 nm to the NIR emission at 760 nm observed in Ho:LiNbO3 was attributed to the efficient cross relaxation process of5G4+5I8→5F4/5S2+5I6.The studies on the ultraviolet-visible-near infrared (UV-Vis-NIR) absorption spectra indicate that Ho3+ ions may enter into Nb sites in LiNbO3 crystals doped with 0.3 mol% and 0.5 mol% Ho3+ ions.   Key Words :Ho:LiNbO3 crystal; Upconversion; Ultraviolet and violet   1. Introduction   The upconversion (UC) emission arising from the activated rare-earth (RE) ions is important for practical applications such as solar cells, UC laser, biological imaging, temperature sensors and DNA detection [1-4].In particular, the solid-state lasers working in the ultraviolet (UV) spectral range have attributed much attention since the UV lasers have great potential applications of optical data storage, color displays, environmental monitoring, etc.[5-7]. Therefore, many efforts have been expanded to obtain the efficient UC-UV emission. G. Y. Chen[8] reported that the blue and violet UC emissions of Er3+ at 409 nm (2H9/2→4I15/2) and 390 nm (4G11/2→4I15/2) can be observed in Yb3+/Er3+:Y2O3 nanocrystals under 980 nm exci

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