Luminescence of LuCl3: Pr3+ under interconfigurational (4f2 → 4f15d1) and band gap excitations

被引：22

作者：

Srivastava, A. M. ^{[1
]}

Happek, U. ^{[2
]}

Schmidt, P. ^{[2
]}

机构：

[1] GE Global Res, Niskayuna, NY 12309 USA

[2] Univ Georgia, Dept Phys & Astron, Athens, GA 30602 USA

来源：

OPTICAL MATERIALS | 2008年 / 31卷 / 02期

关键词：

Luminescence; LuCl3; Pr3+; UV and X-ray excitation; Charge transfer;

D O I：

10.1016/j.optmat.2008.03.011

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

The optical properties of Pr3+ activated LuCl3 under interconfigurational 4f(2) -> 4f(1)5d(1) and band gap (lambda(ex) = 193 nm; X-ray) excitations have been evaluated. The luminescence of LuCl3:Pr3+ is found to be strongly dependent on the excitation energy: for energies less than the absorption edge of the host, the luminescence of LuCl3:Pr3+ is dominated by the 4f(1)5d(1) -> 4f(2) interconfigurational optical transitions. When luminescence is excited by photons with energies corresponding to the absorption edge or the band gap of the host, the emission spectrum is dominated by the Pr3+ 4f(2) -> 4f(2) intraconfigurational optical transitions. A model to account for the dependence of the emission behavior on the excitation energy is presented. The Cl- -> Pr3+ charge transfer band is identified in the excitation spectrum of LuCl3:Pr3+. A comparitive study of the Pr3+ luminescence in LuCl3 and LaBr3 is offered. (C) 2008 Elsevier B.V. All rights reserved.

引用

页码：213 / 217

页数：5

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[11] CRYSTAL STRUCTURES OF ANHYDROUS RARE-EARTH CHLORIDES [J].