Published October 6, 2008 | Version v1
Journal article

Long lasting phosphorescence of Gd2O2S:Eu,Ti,Mg nanorods via a hydrothermal routine

  • 1. State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Jiaotong University, 1954 Huashan Road, Shanghai 200030 (China)

Description

This paper reports a novel hydrothermal method to synthesize nanorod like Gd2O2S:Eu,Ti,Mg persistent phosphor and the characterization of the same. Hydrothermally prepared Gd(OH)3 nanorod precursor, codoped with Eu, Ti and Mg, was converted into the aimed phosphor by calcinating the precursor in CS2 atmosphere. XRD investigation revealed a pure phase of Gd2O2S, indicating that the codoped ions, Eu, Ti and Mg, occupy the lattice position within Gd2O2S crystal, rather than form secondary phase in the obtained phosphor powder. SEM observation showed that the phosphor calcined in CS2 atmosphere inherited the rod-like shape from the precursor, indicating the advantage of the CS2 routine in controlling the phosphor morphology. HRTEM investigation further revealed a crystalline nature of the nanorods, as well as a preferred growth along c axis. When the nanorods were exposed to UV illumination, bright orange emission was generated, due to the intrinsic transitions of Eu3+. The Eu3+ concentration and the calcination temperature were two key factors that greatly influent the photo luminescent behavior of the prepared Gd2O2S:Eu,Ti,Mg phosphor. Persistent luminescence was readily observed after the UV source was switched off, due to the formation of electron traps with suitable trap depth within the matrix by the codoped Ti4+ and Mg2+ ions

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2007.10.119

Additional details

Identifiers

DOI
10.1016/j.jallcom.2007.10.119;
PII
S0925-8388(07)02039-7;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
465
Journal Issue
1-2
Journal Page Range
p. 367-374
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.