Published July 15, 2003 | Version v1
Journal article

Luminescence behavior of the europium (III) complexes with hexafluoracetylacetonate in the ORMOSIL matrices

Description

The luminescence behavior of the europium (Eu) complexes with hexafluoracetylacetonate (HFA:Eu3+ complexes) in the ORMOSIL matrices has been investigated. The steady-state excitation and emission spectra of the 1 mol.% EuCl3 and the 3 mol.% hexafluoracetylacetonate (HFA) co-doped gel were similar to that of the HFA:Eu3+ complexes powders which were synthesized in ethanol solution, which indicated that the HFA:Eu3+ complexes have been synthesized in the 1 mol.% EuCl3 and the 3 mol.% HFA co-doped gel. The time-resolved spectra of the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gel exhibited the ligand-to-metal energy transfer process, which also confirmed the synthesis of the HFA:Eu3+ complexes in the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gel. The decay curves of the luminescence 5D0 state obtained by monitoring the 5D0→7F2 emission line for the HFA:Eu3+ complexes powders and for the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gel could both be fitted to a single-exponential fitting function. The temperature of heat treatment has significant influence on the luminescence behavior of the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gel. The luminescence intensities of the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gel reached a maximum at approximately 110 deg. C and decreased gradually with increasing temperature. However, the 5D0 excited-state lifetimes of the Eu3+ ions in the 1 mol.% EuCl3 and 3 mol.% HFA co-doped gels increased gradually with increasing temperature

Additional details

Identifiers

DOI
10.1016/S0921-5107;
PII
S0921510703000886;

Publishing Information

Journal Title
Materials Science and Engineering. B, Solid-State Materials for Advanced Technology
Journal Volume
100
Journal Issue
2
Journal Page Range
p. 147-151
ISSN
0921-5107
CODEN
MSBTEK

Optional Information

Copyright
Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.