Published December 2011 | Version v1
Journal article

Excellent red phosphors of double perovskite Ca2LaMO6:Eu (M=Sb, Nb, Ta) with distorted coordination environment

  • 1. State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China)
  • 2. College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)
  • 3. Key Laboratory of Functional Crystals and Laser Technology, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190 (China)

Description

Double perovskite Ca2LaSbO6, successfully synthesized by solid state reaction method, was identified by Rietveld refinements to crystallize in the monoclinic space group P21/n, which is isostructural to Ca2LaMO6 (M=Nb, Ta). Excellent red luminescence of Eu-doped Ca2LaMO6 (M=Sb, Nb, Ta) can be obtained and no luminescence quenching effect was observed when Eu-doping level reached 40%. For Ca2La0.6NbO6:0.4Eu3+, quantum efficiencies of 20.9% and 27.7% were reached to show high light conversion and bright red emission excited at 465 nm (blue light) and 534 nm (green light), respectively, comparable to the commercial phosphors. Through systemic investigation for the series of double perovskite compounds, the excellent red emission in Ca2LaMO6 is attributed to highly distorted polyhedra of EuO8 (low tolerance factor of the pervoskite), and large bond distances of La−O (low crystal field effect of the activator). - Graphical Abstract: Eu3+ doped double-perovskite compounds A2LnMO6 (A=Ca, Sr, Ba; Ln=La, Gd, Y; M=Sb, Nb, Ta) show the dependence of luminescence intensity on the crystal structure. Highlights: ► A series of double perovskite compounds were synthesized by solid state reaction. ► Eu3+ doped samples display intense red emission when excited by blue or green light. ► High quantum efficiency was obtained, comparable to the commercial phosphors. ► Luminescence properties were ascribed to crystal distortion and large Ln–O distance.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2011.10.032

Additional details

Identifiers

DOI
10.1016/j.jssc.2011.10.032;
PII
S0022-4596(11)00574-3;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
184
Journal Issue
12
Journal Page Range
p. 3324-3328
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.