Published March 2011 | Version v1
Journal article

Influence of Mg2+ on luminescence efficiency and charge compensating mechanism in phosphor CaAl12O19:Mn4+

  • 1. Nanomaterials and Chemistry Key Laboratory, Wenzhou University, Wenzhou 325027 (China)
  • 2. Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, IL 60439 (United States)

Description

Synthesized by a modified solid state method in air and mixed with MgO, the red phosphor of CaAl12O19:yMn4+ (y=0.001-1.5%) enhanced its photoluminescence efficiency by 3.5 times. The influence of MgO on crystal phases, luminescence intensity and spectral characteristics of the composition modified phosphor has been investigated by spectroscopic experiments and luminescence decay measurements. It is observed that the decay time of Mn4+ luminescence prolongs linearly with increase of MgO in the composition, indicating that the excitation energy transfer and non-radiative relaxation between Mn4+-Mn4+ pairs decrease. The presence of Mg2+ leads to a transformation of Mn4+-Mn4+ pairs connected with interstitial O2- to isolated Mn4+ ions and therefore eliminates energy transfer and provides charge compensation as well. - Research highlights: → Enhancement of phosphor efficiency via composition modification. → Investigation of charge compensation, energy transfer and non-radiative relaxation mechanisms in Mn4+ activated red phosphors. → Demonstration of the role of MgO in elimination of Mn4+-Mn4+ pair formation and luminescence enhancement.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jlumin.2010.11.014

Additional details

Identifiers

DOI
10.1016/j.jlumin.2010.11.014;
PII
S0022-2313(10)00490-4;

Publishing Information

Journal Title
Journal of Luminescence
Journal Volume
131
Journal Issue
3
Journal Page Range
p. 465-468
ISSN
0022-2313
CODEN
JLUMA8

Conference

Title
17. international conference on dynamical processes in excited states of solids
Acronym
DPC'10
Dates
20-25 Jun 2010
Place
Argonne, IL (United States)

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.