Published October 2014 | Version v1
Journal article

Optical spectroscopy of erbium-doped SrTiO3 crystals

  • 1. Czech Technical University in Prague, Faculty of Nuclear Sciences and Physical Engineering, Trojanova 13, CZ-120 00 Praha 2 (Czech Republic)
  • 2. Ioffe Physical-Technical Institute of the RAS, 194 021 Saint-Petersburg (Russian Federation)
  • 3. Institute of Physics AS CR, v. v. i., Na Slovance 2, CZ-182 21 Praha 8 (Czech Republic)

Description

Results of a detailed study of optical absorption and photoluminescence of slightly erbium-doped (∼50 ppm) strontium titanate (SrTiO3) single crystals are presented. This study allowed us to specify the structure of energy levels that determine the main internal optical transitions within the 4f11 electron configuration of Er3+ ions in SrTiO3:Er crystals at temperatures below the transition from cubic to tetragonal phase. The numbers of energy levels of the studied multiplets obtained at 2 K correspond exactly to the theoretically expected numbers of crystal field levels for multiplets of only one type of Er3+ centers with non-cubic symmetry. Experimental results indicate that Er3+ ions most probably substitute for Sr2+ ions acting in SrTiO3 as ionized donors. Such location of Er3+ ions is consistent with both n-type conductivity and substantial free charge carrier absorption in the infrared spectral region observed in the studied SrTiO3:Er single crystals at room temperature. - Highlights: • For the first time observed absorption lines of Er3+ in SrTiO3:Er single crystals. • Only one type of Er3+ centers of non-cubic symmetry was found in the crystals. • Structure of 4f electron energy levels at 2 K was determined for the Er3+ center. • Er-doping results in pronounced free charge carrier absorption in the IR region

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jlumin.2014.05.021

Additional details

Identifiers

DOI
10.1016/j.jlumin.2014.05.021;
PII
S0022-2313(14)00304-4;

Publishing Information

Journal Title
Journal of Luminescence
Journal Volume
154
Journal Page Range
p. 437-444
ISSN
0022-2313
CODEN
JLUMA8

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.