Published July 29, 2016 | Version v1
Journal article

Mechanism of enhanced photoluminescence of Tb ions in hydrogenated silicon-rich silicon oxide films

  • 1. Department of Experimental Physics, Wroclaw University of Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw (Poland)
  • 2. Department of Engineering Physics and Centre for Emerging Device Technologies, McMaster University, 1280 Main St. W, Hamilton, Ontario L8S 4L7 (Canada)

Description

Terbium-doped silicon-rich silicon oxide films were deposited and hydrogenated at elevated temperatures. The influence of hydrogenation on defects-mediated non-radiative recombination of excited Tb3+ ions was investigated by means of photoluminescence and photoluminescence decay measurements. An increase in photoluminescence intensity and photoluminescence decay time was observed upon hydrogenation for the main 5D47F5 transition of Tb3+ ions. This observation was ascribed to saturation of non-radiative recombination defect centers with hydrogen. It was found that the number of emitted photons increases upon passivation as a result of two effects: (1) a reduction of the non-radiative recombination rate, and (2) optical activation of new Tb3+ emitters. Based on the obtained results and literature data, Förster energy-transfer was suggested as the interaction responsible for the non-radiative coupling between Tb3+ ions and defects. - Highlights: • Tb-doped silicon-rich silicon oxide films were deposited and hydrogenated. • The influence of defect passivation on Tb emission properties was investigated. • Enhancement of Tb photoluminescence intensity was observed upon passivation. • Longer Tb3+ lifetime in the 5D4 excited state was observed upon passivation. • Optical activation of new Tb3+ emitters was observed after hydrogenation.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tsf.2016.04.050

Additional details

Identifiers

DOI
10.1016/j.tsf.2016.04.050;
PII
S0040-6090(16)30142-0;

Publishing Information

Journal Title
Thin Solid Films
Journal Volume
611
Journal Page Range
p. 62-67
ISSN
0040-6090
CODEN
THSFAP

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.