Published October 15, 2014 | Version v1
Journal article

A study on the crystallization behavior of Sn-doped amorphous Ge2Sb2Te5 by ultraviolet laser radiation

  • 1. Institute of Laser Engineering, Beijing University of Technology, 100124, Beijing (China)
  • 2. State Key Laboratory of Solidification Processing, Northwestern Poly technical University (China)
  • 3. Electrical and Computer Engineering Department, Northeastern University, MA 02115 (United States)

Description

Highlights: • The Raman peaks of Sn doped GST moved towards lower wavenumbers compared to GST. • The crystallization fluence for Sn doped GST was smaller than that for pure GST. • The optical contrast increased from 15% to 40% with the addition of Sn. • Optical contrast changed little with the variation of laser fluence. - Abstract: In this paper, the influence of Sn doping (0%, 8% and 14%) on the crystallization of Ge2Sb2Te5 was studied with the aid of an ultraviolet laser. The XRD analyses revealed that the addition of Sn maintained the NaCl-type structure of Ge2Sb2Te5 after crystallization but expanded the lattice parameter due to the smaller atomic radii of Ge replaced by Sn. Raman peaks (123, 150 and 110 cm−1) moved towards lower wavenumbers (118, 137 and 104 cm−1), which can be explained by the remarkable decrease of the binding energy from Ge–Te to Sn–Te. A remarkable increase in optical contrast from 15% to 40% was observed in the Sn-doped Ge2Sb2Te5 film after crystallization with both the isothermal annealing and laser radiance. While the optical contrast changed little for a fixed volume fraction of Sn-doped sample with the variation of laser fluence which is attributed to the crystallization mechanism induced by laser under different fluences is the same

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2014.08.007

Additional details

Identifiers

DOI
10.1016/j.apsusc.2014.08.007;
PII
S0169-4332(14)01739-5;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
316
Journal Page Range
p. 202-206
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

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