Published June 16, 2011 | Version v1
Journal article

CuInSe2 nano-crystallite reaction kinetics using solid state reaction from Cu2Se and In2Se3 powders

  • 1. Department of Resources Engineering, Particulate Materials Research Center, National Cheng Kung University, Tainan 70101, Taiwan (China)

Description

Highlights: → CuInSe2 phase increased gradually accompanied with a decrease in γ-In2Se3 and no intermediate phase during calcination. → CuInSe2 formation from Cu2Se and In2Se3 powders follows a one-dimensional diffusion-controlled reaction with apparent activation energy of about 122.5 kJ/mol. → The solid reaction kinetics may be dominated by the diffusion of In3+ ions. - Abstract: The reaction mechanism and CuInSe2 formation kinetics using a solid state reaction from Cu2Se and In2Se3 powders synthesized using a heating up process were investigated using X-ray diffractomy (XRD) and transmission electron microscopy (TEM). It was observed that the CuInSe2 phase increased gradually, accompanied with a decrease in γ-In2Se3 with no intermediate phase as the calcination temperature and soaking time were increased. The reaction kinetics was analyzed using the Avrami and polynomial kinetic model, suggesting that CuInSe2 formation from Cu2Se and In2Se3 powders follows a diffusion-controlled reaction with an apparent activation energy of about 122.5-182.3 kJ/mol. Cu2Se and In2Se3 phases react and directly transform into CIS without the occurrence of any intermediate phase and the size of the newly formed CuInSe2 crystallites was close to that of the Cu2Se reactant particle based on the TEM results, which indicated that the solid reaction kinetics may be dominated by the diffusion of In3+ ions.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2011.04.009

Additional details

Identifiers

DOI
10.1016/j.jallcom.2011.04.009;
PII
S0925-8388(11)00829-2;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
509
Journal Issue
24
Journal Page Range
p. 6950-6954
ISSN
0925-8388
CODEN
JALCEU

Optional Information

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