Published January 1, 2012 | Version v1
Journal article

The electrocatalytic properties of an IrO2/SnO2 catalyst using SnO2 as a support and an assisting reagent for the oxygen evolution reaction

  • 1. Department of Physical Chemistry, University of Science and Technology Beijing, 30 College Road, Beijing 100083 (China)
  • 2. State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing, 30 College Road, Beijing 100083 (China)

Description

Highlights: ► Enhanced performance was attributed to high surface area and desorption of hydroxy. ► Optimum condition was found at the mass ratio of iridium to tin was 2:1. ► Terminal voltage of water electrolysis was 1.70 V at 80 °C and 2 A cm−2. - Abstract: Electrocatalysts made of IrO2/SnO2 were prepared using the Adams method for solid polymer electrolyte (SPE) water electrolysis. The physicochemical properties of the catalyst were characterized via X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical properties of the catalyst were investigated using cyclic voltammetry (CV), electrochemical impendence spectroscopy (EIS), chronopotentiometry and Tafel curve measurements in 0.1 mol L−1 H2SO4 at room temperature. The test results showed that the catalytic properties of IrO2/SnO2 depended on the mass ratio of iridium to tin, and that the optimal mass ratio was 2:1. The optimized catalyst was applied to a membrane electrode assembly (MEA), and the stationary current–potential relationships were determined. With an IrO2/SnO2 (2:1) anode, a 40% Pt/C cathode and a total noble metal (Ir, Pt) loading of 1.2 mg cm−2, the terminal applied potential difference of the water electrolysis was 1.70 V at 2 A cm−2 and 80 °C.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2011.10.044

Additional details

Identifiers

DOI
10.1016/j.electacta.2011.10.044;
PII
S0013-4686(11)01548-9;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
59
Journal Page Range
p. 105-112
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

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