CO and methanol electrooxidation on Pt/Ir/Pt multilayers electrodes

Author(s)

Freitas‚ RG ; Antunes‚ EP ; Pereira‚ EC

• Document type: Journal article
• Source: Electrochimica Acta; v. 54, n. 7, p. 1999-2003, 2009.

Abstract

This work describes the CO and methanol electrooxidation over an Ir/Pt bilayer electrodeposited on a platinum polycrystalline substrate. In the blank acidic solution it was observed that the electrochemical behavior of both the polycrystalline Pt and Pt/Ir/Pt nanostructured electrodes were very similar. The electroactive area, calculated using the hydrogen desorption method, are the same for both materials. In order to investigate the effect of the thickness change of Ir interlayer, two different samples were prepared. One with 1 Ir monolayer and the second with 3 monolayers thick. CO stripping voltammograms showed a shift in the anodic peak potential towards the negative direction of 160 and 180 mV for Pt/Ir/Pt 3:1 and 1:1 ML, respectively, compared to polycrystalline Pt. Besides, for methanol electrooxidation, the Pt/Ir/Pt electrodes presented an increase of 170% in the peak current density compared to polycrystalline Pt. These results are in agreement with the calculated activation energies which were 31.5, 39.0 and 43.5 kJ mol(-1) for Pt/Ir/Pt 1:1, 3:1 ML and polycrystalline Pt electrodes, respectively. Using the electrochemical impedance spectroscopy, surprisingly, the Pt/Ir/Pt electrodes, did not exhibit the inductive arc which means that the poisoning of the electrode surface is not important in this case. (C) 2008 Elsevier Ltd. All rights reserved. (AU)

• FAPESP's process: 03/09933-8 - Center for Excellence in Electrochemically Synthesized Nanostructures
• Grantee: Ernesto Chaves Pereira de Souza
• Support Opportunities: PRONEX Research - Thematic Grants