Issue 36, 2011

Near-surface ion distribution and buffer effects during electrochemical reactions

Abstract

The near-surface ion distribution at the solid–liquid interface during the Hydrogen Oxidation Reaction (HOR)/Hydrogen Evolution Reaction (HER) on a rotating platinum disc electrode is demonstrated in this work. The relation between reaction rate, mass transport and the resulting surface pH-value is used to theoretically predict cyclic voltammetry behaviour using only thermodynamic and diffusion data obtained from the literature, which were confirmed by experimental measurements. The effect of buffer addition on the current signal, the surface pH and the ion distribution is quantitatively described by analytical solutions and the fragility of the surface pH during reactions that form or consume H+ in near-neutral unbuffered solutions or poorly buffered media is highlighted. While the ideal conditions utilized in this fundamental study cannot be directly applied to real scenarios, they do provide a basic understanding of the surface pH concept for more complex heterogeneous reactions.

Graphical abstract: Near-surface ion distribution and buffer effects during electrochemical reactions

Article information

Article type
Paper
Submitted
26 May 2011
Accepted
25 Jul 2011
First published
11 Aug 2011

Phys. Chem. Chem. Phys., 2011,13, 16384-16394

Near-surface ion distribution and buffer effects during electrochemical reactions

M. Auinger, I. Katsounaros, J. C. Meier, S. O. Klemm, P. U. Biedermann, A. A. Topalov, M. Rohwerder and K. J. J. Mayrhofer, Phys. Chem. Chem. Phys., 2011, 13, 16384 DOI: 10.1039/C1CP21717H

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