Recent Progress in Hydrogen Electrocatalysis

PAOLA QUAINO; ELIZABETH SANTOS; GERMÁN JOSÉ SOLDANO; WOLFGANG SCHMICKLER

Advances in Physical Chemistry

Hindawi Publishing Corporation Country

Año: 2011 vol. 2011 p. 1 - 14

1687-7985

Recently, we have proposed a unified model for electrochemical electron transfer reactions which explicitly accounts for the electronic structure of the electrode. It provides a framework describing the whole course of bond-breaking electron transfer, which explains catalytic effects caused by the presence of surface d bands. In application on real systems, the parameters of this model interaction strengths, densities of states, and energies of reorganization are obtained from density functional theory (DFT). In this opportunity, we review our main achievements in applying the theory of electrocatalysis. Particularly, we have focused on the electrochemical adsorption of a proton from the solution (the Volmer reaction) on a variety of systems of technological interest, such as bare single crystals and nanostructured surfaces. We discuss in detail the interaction of the surface metal d band with the valence orbital of the reactant and its effect on the catalytic activity as well as other aspects that influence the surface-electrode reactivity such as strain and chemical factors.