Transition heterogeneous electrocatalysis

Scherson, Palenscar, Tolmachev and Stefan provide a critical review of transition metal macrocycles, in both intact and thermally activated forms, as electrocatalysts for dioxygen reduction in aqueous electrolytes. An introduction is provided to fundamental aspects of electrocatalysis, oxygen reduction, and transition metal macrocydes. Since the theoretical and experimental tools used for investigation of homogeneous and heterogeneous electrocatalysis are considerably different, these topics are given separate discussion. The influence of the electrode surface on adsorbed macrocydes, and their influence on mechanism and rates of 02 reduction is treated in detail. Issues related to pyrolyzed macrocydes are also described. 

In recent years, much attention has been focused on electrochemical studies of metalloporphyrins, not only as mimetic compounds of the iron porphyrin unit in heme proteins but also as potential electrocatalysts . Metalloporphyrins have been found to be applicable in both homogeneous and heterogeneous catalysis - and, because oxygen can be reduced directly through a 4-electron pathway on some transition metal porphyrins, catalysis in the heterogeneous electrochemical oxygen reduction reaction has received particular attention The application of metalloporphyrins to heterogeneous electrocatalysis requires their attachment to solid electrodes which can be realized based on chemisorption, chemical reactions with previously functionalized electrodes, chemical reactions with a functionalized polymer, incorporation of the porphyrin with the polymer film and electrochemical polymerization. 

This series covers recent advances in electrocatalysis and electrochemistry and depicts prospects for their contribution into the present and future of the industrial world. It illustrates the transition of electrochemical sciences from a solid chapter of physical electrochemistry (covering mainly electron transfer reactions, concepts of electrode potentials and stmcture of the electrical double layer) to the field in which electrochemical reactivity is shown as a unique chapter of heterogeneous catalysis, is supported by high-level theory, connects to other areas of science, and includes focus on electrode surface structure, reaction environment, and interfacial spectroscopy. 

The electrical, magnetic, optical, and catalytic properties of transition metal nanoparticles differ decisively from those of the bulk phase. The peculiar effects of nanoparticle size, shape, and electronic structure are of interest both from the perspective of fundamental research and applications in energy research (Roduner, 2006 Yaca-man et al., 2001). Specific phenomena at particle sizes below 2 nm arise from the confinement of (quasi)-free electrons and the increasingly discrete nature of the electronic structure (Halperin, 1986). In electrocatalysis, the primary interests are to understand (i) the classical effects of atom arrangement and (ii) the heterogeneous electronic structure at the nanoparticle surface, controlling interfacial adsorption and charge transfer phenomena. 

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