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Phys Chem Chem Phys. 2015 Feb 14;17(6):4505-15. doi: 10.1039/c4cp03783a.

Oxygen-induced changes to selectivity-determining steps in electrocatalytic CO2 reduction.

Physical chemistry chemical physics : PCCP

Yin-Jia Zhang, Andrew A Peterson

Affiliations

  1. Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA.

PMID: 25582895 DOI: 10.1039/c4cp03783a

Abstract

The state of the electrocatalyst surface-including the oxidation state of the catalyst and the presence of spectator species-is investigated on Cu surfaces with density functional theory in order to understand predicted ramifications on the selectivity and efficiency of CO2 reduction. We examined the presence of oxygen-based species, including the fully oxidized Cu2O surface, the partially oxidized Cu(110)-(2 × 1)O surface, and the presence of OH spectators. The relative oxygen binding strength among these surfaces can help to explain the experimentally observed selectivity change between CH4 and CH3OH on these electrodes; this suggests that the oxygen-binding strength may be a key parameter which predicts the thermodynamically preferred selectivity for pathways proceeding through a methoxy (CH3O) intermediate. This study shows the importance of the local surface environment in the product selectivity of electrocatalysis, and suggests a simple descriptor that can aid in the design of improved electrocatalytic materials.

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