Molecular Transition Metal Oxide Electrocatalysts for the Reversible Carbon Dioxide-Carbon Monoxide Transformation.

Abstract

Carbon monoxide dehydrogenase (CODH) enzymes are active for the reversible CO oxidation-CO2 reduction reaction and are of interest in the context of CO2 abatement and carbon-neutral solar fuels. Bioinspired by the active-site composition of the CODHs, polyoxometalates triply substituted with first-row transition metals were modularly synthesized. The polyanions, in short, {SiM3 W9 } and {SiM'2 M''W9 }, M, M', M''=CuII , NiII , FeIII are shown to be electrocatalysts for reversible CO oxidation-CO2 reduction. A catalytic Tafel plot showed that {SiCu3 W9 } was the most reactive for CO2 reduction, and electrolysis reactions yielded significant amounts of CO with 98 % faradaic efficiency. In contrast, Fe-Ni compounds such as {SiFeNi2 W9 } preferably catalyzed the oxidation of CO to CO2 similar to what is observed for the [NiFe]-CODH enzyme. Compositional control of the heterometal complexes, now and in the future, leads to control of reactivity and selectivity for CO2 electrocatalytic reduction.