4.8 Article

Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide

Journal

CHEMICAL SCIENCE
Volume 6, Issue 4, Pages 2405-2410

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5sc00032g

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Funding

  1. UNC EFRC: Center for Solar Fuels, an Energy Frontier Research Center by the U.S. Department of Energy, Office of Science, Office of Basic Energy [DE-SC0001011]

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The tris(2-pyridyl)phosphine oxide (Py3PO) complex [Ru(Py3PO)(bpy)(OH2)](2+) (bpy is 2,2'-bipyridine) is a pH-dependent water oxidation electrocatalyst that accelerates dramatically with increasing pH-up to 780 s(-1) at pH 10 (similar to 1 V overpotential). Despite retaining the pentakis(pyridine) ligand arrangement common to previously reported catalysts, the tripodal Py3PO ligand framework supports much faster electrocatalysis. The early stages of the catalytic cycle are proposed to follow the typical pattern of single-site ruthenium catalysts, with two sequential 1H(+)/1e(-) proton-coupled electron transfer (PCET) oxidations, but the pH-dependent onset of catalysis and rapid rates are distinguishing features of the present system.

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