4.7 Article

Effects of aqueous buffers on electrocatalytic water oxidation with an iridium oxide material electrodeposited in thin layers from an organometallic precursor

Journal

DALTON TRANSACTIONS
Volume 42, Issue 10, Pages 3617-3622

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt32326e

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Funding

  1. Argonne-Northwestern Solar Energy Research (ANSER) Center
  2. Energy Frontier Research Center
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001059]
  4. U.S. DOE [DE-FG02-84ER13297]
  5. U.S. Department of Energy (DOE) [DE-FG02-84ER13297] Funding Source: U.S. Department of Energy (DOE)

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A thin layer of an amorphous, mixed-valence iridium oxide (electrodeposited from an organometallic precursor, [Cp*Ir(H2O)(3)](2+)) is a heterogeneous catalyst among the most active and stable currently available for electrochemical water oxidation. We show that buffers can improve the oxygen-evolution activity of such thin-layer catalysts near neutral pH, but that buffer identity and concentration, as well as the solution pH, remain key determinants of long-term electrocatalyst activity and stability; for example, phosphate buffer can reduce the overpotential by up to 173 mV.

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