4.8 Article

Operando X-Ray Absorption Spectroscopy Shows Iron Oxidation Is Concurrent with Oxygen Evolution in Cobalt-Iron (Oxy)hydroxide Electrocatalysts

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 39, Pages 12840-12844

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201808818

Keywords

electrocatalysts; heterogeneous catalysis; oxygen evolution; water electrolysis; X-ray absorption spectroscopy

Funding

  1. National Science Foundation [CHE-1566348]
  2. Nancy and Stephen Grand Technion Energy Program (GTEP)
  3. Ministry of Science and Technology (MOST), Israel
  4. DOE Office of Science User Facility [DE-AC02-05CH11231]

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Iron cations are essential for the high activity of nickel and cobalt-based (oxy)hydroxides for the oxygen evolution reaction, but the role of iron in the catalytic mechanism remains under active investigation. Operando X-ray absorption spectroscopy and density functional theory calculations are used to demonstrate partial Fe oxidation and a shortening of the Fe-O bond length during oxygen evolution on Co(Fe)OxHy. Cobalt oxidation during oxygen evolution is only observed in the absence of iron. These results demonstrate a different mechanism for water oxidation in the presence and absence of iron and support the hypothesis that oxidized iron species are involved in water-oxidation catalysis on Co(Fe)OxHy.

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