Journal Article PUBDB-2026-00936

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Role of Defects in Reversible Surface Restructuring and Activity of Co$_3$O$_4$ Oxygen Evolution Electrocatalysts

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2026
ACS Catalysis Washington, DC

ACS catalysis 16(5), 4877 - 4891 () [10.1021/acscatal.5c08785]
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Abstract: Overcoming the slow kinetics of the oxygen evolution reaction at the anode is a key challenge for the production of hydrogen via electrolysis. This reaction operates at very positive potentials, where the electrocatalyst is exposed to highly oxidative conditions and prone to potential-dependent transformation of the near-surface region. While substantial evidence for such surface restructuring exists, its extent and relevance for the catalyst’s activity are unclear. We address this topic for the case of Co$_3$O$_4$, one of the best-known electrocatalysts exhibiting surface restructuring, by studies of epitaxial (111)-ordered electrodeposited films with combined operando X-ray surface diffraction and absorption spectroscopy, electrochemical impedance spectroscopy, and electrochemical measurements on rotating disk electrodes. Comparison of the as-prepared and annealed state of the same samples, which both are stable even under long-term oxygen evolution conditions, provides clear insight into the role of surface defects. Our results show that defect-free annealed Co$_3$O$_4$(111) surfaces are structurally stable over a wide potential range and hydroxylate via adsorption at surface oxygen and Co sites. Potential-induced surface restructuring of the Co$_3$O$_4$ lattice occurs only in the presence of surface defects, leading to the formation of the well-known nanometer-thick oxyhydroxide skin layer. The presence of this skin layer promotes oxygen evolution at low overpotentials but results in higher Tafel slopes. As a result, highly ordered Co$_3$O$_4$(111) surfaces are more active at high current densities than defective Co$_3$O$_4$ surfaces that undergo surface restructuring. These results highlight that strategies for catalyst surface defect engineering need to be application-oriented.

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Contributing Institute(s):
  1. DOOR-User (DOOR ; HAS-User)
  2. Uni Kiel (UKiel)
  3. CNRS (CNRS)
  4. Ruhr-Universität Bochum (U Bochum)
Research Program(s):
  1. 6G3 - PETRA III (DESY) (POF4-6G3) (POF4-6G3)
  2. DFG project G:(GEPRIS)388390466 - TRR 247: Heterogene Oxidationskatalyse in der Flüssigphase – Materialien und Mechanismen in der thermischen, Elektro- und Photokatalyse (388390466) (388390466)
  3. FS-Proposal: I-20220824 (I-20220824) (I-20220824)
  4. FS-Proposal: I-20230748 (I-20230748) (I-20230748)
Experiment(s):
  1. PETRA Beamline P23 (PETRA III)

Appears in the scientific report 2026
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; Essential Science Indicators ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2026-03-09, last modified 2026-03-23