Preprint PUBDB-2025-05645

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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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2025

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Abstract: Overcoming the slow kinetics of the oxygen evolution reaction at the anode is a key challenge for the sustainable 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 surface structural transformations. While substantial evidence for such surface restructuring exists, its extent and relevance for the catalysts’ activity is unclear. We address this topic for the case of Co$_3$O$_4$, one of the best known electrocatalysts exhibiting surface transformations, by studies of epitaxial (111)-ordered electrodeposited films with combined operando surface X-ray diffraction, electrochemical impedance spectroscopy, and electrochemical measurements on rotating disk electrodes. Comparison of the as-prepared and the 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 only occurs 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 transformation. These results highlight that strategies for catalyst surface defect engineering need to be application-oriented.


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

Appears in the scientific report 2025
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Creative Commons Attribution-NonCommercial-NoDerivs CC BY-NC-ND 4.0 ; OpenAccess
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Private Collections > >DESY > >Others > >UNI > UKiel
Private Collections > >Extern > >HAS-User > HAS-User
Private Collections > >Extern > U Bochum
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Private Collections > >Extern > EPTFR
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 Record created 2025-12-17, last modified 2026-02-09