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March 18, 2026ACS Materials Letters3 citations

Activating High-Valent Cu III Species via Co-Doping in Covellite CuS for Water Oxidation

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FYFulin YangRHR F HeSWS. X. Wang

Key Points

  • This research aims to develop more efficient Cu-based catalysts for the oxygen evolution reaction by activating high-valent CuIII species.
  • Synthesize Co-doped CuS supported on graphene (Co-CuS/G).
  • Analyze the surface reconstruction processes under potential application.
  • Perform theoretical calculations to assess adsorption strength of oxygenated intermediates.
  • Co-CuS/G activates CuIII species at ~1.35 V, significantly lower than typical Cu-based catalysts.
  • Theoretical models confirm strong synergy between CuIII and Co dopants.
  • Co-CuS/G exhibits superior catalytic ability and durability over both undoped CuS and commercial IrO2.

Abstract

Developing Cu-based catalysts for the oxygen evolution reaction (OER) holds great promise as an alternative to noble-metal catalysts yet is hampered by the large energy cost required for generating active CuIII species. Here, we uncover a surface reconstruction of the graphene-supported CuS enabled by Co-doping (Co-CuS/G) that can effectively activate and stabilize high-valent CuIII species for OER. Unlike undoped CuS that partially converts into CuO, Co-CuS/G undergoes deep reconstruction into Cu(OH)2 and subsequently to the active phase CuOOH at ∼1.35 V vs RHE, much lower than the most reported Cu-based catalysts (≥1.62 V vs RHE). Theoretical calculations further confirm that CuIII species and Co dopants synergistically strengthen the adsorption of key oxygenated intermediates, lowering the energy barrier of the rate-determining step. Therefore, Co-CuS/G achieves good catalytic ability and durability, outperforming both undoped CuS and even commercial IrO2. This work offers a strategy to lower the energetic threshold for CuIII generation in Cu-based OER catalysts.

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Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/69ba42cf4e9516ffd37a3581https://doi.org/10.1021/acsmaterialslett.6c00138
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