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March 14, 2026The Journal of Physical Chemistry C0 citations

Synthetic CuS x O 1– x Copper Oxysulfides Nanosheets by Redox Reaction for Efficient Oxygen Evolution Reaction

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HLHui LiMGMingzheng GuJWJuan Wang

Key Points

  • To investigate the performance of copper oxysulfide nanoflowers in the oxygen evolution reaction (OER).
  • Synthesis of copper oxysulfide nanoflowers via redox reaction.
  • Assessment of OER activity and stability through electrochemical measurements.
  • In situ ATR-IR measurements for monitoring reconstruction during OER.
  • Copper oxysulfide exhibited a low overpotential of 206 mV at 10 mA cm–2 for the OER.
  • Nanoflowers showed superior stability compared to original CuS.
  • Enhanced performance attributed to facilitated formation of reaction intermediates and accelerated kinetics.

Abstract

Copper-based electrocatalysts are regarded as highly efficient electrocatalysts due to their low cost and environmental friendliness. However, their practical application in water splitting remains severely limited by intrinsic drawbacks such as inferior electron transfer kinetics and moderate catalytic activity. Herein, we synthesized copper oxysulfide (CuSxO1–x) flake-like nanoflowers through a redox reaction and explored their application as efficient electrocatalysts for the oxygen evolution reaction. As expected, compared to the original CuS, the copper oxysulfides exhibited superior OER activity and stability, showing a remarkably low overpotential of 206 mV at a benchmark current density of 10 mA cm–2 for the OER. This study elucidates the reconstruction of copper oxysulfide electrocatalysts during the oxygen evolution reaction through in situ ATR-IR measurements. The facilitated formation of reaction intermediates and accelerated reconstruction kinetics during the structural evolution of copper oxysulfide synergistically contribute to its enhanced oxygen evolution reaction performance.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69b4b9db18185d8a398020e0https://doi.org/10.1021/acs.jpcc.6c00817
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