Neighbouring Synergy in High‐Density Single Ir Atoms on CoGaOOH for Efficient Alkaline Electrocatalytic Oxygen Evolution

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Abstract
The catalytic performance of single‐atom catalysts was strictly limited by isolated single‐atom sites. Fabricating high‐density single atoms to realize the synergetic interaction in neighbouring single atoms could optimize the adsorption behaviors of reaction intermediates, which exhibited great potential to break performance limitations and deepen mechanistic understanding of electrocatalysis. However, the catalytic behavior governed by neighbouring single atoms is particularly elusive and has yet to be understood. Herein, we revealed that the synergetic interaction in neighbouring single atoms contributes to superior performance for oxygen evolution relative to isolated Ir single atoms. Neighbouring single atoms was achieved by fabricating high‐density single atoms to narrow the distance between single atoms. Electrochemical measurements demonstrated that the Nei‐Ir1/CoGaOOH with neighbouring Ir single atoms exhibited a low overpotential of 170 mV at a current density of 10 mA cm−2, and long‐durable stability over 2000 h for oxygen evolution. Mechanistic studies revealed that neighbouring single atoms synergetic stabilized the *OOH intermediates via extra hydrogen bonding interactions, thus significantly reducing the reaction energy barriers, as compared to isolated Ir single atoms. The discovery of the synergetic interaction in neighbouring single atoms could offer guidance for the development of efficient electrocatalysts, thus accelerating the world‘s transition to sustainable energy.
Funding Information
  • National Natural Science Foundation of China (12241502, 22202192)
  • Fundamental Research Funds for the Central Universities (20720220010)
  • National Key Research and Development Program of China (2019YFA0405602)

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