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• W4282576869 abstract "Abstract A large number of highly active Ru‐based electrocatalysts have been reported for the hydrogen evolution reaction (HER). The utilization of synergistic effects for promoting HER performance remains inadequate, especially for corresponding potential‐driven reactive sites at the atomic level. Herein, a Co‐substituted RuRu 2 P structure is employed as a model system to reveal the synergistic effect on Ru‐based electrocatalysts and to realize the potential‐driven reactive sites during the HER. Optimized RuRu 2 P @ Co 0.6 exhibits a superior catalytic performance in alkaline electrolytes, achieving a low overpotential of 9 mV at a current density of 10 mA cm –2 . To precisely describe the geometrical nature of surface moiety of Co( µ ‐O) 2 Ru, an indicator (β) is established to quantify the strain of Co( µ ‐O) 2 Ru moieties through calculating the LCoL (L = P or O) angles through employing in situ X‐ray absorption spectroscopy. Both bond strain and corresponding metal‐metal distance of CoRu in Co( µ ‐O) 2 Ru moiety can significantly affect the structural tolerance and facilitate the coupling of adsorbed hydrogen atoms during HER. It is believed that the perspective raised in the present work will provide a new avenue to the design of highly active HER catalysts at the atomic scale." @default.
• W4282576869 created "2022-06-14" @default.
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• W4282576869 date "2022-06-13" @default.
• W4282576869 modified "2023-10-16" @default.
• W4282576869 title "Dynamic Co( <i>µ</i> ‐O) ₂ Ru Moiety Endowed Efficiently Catalytic Hydrogen Evolution" @default.
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• W4282576869 doi "https://doi.org/10.1002/aenm.202200079" @default.
• W4282576869 hasPublicationYear "2022" @default.
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