4.8 Article

Rationally Modulating the Functions of Ni3Sn2-NiSnOx Nanocomposite Electrocatalysts towards Enhanced Hydrogen Evolution Reaction

Journal

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202301562

Keywords

Alkaline Hydrogen Evolution; All Pertinent Intermediates; Multiple Functions; Mutual Coordination; Nanocomposite Electrocatalysts

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In this study, Ni3Sn2-NiSnOx nanocomposites were designed to address the challenge of efficient alkaline hydrogen evolution reaction (HER) by enabling easy dissociation of water, rapid transformation of hydroxyl, and facile hydrogen-hydrogen bond formation. The results showed that Ni3Sn2 exhibited ideal hydrogen adsorption and low hydroxyl adsorption abilities, while NiSnOx facilitated water dissociation and hydroxyl transfer process. The fine-tuned interplay of the two functional parts significantly boosted HER kinetics, with current densities of 10 and 1000 mA cm(-2) obtained at overpotentials of 14 and 165 mV on the optimized catalyst. This work highlights the importance of considering intrinsic interactions between active sites and all pertinent intermediates in obtaining promising electrocatalysts.
Identifying electrocatalysts with functions of easy dissociation of water, rapid transformation of hydroxyl and facile hydrogen-hydrogen bond formation are indispensable while challenge for realizing efficient alkaline hydrogen evolution reaction (HER). Herein, we presented the design of Ni3Sn2-NiSnOx nanocomposites towards addressing this challenge. We showed that Ni3Sn2 possessed ideal hydrogen adsorption and low hydroxyl adsorption abilities and NiSnOx facilitated water dissociation and hydroxyl transfer process, respectively. Consequently, the fine-tuned interplay of the two functional parts realized the mutual coordination among the multiple functions and led to significantly boosted HER kinetics. Current densities of 10 and 1000 mA cm(-2) were obtained at overpotentials of 14 and 165 mV on the optimized catalyst. This work highlights the significance of considering intrinsic interactions between active sites and all pertinent intermediates on obtaining promising electrocatalysts.

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