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MoN/NiS异质结阵列的界面电子调制促进电催化碱性全水解

Interfacial Electronic Modulation of MoN/NiS Heterojunction Array Boosts Electrocatalytic Alkaline Overall Water Splitting.

作者信息

Fang Bin, Jin Jutao, Li Yanqin, Dang Haifeng, Shao Mengmeng, Zhao Liyuan, Yin Nianliang, Wang Wenlong

机构信息

School of Materials Science and Engineering, Dongguan University of Technology, Dongguan, Guangdong, 523808, P. R. China.

School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.

出版信息

Small. 2024 Jul;20(29):e2310825. doi: 10.1002/smll.202310825. Epub 2024 Feb 11.

Abstract

Bifunctional electrocatalysts with excellent activity and durability are highly desirable for alkaline overall water splitting, yet remain a significant challenge. In this contribution, palm-like MoN/NiS heterojunction arrays anchored in conductive Ni foam (denoted as MoN-NiS HNPs/NF) are developed. Benefiting from the optimized electronic structure configuration, hierarchical branched structure and abundant heterogeneous interfaces, the as-synthesized MoN-NiS HNPs/NF electrode exhibits remarkably stable bifunctional electrocatalytic activity in 1 m KOH solution. It only requires ultralow overpotentials of 59 and 190 mV to deliver a current density of 10 mA cm for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1 m KOH solution, respectively. Importantly, the overall water splitting electrolyzer assembled by MoN-NiS HNPs/NF exhibits an exceptionally low cell voltage (1.48 V@10 mA cm) and outstanding durability, surpassing most of the reported Ni-based bifunctional materials. Density functional theory (DFT) further confirms the heterostructure can optimize the Gibbs free energies of H and O-containing intermediates (OH, O, OOH) during HER and OER processes, thereby accelerating the catalytic kinetics of electrochemical water splitting. The findings provide a new design strategy toward low-cost and excellent catalysts for overall water splitting.

摘要

具有优异活性和耐久性的双功能电催化剂对于碱性全水解非常理想,但仍然是一个重大挑战。在本研究中,制备了锚定在导电泡沫镍上的棕榈状MoN/NiS异质结阵列(记为MoN-NiS HNPs/NF)。得益于优化的电子结构配置、分级分支结构和丰富的异质界面,所合成的MoN-NiS HNPs/NF电极在1 m KOH溶液中表现出显著稳定的双功能电催化活性。在1 m KOH溶液中,析氢反应(HER)和析氧反应(OER)分别仅需59和190 mV的超低过电位即可实现10 mA cm的电流密度。重要的是,由MoN-NiS HNPs/NF组装的全水解电解槽表现出极低的电池电压(1.48 V@10 mA cm)和出色的耐久性,超过了大多数已报道的镍基双功能材料。密度泛函理论(DFT)进一步证实,异质结构可以优化HER和OER过程中含H和O中间体(OH、O、OOH)的吉布斯自由能,从而加速电化学水分解的催化动力学。这些发现为全水解低成本优异催化剂提供了一种新的设计策略。

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