过电位
海水
催化作用
法拉第效率
电解质
异质结
材料科学
化学工程
纳米技术
化学
电极
电化学
光电子学
物理化学
地质学
工程类
海洋学
生物化学
作者
Xiuming Bu,Xinwen Liang,Yu Bu,Quan Quan,You Meng,Zhengxun Lai,Wei Wang,Chuntai Liu,Jian Lü,Chi‐Man Lawrence Wu,Johnny C. Ho
标识
DOI:10.1016/j.cej.2022.135379
摘要
Designing highly efficient and stable electrocatalysts for hydrogen evolution reaction (HER), particularly in seawater, still remains a challenging task. Herein, the unique heterostructures composed of 1D NiMo cores and 2D C3N5 shells ([email protected]3N5) are rationally designed and demonstrated as the robust HER catalysts in both alkaline electrolytes and natural seawater, where the carbon-based shell can effectively protect the catalyst core from seawater poisoning. Based on the experimental investigation and density functional theory calculation, multiple electronic transmission channels were found to establish at the interface between NiMo cores and C3N5 shells, thus providing efficiently optimized HER pathways to achieve minimized overpotential with a reduced energy barrier of the rate-determining step. More importantly, the [email protected]3N5 hybrids exhibit stable HER performance with a high Faradaic efficiency of 94.8% in seawater, which is superior to that of commercial Pt/C. All these results can evidently highlight a feasible strategy to develop high-performance HER electrocatalysts via interface engineering.
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