电催化剂
镍
异质结
分解水
材料科学
纳米技术
化学工程
光电子学
化学
催化作用
电化学
冶金
光催化
电极
物理化学
工程类
生物化学
作者
Yuanyuan Wang,Rui Yin,Lei Yuan,Xingmei Guo,Xiangjun Zheng,Qianqian Fan,Zhongyao Duan,Yuanjun Liu,Junhao Zhang,Shenglin Xiong
标识
DOI:10.1021/acsenergylett.4c03097
摘要
Exploring a general method for constructing uniform heterostructures with sub-5 nm crystallites and dense interfaces is crucial yet challenging for advancing water electrocatalysis. Herein, a bottom-up cocrystallization strategy, involving in situ transformation of amorphous Ni–P through gas–solid reactions, is proposed to synthesize a series of nickel-based heterojunctions on carbon cloth (CC). Thereinto, interface-wealthy NiS2-Ni2P/CC with densely packed 3–4 nm crystallites demonstrates superb catalytic performance for both hydrogen and oxygen evolution. The electrolyzer merely requires cell voltages of 1.79 and 1.89 V to propel overall water splitting currents of 200 and 400 mA cm–2, respectively, outperforming the vast majority of reported nickel-based heterojunctions. Theoretical calculations reveal that charge redistribution and electronic structure modulation optimize the hydrogen and oxygen evolution pathways at the NiS2 and Ni2P sides of the interfaces, respectively. Moreover, uniform hybridization with densely distributed heterointerfaces offers abundant active sites for electrocatalysis, pioneering an extendable approach for constructing advanced heterojunction catalysts for green hydrogen production.
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