材料科学
催化作用
分解水
碳纤维
异质结
化学工程
纳米技术
化学
复合数
复合材料
光电子学
生物化学
光催化
工程类
作者
Yajie Chen,Zhiyu Ren,Huiying Fu,Xin Zhang,Guohui Tian,Honggang Fu
出处
期刊:Small
[Wiley]
日期:2018-05-27
卷期号:14 (25): e1800763-e1800763
被引量:227
标识
DOI:10.1002/smll.201800763
摘要
Abstract Fabricating cost‐effective, bifunctional electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in basic media is critical for renewable energy generation. Here, NiSe/CP, Ni 0.85 Se/CP, and NiSe‐Ni 0.85 Se/CP heterostructure catalysts with different phase constitutions are successfully prepared through in situ selenylation of a NiO nanoflake array oriented on carbon paper (CP) by tuning the original Ni/Se molar ratio of the raw materials. The relationship between the crystal phase component and electrocatalytic activity is systematically studied. Benefiting from the synergetic effect of the intrinsic metallic state, facile charge transport, abundant catalytic active sites, and multiple electrolyte transmission paths, the optimized NiSe‐Ni 0.85 Se/CP exhibits a remarkably higher catalytic activity for both the HER and OER than single‐phase NiSe/CP and Ni 0.85 Se/CP. A current density of 10 mA cm −2 at 1.62 V and a high stability can be obtained by using NiSe‐Ni 0.85 Se/CP as both the cathode and anode for overall water splitting under alkaline conditions. Density functional theory calculations confirm that H and OH − can be more easily adsorbed on NiSe‐Ni 0.85 Se than on NiSe and Ni 0.85 Se. This study paves the way for enhancing the overall water splitting performance of nickel selenides by fabricating heterophase junctions using nickel selenides with different phases.
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