过电位
X射线光电子能谱
材料科学
电催化剂
氢
接口(物质)
密度泛函理论
化学物理
再分配(选举)
分解水
催化作用
化学工程
纳米技术
化学
电极
物理化学
光催化
计算化学
有机化学
复合材料
工程类
政治
电化学
毛细管数
毛细管作用
法学
政治学
作者
Zhijie Zhang,Jing Zhao,Mengchen Wu,Qinghua Lu,Rui Liu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-11-09
卷期号:16 (4): 4706-4714
被引量:29
标识
DOI:10.1007/s12274-022-5140-6
摘要
Exploring superior electrocatalyst for hydrogen evolution reaction (HER) is an urgent need for hydrogen production based on water splitting. The redistribution of electrons and the increase of active sites through multi-interface designing of electrocatalyst are powerful strategies to improve the catalytic efficiency. Herein, a three-phase interface structure of N,P co-doped carbon tube embedded with MoO2/Mo2C (MoO2/Mo2C-CT) was fabricated via a cooperative polymerizing-embedding and pyrolysis strategy. Work function and X-ray photoelectron spectroscopy (XPS) verified that the interfacial charge was quantificationally modulated, achieving an intrinsically enhanced charge transfer by an induced built-in electric field. Theoretical study of density functional theory (DFT) illustrated that triple-interface structure showed a lower energy for H* + H2O* than that of single-interface counterparts. The triple-interface MoO2/Mo2C-CT delivered a lower overpotential of 129 mV at 10 mA·cm−2 than that of either single-interface MoO2-CT or Mo2C-CT catalyst. This work may put forward an attractive approach for modulating electronic structure and provide insights into the understanding of triple-interface structure towards HER.
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