磷化物
化学
催化作用
电催化剂
X射线光电子能谱
无机化学
吸附
氧化物
分解水
可逆氢电极
化学工程
电化学
光催化
电极
工作电极
物理化学
有机化学
工程类
作者
Biao Zhang,Hongye Qin,Lechen Diao,Naiqin Zhao,Chunsheng Shi,Enzuo Liu,Chunnian He
标识
DOI:10.1016/j.jcat.2019.08.007
摘要
Exploring and developing highly efficient, cost-efficient and stable electrocatalyst for hydrogen evolution reaction (HER) in alkaline solutions is a meaningful but challenging task. Herein, we present the design and synthesis of a novel hollow-cerium oxide/nickel phosphide heterostructure encapsulated by ultrathin nitrogen-doped carbon layer (H-CeO2-x/Ni2[email protected]) as efficient electrocatalysts for HER in alkaline media. Both experimental and theoretical analysis suggests that the presence of CeO2-x not only serves as a site for adsorption of water molecules, but also has a strong ability to cleave H-O bonds in H2O molecules. More importantly, X-ray photoelectron spectroscopy (XPS) and differential charge density showed that the strong interaction between the components caused the change of charge distribution at the interface, that is, the charge accumulated to the phosphorus atoms. And that will greatly optimize the adsorption strength of the hydrogen intermediate species on the Ni2P surface. In addition, the nitrogen-doped ultrathin carbon layer on the outer surface can not only effectively accelerate the electron transfer to the active site, but avoid the catalyst deactivation caused by the falling off or segregation of the active species. Therefore, the as-prepared H-CeO2-x/Ni2[email protected] ternary hybrid electrode exhibit outstanding HER catalytic performance with low onset potential, high catalytic activity and excellent stability. Our work might shed some new lights on the design of efficient and robust three-dimensional hybrid catalyst for a variety of electrochemical applications.
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