In situ construction of layered transition metal phosphides/sulfides heterostructures for efficient hydrogen evolution in acidic and alkaline media

被引:13
|
作者
Qian, Yongteng [1 ]
Sun, Yue [2 ]
Zhang, Fangfang [1 ]
Luo, Xiaohui [1 ]
Li, Kangning [1 ]
Shen, Lin [3 ]
Shi, Hu [2 ]
Kang, Dae Joon [3 ]
Pang, Huan [4 ]
机构
[1] Jinhua Polytech, Coll Pharm, Jinhua 321007, Zhejiang Provin, Peoples R China
[2] Shanxi Univ, Inst Mol Sci, Sch Chem & Chem Engn, Taiyuan 030006, Peoples R China
[3] Sungkyunkwan Univ, Dept Phys, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[4] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Re2P; ReS2; Heterostructures; Intrinsic activity; Hydrogen evolution reaction; RES2;
D O I
10.1016/j.cej.2024.151693
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Construction of electrocatalysts with exceptional intrinsic activity and rich active sites has proved to be an effective strategy for remarkably enhancing the activity of the hydrogen evolution reaction (HER). In this work, durable and highly efficient layered Re 2 P/ReS 2 (RePS) heterostructures were successfully fabricated by an in -situ phosphating layered ReS 2 . Taking advantage of the unique layered structure can provide abundant reaction active sites and the strong electronic interaction between ReS 2 and Re 2 P can enhance the intrinsic activity, the optimized RePS electrocatalysts show superior catalytic activities of 69 and 57 mV at 10 mA cm -2 for HER in alkaline and acidic media, respectively. The density functional theory results suggest that the formed heterostructures between ReS 2 and Re 2 P play an important role in optimizing the catalytic kinetics of the electrocatalysts. This work not only demonstrates that modulation of the electronic structure of catalysts is an efficient way to improve the HER activity but also confirms that the layered RePS heterostructure is a promising candidate for robust and high performance HER catalysts.
引用
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页数:7
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