Pt Single-Atom collaborate with Pt Atom-Clusters by an In-Situ confined strategy for accelerating electrocatalytic hydrogen evolution

被引:21
作者
Liu, Xingyan [1 ]
Song, Xueting [1 ]
Jiang, Guangmei [1 ]
Tao, Liujun [1 ]
Jin, Zhaoyu [2 ]
Li, Fukun [1 ]
He, Youzhou [1 ]
Dong, Fan [2 ]
机构
[1] Chongqing Technol & Business Univ, Coll Environm & Resources, Chongqing Key Lab Catalysis & New Environm Mat, Chongqing 400067, Peoples R China
[2] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Peoples R China
基金
中国国家自然科学基金;
关键词
UiO-66-PtTCPP precursor; Pt single-atom; Pt atom-clusters; Mass activity; Hydrogen evolution reaction; METAL-ORGANIC FRAMEWORKS; CATALYSTS;
D O I
10.1016/j.cej.2023.148430
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterogeneous catalysts with atomic dispersion play an important role in electrocatalysis. In addition to the single-atom, modifying the intrinsic catalytic capacity of single-atom catalysts through cooperative atom-clusters is an effective way to increase active sites and improve mass activity. Herein, a composite electrocatalytic material (PtM@CN) with partial Pt single-atoms and partial Pt atom-clusters was obtained by pyrolysis of the thermostable UiO-66-PtTCPP precursor. Remarkably, beneficial to the synergistic effect of Pt single-atom and Pt atom-clusters as well as the strong metal-support interaction, the PtM@CN catalyst showed excellent hydrogen evolution reaction (HER) activity and stability in both acidic and alkaline electrolytes. Moreover, X-ray photoelectron spectroscopy (XPS) and density functional theory (DFT) calculations shows that the existence of Pt single-atom and Pt atom-clusters could rationally adjust electronic structure of supported metals and impact adsorption energy of reaction intermediates, which play an essential role in enhancing the electrocatalytic activity of HER.
引用
收藏
页数:10
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