Rational construction of Pt/PtTex interface with optimal intermediate adsorption energy for efficient hydrogen evolution reaction

被引:72
作者
Chen, Jiadong [1 ]
Qin, Minkai [1 ]
Ma, Shuangxiu [1 ]
Fan, Ruxue [1 ]
Zheng, Xiaozhong [1 ]
Mao, Shanjun [1 ]
Chen, Chunhong [1 ]
Wang, Yong [1 ,2 ]
机构
[1] Zhejiang Univ, Inst Catalysis, Dept Chem, Adv Mat & Catalysis Grp, Hangzhou 310028, Peoples R China
[2] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Intermediates adsorption modulation; Pt/PtTex heterojunctions; Hydrogen evolution reaction; Long-term stability; PLATINUM; SURFACE; RU;
D O I
10.1016/j.apcatb.2021.120640
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Increasing OH* adsorption to promote water dissociation while reducing H* adsorption to accelerate hydrogen generation kinetics is an effective solution to further improve the HER activity of Pt-based catalysts. Herein, we have successfully constructed a Pt/PtTex heterogeneous catalysis interface by electrochemical activation of PtTe2 nanorods (NRs). The reduction of H* adsorption and significant increase of OH* adsorption was observed on Pt/PtTex heterojunction via cyclic voltammetry method. Theoretical calculations indicate that Gibbs free energy change (Delta G) of H* is closer to 0.00 eV and Delta G of OH* decreased from 1.36 eV of Pt (111) to -0.40 eV of Pt/ PtTex, which reinforces the experimental results. The rational modulation of adsorbed intermediates endows Pt/PtTex NRs with exceptionally lower Tafel slopes of 16 and 23 mV dec(-1) in 0.5 M H2SO4 and 1.0 M KOH electrolytes, which is among the best reported HER electrocatalysts.
引用
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页数:10
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