Boosting Hydrogen Evolution in Neutral Medium by Accelerating Water Dissociation with Ru Clusters Loaded on Mo2CTx MXene

被引:55
|
作者
Wu, Yanze [1 ]
Wang, Lin [1 ]
Bo, Tao [2 ]
Chai, Zhifang [1 ]
Gibson, John K. [3 ]
Shi, Weiqun [1 ]
机构
[1] Chinese Acad Sci, Inst High Energy Phys, Lab Nucl Energy Chem, Beijing 100049, Peoples R China
[2] Chinese Acad Sci, Engn Lab Adv Energy Mat Ningbo Inst Mat Technol &, Ningbo 315201, Peoples R China
[3] Chem Sci Div, Lawrence Berkeley Natl Lab LBNL, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
hydrogen evolution reaction; neutral medium; noble metals; water dissociation; MO2CTX MXENE; EFFICIENT; ELECTROCATALYSTS; ENERGY; TRANSITION; GOLD;
D O I
10.1002/adfm.202214375
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic hydrogen evolution reaction (HER) in mild neutral medium is a compelling goal for environmentally sustainable energy conversion, but its development is greatly limited by slow kinetics. Platinum group noble metals exhibit ultra-high HER activities, but their scarcity and performance instability restrict wide application. Herein, taking advantage of excellent catalyst carrier properties of 2D-layered transition metal carbides (MXenes), highly dispersed of Ru clusters anchored on Mo2CTx MXene are demonstrated as a superior HER electrocatalyst, which is prepared by a facile in situ reduction strategy. The as-prepared Ru/Mo2CTx catalyst exhibits a very low overpotential of 73 mV to achieve a current density of -10 mA cm(-2) and Tafel slope of 57 mV dec(-1) in neutral medium, surpassing performance of most previously reported MXene-based catalysts. In addition, Ru/Mo2CTx catalyst also presents superior stability compared to commercial Pt/C. Experimental results and theoretical calculations indicate that the interaction between Ru clusters modulates the electronic structure of active sites and promotes H2O dissociation and hydrogen desorption.
引用
收藏
页数:7
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