Highly active and durable nanostructured molybdenum carbide electrocatalysts for hydrogen production

被引:865
作者
Chen, W. -F. [1 ]
Wang, C. -H. [1 ,2 ]
Sasaki, K. [1 ]
Marinkovic, N. [3 ]
Xu, W. [1 ]
Muckerman, J. T. [1 ]
Zhu, Y. [2 ]
Adzic, R. R. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Condensed Matter Phys & Mat Sci Dept, Upton, NY 11973 USA
[3] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
关键词
TUNGSTEN CARBIDE; CATALYTIC-ACTIVITY; THERMAL-DECOMPOSITION; EVOLUTION REACTION; NANOPARTICLES; NANOTUBES; EFFICIENT; SURFACES; SULFIDE; MO2C;
D O I
10.1039/c2ee23891h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In an attempt to tailor low-cost, precious-metal-free electrocatalysts for water electrolysis in acid, molybdenum carbide (beta-Mo2C) nanoparticles are prepared by in situ carburization of ammonium molybdate on carbon nanotubes and XC-72R carbon black without using any gaseous carbon source. The formation of Mo2C is investigated by thermogravimetry and in situ X-ray diffraction. X-ray absorption analysis reveals that Mo2C nanoparticles are inlaid or anchored into the carbon supports, and the electronic modification makes the surface exhibit a relatively moderate Mo-H bond strength. It is found that carbon nanotube-supported Mo2C showed superior electrocatalytic activity and stability in the hydrogen evolution reaction (HER) compared to the bulk Mo2C. An overpotential of 63 mV for driving 1 mA cm(-2) of current density was measured for the nanotube-supported Mo2C catalysts; this exceeds the activity of analogous Mo2C catalysts. The enhanced electrochemical activity is facilitated by unique effects of the anchored structure coupled with the electronic modification.
引用
收藏
页码:943 / 951
页数:9
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