Nanostructured cobalt-modified molybdenum carbides electrocatalysts for hydrogen evolution reaction

被引:43
作者
Bukola, Saheed [1 ]
Merzougui, Belabbes [2 ]
Creager, Stephen E. [1 ]
Qamar, Mohammad [3 ]
Pederson, Larry R. [2 ]
Noui-Mehidi, Mohamed N. [4 ]
机构
[1] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
[2] Hamad Bin Khalifa Univ, Qatar Fdn, QEERI, Doha 5825, Qatar
[3] King Fahd Univ Petr & Minerals, Ctr Nanotechnol CENT, Dhahran 31261, Eastern Provinc, Saudi Arabia
[4] EXPEC Adv Res Ctr, Saudi Aramco, Saudi Arabia
关键词
Electrocatalyst; Hydrogen evolution reaction; Brine water; Molybdenum carbide; Sustainable fuel; TUNGSTEN CARBIDE; ELECTROCHEMICAL IMPEDANCE; OXYGEN REDUCTION; CATALYSTS; NI; CO; KINETICS; FE; NANOPARTICLES; GENERATION;
D O I
10.1016/j.ijhydene.2016.10.017
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
A series of nanostructured catalysts based on cobalt-modified molybdenum carbides, intended as alternative replacement for platinum has been developed for the hydrogen evolution reaction (HER) from brine. The catalysts were synthesized by simple impregnation of the metal salts on carbon support and followed by pyrolysis in CH4 atmosphere. The obtained catalysts show impressive HER activities in both brine and alkaline media. At current density of -7.0 mA cm(-2), the overpotential for Co modified Mo/C catalysts was greater than that obtained with a commercial Pt/C catalyst by 63-89 mV and 15-148 mV for brine and alkaline solution, respectively. Our findings for HER in both media are consistent with electrochemical desorption of hydrogen gas following the Volmer-Heyrovsky mechanism as the rate-determining step. The HER activities of the catalysts were correlated to their high mesopore surface areas with active pores, nanocrystallites, and low charge transfer resistances as confirmed by electrochemical impedance spectroscopy. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:22899 / 22912
页数:14
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