过电位
材料科学
塔菲尔方程
石墨烯
碳纳米管
催化作用
化学工程
电极
无定形碳
钼
无定形固体
纳米技术
无机化学
电化学
冶金
化学
有机化学
物理化学
工程类
作者
Kien-Cuong Pham,Yung‐Huang Chang,David S. McPhail,Cecilia Mattevi,Andrew T. S. Wee,Daniel H. C. Chua
标识
DOI:10.1021/acsami.5b09690
摘要
In this study, we report on the deposition of amorphous molybdenum sulfide (MoSx, with x ≈ 3) on a high specific surface area conductive support of Graphene–Carbon Nanotube hybrids (GCNT) as the Hydrogen Evolution Reaction (HER) catalysts. We found that the high surface area GCNT electrode could support the deposition of MoSx at much higher loadings compared with simple porous carbon paper or flat graphite paper. The morphological study showed that MoSx was successfully deposited on and was in good contact with the GCNT support. Other physical characterization techniques suggested the amorphous nature of the deposited MoSx. With a typical catalyst loading of 3 mg cm–2, an overpotential of 141 mV was required to obtain a current density of 10 mA cm–2. A Tafel slope of 41 mV decade–1 was demonstrated. Both measures placed the MoSx-deposited GCNT electrode among the best performing molybdenum sulfide-based HER catalysts reported to date. The electrode showed a good stability with only a 25 mV increase in overpotential required for a current density of 10 mA cm–2, after undergoing 500 potential sweeps with vigorous bubbling present. The current density obtained at −0.5 V vs SHE (Standard Hydrogen Electrode potential) decreased less than 10% after the stability test. The deposition of MoSx on high specific surface area conductive electrodes demonstrated to be an efficient method to maximize the catalytic performance toward HER.
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