过电位
材料科学
催化作用
塔菲尔方程
双金属片
钼
掺杂剂
化学工程
制氢
过渡金属
电催化剂
无机化学
电化学
氢
金属
兴奋剂
物理化学
冶金
化学
有机化学
电极
光电子学
工程类
作者
Di Gao,Jiangna Guo,Xun Cui,Lin Yang,Yang Yang,Huichao He,Peng Xiao,Yunhuai Zhang
标识
DOI:10.1021/acsami.7b04009
摘要
First-row (3d) transition-metal catalysts, such as bimetallic Ni-Co, represent an emerging class of electrocatalysts for HER, but they usually suffer from a large overpotential significantly above thermodynamic demands. Here, we doped NiCo catalyst with non3d metals molybdenum (Mo) for improvement in catalyzing the hydrogen evolution reaction. The ternary catalyst was readily obtained by a one-pot process via the sequential electrodeposition of Ni, Co, and Mo precursors on titanium (Ti) support. By tailing the deposition conditions, we fabricated NiCoMo catalysts with three-dimensional dendritic structures, exhibiting large amounts of electrochemically active sites. To attain the benchmark HER current density of -10 mA cm-2, an overpotential of ∼132 mV is required in 0.1 M KOH for the Mo-doped NiCo (5 atom % Mo in bath), and they produced the decreasing in Tafel slope of ∼108 mV decade-1 exceeding those of binary NiCo alloy catalysts and other contents of Mo doping. In a synergistic effect, dopant incorporation of Mo element may provide near-optimal adsorption energies for HER intermediates promoting the process of water dissociation and hydrogen intermediates production and binding into molecular hydrogen.
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