Bingxin Zhao , Yuxin Zhao , Wenyue Jiang , Ziting Li , Peng Zhou , Jinping Wang , Rui Yang , Chunling Zuo , Xiaoshuang Chen
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引用次数: 0
摘要
设计高效节能制氢系统的关键在于开发高催化、低成本的非贵金属催化剂。同时,通过涉及小分子的反应取代耗能大的析氧在阳极容易氧化。本文报道了共掺杂Ni/ mon4 (Co-Ni/ mon4)异质结构的多组分金属间化合物,并将其作为尿素助水分解电催化剂直接集成在导电泡沫镍上。Co-Ni/MoNi4产物具有三维火山岩状结构,表面呈多层粗糙珊瑚状,在水裂解领域表现出满意的电催化效果。结果表明,在低过电位46.8 mV下,析氢反应(HER)的电流密度为10 mA cm-2;在低过电位下,尿素氧化反应(UOR)的电流密度为1.33 V,为10 mA cm-2。Co-Ni/MoNi4的HER和UOR的Tafel斜率分别为72.2和29.1 mV / dec-1。此外,Co-Ni/MoNi4偶联电解槽仅需1.40 V的电池电压即可达到10 mA cm-2,且对尿素电解具有良好的稳定性。
3D volcanic-rock-like structure of Co-doped Ni/MoNi4 heterostructure with corallite pattern surface as bifunctional electrocatalysts for urea-assisted water splitting
The key to the design of energy-efficient hydrogen production system lies in the development of highly catalytic, low-cost and non-precious metal catalysts. Meanwhile, the replacement of great-energy-consuming oxygen evolution through the reactions involving small molecules is easily oxidizable at the anode. Herein, we report the multicomponent intermetallic of Co-doped Ni/MoNi4 (Co-Ni/MoNi4) heterostructure, which is directly integrated on conductive nickel foam as an urea-assisted water splitting electrocatalyst. The Co-Ni/MoNi4 product possesses 3D volcanic-rock-like architecture with multideck and scabrous corallite pattern surface, which presents satisfactory electrocatalysis in water splitting territory. It demonstrates a low overpotential of 46.8 mV to achieve the current density of 10 mA cm−2 for hydrogen evolution reaction (HER), and showcases a potential of 1.33 V for urea oxidation reaction (UOR) at 10 mA cm−2. The Tafel slopes of HER and UOR for Co-Ni/MoNi4 are 72.2 and 29.1 mV dec−1, respectively. What's more, the Co-Ni/MoNi4 couple electrolyzer only requires a cell voltage of 1.40 V to attain 10 mA cm−2 and exhibits good stability for urea electrolysis.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.