Xue Sen, Liu Zhibo, Ma Chaoqun, Cheng Hui-Ming, Ren Wencai
School of Materials Science and Engineering, Northeastern University, Shenyang 110819, China; Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China.
Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China.
Sci Bull (Beijing). 2020 Jan 30;65(2):123-130. doi: 10.1016/j.scib.2019.10.024. Epub 2019 Nov 5.
Splitting water under large current density is essential for efficient large-scale production and commercial utilization of hydrogen. However, the performance of the available electrocatalysts for hydrogen evolution reaction (HER) is far from satisfactory under large current density in alkaline electrolyte. Here we report a remarkably active and durable electrocatalyst, long and dense MoS/NiS co-axial heterostructure nanowires on nickel foam (NF). Notably, it requires only 182 and 200 mV overpotential to achieve large current density of 500 and 1000 mA cm, respectively, in alkaline solution, which are far superior to those of Pt/C-NF (281 and 444 mV) and the reported best non-noble metal catalysts (191 and 220 mV). The physical origin for this extraordinary HER performance is analyzed, which provides a useful guide for structure design of electrocatalysts to further improve their performance.
在大电流密度下分解水对于高效大规模制氢及氢能的商业利用至关重要。然而,现有用于析氢反应(HER)的电催化剂在碱性电解液大电流密度下的性能远不能令人满意。在此,我们报道一种具有卓越活性和耐久性的电催化剂,即生长在泡沫镍(NF)上的长且致密的MoS/NiS同轴异质结构纳米线。值得注意的是,在碱性溶液中,分别实现500和1000 mA cm的大电流密度时,它仅需182和200 mV的过电位,这远远优于Pt/C-NF(281和444 mV)以及已报道的最佳非贵金属催化剂(191和220 mV)。分析了这种优异析氢性能的物理根源,这为电催化剂的结构设计提供了有用的指导,以进一步提升其性能。