Zhanhua Su , Rui Sun , Zhifeng Zhao , Tingyu Yan , Shuangyan Lin , Yongchen Shang , Jingxiang Zhao
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引用次数: 0
Abstract
Exploiting low-cost and highly effective electrocatalysts is crucial to enhancing water splitting and developing the environmental hydrogen economy. Herein, the NiS/Ni3S2@V2O5 nanoarrays grown in situ on Ni foam (NF) are fabricated by a simple hydrothermal process for different reaction times. The V2O5 acts as a shell and Ni-based sulfides act as cores. Interestingly, the NiS/Ni3S2@V2O5/NF-16h reveals superb electrocatalytic activity and stability in an alkaline media, the overpotentials for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are only 32 and 182 mV at 10 mA cm−2, respectively, and eminent durability over 100 h. Moreover, the cell voltage for the hydrolysis process requires only 1.46 V at 10 mA cm−2. According to density functional theory (DFT) computations, the strong interfacial effect modulates the electronic properties of Ni and S atoms, endowing them with optimal binding strength to *H and oxygenated intermediates, thus leading to their outstanding catalytic performance for water splitting. This study offers a promising strategy for constructing cost-efficient bifunctional electrocatalysts.
开发低成本、高效的电催化剂是提高水分解效率和发展环境氢经济的关键。本文采用简单的水热法制备了不同反应时间在Ni泡沫(NF)上原位生长的NiS/Ni3S2@V2O5纳米阵列。V2O5作为壳层,镍基硫化物作为核。有趣的是,NiS/Ni3S2@V2O5/NF-16h在碱性介质中表现出极好的电催化活性和稳定性,析氢反应(HER)和析氧反应(OER)的过电位在10 mA cm - 2时分别仅为32和182 mV,并且在100小时内具有优异的耐久性。此外,水解过程的电池电压在10 mA cm - 2时仅为1.46 V。根据密度泛函理论(DFT)计算,强界面效应调节了Ni和S原子的电子性质,赋予它们与氢和含氧中间体的最佳结合强度,从而导致它们具有出色的水裂解催化性能。该研究为构建具有成本效益的双功能电催化剂提供了一种有前景的策略。
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.