Liu Qianqian, Huang Jianfeng, Liu Kehan, Du Huiling, Kang Le, Yang Dan, Niu Mengfan, Li Guodong, Cao Liyun, Feng Liangliang
School of Material Science and Engineering, Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology, Xi'an 710021, China.
College of Materials Science and Engineering, Xi'an University of Science and Technology, Xi'an 710054, China.
Dalton Trans. 2022 May 10;51(18):7234-7240. doi: 10.1039/d2dt00157h.
The synergistic effect of a highly active surface/interface and an optimized electronic structure of electrocatalysts is of great significance to improve the performance of the hydrogen evolution reaction. Herein, a superhydrophilic core@shell heterostructure nanorod-integrated electrode composed of an amorphous VO nanoshell (3-7 nm) and a crystalline NiS core supported on Ni foam (CS-NS/NF) was prepared by an conversion method. We prove that the amorphous VO not only helps to kinetically decouple the adsorption/dissociation of hydroxyl/water, but also enriches the active sites, thereby significantly enhancing the electron transfer efficiency and electrocatalytic activity toward the hydrogen evolution reaction (HER). The optimized CS-NS/NF has excellent hydrogen production performance, with overpotentials of 335 and 394 mV at current densities of 500 and 1000 mA cm, respectively, as well as superior durability for over 68 h in 1 M KOH.
高活性表面/界面与电催化剂优化电子结构的协同效应对于提高析氢反应性能具有重要意义。在此,通过一种转化方法制备了一种由非晶态VO纳米壳(3 - 7纳米)和负载在泡沫镍上的结晶NiS核组成的超亲水核壳异质结构纳米棒集成电极(CS - NS/NF)。我们证明,非晶态VO不仅有助于在动力学上解耦羟基/水的吸附/解离,还能丰富活性位点,从而显著提高电子转移效率和对析氢反应(HER)的电催化活性。优化后的CS - NS/NF具有优异的产氢性能,在电流密度为500和1000 mA cm时的过电位分别为335和394 mV,并且在1 M KOH中具有超过68小时的优异耐久性。