Zheng Yunhua, Xu Jinchao, Zhu Yao, Zhang Tao, Yang Dongya, Qiu Fengxian
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, 212013 Jiangsu Province, China.
Inorg Chem. 2022 Apr 4;61(13):5352-5362. doi: 10.1021/acs.inorgchem.2c00133. Epub 2022 Mar 20.
The hydrogen evolution reaction (HER) is significantly influenced by the evolved H bubble diffusion rate on the surface of the electrode, which involves the blocking and release of the active site at the catalytic interface. Rational design of nanostructured catalysts could not only sharply enhance the specific surface area but also provide large amounts of channels for gas release. Herein, NiCo-nanowire-derived multimetal chalcogenides grown on carbon cloth [denoted as (NiCo)S@MoS/CC] are presented by serial hydrothermal methods. The obtained hierarchical nanowire array architecture affords abundant surface-active sites and is conducive to permeate electrolytes. The surface adsorption/desorption behavior of the heterostructure catalyst was optimized through regulating MoS concentration. Owing to the synergistic effect of metal Ni and Co and the interaction of the (NiCo)S@MoS heterostructure, (NiCo)S@MoS/CC-2 delivers a relatively low overpotential of 74 mV at a current density of 10 mA cm and displays a small Tafel slope of 54 mV dec for HER catalysis, surpassing that of the recently reported MoS-based electrocatalysts. Such a strategy through nanostructure optimization and electron interaction of the heterostructure could improve the electrocatalytic HER performance for multimetal chalcogenides in an alkaline medium.
析氢反应(HER)受到电极表面析出的氢气泡扩散速率的显著影响,这涉及催化界面处活性位点的阻塞和释放。合理设计纳米结构催化剂不仅可以大幅提高比表面积,还能提供大量气体释放通道。在此,通过一系列水热法制备了生长在碳布上的镍钴纳米线衍生的多金属硫族化物[记为(NiCo)S@MoS/CC]。所获得的分级纳米线阵列结构提供了丰富的表面活性位点,有利于电解质渗透。通过调节MoS浓度优化了异质结构催化剂的表面吸附/解吸行为。由于金属Ni和Co的协同效应以及(NiCo)S@MoS异质结构的相互作用,(NiCo)S@MoS/CC-2在电流密度为10 mA cm时具有相对较低的74 mV过电位,并且在HER催化中显示出54 mV dec的小塔菲尔斜率,超过了最近报道的基于MoS的电催化剂。这种通过纳米结构优化和异质结构的电子相互作用的策略可以提高多金属硫族化物在碱性介质中的电催化HER性能。