Wu Wenzhuo, Niu Chunyao, Wei Cong, Jia Yu, Li Chong, Xu Qun
College of Materials Science and Engineering, Zhengzhou University, Zhengzhou, 450052, China.
International Laboratory for Quantum Functional Materials of Henan, School of Physics and Engineering, Zhengzhou University, Zhengzhou, 450001, P. R. China.
Angew Chem Int Ed Engl. 2019 Feb 11;58(7):2029-2033. doi: 10.1002/anie.201812475. Epub 2019 Jan 18.
Molybdenum disulfide (MoS ) has been widely studied as a potential earth-abundant electrocatalyst for the hydrogen-evolution reaction (HER). Defect engineering and heteroelemental doping are effective methods to enhance the catalytic activity in the HER, so exploring an efficient route to simultaneously achieve in-plane vacancy engineering and elemental doping of MoS is necessary. In this study, Zinc, a low-cost and moderately active metal, has been used to realize this strategy by generation of sulfur vacancies and zinc doping on MoS in one step. Density functional theory calculations reveal that the zinc atoms not only lower the formation energy of S vacancies, but also help to decrease ΔG of S-vacancy sites near the Zn atoms. At an optimal zinc-reduced MoS (Zn@MoS ) example, the activated basal planes contribute to the HER activity with an overpotential of -194 mV at 10 mA cm and a low Tafel slope of 78 mV/dec.
二硫化钼(MoS₂)作为一种潜在的储量丰富的析氢反应(HER)电催化剂已得到广泛研究。缺陷工程和异质元素掺杂是提高HER催化活性的有效方法,因此探索一条同时实现MoS₂面内空位工程和元素掺杂的有效途径很有必要。在本研究中,锌这种低成本且活性适中的金属已被用于通过一步在MoS₂上产生硫空位和锌掺杂来实现这一策略。密度泛函理论计算表明,锌原子不仅降低了S空位的形成能,还有助于降低锌原子附近S空位位点的ΔG。在一个最佳的锌还原MoS₂(Zn@MoS₂)实例中,活化的基面有助于HER活性,在10 mA cm⁻²时过电位为 -194 mV,塔菲尔斜率低至78 mV/dec。