College of Materials and Textiles, Key Laboratory of Advanced Textile Materials and Manufacturing Technology of the Ministry of Education, Zhejiang Sci-Tech University, Hangzhou, 310018, People's Republic of China.
Nanotechnology. 2018 Sep 21;29(38):385602. doi: 10.1088/1361-6528/aacfd7. Epub 2018 Jun 28.
A facile method to prepare nitrogen anion-decorated cobalt tungsten disulfides solid solutions, retaining ultra-thin WS-like nanosheet structures (The N-Co W S) anchored on carbon nanofibers (CNFs), is developed. The synergistic effect of the WS nanosheets provides a secure framework for stabilizing the amorphous Co-S clusters, CNFs substrate and nitrogen anion-decoration significantly enhances the inherent conductivity of the catalyst, resulting in a significantly promoted hydrogen evolution reaction activity and stable performance compared to pure CoS nanoparticles or ultra-thin WS nanosheets. The N-Co W S electrode demonstrates the excellent electrocatalytic performance, with current density of 10 mA cm at a low overpotential of 93 mV and Tafel slope of 85 mV dec, as well as the long-term stability in acid electrolyte. The present investigation may provide a feasible strategy for incorporating other heteroatoms into transitional metal disulfides materials to design catalysts with highly active and stable performance for water splitting.
一种简便的方法可制备氮阴离子修饰的钴钨二硫化物固溶体,保留了超薄 WS 类似的纳米片结构(N-CoW S)锚定在碳纳米纤维(CNF)上。WS 纳米片的协同效应为稳定非晶态 Co-S 簇、CNF 基底和氮阴离子修饰提供了一个安全的框架,显著提高了催化剂的固有导电性,与纯 CoS 纳米粒子或超薄 WS 纳米片相比,析氢反应活性和稳定性显著提高。N-CoW S 电极表现出优异的电催化性能,在低过电势 93 mV 时电流密度为 10 mA cm-2,塔菲尔斜率为 85 mV dec-1,在酸性电解质中具有长期稳定性。本研究可能为将其他杂原子引入过渡金属二硫化物材料中提供了一种可行的策略,以设计具有高活性和稳定性能的析氢反应催化剂。