Peng Zehui, Lou Shuai, Gao Yuan, Kong Lijun, Yan Shancheng, Wang Ka, Song Haizeng
School of Geography and Biological Information, Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Department of Materials Science and Engineering, University of California, Berkeley, CA 94720, USA.
Nanomaterials (Basel). 2021 May 8;11(5):1245. doi: 10.3390/nano11051245.
There are abundant water resources in nature, and hydrogen production from electrolyzed water can be one of the main ways to obtain green and sustainable energy. Traditional water electrolysis uses precious metals as catalysts, but it is difficult to apply in massive volumes due to low reserves and high prices. It is still a challenge to develop hydrogen electrocatalysts with excellent performance but low cost to further improve the efficiency of hydrogen production. This article reported a potential candidate, the Co-NiS/CoS (material is based on NiS, and after Co doping, The NiS/CoS heterostructure is formed) heterostructures, prepared by hydrothermal method with carbon paper as the substrate. In a 0.5 M sulfuric acid solution, the hydrogen evolution reaction with Co-NiS/CoS as the electrode showed excellent catalytic performance. When the Co (Cobalt) doping concentration is increased to 27%, the overpotential is -133.3 mV, which is a drop of 81 mV compared with -214.3 mV when it is not doped. The heterostructure formed after doping also has good stability. After 800 CV cycles, the difference in overpotential is only 3 mV. The significant improvement of the catalytic performance can be attributed to the significant changes in the crystal structure and properties of the doped heterostructures, which provide an effective method for efficient electrocatalytic hydrogen production.
自然界中水资源丰富,电解水制氢可成为获取绿色可持续能源的主要途径之一。传统水电解使用贵金属作为催化剂,但由于储量低、价格高,难以大规模应用。开发具有优异性能但低成本的氢电催化剂以进一步提高制氢效率仍是一项挑战。本文报道了一种潜在的候选材料,即通过水热法以碳纸为基底制备的Co-NiS/CoS(材料基于NiS,Co掺杂后形成NiS/CoS异质结构)异质结构。在0.5M硫酸溶液中,以Co-NiS/CoS为电极的析氢反应表现出优异的催化性能。当Co(钴)掺杂浓度增加到27%时,过电位为-133.3mV,与未掺杂时的-214.3mV相比下降了81mV。掺杂后形成的异质结构也具有良好的稳定性。经过800次循环伏安循环后,过电位差异仅为3mV。催化性能的显著提高可归因于掺杂异质结构的晶体结构和性能的显著变化,这为高效电催化制氢提供了一种有效方法。