Zhang Wenxiu, Liu Maosheng, Liang Hui, Cui Liang, Yang Wenrong, Razal Joselito M, Liu Jingquan
College of Materials Science and Engineering, Institute for Graphene Applied Technology Innovation, Qingdao University, Qingdao 266071, China.
College of Materials Science and Engineering, Linyi University, Linyi 276000, Shandong, China.
J Colloid Interface Sci. 2021 Apr;587:650-660. doi: 10.1016/j.jcis.2020.11.025. Epub 2020 Nov 12.
Hydrogen generation through electrochemical water decomposition is a promising method to address the global energy crisis. Herein, we report the synthesis of a series of flower-like MoS/CoS composites on Co foil (MoS/CoS@CF) as high-performance electrochemical water-splitting catalysts in an alkaline environment. The flower-like array structure of MoS/CoS@CF not only increases the electrochemically active surface area of the catalyst, but also facilitates the release of bubbles generated, resulting in enhanced catalytic activity. For the hydrogen evolution reaction, the MoS/CoS@CF electrode exhibits good stability and excellent catalytic activity in 1.0 M KOH (η = 105 mV), 1.0 M PBS (η = 92 mV) and 0.5 M HSO (η = 68 mV) solutions. For the oxygen evolution reaction, the electrode displays excellent stability and catalytic activity in 1.0 M KOH solution (η = 215 mV). When used for overall water splitting in 1.0 M KOH solution, MoS/CoS@CF achieves a current density of 10 mA cm at a low potential of 1.58 V and maintains it stably for 40 h. This study presents a simple method for preparing transition metal-based bimetallic composite catalysts for efficient hydrogen production.
通过电化学水分解制氢是解决全球能源危机的一种很有前景的方法。在此,我们报道了在钴箔(MoS/CoS@CF)上合成一系列花状MoS/CoS复合材料,作为碱性环境中高性能的电化学水分解催化剂。MoS/CoS@CF的花状阵列结构不仅增加了催化剂的电化学活性表面积,还促进了产生的气泡的释放,从而提高了催化活性。对于析氢反应,MoS/CoS@CF电极在1.0 M KOH(η = 105 mV)、1.0 M PBS(η = 92 mV)和0.5 M HSO(η = 68 mV)溶液中表现出良好的稳定性和优异的催化活性。对于析氧反应,该电极在1.0 M KOH溶液(η = 215 mV)中表现出优异的稳定性和催化活性。当用于1.0 M KOH溶液中的全水分解时,MoS/CoS@CF在1.58 V的低电位下实现了10 mA cm的电流密度,并稳定维持40小时。本研究提出了一种制备用于高效制氢的过渡金属基双金属复合催化剂的简单方法。