Mushtaq Nouraiz, Wang Zhitao, Tabassum Hassina, Tahir Muhammad, Han Zhanli, Zhu Youqi, Younas Waqar, Ma Xilan, Cao Chuanbao
Research Center of Materials Science, Beijing Key Laboratory of Construction Tailorable Advanced Functional Materials and Green Applications, Beijing Institute of Technology, Beijing 100081, China.
Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, New York 14260, USA.
Dalton Trans. 2022 Apr 20;51(16):6285-6292. doi: 10.1039/d2dt00019a.
The engineering of inexpensive, high-efficiency and stable electrodes related to both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is highly desired for full water splitting devices to promote future advances in this energy technology. Therefore, a large surface area, rich in exposed surface atoms, and mesoporosity are very effective parameters in electrochemical reactions. Herein, we have, for the first time, synthesized free-standing mesoporous FeS nanosheets with a large surface area of 129.65 m g through a microwave-assisted synthetic technique. Our present synthesis strategy demonstrates a facile and cost-effective method to overcome the obstacles of fabricating ultrathin two-dimensional graphene-like transition metal sulfide nanosheets. The as-synthesized FeS nanosheets are applied as both cathodic and anodic electrodes for full water electrolysis. Remarkably, FeS nanosheets can exhibit a small overpotential ( = 103 mV) to provide the required 10 mA cm current density during the HER process. Meanwhile, a low overpotential of 230 mV is also exhibited for the OER process to allow a 10 mA cm current density. Furthermore, the assembled full water splitting device can achieve potentials of 1.43 and 1.65 V at 10 and 100 mA cm current densities, respectively, in an alkaline electrolyte with excellent cycling stability over 24 h. Our current study may provide an advanced channel for transition metal sulfide catalysts towards commercial water splitting applications.
对于全水解装置而言,迫切需要设计出与析氧反应(OER)和析氢反应(HER)相关的廉价、高效且稳定的电极,以推动这种能源技术的未来发展。因此,大表面积、富含暴露表面原子以及具有介孔性是电化学反应中非常有效的参数。在此,我们首次通过微波辅助合成技术合成了具有129.65 m²/g大表面积的独立介孔FeS纳米片。我们目前的合成策略展示了一种简便且经济高效的方法,以克服制备超薄二维类石墨烯过渡金属硫化物纳米片的障碍。所合成的FeS纳米片被用作全水电解的阴极和阳极电极。值得注意的是,FeS纳米片在HER过程中能够表现出较小的过电位(η = 103 mV)以提供所需的10 mA/cm²电流密度。同时,在OER过程中也表现出230 mV的低过电位以实现10 mA/cm²电流密度。此外,组装的全水解装置在碱性电解质中,在10和100 mA/cm²电流密度下分别可实现1.43和1.65 V的电位,并且在超过24小时的时间内具有出色的循环稳定性。我们目前的研究可能为过渡金属硫化物催化剂用于商业水分解应用提供一条先进的途径。