Shamloofard Maryam, Shahrokhian Saeed
Department of Chemistry, Sharif University of Technology, Tehran 11155-9516, Iran.
Institute for Nanoscience and Technology, Sharif University of Technology, Tehran, Iran.
Nanoscale. 2021 Oct 28;13(41):17576-17591. doi: 10.1039/d1nr04374a.
Although important advances have been acquired in the field of electrocatalysis, the design and fabrication of highly efficient and stable non-noble earth-abundant metal catalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) remain a significant challenge. In this study, we have designed a superior bifunctional catalyst for OER and HER in alkaline media based on the Co-Mo-P/Zn-Co-S multicomponent heterostructure. The as-prepared multicomponent heterostructure was successfully obtained a simple three-step hydrothermal-sulfidation-electrodeposition process consisting of star-like Co-Zn-S covered with Co-Mo-P. The structure and morphology evaluation of the prepared catalysts were performed Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy, field emission scanning electron microscopy, X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, and elemental mapping techniques. The electrochemical tests show that Co-Mo-P/Co-Zn-S exhibits outstanding activity toward both OER and HER with OER overpotentials of 273 mV and 312 mV to drive the benchmark current densities of 10 and 50 mA cm, respectively, with a Tafel slope of 41 mV dec. In addition, the HER overpotentials of 120 mV and 165 mV were required to reach the benchmark current densities of 10 and 50 mA cm, respectively, with a Tafel slope of 61.7 mV dec that outperforms most other state-of-the-art catalysts. In the case of HER, the prepared catalyst required an overpotential of 202 mV to reach the current density of 200 mA cm that was much lower than the overpotential of Pt/C (286 mV) to achieve the same current density. Co-Mo-P/Co-Zn-S also exhibits a suitable stability length of 10 h for OER and HER during the chronoamperometric tests. The superior performance of the Co-Mo-P/Co-Zn-S multicomponent heterostructure toward OER and HER may be related to the large specific surface area, accelerated mass and electron transport, and synergistic effect of multiple hybrid materials. These merits suggest that Co-Mo-P/Co-Zn-S can be considered as a promising catalyst for bi-functional OER and HER, and can be offered a great promise for future applications.
尽管在电催化领域已取得重要进展,但设计和制备用于析氧反应(OER)和析氢反应(HER)的高效且稳定的非稀土丰富金属催化剂仍然是一项重大挑战。在本研究中,我们基于Co-Mo-P/Zn-Co-S多组分异质结构设计了一种在碱性介质中用于OER和HER的优异双功能催化剂。通过由覆盖有Co-Mo-P的星状Co-Zn-S组成的简单三步水热-硫化-电沉积过程成功获得了所制备的多组分异质结构。使用傅里叶变换红外光谱、X射线衍射光谱、场发射扫描电子显微镜、X射线光电子能谱、能量色散X射线光谱和元素映射技术对所制备催化剂的结构和形态进行了评估。电化学测试表明,Co-Mo-P/Co-Zn-S对OER和HER均表现出出色的活性,其OER过电位分别为273 mV和312 mV,以驱动10和50 mA cm²的基准电流密度,塔菲尔斜率为41 mV dec⁻¹。此外,HER过电位分别为120 mV和165 mV才能达到10和50 mA cm²的基准电流密度,塔菲尔斜率为61.7 mV dec⁻¹,优于大多数其他先进催化剂。在HER方面,所制备的催化剂达到200 mA cm²的电流密度需要202 mV的过电位,这远低于Pt/C达到相同电流密度所需的过电位(286 mV)。在计时电流测试期间,Co-Mo-P/Co-Zn-S对OER和HER还表现出合适的10 h稳定性时长。Co-Mo-P/Co-Zn-S多组分异质结构对OER和HER的优异性能可能与大比表面积、加速的质量和电子传输以及多种混合材料的协同效应有关。这些优点表明Co-Mo-P/Co-Zn-S可被视为一种有前途的双功能OER和HER催化剂,并为未来应用提供了巨大潜力。