Dual-electrocatalysis behavior of star-like zinc–cobalt-sulfide decorated with cobalt–molybdenum-phosphide in hydrogen and oxygen evolution reactions

塔菲尔方程 过电位 电催化剂 析氧 材料科学 催化作用 X射线光电子能谱 磷化物 双功能 分解水 化学工程 无机化学 电化学 化学 物理化学 电极 光催化 工程类 生物化学
作者
Maryam Shamloofard,Saeed Shahrokhian
出处
期刊:Nanoscale [Royal Society of Chemistry]
卷期号:13 (41): 17576-17591 被引量:36
标识
DOI:10.1039/d1nr04374a
摘要

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 via 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 via 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-2, respectively, with a Tafel slope of 41 mV dec-1. 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-2, respectively, with a Tafel slope of 61.7 mV dec-1 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-2 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.
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