Nickel–cobalt bimetallic sulfide NiCo2S4 nanostructures for a robust hydrogen evolution reaction in acidic media

塔菲尔方程 过电位 双金属片 材料科学 交换电流密度 结晶度 催化作用 化学工程 硫化钴 介电谱 电催化剂 双层电容 电化学 无机化学 化学 金属 电极 冶金 物理化学 复合材料 有机化学 工程类
作者
Umair Aftab,Aneela Tahira,Raffaello Mazzaro,Vittorio Morandi,Muhammad Ishaque Abro,Muhammad Moazam Baloch,Cong Yu,Zafar Hussain Ibupoto
出处
期刊:RSC Advances [The Royal Society of Chemistry]
卷期号:10 (37): 22196-22203 被引量:11
标识
DOI:10.1039/d0ra03191g
摘要

There are many challenges associated with the fabrication of efficient, inexpensive, durable and very stable nonprecious metal catalysts for the hydrogen evolution reaction (HER). In this study, we have designed a facile strategy by tailoring the concentration of precursors to successfully obtain nickel-cobalt bimetallic sulfide (NiCo2S4) using a simple hydrothermal method. The morphology of the newly prepared NiCo2S4 comprised a mixture of microparticles and nanorods, which were few microns in dimension. The crystallinity of the composite sample was found to be excellent with a cubic phase. The sample that contained a higher amount of cobalt compared to nickel and produced single-phase NiCo2S4 exhibited considerably improved HER performance. The variation in the salt precursor concentration during the synthesis of a material is a simple methodology to produce a scalable platinum-free catalyst for HER. The advantageous features of the multiple active sites of cobalt in the CN-21 sample as compared to that for pristine CoS and NiS laid the foundation for the provision of abundant active edges for HER. The composite sample produced a current density of 10 mA cm-2 at an overpotential of 345 mV. Also, it exhibited a Tafel value of 60 mV dec-1, which predominantly ensured rapid charge transfer kinetics during HER. CN-21 was highly durable and stable for 30 hours. Electrochemical impedance spectroscopy showed that the charge transfer resistance was 21.88 ohms, which further validated the HER polarization curves and Tafel results. CN-21 exhibited a double layer capacitance of 4.69 μF cm-2 and a significant electrochemically active surface area of 134.0 cm2, which again supported the robust efficiency for HER. The obtained results reveal that our developed NiCo2S4 catalyst has a high density of active edges, and it is a non-noble metal catalyst for the hydrogen evolution reaction. The present findings provide an alternative strategy and an active nonprecious material for the development of energy-related applications.
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