The development of efficient non-noble-metal electrocatalysts is of critical importance for clean energy conversion systems, such as fuel cells, metal–air batteries, and water electrolysis. Herein, uniform Co 9 S 8 @MoS 2 core–shell heterostructures have been successfully prepared via a solvothermal approach, followed by an annealing treatment. Transmission electron microscopy, X-ray absorption near-edge structure, and X-ray photoelectron spectroscopy measurements reveal that the core–shell structure of Co 9 S 8 @MoS 2 can introduce heterogeneous nanointerface between Co 9 S 8 and MoS 2, which can deeply influence its charge state to boost the electrocatalytic performances. Besides, due to the core–shell structure that can promote the synergistic effect of Co 9 S 8 and MoS 2 and provide abundant catalytically active sites, Co 9 S 8 @MoS 2 exhibits a superior hydrogen evolution reaction performance with a small overpotential of 143 mV at 10 mA cm –2 and a small Tafel slope value of 117 mV dec –1 under alkaline solution. Meanwhile, the activity of Co 9 S 8 @MoS 2 toward oxygen evolution reaction is also impressive with a low operating potential (∼1.57 V vs reversible hydrogen electrode) at 10 mA cm –2 . By using Co 9 S 8 @MoS 2 catalyst for full water splitting, an alkaline electrolyzer affords a cell voltage as low as 1.67 V at a current density of 10 mA cm –2 . Also, Co 9 S 8 @MoS 2 reveals robust oxygen reduction reaction performance, making it an excellent catalyst for Zn–air batteries with a long lifetime (20 h). This work provides a new means for the development of multifunctional electrocatalysts of non-noble metals for the highly demanded electrochemical energy technologies.
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Bai et al. (2017) studied this question.
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