摘要
Two-dimensional layered-structure MoS 2 has been explored as the promising cathode materials for magnesium ion batteries benefited by its wide layer distance and satisfactory capacity. However, such strong interaction between Mg 2+ and MoS 2 brings about the sluggish diffusion kinetics and irreversible electrochemical reaction, leading to a decreased specific capacity and poor rate capability. How to adopt its structure engineering and interface engineering to boost the Mg 2+ diffusion kinetics and enhance the electrochemical reversibility of MoS 2 is still a huge challenge. Herein, the amorphous sulfur-rich 1T/2H-MoS 2 mesoporous nanospheres (a-MoS 2+x , 0
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