Abstract
Integrating a highly conductive carbon host and polar inorganic compounds has been widely reported to improve the electrochemical performances for promising low-cost lithium sulfur batteries. Herein, a MoS(2)/mesoporous carbon hollow sphere (MoS(2)/MCHS) structure has been proposed as an efficient sulfur cathode via a simple wet impregnation method and gas phase vulcanization method. Multi-fold structural merits have been demonstrated for the MoS(2)/MCHS structures. On one hand, the mesoporous carbon hollow sphere (MCHS) matrix, with abundant pore structures and high specific surface areas, could load a large amount of sulfur, improve the electronical conductivity of sulfur electrodes, and suppress the volume changes during the repeated sulfur conversion processes. On the other hand, ultrathin multi-layer MoS(2) nanosheets are revealed to be uniformly distributed in the mesoporous carbon hollow spheres, enhancing the physical adsorption and chemical entrapment functionalities towards the soluble polysulfide species. Having benefited from these structural advantages, the sulfur-impregnated MoS(2)/MCHS cathode presents remarkably improved electrochemical performances in terms of lower voltage polarization, higher reversible capacity (1094.3 mAh g(-1)), higher rate capability (590.2 mAh g(-1) at 2 C), and better cycling stability (556 mAh g(-1) after 400 cycles at 2 C) compared to the sulfur-impregnated MCHS cathode. This work offers a novel delicate design strategy for functional materials to achieve high performance lithium sulfur batteries.