硫黄
化学工程
碳纤维
电解质
无机化学
溶解
阴极
锂(药物)
碳化
材料科学
金属有机骨架
熔盐
化学
有机化学
电极
吸附
复合数
冶金
复合材料
医学
物理化学
工程类
内分泌学
作者
Dae Kyom Kim,Jin Seul Byun,San Moon,Junyoung Choi,Joon Ha Chang,Jungdon Suk
标识
DOI:10.1016/j.cej.2022.135945
摘要
Lithium-sulfur (Li-S) batteries have attracted significant attention as next-generation energy storage systems owing to their high theoretical specific capacity (1675 mAh g−1) and energy density (2567 Wh kg−1). However, the low electrical conductivity of S and the dissolution of polysulfides in organic electrolytes pose significant challenges for their industrial applications. Herein, we report a facile, scalable, and solvent-free synthetic method based on metal–organic-framework (MOF) for synthesizing N-doped carbon-based materials with hierarchical porous structures and large specific surface areas (2297 m2 g−1) as efficient cathode hosts for Li-S batteries. The cathode materials were synthesized via solvent-free mixing, followed by the direct carbonization of adenine and tetracarboxylic acid with zinc acetate using the molten salt method. Zinc salt was employed as a template for mesopores as well as binding sites for other organic materials. The irregular surface morphology and N-doping of the resulting porous carbons act as physical barriers to confine polysulfides within the carbon matrix. The S-loaded cathode was stable and exhibited a discharge capacity of 555 mAh g−1 over 290 cycles at a current density of 0.5C, corresponding to the capacity retention of 63%. The facile modified MOF synthetic strategy, assisted by molten salt processing, holds promise for the synthesis of noble cathode materials for high-performance Li-S batteries.
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