材料科学
多硫化物
纳米技术
石墨烯
纳米纤维
硫黄
碳纳米纤维
合理设计
储能
纳米颗粒
锂(药物)
碳纤维
催化作用
氧化还原
化学工程
阳极
电极
纳米
对偶(语法数字)
纳米线
能量转换
工作(物理)
法拉第效率
作者
Wenrui Zheng,Yonghui Xie,Yinlong Lin,Jing Zhu,Jinling Yu,Zhong‐Zhen Luo,Xinghui Wang
标识
DOI:10.1021/acsami.5c21319
摘要
The practical application of lithium-sulfur batteries is limited by the severe shuttle effect of lithium polysulfides (LiPSs) and slow sulfur conversion kinetics, resulting in accelerated capacity decay and limited cycle life. To address these challenges, we designed a multifunctional sulfur host, named VGS@MoC/NCNF, in which MoC-modified, nitrogen-doped carbon nanofibers are coated with a layer of vertically aligned graphene sheets. The hierarchically designed dual-carbon architecture provides sufficient sulfur loading space and establishes efficient pathways for rapid electron/ion transport, while the uniformly dispersed MoC nanoparticles provide dual adsorption-catalysis functions. The VGS@MoC/NCNF-S effectively confines LiPSs through combined physical-chemical interactions and catalytically accelerates LiPS redox kinetics. Consequently, the VGS@MoC/NCNF-S displays an initial capacity of 1070.8 mAh g-1 and maintains a capacity of 798.5 mAh g-1 after 400 cycles with only 0.063% capacity fade per cycle at 1 C rate, presenting excellent cycling stability. This work provides a rational design strategy for designing high-efficiency sulfur hosts with the integrated functionality of polysulfide confinement and catalytic conversion for advanced lithium-sulfur batteries.
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