法拉第效率
材料科学
杂原子
介孔材料
硫黄
碳纤维
纳米技术
化学工程
阴极
纳米结构
多孔性
催化作用
锂(药物)
兴奋剂
吸附
电极
化学
电化学
有机化学
光电子学
复合材料
复合数
工程类
医学
戒指(化学)
物理化学
冶金
内分泌学
作者
Jinlong Hu,Qingqing Chen,Qi Xia,Lingzhi Zhang
标识
DOI:10.1016/j.apsusc.2022.153951
摘要
Heteroatom-doped hollow carbon nanostructures are one of the most promising sulfur hosts for high-performance lithium-sulfur (Li-S) batteries. However, finding a facile and controllable synthesis and enhancing their immobilization effect on polysulfides have been challenging. Herein, we propose a one-step in-situ reaction approach to synthesize N/F dual-doped hollow micro/mesoporous carbon nanospheres (NFHCs) as multifunctional sulfur host, which integrates the physical confinement of hollow porous structure and chemical adsorption/catalytic ability of N/F active sites to realize strong anchoring and accelerated conversion of polysulfides. This sulfur cathode based on NFHCs host with a high sulfur content of 80 wt% enables a superior high-rate capacity of 689 mAh g−1 at 3C, accompanied by outstanding cycle life over 500 cycles at 2C with a capacity decay of only 0.05% per cycle and nearly 100% Coulombic efficiency. This work opens up new horizons to design nanostructured functional hollow carbons for advanced Li-S batteries.
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