化学
硫黄
介孔材料
锂(药物)
阴极
多孔性
碳纤维
电池(电)
阳极
电化学
锂硫电池
电导率
催化作用
基质(水族馆)
化学工程
扩散
储能
纳米技术
电极
有机化学
物理化学
复合数
复合材料
内分泌学
工程类
功率(物理)
地质学
物理
材料科学
海洋学
热力学
医学
量子力学
作者
Xinan Chen,Zhengju Zhu,Elif Vargün,Yiwen Li,Petr Sáha,Qilin Cheng
标识
DOI:10.1016/j.jelechem.2022.117046
摘要
Lithium-sulfur (Li-S) battery is the promising next-generation energy storage device owing to its ultra-high theoretical energy density and low cost. Unfortunately, its practical performance is significantly hindered by the poor conductivity of sulfur, huge volume change, and soluble lithium polysulfides (LiPSs). To address above issues, single iron (Fe) atoms anchored on hierarchically porous carbon substrate configured by ordered macropores and widespread mesopores/micropores (FeNC/OC) are synthesized and acted as carbon hosts for sulfur cathodes. Single Fe atoms in Fe-N4 moieties serve as active sites to accelerate conversion kinetics of LiPSs due to strong catalytic ability, thereby the shuttle effect being obviously restrained. Meanwhile, the trimodal-porous structure provides continuous carbon framework for enhanced electrical conductivity, ordered macroporous channels bridged by mesopores for rapid Li+ diffusion, and adequate spaces to reserve sulfur volume oscillation. Consequently, sulfur-loaded FeNC/OC (FeNC/OC/S) cathodes exhibit an impressive specific capacity of 1442 mAh g−1 at 0.1C and maintain the capacity retention of 89.2 % after 300 cycles at 1C. It offers fresh insights for designing efficient sulfur hosts to enhance the performance of Li-S batteries.
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