材料科学
动力学
锂(药物)
催化作用
氧化还原
硫黄
固溶体
化学工程
密度泛函理论
纳米颗粒
纳米技术
有机化学
冶金
化学
计算化学
工程类
内分泌学
物理
医学
量子力学
作者
Xintao Zuo,Mengmeng Zhen,Dapeng Liu,Haohan Yu,Xilan Feng,Wei Zhou,Hua Wang,Yu Zhang
标识
DOI:10.1002/adfm.202214206
摘要
Abstract The theoretically high‐energy‐density lithium–sulfur batteries (LSBs) are seriously limited by the disadvantages including the shuttle effect of soluble lithium polysulfides (LiPSs) and the sluggish sulfur redox kinetics, especially for the most difficult solid–solid conversion of Li 2 S 2 to Li 2 S. Herein, a multifunctional catalytic interlayer to improve the performance of LSBs is tried to introduce, in which Fe 1– x S/Fe 3 C nanoparticles are embedded in the N/S dual‐doped carbon network (NSC) composed by nanosheets and nanotubes (the final product is named as FeSC@NSC). The well‐designed 3D NSC network endows the interlayer with a satisfactory LiPSs capture‐catalytic ability, thus ensuring fast redox reaction kinetics and suppressing LiPSs shuttling. The density functional theory calculations disclose the catalytic mechanisms that FeSC@NSC greatly improves the liquid–solid (LiPSs to Li 2 S 2 ) conversion and unexpectedly the solid–solid (Li 2 S 2 to Li 2 S) one. As a result, the LSBs based on the FeSC@NSC interlayer can achieve a high specific capacity of 1118 mAh g −1 at a current density of 0.2 C, and a relatively stable capacity of 415 mAh g −1 at a large current density of 2.0 C after 700 cycles as well as superior rate performance.
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