材料科学
阳极
硫黄
阴极
催化作用
化学工程
电极
锂硫电池
扩散
锂(药物)
纳米技术
电化学
物理化学
化学
有机化学
内分泌学
热力学
冶金
医学
物理
工程类
作者
Kunyang Zou,Tengfei Zhou,Yuanzhen Chen,Xuyang Xiong,Weitao Jing,Xin Dai,Ming Shi,Na Li,Junjie Sun,Shilin Zhang,Chaofeng Zhang,Yongning Liu,Zhanhu Guo
标识
DOI:10.1002/aenm.202103981
摘要
Abstract The decay of lithium–sulfur (Li–S) batteries is mainly due to the shuttle effect caused by intermediate polysulfides (LiPSs). Herein, a multiple confined cathode architecture is prepared by filling graphitized Pinus sylvestris with carbon nanotubes and defective LaNiO 3− x (LNO‐V) nanoparticles. The composite electrode with high areal sulfur loading of 11.6 mg cm −2 shows a high areal specific capacity of 8.5 mAh cm −2 at 1 mA cm −2 (0.05 C). Both experimental results and theoretical calculations reveal that this unique structure not only provides physical restriction on LiPSs within microchannels but also offers strong chemical immobilization and catalytic conversion of LiPSs attributed to the spin density around oxygen vacancies of LaNiO 3− x . These oxygen vacancies elongate the SS and LiS bonds and make them easy to break. Furthermore, the lengthwise channels derived from cytoderm restrict the transverse diffusion of polysulfides, leading to a uniform areal current and thus homogeneous lithium infiltration. This suppresses the corrosion of the lithium anode due to polysulfides confinement. The discovery of the multiple confined structure that provides chemical adsorption, fast diffusion, and catalytic conversion for polysulfides can broaden the application of biomass materials and offer a new strategy to achieve robust Li–S batteries.
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