多硫化物
氧化还原
异质结
电化学
锂(药物)
阳极
化学吸附
催化作用
材料科学
化学工程
阴极
硫黄
化学
无机化学
纳米技术
电极
电解质
有机化学
冶金
光电子学
医学
物理化学
工程类
内分泌学
作者
Guo Liu,Qi Zeng,Xiaohui Hua,Ziye Fan,Xueliang Lv,Wenjian Zhang,Zhenxing Zhang
标识
DOI:10.1016/j.matchemphys.2021.125578
摘要
Polysulfide shutting between cathode and anode and sluggish redox of solid-liquid-solid conversion largely impede the commercial applications of lithium-sulfur (Li–S) batteries. Herein, a novel V2O3/VN heterostructure has been designed as an efficient adsorbent and catalyst to promote polysulfide trapping and redox kinetics. Such synchronous advantages of each part of V2O3/VN can efficiently alleviate shuttling and accelerate polysulfide conversion, thus improve electrochemical performances. Benefited from this synergistic effect, the assembled full cells with V2O3/VN heterostructure exhibit an initial capacity of about 1100 mAh g−1 at 0.1C and an outstanding rate performance of 612 mAh g−1 at 2C. After 100 cycling tests at 0.2C, the specific capacity still maintains about 670 mAh g−1. Our approach would provide a new viewpoint of designing efficient sulfur additives to improve the redox kinetics for high-performance lithium-sulfur batteries.
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