硫黄
电解质
材料科学
催化作用
阴极
锂(药物)
氧化还原
位阻效应
化学工程
铜
无机化学
电极
有机化学
化学
物理化学
冶金
工程类
内分泌学
医学
作者
Zhihao Yu,Xiehe Huang,Mengting Zheng,Shanqing Zhang,Ying Yang,Jun Lü
标识
DOI:10.1002/adma.202300861
摘要
Abstract The practical viability of high‐energy‐density lithium–sulfur (Li–S) batteries stipulates the use of a high‐loading cathode and lean electrolyte. However, under such harsh conditions, the liquid–solid sulfur redox reaction is much retarded due to the poor sulfur and polysulfides utilization, leading to low capacity and fast fading. Herein, a self‐assembled macrocyclic Cu(II) complex (CuL) is designed as an effective catalyst to homogenize and maximize the liquid‐involving reaction. The Cu(II) ion coordinated with four N atoms features a planar hybridization, showing a strong bonding affinity toward lithium polysulfides (LiPSs) along the orbital via steric effects. Such a structure not only lowers the energy barrier of the liquid–solid conversion (Li 2 S 4 to Li 2 S 2 ) but also guides a 3D deposition of Li 2 S 2 /Li 2 S. As such, with a 1 wt% electrolyte additive of CuL, a high initial capacity of 925 mAh g −1 and areal capacity of 9.62 mAh cm −2 with a low decay of 0.3%/cycle can be achieved under a high sulfur loading of 10.4 mg cm −2 and low electrolyte/sulfur ratio of 6 µL mg s −1 . This work is expected to inspire the design of homogenous catalysts and accelerate the uptake of high‐energy‐density Li–S batteries.
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