材料科学
钇
硫黄
成核
锂(药物)
化学工程
储能
氢氧化物
化学吸附
电解质
动力学
阴极
纳米技术
无机化学
催化作用
化学
电极
冶金
物理化学
有机化学
氧化物
医学
功率(物理)
物理
量子力学
工程类
内分泌学
作者
Tengfei Yang,Xiao Sun,Jingshuai Xiao,Yan Song,Chaozheng He
标识
DOI:10.1016/j.matlet.2023.135583
摘要
Rechargeable lithium–sulfur (Li–S) batteries reveal promising prospect as high energy storage systems because of the extraordinary theoretical specific energy density. However, the shuttle effect and sluggish reaction kinetics of polysulfides hamper the commercialization applications of high energy density Li-S batteries. Herein, a novel and efficient sulfur host material of yttrium hydroxide (Y(OH)3) has rationally been achieved for Li–S batteries. Y(OH)3 host not only suppress shuttle effect of polysulfides by physical confinement and chemisorption, but also decline Li2S nucleation and deposition reaction barriers and expedite chemical reaction kinetics. Consequently, the prepared Y(OH)3/S cathodes achieve a high initial specific capacity of 1295 mAh g−1 at 0.1 C and improved cycling stability with a low capacity decay rate of 0.019% per cycle over 1000 cycles at 2.0 C. The enhanced performances confirm a potential host material for facilitating practical implementation of Li–S batteries.
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