多硫化物
材料科学
吸附
储能
化学工程
锂(药物)
硫黄
电极
电化学
电池(电)
锂硫电池
电解质
色谱法
膜
有机化学
化学
物理化学
功率(物理)
医学
冶金
工程类
生物化学
量子力学
内分泌学
物理
作者
Yuxiao Wang,Ying Yu,Yeqiang Tan,Tianyu Li,Yanbing Chen,Shuang Wang,Kunyan Sui,Hongzhang Zhang,Yang Luo,Xianfeng Li
标识
DOI:10.1002/aenm.201903233
摘要
Abstract Lithium–sulfur (Li–S) batteries are promising candidates for energy storage, but suffer from capacity and cycling challenges caused by the serious shuttling effect of polysulfide (PS) ions. To address these issues, a sodium alginate (SA)‐derived affinity laminated chromatography membrane built‐in electrode is designed. This is the first attempt to utilize this type of membrane, which is widely used for the selective adsorption of proteins, in the battery field. An ordered multilayer structure throughout the electrode can easily be obtained, and the number of membrane layers can be also conveniently controlled by varying the cross‐linking time of SA. The PS shuttling effect is efficiently suppressed and the permeability of PSs is reduced by enveloping the carbon/sulfur powder in ultrathin laminated chromatography membranes. As a result, these designed electrodes deliver a superhigh initial capacity of 1492 mA h g −1 , with a capacity retention almost 20% higher than the contrast. This low‐cost and easily mass‐producible strategy inspired by affinity chromatography is expected to effectively solve the PS shuttling problem toward high‐loading and long‐lifetime Li–S batteries in practice.
科研通智能强力驱动
Strongly Powered by AbleSci AI