多硫化物
阴极
锂(药物)
胶粘剂
储能
硫黄
材料科学
聚合物
溶解
粘附
吸附
锂硫电池
化学
化学工程
电极
纳米技术
复合材料
电化学
电解质
有机化学
冶金
工程类
图层(电子)
功率(物理)
物理化学
内分泌学
物理
医学
量子力学
作者
Yong Wen,Xiangyu Lin,Xingshen Sun,Shanshan Wang,Jie Wang,He Liu,Xu Xu
标识
DOI:10.1016/j.jcis.2024.01.092
摘要
Although lithium-sulfur (Li-S) batteries have attracted a great deal of attention due to their ultrahigh energy density, the significant dissolution and shuttle of polysulfides, coupled with the unstable electrode structure, result in a substantial decline in capacity, thereby hindering their practical application in rapidly advancing energy storage systems. In this work, we prepare an environmentally friendly binder (LA-GA) that possesses self-healing abilities and high adhesion by combining dynamic disulfide (S-S) bonds with abundant polar functional groups. Significantly, the self-healing capability provided by S-S bonds facilitates the repair of cracks resulting from cathode volume expansion. Simultaneously, the polar functional groups (carboxyl and pyrogallol) not only enhance adhesion, preserving cathode integrity, but also effectively participate in lithium polysulfide adsorption, thereby inhibiting the shuttle effect. As a result, sulfur cathodes incorporating the LA-GA binder demonstrate favorable cycling stability, with a high capacity retention of 81.9% when tested at 0.2 C for 100 cycles. Additionally, the long-term cycling performance is satisfactory, showing a small capacity decline rate of 0.0469% per cycle over 700 cycles at 1.0 C.
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