材料科学
电极
聚偏氟乙烯
电池(电)
范德瓦尔斯力
锂(药物)
纳米技术
合理设计
密度泛函理论
电化学
储能
表面改性
能量密度
电化学储能
工程物理
化学工程
复合材料
聚合物
超级电容器
分子
功率(物理)
化学
工程类
内分泌学
计算化学
物理化学
物理
有机化学
医学
量子力学
作者
Yun Zhao,Zheng Liang,Yuqiong Kang,Yunan Zhou,Yanxi Li,Xiangming He,Li Wang,Weicong Mai,Xianshu Wang,Guangmin Zhou,Junxiong Wang,Jiangang Li,Naser Tavajohi,Baohua Li
标识
DOI:10.1016/j.ensm.2020.11.021
摘要
Binders, which maintain the structural integrity of electrodes, are critical components of lithium-based rechargeable batteries (LBRBs) that significantly affect battery performances, despite accounting for 2 to 5 wt% (up to 5 wt% but usually 2 wt%) of the entire electrode. Traditional polyvinylidene fluoride (PVDF) binders that interact with electrode components via weak van der Waals forces are effective in conventional LBRB systems (graphite/LiCoO2, etc.). However, its stable fluorinated structures limit the potential for further functionalization and inhibit strong interactions towards external substances. Consequently, they are unsuitable for next-generation battery systems with high energy density. There is thus a need for new functional binders with facile features compatible with novel electrode materials and chemistries. Here in this review we consider the strategies for rationally designing these functional binders. On the basis of fundamental understandings of the issues for high-energy electrode materials, we have summarized seven desired functions that binders should possess depending on the target electrodes where the binders will be applied. Then a variety of leading-edge functional binders are reviewed to show how their chemical structures realize these above functions and how the employment of these binders affects the cell's electrochemical performances. Finally the corresponding design strategies are therefore proposed, and future research opportunities as well as challenges relating to LBRB binders are outlined.
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