材料科学
离子电导率
电解质
极地的
延伸率
聚合物
电导率
Boosting(机器学习)
化学工程
离子键合
聚合物电解质
电压
纳米技术
复合材料
离子
有机化学
电极
电气工程
物理化学
极限抗拉强度
机器学习
物理
工程类
化学
计算机科学
天文
作者
Junlei Liu,Yu‐Sheng Chen,Zhiqiang Zhou,Weiwei Hou,Dianyu Tang,Abolhassan Noori,Wentao Chi,Yihu Liu,Chenze Wang,Bingbing Han,Mir Fazlollah Mousavi,Cheng Zhang
标识
DOI:10.1021/acsami.4c19721
摘要
Poly(ethylene oxide) (PEO) has been widely studied as an electrolyte owing to its excellent lithium compatibility and good film-forming properties. However, its electrochemical performance at room temperature remains a significant challenge due to its low ionic conductivity, narrow electrochemical window, and continuous decomposition. Herein, we prepare a multifunctional polar polymer to optimize PEO’s electrochemical properties and cycling stability. PEO’s crystallinity is disrupted with the addition of polar polymer, and the amorphous polymer segments create more transfer pathways for Li-ion. More importantly, the polar groups enhance PEO’s Li-ion transference number by facilitating lithium salt dissociation through Lewis acid–base interactions and weaken the coordination between Li-ion and ether oxygen, thereby expediting Li-ion migration. In addition, the trifluoromethyl groups promote TFSI – defluorination, forming LiF-rich solid electrolyte interphase layers that prevent continuous decomposition of PEO. The resulting composite electrolyte exhibits excellent room temperature ionic conductivity (2.06 × 10 –4 S cm –1 ) and Li-ion transference number (0.30) and outstanding voltage (4.9 V). The assembled symmetric lithium battery could perform stably for 620 h at 0.1 mA cm –2 . Li||LiFePO 4 cells exhibit excellent capacity retention (87.81%) and Coulombic efficiency (100.0%) at 0.5 C over 700 cycles.
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