材料科学
离子电导率
锂(药物)
离子液体
辛烷值
达布科
电解质
单体
快离子导体
化学工程
高分子化学
热稳定性
聚合物
有机化学
物理化学
化学
复合材料
电极
医学
工程类
内分泌学
催化作用
作者
Sumana Bandyopadhyay,Aashish Joshi,Amit Kumar Gupta,Rajiv K. Srivastava,Bhanu Nandan
标识
DOI:10.1021/acsami.3c11377
摘要
Solid polymer electrolytes (SPEs) have emerged as a viable alternative to traditional organic liquid-based electrolytes for high energy density and safer lithium batteries. Poly(ethylene oxide) (PEO)-based SPEs are considered one of the mainstream SPE materials with excellent dissociation ability of lithium salts. However, the inferior ionic conductivity at room temperature and poor dimensional stability at high temperature limit their utilization. In this work, a semi-interpenetrating polymer network (semi-IPN) forming a precursor based on an ionic liquid (IL) monomer and linear PEO chains were introduced into an electrospun poly(acrylonitrile) (PAN) fibrous mat with subsequent thermal-initiated cross-linking. 1,4-Diazabicyclo [2.2.2] octane (DABCO) and 4-(chloromethyl) styrene were used to synthesize the styrenic-DABCO-based IL monomer with bis(trifluoromethane sulfonyl)imide (TFSI – ) or bis(fluoromethane sulfonyl)imide (FSI – ) as the anion, named as SDTFSI and SDFSI, respectively. Together, the FSI – and TFSI – anions demonstrate a synergistic effect in providing ion-conductive LiF and Li 3 N-rich inorganic SEI layer with enhanced lithium dendrite suppression ability. The twofold reinforcement effect is achieved collectively from the semi-IPN structure and the three-dimensional (3D) PAN network that help to construct highly efficient and uniform ion transport channels with excellent flexibility, further suppressing the lithium dendrite growth. The SPEs were dimensionally stable even at elevated temperatures of 150 °C. Moreover, the SPEs show an ionic conductivity of 4.4 × 10 –4 S cm –1 at 25 °C and 1.81 × 10 –3 S cm –1 at 55 °C and a lithium-ion transference number of 0.56. The favorable electrochemical performance of the SPEs was verified by operating LiFePO 4 /Li and NMC/Li cells.
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