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SiO2-Decorated-Montmorillonite reinforced Poly(1,3-dioxolane) as a multifunctional solid electrolyte for High-Performance lithium batteries

蒙脱石 锂(药物) 离子电导率 电解质 电化学 电导率 材料科学 法拉第效率 快离子导体 化学工程 复合数 化学 复合材料 工程类 电极 物理化学 内分泌学 医学
作者
Guojian Lin,Tianqi Yang,Haiyuan Zhang,Hongjie Wang,Wenkui Zhang,Hui Huang,Yang Xia,Xinhui Xia,Xinyong Tao,Jun Zhang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:488: 151161-151161 被引量:18
标识
DOI:10.1016/j.cej.2024.151161
摘要

Solid polymer electrolytes (SPEs) have garnered considerable attention owing to their remarkable flexibility, manufacturability, and cost-effectiveness. However, SPEs are hampered by critical limitations such as inadequate ionic conductivity at room temperature and issues related to lithium-ion migration, which curtail their practical applications. To tackle these challenges, the incorporation of inorganic additives into SPEs is considered as an effective strategy. Montmorillonite (MMT), a typical two-dimensional material, has emerged as an advanced filler for SPEs, displaying increased ionic conductivity, lithium-ion transference, and electrochemical stability. Herein, siliconized-modified montmorillonite (SiO2-MMT) nanosheets are synthesized and incorporated into poly(1,3-dioxolane) (PDOL)-based SPEs, resulting in a multifunctional composite solid electrolyte (CSE). The CSE shows an ionic conductivity as high as 5.58 × 10−4 S cm−1 at 30 °C, with a lithium-ion transference number close to 0.58. Symmetrical Li||Li cells utilizing the CSE exhibits stable performance for over 1200 h at a current density of 0.2 mA cm−2. Additionally, the CSE contributes to the stability of electrolytes, facilitates superior Li+ mobility and uniform deposition, thereby forming a stable solid electrolyte interface (SEI). Density functional theory (DFT) simulation confirms that SiO2-MMT, containing a large number of adsorption sites, facilitated fast reaction kinetics and effective anchoring of lithium polysulfides (LiPSs). As a result, the composite electrolyte is cycled in Lithium-sulfur (Li-S) batteries at 200 mA g−1 and 30 °C for 250 cycles, achieving a high coulombic efficiency (CE > 99.4 %) and a capacity decay rate of 0.15 %. Additionally, when paired with high-voltage Li(Ni0.8Co0.1Mn0.1)O2 (NCM811) cathodes and LiFePO4 (LFP) cathodes, both display excellent electrochemical performance. This research presents a highly promising approach for constructing multifunctional solid electrolytes for high-performance lithium batteries.
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