Polymer-coated silica dual functional fillers to improve the performance of poly(ethylene oxide)-based solid electrolytes

被引:13
|
作者
Chen, Zehan [1 ]
Jia, He [1 ]
Yan, Shanshan [1 ]
Gohy, Jean-Francois [1 ]
机构
[1] Catholic Univ Louvain, Inst Condensed Matter & Nanosci IMCN, Pl L Pasteur 1, B-1348 Louvain La Neuve, Belgium
关键词
Three-dimensional coating; Silica filler; Poly(ethylene oxide); Composite solid electrolyte; Lithium metal battery; IONIC-CONDUCTIVITY; TRANSPORT-PROPERTIES; PEO;
D O I
10.1016/j.nanoen.2023.108637
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The application of solid polymer electrolytes (SPEs) is mainly hindered by their low ionic conductivity and the limited mechanical properties. Adding functional small molecules and inorganic fillers are two of the simplest and most effective ways to improve the performance of SPEs. However, most of the time, both methods cannot be implemented concomitantly, and may even inhibit each other. Here, an original dual functional filler, consisting of hollow porous SiO2 nanospheres three-dimensionally wrapped by poly(2,2,6,6-tetramethylpiperidin-4-yl methacrylate) (PTMPM), is blended with poly(ethylene oxide) (PEO) and LiClO4 to obtain a composite solid electrolyte (CSE). Compared to the reference PEO SPE, the room-temperature ionic conductivity of the synthe-sized CSE is improved by 4 orders of magnitude reaching 1.3 x 10-4 S cm-1. Moreover, a lithium ion trans-ference number value as high as 0.81 is obtained. The CSE membrane is further assembled with a Li anode and a standard LiFePO4 cathode to obtain an all-solid-state battery showing high capacity (149.3 mAh g-1 at 0.1 C) and long-term stability (0.68 & PTSTHOUSND; loss of capacity per cycle, over 100 cycles). The peculiar structure of the PEO/PTMPM interface is thought to be at the origin of the enhanced LiClO4 dissociation and mobility of lithium ions. Remarkably, the well-known toughening effect of SiO2 fillers is preserved in the CSE.
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页数:9
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