Sångeland Christofer, Tjessem Trine, Mindemark Jonas, Brandell Daniel
Department of Chemistry - Ångström Laboratory, Uppsala University, Lägerhyddsvägen 1, SE-751 21 Uppsala, Sweden.
J Phys Chem Lett. 2021 Mar 25;12(11):2809-2814. doi: 10.1021/acs.jpclett.1c00366. Epub 2021 Mar 12.
Double-layer solid polymer electrolytes (DLSPEs) comprising one layer that is stable toward lithium metal and one which is stable against a high-voltage cathode are commonly suggested as a promising strategy to achieve high-energy-density lithium batteries. Through in-depth EIS analysis, it is here concluded that the polymer-polymer interface is the primary contributor to electrolyte resistance in such DLSPEs consisting of polyether-, polyester-, or polycarbonate-bad SPEs. In comparison to the bulk ionic resistance, the polymer-polymer interface resistance is approximately 10-fold higher. Nevertheless, the interfacial resistance was successfully lowered by doubling the salt concentration from 25 to 50 wt % LiTFSI owing to improved miscibility at the interface of the two polymer layers.
包含一层对锂金属稳定且另一层对高压阴极稳定的双层固体聚合物电解质(DLSPEs)通常被认为是实现高能量密度锂电池的一种有前景的策略。通过深入的电化学阻抗谱(EIS)分析,本文得出结论,在由聚醚、聚酯或聚碳酸酯基固态聚合物电解质(SPEs)组成的此类DLSPEs中,聚合物 - 聚合物界面是电解质电阻的主要贡献因素。与本体离子电阻相比,聚合物 - 聚合物界面电阻大约高10倍。然而,由于两层聚合物界面处的混溶性提高,通过将盐浓度从25 wt% LiTFSI加倍至50 wt% LiTFSI,界面电阻成功降低。