Mao Yuezhen, Mi Fanghui, Zhang Wei, Zhang Zhijun, Sun Chunwen
School of Chemical & Environmental Engineering, China University of Mining and Technology-Beijing, Beijing 100083, PR China.
School of Chemical & Environmental Engineering, China University of Mining and Technology-Beijing, Beijing 100083, PR China.
J Colloid Interface Sci. 2025 Sep 30;703(Pt 1):139143. doi: 10.1016/j.jcis.2025.139143.
Composite solid electrolytes (CSEs) based on garnet LiLaZrO (LLZO) are promising for solid-state batteries due to high ionic conductivity and flexibility. However, interfacial instability with lithium metal anodes promotes dendrite growth and side reactions. To address this issue, an in situ polymerized interfacial layer (TPELL layer) was constructed by copolymerizing trimethyl phosphate (TMP) and ethylene carbonate (EC) between the Li anode and CSE. The copolymerization of EC and TMP effectively regulates the solvent structure within the interfacial layer, which in turn modulates the Li coordination environment and enhances the mechanical robustness of the interface. Furthermore, the incorporation of EC and LiPF promotes the formation of a more stable lithium metal anode/electrolyte interface. Consequently, the Li||LiFePO battery with CSE containing interfacial layer formed by copolymerization of TMP and EC exhibits a capacity retention of 93.83 % after 750 cycles at 1C and the Li||LiNiCoMnO battery maintains 130.1 mAh g after 350 cycles at 0.5C. Post-cycling analysis indicates that the preserved integrity of the cathode structure can be ascribed to the formation of a multifunctional cathode electrolyte interphase (CEI) derived from TPELL components, which effectively suppresses transition-metal dissolution and alleviates interfacial resistance. Moreover, this in situ polymerization strategy facilitates intimate interfacial contact at both the anode and cathode, thereby providing a promising pathway to address the persistent electrode/electrolyte interfacial challenges in solid-state lithium metal batteries.
基于石榴石型LiLaZrO(LLZO)的复合固体电解质(CSEs)因其高离子电导率和柔韧性而在固态电池领域颇具潜力。然而,与锂金属负极的界面不稳定性会促进枝晶生长和副反应。为解决这一问题,通过在锂负极和CSE之间使磷酸三甲酯(TMP)和碳酸亚乙酯(EC)共聚,构建了原位聚合界面层(TPELL层)。EC和TMP的共聚有效调节了界面层内的溶剂结构,进而调节了锂的配位环境并增强了界面的机械稳定性。此外,EC和LiPF的加入促进了更稳定的锂金属负极/电解质界面的形成。因此,含有由TMP和EC共聚形成的界面层的CSE的Li||LiFePO电池在1C下循环750次后容量保持率为93.83%,Li||LiNiCoMnO电池在0.5C下循环350次后保持130.1 mAh g。循环后分析表明,阴极结构的完整性得以保留可归因于源自TPELL组分的多功能阴极电解质界面(CEI)的形成,其有效抑制了过渡金属溶解并减轻了界面电阻。此外,这种原位聚合策略促进了阳极和阴极处的紧密界面接触,从而为解决固态锂金属电池中长期存在的电极/电解质界面挑战提供了一条有前景的途径。