Ma Xinyu, Yu Jiangtao, Zou Xiuyang, Wang Xiaoliang, Wang Huihui, Hu Yin, Duan Minzhi, Tao Songlin, Sun Shipeng, Shen Yanbin, Yan Feng
Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Suzhou Key Laboratory of Soft Material and New Energy, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, P.R. China.
School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, P.R. China.
Angew Chem Int Ed Engl. 2025 Jun 2;64(23):e202505035. doi: 10.1002/anie.202505035. Epub 2025 Apr 2.
The practical use of all-solid-state batteries (ASSBs) is hindered by the intractable electrolyte/electrode interfacial resistance and discontinuous ion transport networks within electrodes. Ionic plastic crystals offer a potential solution to these challenges due to their melt-permeable properties to the electrodes. However, their limited ionic conductivity restricts their application. Here, we propose a design principle for solid-state electrolytes based on an electric field-induced strategy by using ionic plastic crystals with low self-migrating and high conductivity toward target ions. Through the external potential difference, an ordered internal electric field is generated within the ionic plastic crystal-based solid-state electrolytes (IPCEs), which mitigates the coordination limitations of anions on target ions to facilitate rapid ion conduction. The prepared IPCE demonstrates high ionic conductivity (1.08 × 10 S cm at 25 °C) and a Li transfer number (0.77), enabling the application of ASSBs over a wide temperature range (from 0 to 60 °C). Furthermore, the assembled Li||LiNiCoMnO ASSBs exhibit stable cycling, maintaining 97.5% capacity retention after 500 cycles at 25 °C. This work provides a fresh perspective on the practical application of ASSBs, highlighting the potential of IPCEs in enhancing battery performance.
全固态电池(ASSB)的实际应用受到难以解决的电解质/电极界面电阻以及电极内不连续离子传输网络的阻碍。离子塑性晶体因其对电极具有熔体可渗透特性,为这些挑战提供了一种潜在的解决方案。然而,它们有限的离子电导率限制了其应用。在此,我们提出一种基于电场诱导策略的固态电解质设计原理,通过使用对目标离子具有低自迁移率和高电导率的离子塑性晶体。通过外部电势差,在基于离子塑性晶体的固态电解质(IPCE)中产生有序的内部电场,这减轻了阴离子对目标离子的配位限制,以促进快速离子传导。制备的IPCE表现出高离子电导率(25℃时为1.08×10 S cm)和锂迁移数(0.77),使得ASSB能够在较宽温度范围(从0到60℃)内应用。此外,组装的Li||LiNiCoMnO ASSB表现出稳定的循环性能,在25℃下500次循环后容量保持率为97.5%。这项工作为ASSB的实际应用提供了新的视角,突出了IPCE在提高电池性能方面的潜力。