| Institution: | 1. College of Chemistry & Green Catalysis Center, Zhengzhou University, Zhengzhou, 450001 Henan, P. R. China
These authors contributed equally to this work.;2. College of Chemistry & Green Catalysis Center, Zhengzhou University, Zhengzhou, 450001 Henan, P. R. China;3. Leeds Institute of Textiles and Colour (LITAC), School of Design, Woodhouse Lane, University of Leeds, Leeds, LS2 9JT UK |
| Abstract: | Polymer electrolytes provide a visible pathway for the construction of high-safety quasi-solid-state batteries due to their high interface compatibility and processability. Nevertheless, sluggish ion transfer at room temperature seriously limits their applications. Herein, a triangular synergy strategy is proposed to accelerate Na-ion conduction via the cooperation of polymer-salt, ionic liquid, and electron-rich additive. Especially, PVDF-HFP and NaTFSI salt acted as the framework to stably accommodate all the ingredients. An ionic liquid (Emim+-FSI−) softened the polymer chains through a weakening molecule force and offered additional liquid pathways for ion transport. Physicochemical characterizations and theoretical calculations demonstrated that electron-rich Nerolin with π-cation interaction facilitated the dissociation of NaTFSI and effectively restrained the competitive migration of large cations from EmimFSI, thus lowering the energy barrier for ion transport. The strategy resulted in a thin F-rich interphase dominated by NaTFSI salt's decomposition, enabling rapid Na+ transmission across the interface. These combined effects resulted in a polymer electrolyte with high ionic conductivity (1.37×10−3 S cm−1) and tNa+ (0.79) at 25 °C. The assembled cells delivered reliable rate capability and stability (200 cycles, 99.2 %, 0.5 C) with a good safety performance. |
