Effects of Polymer Side Chains on Ion Transport Properties of Gel Electrolytes Containing High Concentration Li Salt Solution

Highly concentrated Li salt electrolyte solutions have attracted attention recently due to the unique physicochemical and electrochemical properties. 1 Recently, our group reported that highly concentrated Li salt/sulfolane electrolytes exhibit Li + ion hopping conduction mechanism. 2 Gel electrolytes, which incorporate liquid electrolytes within polymer network generally maintain ion transport properties derived from liquid electrolytes. The gelation of liquid electrolytes can prevent the leakage of liquids and improve the safety of batteries. However, certain gel electrolytes containing high concentration Li salt solution have been reported that the ion transport properties can be affected by the participation of the polymer matrix in the solvation structure. 3 In this study, we focused on the effects of polymer side chains on ion transport properties of gels. We prepared novel gel electrolytes using polymers with different side chains as a polymer matrix containing high concentration Li salt/sulfolane solutions. Gel electrolytes incorporating lithium bis(trifluoromethanesulfonyl)amide (LiTFSA) and sulfolane (SL) at 1:3 molar ratio, which exhibits a high Li + ion transference number ( t Li + ), were prepared by free radical polymerization using four types of methacrylate monomers (methyl methacrylate: MMA, propyl methacrylate: PMA, 2,2,3,3-tetrafluoropropyl methacrylate: TFPMA, diethylene glycol monomethyl ether methacrylate: DEGMA). Ionic conductivity and of PMMA gel were comparable to those of PPMA gel with extended alkyl side chains, while in PDEGMA gel with multiple coordination sites for Li + showed lower t Li + because Li + ions were trapped by the ether moiety of the side chain. On the other hand, PTFPMA gel with partially fluorinated propyl side chains showed a higher t Li + . The self-diffusion coefficients of Li + , TFSA − , and SL in PTFPMA gel measured with pulsed field gradient (PFG) NMR suggested lower diffusivity of TFSA − compared to that in PPMA gel. Moreover, 19 F NMR revealed that the signal derived from TFSA − shifted to downfield side in PPMA gel and upfield shift in PTFPMA gel compared to that in the liquid electrolyte of [LiTFSA]/[SL] =1:3, indicating a change of solvation structure due to the polymer side chain. Finally, we demonstrated rate capability tests for gel electrolytes with LiCoO 2 /Li cells and found that the cell with PTFPMA gel having high t Li + exhibited better rate performance than one with PPMA gel. Acknowledgements This study was partially supported by Japan Science and Technology Agency (JST) GteX Program (Grant No. JPMJGX23S0) and JSPS KAKENHI (Grant No. 22H00340) from the Japan Society for the Promotion of Science (JSPS). References Yamada and A. Yamada, Review—Superconcentrated Electrolytes for Lithium Batteries, J. Electrochem. Soc. , 2015, 162 , A2406–A2423. Dokko, D. Watanabe, Y. Ugata, M. L. Thomas, S. Tsuzuki, W. Shinoda, K. Hashimoto, K. Ueno, Y. Umebayashi and M. Watanabe, Direct Evidence for Li Ion Hopping Conduction in Highly Concentrated Sulfolane-Based Liquid Electrolytes, J. Phys. Chem. B , 2018, 122 , 10736–10745. Tasaki, Y. Ugata, K. Hashimoto, H. Kokubo, K. Ueno, M. Watanabe and K. Dokko, Tetra-arm poly(ethylene glycol) gels with highly concentrated sulfolane-based electrolytes exhibiting high Li-ion transference numbers, Phys. Chem. Chem. Phys. , 2023, 25 , 17793–17797.