Affiliation:
1. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 P.R. China
2. Hubei Longzhong Laboratory Wuhan University of Technology (Xiangyang Demonstration Zone) Xiangyang 441000, Hubei P.R. China
3. Hainan Institute Wuhan University of Technology Sanya 572000 P.R. China
Abstract
AbstractDeep eutectic electrolytes (DEEs) are regarded as one of the next‐generation electrolytes to promote the development of lithium metal batteries (LMBs) due to their unparalleled advantages compared to both liquid electrolytes and solid electrolytes. However, its application in LMBs is limited by electrode interface compatibility. Here, we introduce a novel solid dimethylmalononitrile (DMMN)‐based DEE induced by N coordination to dissociate LiTFSI. We confirmed that the DMMN molecule can promote the dissociation of LiTFSI by the interaction between the N atom and Li+, and form the hydrogen bond with TFSI− anion, which can promote the dissociation of LiTFSI to form DEE. More importantly, due to the absence of active α‐hydrogen, DMMN exhibits greatly enhanced reduction stability with Li metal, resulting in favorable electrode/electrolyte interface compatibility. Polymer electrolytes based on this DEE exhibit high ionic conductivity (0.67 mS cm−1 at 25 °C), high oxidation voltage (5.0 V vs. Li+/Li), favorable interfacial stability, and nonflammability. Li‖LFP and Li‖NCM811 full batteries utilizing this DEE polymer electrolyte exhibit excellent long‐term cycling stability and excellent rate performance at high rates. Therefore, the new DMMN‐based DEE overcomes the limitations of traditional electrolytes in electrode interface compatibility and opens new possibilities for improving the performance of LMBs.