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用于高性能锂金属电池的一种高度稳定且不易燃的深共晶电解质

A Highly Stable and Non-Flammable Deep Eutectic Electrolyte for High-Performance Lithium Metal Batteries.

作者信息

Zhao Li, Xu Ao, Cheng Yu, Xu Hantao, Xu Lin, Mai Liqiang

机构信息

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.

Hubei Longzhong Laboratory, Wuhan University of Technology (Xiangyang Demonstration Zone), Xiangyang, 441000, Hubei, P.R. China.

出版信息

Angew Chem Int Ed Engl. 2024 Oct 21;63(43):e202411224. doi: 10.1002/anie.202411224. Epub 2024 Sep 13.

Abstract

Deep 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 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.

摘要

深共晶电解质(DEEs)因其与液体电解质和固体电解质相比具有无与伦比的优势,被视为推动锂金属电池(LMBs)发展的下一代电解质之一。然而,其在LMBs中的应用受到电极界面兼容性的限制。在此,我们引入了一种由N配位诱导的新型基于固体二甲基丙二腈(DMMN)的DEE来解离双三氟甲烷磺酰亚胺锂(LiTFSI)。我们证实,DMMN分子可通过N原子与Li之间的相互作用促进LiTFSI的解离,并与TFSI阴离子形成氢键,从而促进LiTFSI的解离以形成DEE。更重要的是,由于不存在活性α-氢,DMMN与锂金属的还原稳定性大大增强,从而实现了良好的电极/电解质界面兼容性。基于这种DEE的聚合物电解质具有高离子电导率(25℃时为0.67 mS cm)、高氧化电压(相对于Li/Li为5.0 V)、良好的界面稳定性和不可燃性。使用这种DEE聚合物电解质的Li‖磷酸铁锂(LFP)和Li‖镍钴锰酸锂(NCM811)全电池在高倍率下表现出优异的长期循环稳定性和倍率性能。因此,新型基于DMMN的DEE克服了传统电解质在电极界面兼容性方面的局限性,并为提高LMBs的性能开辟了新的可能性。

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