Guoyu Wang , Qiang Ma , Tong Zhang , Yonghong Deng , Guangzhao Zhang
{"title":"锂金属电池快速充电用强/弱溶剂共溶剂化电解质","authors":"Guoyu Wang , Qiang Ma , Tong Zhang , Yonghong Deng , Guangzhao Zhang","doi":"10.1016/j.nanoen.2025.111064","DOIUrl":null,"url":null,"abstract":"<div><div>Electrolyte engineering has improved the cycling life and energy density of lithium metal batteries (LMBs) by simultaneously stabilizing Li anodes and high voltage cathodes (such as LiNi<sub>0.6</sub>Co<sub>0.2</sub>Mn<sub>0.2</sub>O<sub>2</sub>, NCM622). However, these electrolytes often compromise the fast-charging performance due to relatively low Li<sup>+</sup> transport kinetics and sluggish interfacial dynamics. Herein, we introduce a strong/weak solvents co-solvation strategy designed to construct an electrolyte with anion-rich clusters and rapid Li<sup>+</sup> transport kinetics for fast-charging and energy-dense LMBs. In this approach, N,N-dimethylsulfamoyl fluoride (FSN) serves as the weak solvent, co-coordinating Li<sup>+</sup> together with the strong solvent 1,2-dimethoxyethane (DME) to form an anion-rich first solvation sheath, while the remaining DME molecules distribute externally to facilitate Li<sup>+</sup> transport. The resulting FSN-DME electrolyte exhibits an impressive ionic conductivity of 7.43 mS cm<sup>−1</sup> and an exceptional Li metal efficiency of 99.6 %. When applied in 1-Ah NCM622||Li pouch cells, the FSN-DME electrolyte enables stable operation of 300 cycles at 0.2/0.5 C and 100 cycles at 1 C charge/discharge rates under stringent conditions (cathode areal loading: 3.75 mAh cm<sup>−2</sup>, electrolyte: 3.0 g Ah<sup>−1</sup>). This breakthrough in strong/weak solvents co-solvation electrolytes, along with the development of Li<sub>2</sub>O-rich SEI interfacial layers, provides a robust foundation for designing next-generation electrolyte materials that support both fast-charging and long-life LMBs.</div></div>","PeriodicalId":394,"journal":{"name":"Nano Energy","volume":"140 ","pages":"Article 111064"},"PeriodicalIF":16.8000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A strong/weak solvents co-solvation electrolyte for fast-charging lithium metal batteries\",\"authors\":\"Guoyu Wang , Qiang Ma , Tong Zhang , Yonghong Deng , Guangzhao Zhang\",\"doi\":\"10.1016/j.nanoen.2025.111064\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Electrolyte engineering has improved the cycling life and energy density of lithium metal batteries (LMBs) by simultaneously stabilizing Li anodes and high voltage cathodes (such as LiNi<sub>0.6</sub>Co<sub>0.2</sub>Mn<sub>0.2</sub>O<sub>2</sub>, NCM622). However, these electrolytes often compromise the fast-charging performance due to relatively low Li<sup>+</sup> transport kinetics and sluggish interfacial dynamics. Herein, we introduce a strong/weak solvents co-solvation strategy designed to construct an electrolyte with anion-rich clusters and rapid Li<sup>+</sup> transport kinetics for fast-charging and energy-dense LMBs. In this approach, N,N-dimethylsulfamoyl fluoride (FSN) serves as the weak solvent, co-coordinating Li<sup>+</sup> together with the strong solvent 1,2-dimethoxyethane (DME) to form an anion-rich first solvation sheath, while the remaining DME molecules distribute externally to facilitate Li<sup>+</sup> transport. The resulting FSN-DME electrolyte exhibits an impressive ionic conductivity of 7.43 mS cm<sup>−1</sup> and an exceptional Li metal efficiency of 99.6 %. When applied in 1-Ah NCM622||Li pouch cells, the FSN-DME electrolyte enables stable operation of 300 cycles at 0.2/0.5 C and 100 cycles at 1 C charge/discharge rates under stringent conditions (cathode areal loading: 3.75 mAh cm<sup>−2</sup>, electrolyte: 3.0 g Ah<sup>−1</sup>). 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引用次数: 0
摘要
电解质工程通过同时稳定Li阳极和高压阴极(如LiNi0.6Co0.2Mn0.2O2, NCM622),提高了锂金属电池(lmb)的循环寿命和能量密度。然而,由于相对较低的Li+传输动力学和缓慢的界面动力学,这些电解质往往会损害快速充电性能。在此,我们引入了一种强/弱溶剂共溶剂化策略,旨在构建一种具有富阴离子簇和快速Li+传输动力学的电解质,用于快速充电和能量密集的lmb。在该方法中,N,N-二甲基磺酰氟(FSN)作为弱溶剂,与强溶剂1,2-二甲氧基乙烷(DME)协同Li+形成一个富含阴离子的第一溶剂鞘,而剩余的二甲氧基乙烷分子则向外分布以促进Li+的运输。得到的FSN-DME电解质具有7.43 mS cm-1的离子电导率和99.6%的锂金属效率。当应用于1- ah的NCM622||锂袋电池时,FSN-DME电解质在严格的条件下(阴极面积负载:3.75 mAh cm-2,电解质:3.0 g Ah-1)能够在0.2/0.5 C下稳定运行300次,在1c充放电速率下稳定运行100次。在强/弱溶剂共溶剂化电解质方面的突破,以及富li20的SEI界面层的发展,为设计支持快速充电和长寿命lmb的下一代电解质材料提供了坚实的基础。
A strong/weak solvents co-solvation electrolyte for fast-charging lithium metal batteries
Electrolyte engineering has improved the cycling life and energy density of lithium metal batteries (LMBs) by simultaneously stabilizing Li anodes and high voltage cathodes (such as LiNi0.6Co0.2Mn0.2O2, NCM622). However, these electrolytes often compromise the fast-charging performance due to relatively low Li+ transport kinetics and sluggish interfacial dynamics. Herein, we introduce a strong/weak solvents co-solvation strategy designed to construct an electrolyte with anion-rich clusters and rapid Li+ transport kinetics for fast-charging and energy-dense LMBs. In this approach, N,N-dimethylsulfamoyl fluoride (FSN) serves as the weak solvent, co-coordinating Li+ together with the strong solvent 1,2-dimethoxyethane (DME) to form an anion-rich first solvation sheath, while the remaining DME molecules distribute externally to facilitate Li+ transport. The resulting FSN-DME electrolyte exhibits an impressive ionic conductivity of 7.43 mS cm−1 and an exceptional Li metal efficiency of 99.6 %. When applied in 1-Ah NCM622||Li pouch cells, the FSN-DME electrolyte enables stable operation of 300 cycles at 0.2/0.5 C and 100 cycles at 1 C charge/discharge rates under stringent conditions (cathode areal loading: 3.75 mAh cm−2, electrolyte: 3.0 g Ah−1). This breakthrough in strong/weak solvents co-solvation electrolytes, along with the development of Li2O-rich SEI interfacial layers, provides a robust foundation for designing next-generation electrolyte materials that support both fast-charging and long-life LMBs.
期刊介绍:
Nano Energy is a multidisciplinary, rapid-publication forum of original peer-reviewed contributions on the science and engineering of nanomaterials and nanodevices used in all forms of energy harvesting, conversion, storage, utilization and policy. Through its mixture of articles, reviews, communications, research news, and information on key developments, Nano Energy provides a comprehensive coverage of this exciting and dynamic field which joins nanoscience and nanotechnology with energy science. The journal is relevant to all those who are interested in nanomaterials solutions to the energy problem.
Nano Energy publishes original experimental and theoretical research on all aspects of energy-related research which utilizes nanomaterials and nanotechnology. Manuscripts of four types are considered: review articles which inform readers of the latest research and advances in energy science; rapid communications which feature exciting research breakthroughs in the field; full-length articles which report comprehensive research developments; and news and opinions which comment on topical issues or express views on the developments in related fields.