Chan-Gyo Kim, Suk Jekal, Jiwon Kim, Ha-Yeong Kim, Gyu-Sik Park, Yoon-Ho Ra, Jungchul Noh, Chang-Min Yoon
{"title":"Ester-based electrolytes for graphite solid electrolyte interface layer stabilization and low-temperature performance in lithium-ion batteries","authors":"Chan-Gyo Kim, Suk Jekal, Jiwon Kim, Ha-Yeong Kim, Gyu-Sik Park, Yoon-Ho Ra, Jungchul Noh, Chang-Min Yoon","doi":"10.1007/s42823-024-00749-7","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, ester co-solvents and fluoroethylene carbonate (FEC) were used as low-temperature electrolyte additives to improve the formation of the solid electrolyte interface (SEI) on graphite anodes in lithium-ion batteries (LIBs). Four ester co-solvents, namely methyl acetate (MA), ethyl acetate, methyl propionate, and ethyl propionate, were mixed with 1.0 M LiPF<sub>6</sub> ethylene carbonate:diethyl carbonate:dimethyl carbonate (1:1:1 by vol%) as the base electrolyte (BE). Different concentrations were used to compare the electrochemical performance of the LiCoO<sub>2</sub>/graphite full cells. Among various ester co-solvents, the cell employing BE mixed with 30 vol% MA (BE/MA30) achieved the highest discharge capacity at − 20 °C. In contrast, mixing esters with low-molecular-weight degraded the cell performance owing to the unstable SEI formation on the graphite anodes. Therefore, FEC was added to BE/MA30 (BE/MA30-FEC5) to form a stable SEI layer on the graphite anode surface. The LiCoO<sub>2</sub>/graphite cell using BE/MA30-FEC5 exhibited an excellent capacity of 127.3 mAh g<sup>−1</sup> at − 20 °C with a capacity retention of 80.6% after 100 cycles owing to the synergistic effect of MA and formation of a stable and uniform inorganic SEI layer by FEC decomposition reaction. The low-temperature electrolyte designed in this study may provide new guidelines for resolving low-temperature issues related to LIBs, graphite anodes, and SEI layers.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":506,"journal":{"name":"Carbon Letters","volume":"34 8","pages":"2113 - 2125"},"PeriodicalIF":5.5000,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Letters","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s42823-024-00749-7","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, ester co-solvents and fluoroethylene carbonate (FEC) were used as low-temperature electrolyte additives to improve the formation of the solid electrolyte interface (SEI) on graphite anodes in lithium-ion batteries (LIBs). Four ester co-solvents, namely methyl acetate (MA), ethyl acetate, methyl propionate, and ethyl propionate, were mixed with 1.0 M LiPF6 ethylene carbonate:diethyl carbonate:dimethyl carbonate (1:1:1 by vol%) as the base electrolyte (BE). Different concentrations were used to compare the electrochemical performance of the LiCoO2/graphite full cells. Among various ester co-solvents, the cell employing BE mixed with 30 vol% MA (BE/MA30) achieved the highest discharge capacity at − 20 °C. In contrast, mixing esters with low-molecular-weight degraded the cell performance owing to the unstable SEI formation on the graphite anodes. Therefore, FEC was added to BE/MA30 (BE/MA30-FEC5) to form a stable SEI layer on the graphite anode surface. The LiCoO2/graphite cell using BE/MA30-FEC5 exhibited an excellent capacity of 127.3 mAh g−1 at − 20 °C with a capacity retention of 80.6% after 100 cycles owing to the synergistic effect of MA and formation of a stable and uniform inorganic SEI layer by FEC decomposition reaction. The low-temperature electrolyte designed in this study may provide new guidelines for resolving low-temperature issues related to LIBs, graphite anodes, and SEI layers.
本研究使用酯类助溶剂和氟碳酸乙烯酯(FEC)作为低温电解质添加剂,以改善锂离子电池(LIB)中石墨阳极上固体电解质界面(SEI)的形成。将四种酯类助溶剂,即醋酸甲酯(MA)、醋酸乙酯、丙酸甲酯和丙酸乙酯,与 1.0 M LiPF6 碳酸乙烯酯:碳酸二乙酯:碳酸二甲酯(体积比为 1:1:1)混合,作为基础电解质(BE)。采用不同的浓度来比较钴酸锂/石墨全电池的电化学性能。在各种酯类助溶剂中,使用混合了 30 Vol% MA 的 BE(BE/MA30)的电池在零下 20 °C 时的放电容量最高。相反,混合低分子量的酯会降低电池性能,因为石墨阳极上会形成不稳定的 SEI。因此,在 BE/MA30 中添加了 FEC(BE/MA30-FEC5),以在石墨阳极表面形成稳定的 SEI 层。使用 BE/MA30-FEC5 的钴酸锂/石墨电池在零下 20 °C 时显示出 127.3 mAh g-1 的出色容量,循环 100 次后容量保持率为 80.6%,这归功于 MA 的协同效应以及 FEC 分解反应形成的稳定、均匀的无机 SEI 层。本研究设计的低温电解液可为解决与 LIB、石墨阳极和 SEI 层有关的低温问题提供新的指导。
期刊介绍:
Carbon Letters aims to be a comprehensive journal with complete coverage of carbon materials and carbon-rich molecules. These materials range from, but are not limited to, diamond and graphite through chars, semicokes, mesophase substances, carbon fibers, carbon nanotubes, graphenes, carbon blacks, activated carbons, pyrolytic carbons, glass-like carbons, etc. Papers on the secondary production of new carbon and composite materials from the above mentioned various carbons are within the scope of the journal. Papers on organic substances, including coals, will be considered only if the research has close relation to the resulting carbon materials. Carbon Letters also seeks to keep abreast of new developments in their specialist fields and to unite in finding alternative energy solutions to current issues such as the greenhouse effect and the depletion of the ozone layer. The renewable energy basics, energy storage and conversion, solar energy, wind energy, water energy, nuclear energy, biomass energy, hydrogen production technology, and other clean energy technologies are also within the scope of the journal. Carbon Letters invites original reports of fundamental research in all branches of the theory and practice of carbon science and technology.