{"title":"通过电解质添加剂和正极材料涂层抑制锰(II)离子沉积对锂离子电池石墨负极的破坏","authors":"Yingying Zeng, Haihui Chen, Changren Xiao, Xiuguang Yi, Wenming Liao, Limin Liu","doi":"10.1002/est2.627","DOIUrl":null,"url":null,"abstract":"<p>SEM and EDS techniques are carried out to demonstrate the variation of morphology and chemical compound on the surface of graphite anode, which suggest a well-accepted concept that the manganese ions have serious influence on the reversible capacity fade of graphite anode in lithium ion batteries. Based the main chemical compounds of the inorganic layer on the graphite surface, the evolution steps of graphite structure damaged by Mn ions are derived. Although the amount of deposited manganese ions is small, these play an important role in the catalytic decomposition of the electrolyte. Moreover, Raman analysis shows that the structure of the graphite anode becomes irregular at initial SEI formation cycles and tends to be stable at subsequent cycles. This structure variation is probably generated from the manganese ion deposition and the solid electrolyte interphase (SEI) film formation. According to the capacity tests, the cycling performance of NCM811/graphite lithium-ion batteries could be improved 50% by FEC additive and B<sub>2</sub>O<sub>3</sub> surface coating. FEC additive maybe benefit graphite forming a stable SEI film in the early stages of cycling to suppress the damage of Mn<sup>2+</sup> ions, then improving the cycling performance.</p>","PeriodicalId":11765,"journal":{"name":"Energy Storage","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Suppressing the damage of deposited Mn(II) ions to graphite anode in lithium-ion batteries by electrolyte additive agent and positive material coating\",\"authors\":\"Yingying Zeng, Haihui Chen, Changren Xiao, Xiuguang Yi, Wenming Liao, Limin Liu\",\"doi\":\"10.1002/est2.627\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>SEM and EDS techniques are carried out to demonstrate the variation of morphology and chemical compound on the surface of graphite anode, which suggest a well-accepted concept that the manganese ions have serious influence on the reversible capacity fade of graphite anode in lithium ion batteries. Based the main chemical compounds of the inorganic layer on the graphite surface, the evolution steps of graphite structure damaged by Mn ions are derived. Although the amount of deposited manganese ions is small, these play an important role in the catalytic decomposition of the electrolyte. Moreover, Raman analysis shows that the structure of the graphite anode becomes irregular at initial SEI formation cycles and tends to be stable at subsequent cycles. This structure variation is probably generated from the manganese ion deposition and the solid electrolyte interphase (SEI) film formation. According to the capacity tests, the cycling performance of NCM811/graphite lithium-ion batteries could be improved 50% by FEC additive and B<sub>2</sub>O<sub>3</sub> surface coating. FEC additive maybe benefit graphite forming a stable SEI film in the early stages of cycling to suppress the damage of Mn<sup>2+</sup> ions, then improving the cycling performance.</p>\",\"PeriodicalId\":11765,\"journal\":{\"name\":\"Energy Storage\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Storage\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/est2.627\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/est2.627","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
通过扫描电子显微镜(SEM)和电离辐射分析(EDS)技术,展示了石墨负极表面形貌和化合物的变化,提出了锰离子严重影响锂离子电池石墨负极可逆容量衰减的公认概念。根据石墨表面无机层的主要化学成分,得出了锰离子破坏石墨结构的演化步骤。虽然沉积的锰离子数量很少,但它们在电解质的催化分解中发挥了重要作用。此外,拉曼分析表明,在最初的 SEI 形成周期中,石墨阳极的结构变得不规则,而在随后的周期中趋于稳定。这种结构变化可能是由锰离子沉积和固体电解质相间(SEI)膜形成引起的。根据容量测试,通过添加 FEC 和 B2O3 表面涂层,NCM811/石墨锂离子电池的循环性能可提高 50%。FEC 添加剂可能有利于石墨在循环初期形成稳定的 SEI 膜,从而抑制 Mn2+ 离子的破坏,进而提高循环性能。
Suppressing the damage of deposited Mn(II) ions to graphite anode in lithium-ion batteries by electrolyte additive agent and positive material coating
SEM and EDS techniques are carried out to demonstrate the variation of morphology and chemical compound on the surface of graphite anode, which suggest a well-accepted concept that the manganese ions have serious influence on the reversible capacity fade of graphite anode in lithium ion batteries. Based the main chemical compounds of the inorganic layer on the graphite surface, the evolution steps of graphite structure damaged by Mn ions are derived. Although the amount of deposited manganese ions is small, these play an important role in the catalytic decomposition of the electrolyte. Moreover, Raman analysis shows that the structure of the graphite anode becomes irregular at initial SEI formation cycles and tends to be stable at subsequent cycles. This structure variation is probably generated from the manganese ion deposition and the solid electrolyte interphase (SEI) film formation. According to the capacity tests, the cycling performance of NCM811/graphite lithium-ion batteries could be improved 50% by FEC additive and B2O3 surface coating. FEC additive maybe benefit graphite forming a stable SEI film in the early stages of cycling to suppress the damage of Mn2+ ions, then improving the cycling performance.