{"title":"Stable Operation of Lithium Metal Batteries with Aggressive Cathode Chemistries at 4.9 V","authors":"Zhihong Piao, Hong-Rui Ren, Gongxun Lu, Kai Jia, Junyang Tan, Xinru Wu, Zhaofeng Zhuang, Zhiyuan Han, Chuang Li, Runhua Gao, Xinyong Tao, Guangmin Zhou, Hui-Ming Cheng","doi":"10.1002/anie.202300966","DOIUrl":null,"url":null,"abstract":"<p>High-voltage lithium metal batteries (LMBs) pose severe challenges for the matching of electrolytes with aggressive electrodes, especially at low temperatures. Here, we report a rational modification of the Li<sup>+</sup> solvation structure to extend the voltage and temperature operating ranges of conventional electrolytes. Ion-ion and ion-dipole interactions as well as the electrochemical window of solvents were tailored to improve oxidation stability and de-solvation kinetics of the electrolyte. Meanwhile, robust and elastic B and F-rich interphases are formed on both electrodes. Such optimization enables Li||LiNi<sub>0.5</sub>Mn<sub>1.5</sub>O<sub>4</sub> cells (90.2 % retention after 400 cycles) and Li||LiNi<sub>0.6</sub>Co<sub>0.2</sub>Mn<sub>0.2</sub>O<sub>2</sub> (NCM622) cells (74.0 % retention after 200 cycles) to cycle stably at an ultra-high voltage of 4.9 V. Moreover, NCM622 cells deliver a considerable capacity of 143.5 mAh g<sup>−1</sup> at −20 °C, showing great potential for practical uses. The proposed strategy sheds light on further optimization for high-voltage LMBs.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"62 15","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2023-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202300966","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 9
Abstract
High-voltage lithium metal batteries (LMBs) pose severe challenges for the matching of electrolytes with aggressive electrodes, especially at low temperatures. Here, we report a rational modification of the Li+ solvation structure to extend the voltage and temperature operating ranges of conventional electrolytes. Ion-ion and ion-dipole interactions as well as the electrochemical window of solvents were tailored to improve oxidation stability and de-solvation kinetics of the electrolyte. Meanwhile, robust and elastic B and F-rich interphases are formed on both electrodes. Such optimization enables Li||LiNi0.5Mn1.5O4 cells (90.2 % retention after 400 cycles) and Li||LiNi0.6Co0.2Mn0.2O2 (NCM622) cells (74.0 % retention after 200 cycles) to cycle stably at an ultra-high voltage of 4.9 V. Moreover, NCM622 cells deliver a considerable capacity of 143.5 mAh g−1 at −20 °C, showing great potential for practical uses. The proposed strategy sheds light on further optimization for high-voltage LMBs.
高压锂金属电池(lmb)对电解质与腐蚀性电极的匹配提出了严峻的挑战,特别是在低温下。在这里,我们报道了一种合理的Li+溶剂化结构的修改,以延长传统电解质的电压和温度工作范围。离子-离子和离子-偶极子相互作用以及溶剂的电化学窗口被定制,以提高电解质的氧化稳定性和脱溶剂动力学。同时,在两个电极上形成了坚固而富有弹性的富B和富f界面。这样的优化使得Li| LiNi0.5Mn1.5O4电池在400次循环后的保留率为90.2%,Li| LiNi0.6Co0.2Mn0.2O2 (NCM622)电池在200次循环后的保留率为74.0%,在4.9 V的超高压下稳定循环。此外,NCM622电池在- 20°C下提供143.5 mAh g - 1的可观容量,显示出实际应用的巨大潜力。提出的策略为高压lmb的进一步优化提供了思路。
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.