{"title":"离子液体添加剂可减轻高电压无阳极金属锂电池的锂损耗和铝腐蚀。","authors":"Minghan Zhou, Weijian Liu, Qili Su, Junfeng Zeng, Xueao Jiang, Xuansheng Wu, Zhengjian Chen, Xiwen Wang, Zhe Li, Haijing Liu, Shiguo Zhang","doi":"10.1021/acsnano.4c13203","DOIUrl":null,"url":null,"abstract":"<p><p>Concentrated electrolytes based on lithium bis(fluorosulfonyl)imide (LiFSI) have been proposed as an effective Li-compatible electrolyte for anode-free lithium metal batteries (AFLMBs). However, these electrolytes suffer from severe aluminum corrosion at an elevated potential. To address this issue, we propose a binary ionic liquid (IL) electrolyte additive comprising the 1-methyl-1-butyl pyrrolidinium cation (Pyr<sub>14</sub><sup>+</sup>), difluoro(oxalate)borate anion (DFOB<sup>-</sup>), and difluorophosphate (PO<sub>2</sub>F<sub>2</sub><sup>-</sup>) anion to mitigate the Li inventory loss and Al corrosion in 4 M LiFSI/DME electrolyte simultaneously. On the anode side, the IL additive facilitates the formation of a robust Li<sub>3</sub>N- and LiF-rich solid electrolyte interphase, promoting highly reversible Li plating/stripping and uniform Li deposition. Additionally, the ILs alter the Li<sup>+</sup> solvation structure, leading to enhanced <i>t</i><sub>Li<sup>+</sup></sub> and rapid Li<sup>+</sup> desolvation kinetics. Concurrently, on the cathode side, the ILs aid in the generation of dense LiF- and AlF-rich passivation films against Al corrosion. By using the IL-added electrolyte, the Cu||LiMn<sub>0.7</sub>Fe<sub>0.3</sub>PO<sub>4</sub> cell operates stably at 4.5 V, and the Cu||NCM613 cell with a high loading of 4.0 mA h cm<sup>-2</sup> sustains 142 cycles until 80% capacity retention. This research contributes to a deeper understanding of the IL additive mechanism at the electrode-electrolyte interfaces and offers a straightforward approach to designing practical high-voltage AFLMB electrolytes.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":" ","pages":"32959-32972"},"PeriodicalIF":15.8000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ionic Liquid Additive Mitigating Lithium Loss and Aluminum Corrosion for High-Voltage Anode-Free Lithium Metal Batteries.\",\"authors\":\"Minghan Zhou, Weijian Liu, Qili Su, Junfeng Zeng, Xueao Jiang, Xuansheng Wu, Zhengjian Chen, Xiwen Wang, Zhe Li, Haijing Liu, Shiguo Zhang\",\"doi\":\"10.1021/acsnano.4c13203\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Concentrated electrolytes based on lithium bis(fluorosulfonyl)imide (LiFSI) have been proposed as an effective Li-compatible electrolyte for anode-free lithium metal batteries (AFLMBs). However, these electrolytes suffer from severe aluminum corrosion at an elevated potential. To address this issue, we propose a binary ionic liquid (IL) electrolyte additive comprising the 1-methyl-1-butyl pyrrolidinium cation (Pyr<sub>14</sub><sup>+</sup>), difluoro(oxalate)borate anion (DFOB<sup>-</sup>), and difluorophosphate (PO<sub>2</sub>F<sub>2</sub><sup>-</sup>) anion to mitigate the Li inventory loss and Al corrosion in 4 M LiFSI/DME electrolyte simultaneously. On the anode side, the IL additive facilitates the formation of a robust Li<sub>3</sub>N- and LiF-rich solid electrolyte interphase, promoting highly reversible Li plating/stripping and uniform Li deposition. Additionally, the ILs alter the Li<sup>+</sup> solvation structure, leading to enhanced <i>t</i><sub>Li<sup>+</sup></sub> and rapid Li<sup>+</sup> desolvation kinetics. Concurrently, on the cathode side, the ILs aid in the generation of dense LiF- and AlF-rich passivation films against Al corrosion. By using the IL-added electrolyte, the Cu||LiMn<sub>0.7</sub>Fe<sub>0.3</sub>PO<sub>4</sub> cell operates stably at 4.5 V, and the Cu||NCM613 cell with a high loading of 4.0 mA h cm<sup>-2</sup> sustains 142 cycles until 80% capacity retention. This research contributes to a deeper understanding of the IL additive mechanism at the electrode-electrolyte interfaces and offers a straightforward approach to designing practical high-voltage AFLMB electrolytes.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\" \",\"pages\":\"32959-32972\"},\"PeriodicalIF\":15.8000,\"publicationDate\":\"2024-11-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsnano.4c13203\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.4c13203","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
基于双(氟磺酰)亚胺锂(LiFSI)的浓缩电解质已被提出作为无阳极锂金属电池(AFLMB)的有效锂兼容电解质。然而,这些电解质在电位升高时会受到严重的铝腐蚀。为解决这一问题,我们提出了一种二元离子液体(IL)电解质添加剂,由 1-甲基-1-丁基吡咯烷阳离子(Pyr14+)、二氟(草酸盐)硼酸阴离子(DFOB-)和二氟磷酸根阴离子(PO2F2-)组成,可同时减轻 4 M LiFSI/DME 电解质中的锂库存损失和铝腐蚀。在阳极侧,IL 添加剂有助于形成稳固的富含 Li3N 和 LiF 的固体电解质互相,促进高度可逆的锂镀层/剥离和均匀的锂沉积。此外,IL 还能改变 Li+ 的溶解结构,从而增强 tLi+ 和快速的 Li+ 解溶解动力学。同时,在阴极侧,IL 有助于生成致密的 LiF- 和富含 AlF 的钝化膜,以防止铝腐蚀。通过使用添加了IL的电解液,Cu||LiMn0.7Fe0.3PO4电池可在4.5 V电压下稳定运行,而高负载为4.0 mA h cm-2的Cu||NCM613电池可维持142个循环,直到容量保持在80%。这项研究有助于加深对电极-电解质界面 IL 添加机制的理解,并为设计实用的高电压 AFLMB 电解质提供了一种直接的方法。
Ionic Liquid Additive Mitigating Lithium Loss and Aluminum Corrosion for High-Voltage Anode-Free Lithium Metal Batteries.
Concentrated electrolytes based on lithium bis(fluorosulfonyl)imide (LiFSI) have been proposed as an effective Li-compatible electrolyte for anode-free lithium metal batteries (AFLMBs). However, these electrolytes suffer from severe aluminum corrosion at an elevated potential. To address this issue, we propose a binary ionic liquid (IL) electrolyte additive comprising the 1-methyl-1-butyl pyrrolidinium cation (Pyr14+), difluoro(oxalate)borate anion (DFOB-), and difluorophosphate (PO2F2-) anion to mitigate the Li inventory loss and Al corrosion in 4 M LiFSI/DME electrolyte simultaneously. On the anode side, the IL additive facilitates the formation of a robust Li3N- and LiF-rich solid electrolyte interphase, promoting highly reversible Li plating/stripping and uniform Li deposition. Additionally, the ILs alter the Li+ solvation structure, leading to enhanced tLi+ and rapid Li+ desolvation kinetics. Concurrently, on the cathode side, the ILs aid in the generation of dense LiF- and AlF-rich passivation films against Al corrosion. By using the IL-added electrolyte, the Cu||LiMn0.7Fe0.3PO4 cell operates stably at 4.5 V, and the Cu||NCM613 cell with a high loading of 4.0 mA h cm-2 sustains 142 cycles until 80% capacity retention. This research contributes to a deeper understanding of the IL additive mechanism at the electrode-electrolyte interfaces and offers a straightforward approach to designing practical high-voltage AFLMB electrolytes.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.