{"title":"混合导电-嗜石-氟化物三重保护界面工程:用于高性能锂金属电池的无枝晶反向锂沉积技术","authors":"","doi":"10.1016/j.jechem.2024.10.002","DOIUrl":null,"url":null,"abstract":"<div><div>Lithium metal batteries (LMBs) with high energy density are impeded by the instability of solid electrolyte interface (SEI) and the uncontrolled growth of lithium (Li) dendrite. To mitigate these challenges, optimizing the SEI structure and Li deposition behavior is the key to stable LMBs. This study novelty proposes a facile synthesis of MgF<sub>2</sub>/carbon (C) nanocomposite through the mechanochemical reaction between metallic Mg and polytetrafluoroethylene (PTFE) powders, and its modified polypropylene (PP) separator enhances LMB performance. The in-situ formed highly conductive fluorine-doped C species play a crucial role in facilitating ion/electron transport, thereby accelerating electrochemical kinetics and altering Li deposition direction. During cycling, the in-situ reaction between MgF<sub>2</sub> and Li leads to the formation of LiMg alloy, along with a LiF-rich SEI layer, which reduces the nucleation overpotential and reinforces the interphase strength, leading to homogeneous Li deposition with dendrite-free feature. Benefiting from these merits, the Li metal is densely and uniformly deposited on the MgF<sub>2</sub>/C@PP separator side rather than on the current collector side. Furthermore, the symmetric cell with MgF<sub>2</sub>/C@PP exhibits superb Li plating/stripping performance over 2800 h at 1 mA cm<sup>−2</sup> and 2 mA h cm<sup>−2</sup>. More importantly, the assembled Li@MgF<sub>2</sub>/C@PP|LiFePO<sub>4</sub> full cell with a low negative/positive ratio of 3.6 delivers an impressive cyclability with 82.7% capacity retention over 1400 cycles at 1 C.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":null,"pages":null},"PeriodicalIF":13.1000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hybrid conductive-lithophilic-fluoride triple protection interface engineering: Dendrite-free reverse lithium deposition for high-performance lithium metal batteries\",\"authors\":\"\",\"doi\":\"10.1016/j.jechem.2024.10.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Lithium metal batteries (LMBs) with high energy density are impeded by the instability of solid electrolyte interface (SEI) and the uncontrolled growth of lithium (Li) dendrite. To mitigate these challenges, optimizing the SEI structure and Li deposition behavior is the key to stable LMBs. This study novelty proposes a facile synthesis of MgF<sub>2</sub>/carbon (C) nanocomposite through the mechanochemical reaction between metallic Mg and polytetrafluoroethylene (PTFE) powders, and its modified polypropylene (PP) separator enhances LMB performance. The in-situ formed highly conductive fluorine-doped C species play a crucial role in facilitating ion/electron transport, thereby accelerating electrochemical kinetics and altering Li deposition direction. During cycling, the in-situ reaction between MgF<sub>2</sub> and Li leads to the formation of LiMg alloy, along with a LiF-rich SEI layer, which reduces the nucleation overpotential and reinforces the interphase strength, leading to homogeneous Li deposition with dendrite-free feature. Benefiting from these merits, the Li metal is densely and uniformly deposited on the MgF<sub>2</sub>/C@PP separator side rather than on the current collector side. Furthermore, the symmetric cell with MgF<sub>2</sub>/C@PP exhibits superb Li plating/stripping performance over 2800 h at 1 mA cm<sup>−2</sup> and 2 mA h cm<sup>−2</sup>. More importantly, the assembled Li@MgF<sub>2</sub>/C@PP|LiFePO<sub>4</sub> full cell with a low negative/positive ratio of 3.6 delivers an impressive cyclability with 82.7% capacity retention over 1400 cycles at 1 C.</div></div>\",\"PeriodicalId\":15728,\"journal\":{\"name\":\"Journal of Energy Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2024-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Energy Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2095495624006922\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Energy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495624006922","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0
摘要
固态电解质界面(SEI)的不稳定性和锂(Li)枝晶的不可控生长阻碍了高能量密度的锂金属电池(LMB)的发展。为了缓解这些挑战,优化 SEI 结构和锂沉积行为是获得稳定 LMB 的关键。本研究通过金属镁和聚四氟乙烯(PTFE)粉末之间的机械化学反应,新颖地提出了一种简便的 MgF2/carbon (C) 纳米复合材料的合成方法,其改性聚丙烯(PP)隔膜提高了 LMB 的性能。原位形成的高导电性掺氟 C 物种在促进离子/电子传输方面发挥了关键作用,从而加速了电化学动力学并改变了锂沉积方向。在循环过程中,MgF2 和锂之间的原位反应会形成锂镁合金以及富含 LiF 的 SEI 层,从而降低了成核过电位并增强了相间强度,导致锂沉积均匀且无枝晶。得益于这些优点,锂金属密集而均匀地沉积在 MgF2/C@PP 分离器一侧,而不是集流器一侧。此外,带有 MgF2/C@PP 的对称电池在 1 mA cm-2 和 2 mA h cm-2 下的 2800 小时内表现出卓越的锂镀层/剥离性能。更重要的是,组装好的 Li@MgF2/C@PP|LiFePO4 全电池的负极/正极比低至 3.6,在 1 C 温度下循环 1400 次,容量保持率达到 82.7%,循环性能令人印象深刻。
Hybrid conductive-lithophilic-fluoride triple protection interface engineering: Dendrite-free reverse lithium deposition for high-performance lithium metal batteries
Lithium metal batteries (LMBs) with high energy density are impeded by the instability of solid electrolyte interface (SEI) and the uncontrolled growth of lithium (Li) dendrite. To mitigate these challenges, optimizing the SEI structure and Li deposition behavior is the key to stable LMBs. This study novelty proposes a facile synthesis of MgF2/carbon (C) nanocomposite through the mechanochemical reaction between metallic Mg and polytetrafluoroethylene (PTFE) powders, and its modified polypropylene (PP) separator enhances LMB performance. The in-situ formed highly conductive fluorine-doped C species play a crucial role in facilitating ion/electron transport, thereby accelerating electrochemical kinetics and altering Li deposition direction. During cycling, the in-situ reaction between MgF2 and Li leads to the formation of LiMg alloy, along with a LiF-rich SEI layer, which reduces the nucleation overpotential and reinforces the interphase strength, leading to homogeneous Li deposition with dendrite-free feature. Benefiting from these merits, the Li metal is densely and uniformly deposited on the MgF2/C@PP separator side rather than on the current collector side. Furthermore, the symmetric cell with MgF2/C@PP exhibits superb Li plating/stripping performance over 2800 h at 1 mA cm−2 and 2 mA h cm−2. More importantly, the assembled Li@MgF2/C@PP|LiFePO4 full cell with a low negative/positive ratio of 3.6 delivers an impressive cyclability with 82.7% capacity retention over 1400 cycles at 1 C.
期刊介绍:
The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
This journal focuses on original research papers covering various topics within energy chemistry worldwide, including:
Optimized utilization of fossil energy
Hydrogen energy
Conversion and storage of electrochemical energy
Capture, storage, and chemical conversion of carbon dioxide
Materials and nanotechnologies for energy conversion and storage
Chemistry in biomass conversion
Chemistry in the utilization of solar energy