• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于极快速充电锂离子电池的光化学驱动固体电解质界面

Photochemically driven solid electrolyte interphase for extremely fast-charging lithium-ion batteries.

作者信息

Baek Minsung, Kim Jinyoung, Jin Jaegyu, Choi Jang Wook

机构信息

School of Chemical and Biological Engineering and Institute of Chemical Processes, Seoul National University, Seoul, Republic of Korea.

Institute of Battery Technology, SK on, Daejeon, Republic of Korea.

出版信息

Nat Commun. 2021 Nov 23;12(1):6807. doi: 10.1038/s41467-021-27095-w.

DOI:10.1038/s41467-021-27095-w
PMID:34815396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8611023/
Abstract

Extremely fast charging (i.e. 80% of storage capacity within 15 min) is a pressing requirement for current lithium-ion battery technology and also affects the planning of charging infrastructure. Accelerating lithium ion transport through the solid-electrolyte interphase (SEI) is a major obstacle in boosting charging rate; in turn, limited kinetics at the SEI layer negatively affect the cycle life and battery safety as a result of lithium metal plating on the electrode surface. Here, we report a γ-ray-driven SEI layer that allows a battery cell to be charged to 80% capacity in 10.8 min as determined for a graphite full-cell with a capacity of 2.6 mAh cm. This exceptional charging performance is attributed to the lithium fluoride-rich SEI induced by salt-dominant decomposition via γ-ray irradiation. This study highlights the potential of non-electrochemical approaches to adjust the SEI composition toward fast charging and long-term stability, two parameters that are difficult to improve simultaneously in typical electrochemical processes owing to the trade-off relation.

摘要

极快速充电(即在15分钟内达到存储容量的80%)是当前锂离子电池技术的迫切需求,也影响着充电基础设施的规划。加速锂离子通过固体电解质界面(SEI)传输是提高充电速率的主要障碍;反过来,SEI层有限的动力学由于锂金属在电极表面镀覆而对电池循环寿命和安全性产生负面影响。在此,我们报道了一种由γ射线驱动的SEI层,对于容量为2.6 mAh cm的石墨全电池,该SEI层能使其在10.8分钟内充电至80%容量。这种卓越的充电性能归因于通过γ射线辐照以盐为主导的分解所诱导的富含氟化锂的SEI。本研究突出了非电化学方法在调整SEI组成以实现快速充电和长期稳定性方面的潜力,这两个参数在典型的电化学过程中由于权衡关系而难以同时提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/6db65179c353/41467_2021_27095_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/4762922b95b6/41467_2021_27095_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/000d50e0333b/41467_2021_27095_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/74cd8b0c87f8/41467_2021_27095_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/d68b613c6431/41467_2021_27095_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/db6496fa8f87/41467_2021_27095_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/6db65179c353/41467_2021_27095_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/4762922b95b6/41467_2021_27095_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/000d50e0333b/41467_2021_27095_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/74cd8b0c87f8/41467_2021_27095_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/d68b613c6431/41467_2021_27095_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/db6496fa8f87/41467_2021_27095_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/8611023/6db65179c353/41467_2021_27095_Fig6_HTML.jpg

相似文献

1
Photochemically driven solid electrolyte interphase for extremely fast-charging lithium-ion batteries.用于极快速充电锂离子电池的光化学驱动固体电解质界面
Nat Commun. 2021 Nov 23;12(1):6807. doi: 10.1038/s41467-021-27095-w.
2
Lithium-Ion Transport Behavior in Thin-Film Graphite Electrodes with SEI Layers Formed at Different Current Densities.在不同电流密度下形成的具有固体电解质界面(SEI)层的薄膜石墨电极中的锂离子传输行为。
ACS Appl Mater Interfaces. 2021 Sep 15;13(36):42662-42669. doi: 10.1021/acsami.1c09559. Epub 2021 Sep 7.
3
Switching Electrolyte Interfacial Model to Engineer Solid Electrolyte Interface for Fast Charging and Wide-Temperature Lithium-Ion Batteries.切换电解质界面模型以设计用于快速充电和宽温度锂离子电池的固体电解质界面
Adv Sci (Weinh). 2022 Sep;9(26):e2201893. doi: 10.1002/advs.202201893. Epub 2022 Jul 17.
4
Inner Lithium Fluoride (LiF)-Rich Solid Electrolyte Interphase Enabled by a Smaller Solvation Sheath for Fast-Charging Lithium Batteries.富氟化锂(LiF)的固体电解质中间相通过较小的溶剂化鞘实现,可用于快速充电锂电池。
ACS Appl Mater Interfaces. 2023 Jan 11;15(1):1201-1209. doi: 10.1021/acsami.2c17628. Epub 2022 Dec 28.
5
Inhibiting Solvent Co-Intercalation in a Graphite Anode by a Localized High-Concentration Electrolyte in Fast-Charging Batteries.通过快速充电电池中的局部高浓度电解质抑制石墨阳极中的溶剂共嵌入
Angew Chem Int Ed Engl. 2021 Feb 15;60(7):3402-3406. doi: 10.1002/anie.202009738. Epub 2020 Dec 15.
6
Long-Life and High-Rate-Charging Lithium Metal Batteries Enabled by a Flexible Active Solid Electrolyte Interphase Layer.通过柔性活性固体电解质界面层实现的长寿命和高倍率充电锂金属电池
ACS Appl Mater Interfaces. 2021 Dec 22;13(50):60678-60688. doi: 10.1021/acsami.1c19952. Epub 2021 Dec 8.
7
Electrochemical Lithiation/Delithiation of ZnO in 3D-Structured Electrodes: Elucidating the Mechanism and the Solid Electrolyte Interphase Formation.三维结构电极中氧化锌的电化学锂化/脱锂:阐明机理及固体电解质界面的形成
ACS Appl Mater Interfaces. 2021 Aug 4;13(30):35625-35638. doi: 10.1021/acsami.1c06135. Epub 2021 Jul 26.
8
Fluorine-Terminated Self-Assembled Monolayers Grafted Graphite Anode Inducing a LiF-Dominated SEI Inorganic Layer for Fast-Charging Lithium-Ion Batteries.氟端基自组装单分子层接枝石墨阳极诱导形成以LiF为主的固体电解质界面无机层用于快速充电锂离子电池。
ACS Appl Mater Interfaces. 2024 Feb 7;16(5):5813-5822. doi: 10.1021/acsami.3c15639. Epub 2024 Jan 25.
9
The Synergetic Effect of Lithium Bisoxalatodifluorophosphate and Fluoroethylene Carbonate on Dendrite Suppression for Fast Charging Lithium Metal Batteries.双草酸硼酸锂与氟代碳酸乙烯酯对快速充电锂金属电池枝晶抑制的协同效应
Small. 2020 Jul;16(30):e2001989. doi: 10.1002/smll.202001989. Epub 2020 Jun 10.
10
The fast-charging properties of micro lithium-ion batteries for smart devices.用于智能设备的微型锂离子电池的快速充电特性。
J Colloid Interface Sci. 2022 Jun;615:141-150. doi: 10.1016/j.jcis.2022.01.105. Epub 2022 Jan 29.

引用本文的文献

1
Detection of the knee point in lithium-ion battery degradation using a state-of-charge-dependent parameter.使用基于荷电状态的参数检测锂离子电池退化中的拐点。
Proc Natl Acad Sci U S A. 2025 Jun 10;122(23):e2424838122. doi: 10.1073/pnas.2424838122. Epub 2025 Jun 3.
2
Data-driven available capacity estimation of lithium-ion batteries based on fragmented charge capacity.基于碎片化充电容量的锂离子电池数据驱动可用容量估计
Commun Eng. 2025 Feb 25;4(1):32. doi: 10.1038/s44172-025-00372-y.
3
Fast-chargeable lithium-ion batteries by μ-Si anode-tailored full-cell design.

本文引用的文献

1
Comparative performance of ex situ artificial solid electrolyte interphases for Li metal batteries with liquid electrolytes.用于含液体电解质的锂金属电池的非原位人工固体电解质界面的性能比较
iScience. 2021 May 21;24(6):102578. doi: 10.1016/j.isci.2021.102578. eCollection 2021 Jun 25.
2
The intrinsic behavior of lithium fluoride in solid electrolyte interphases on lithium.氟化锂在锂固体电解质界面中的本征行为。
Proc Natl Acad Sci U S A. 2020 Jan 7;117(1):73-79. doi: 10.1073/pnas.1911017116. Epub 2019 Dec 17.
3
Before Li Ion Batteries.
通过微硅阳极定制全电池设计实现的可快速充电锂离子电池。
Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2417053121. doi: 10.1073/pnas.2417053121. Epub 2024 Dec 23.
4
Sequential Effect of Dual-Layered Hybrid Graphite Anodes on Electrode Utilization During Fast-Charging Li-Ion Batteries.双层混合石墨负极对锂离子电池快速充电过程中电极利用率的顺序效应
Adv Sci (Weinh). 2024 Aug;11(31):e2403071. doi: 10.1002/advs.202403071. Epub 2024 Jun 13.
5
Rational Design of an In-Situ Polymer-Inorganic Hybrid Solid Electrolyte Interphase for Realising Stable Zn Metal Anode under Harsh Conditions.用于在苛刻条件下实现稳定锌金属负极的原位聚合物-无机混合固体电解质界面的合理设计
Angew Chem Int Ed Engl. 2024 May 21;63(21):e202401987. doi: 10.1002/anie.202401987. Epub 2024 Apr 18.
6
Bismuth-Nanoparticles-Embedded Porous Carbon Derived from Seed Husks as High-Performance for Anode Energy Electrode.源自种壳的铋纳米颗粒嵌入多孔碳作为阳极能量电极的高性能材料
Materials (Basel). 2023 Oct 10;16(20):6628. doi: 10.3390/ma16206628.
7
Hydrogen Stabilization and Activation of Dry-Quenched Coke for High-Rate-Performance Lithium-Ion Batteries.用于高倍率性能锂离子电池的干熄焦的氢稳定化与活化
Nanomaterials (Basel). 2022 Oct 9;12(19):3530. doi: 10.3390/nano12193530.
在锂离子电池之前。
Chem Rev. 2018 Dec 12;118(23):11433-11456. doi: 10.1021/acs.chemrev.8b00422. Epub 2018 Nov 30.
4
Fluorine-donating electrolytes enable highly reversible 5-V-class Li metal batteries.含氟电解质使 5V 级锂金属电池具有高可逆性。
Proc Natl Acad Sci U S A. 2018 Feb 6;115(6):1156-1161. doi: 10.1073/pnas.1712895115. Epub 2018 Jan 19.
5
Graphene-Like-Graphite as Fast-Chargeable and High-Capacity Anode Materials for Lithium Ion Batteries.类石墨烯石墨用作锂离子电池的可快速充电且高容量负极材料
Sci Rep. 2017 Nov 1;7(1):14782. doi: 10.1038/s41598-017-14504-8.
6
Electrolytes and interphases in Li-ion batteries and beyond.锂离子电池及其他电池中的电解质和界面
Chem Rev. 2014 Dec 10;114(23):11503-618. doi: 10.1021/cr500003w. Epub 2014 Oct 29.
7
Gamma sterilization of pharmaceuticals--a review of the irradiation of excipients, active pharmaceutical ingredients, and final drug product formulations.药品的伽马射线灭菌——辅料、活性药物成分及最终药品制剂辐照的综述
PDA J Pharm Sci Technol. 2014 Mar-Apr;68(2):113-37. doi: 10.5731/pdajpst.2014.00955.
8
The Li-ion rechargeable battery: a perspective.锂离子可充电电池:一个展望。
J Am Chem Soc. 2013 Jan 30;135(4):1167-76. doi: 10.1021/ja3091438. Epub 2013 Jan 18.
9
Radical stability and its role in synthesis and catalysis.自由基稳定性及其在合成与催化中的作用。
Org Biomol Chem. 2010 Aug 21;8(16):3609-17. doi: 10.1039/c004166a. Epub 2010 Jun 11.
10
Differentiating contributions to "ion transfer" barrier from interphasial resistance and Li+ desolvation at electrolyte/graphite interface.区分电解质/石墨界面处“离子转移”势垒、相间电阻和 Li+去溶剂化的贡献。
Langmuir. 2010 Jul 6;26(13):11538-43. doi: 10.1021/la1009994.