• 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

通过简便的表面氟化提高 LiTiO 负极材料的倍率性能和低温性能。

Enhanced Rate Capability and Low-Temperature Performance of LiTiO Anode Material by Facile Surface Fluorination.

机构信息

Department of Materials Science, Fudan University , Shanghai 200433, China.

Shanghai Power & Energy Storage Battery System Engineering Tech. Co. Ltd. , Shanghai 200241, China.

出版信息

ACS Appl Mater Interfaces. 2017 May 24;9(20):17145-17154. doi: 10.1021/acsami.7b03489. Epub 2017 May 11.

DOI:10.1021/acsami.7b03489
PMID:28462992
Abstract

A commercial LiTiO material was modified by NHF using a facile and dry method at a low temperature in air. X-ray diffraction reveals that the fluorination did not change the bulk structure of LiTiO. X-ray photoelectron spectroscopy demonstrates that LiF was formed at the surface and Ti was partially changed into Ti. Microscopic images show that some nanoislands were formed on the surface, which enlarged the surface area. Consequently, the NHF-modified LiTiO material exhibited significantly enhanced capacities and rate capabilities, even at low temperatures. The discharge capacity was increased from 149 to 167 mA h g at 1 C, and the capacity retention was increased from 17.8 to 52.0% at 15 C. The capacity retention of NHF-modified LiTiO was greater than that of LiTiO at each low-temperature point. Additionally, the introduction of F can protect the LiTiO material from side reactions with the electrolyte and the atmosphere, enhancing the surface stability and reducing the release of gaseous products. It is believed that the NHF-modified LiTiO with enhanced electrochemical performance is a promising anode material for lithium ion batteries. Furthermore, this facile surface fluorination strategy is amenable to large-scale production.

摘要

采用简单的干法,在低温下,在空气中用 NHF 对商业 LiTiO 材料进行了改性。X 射线衍射表明,氟化没有改变 LiTiO 的体相结构。X 射线光电子能谱表明,在表面形成了 LiF,Ti 部分被转化为 Ti。微观图像显示,表面形成了一些纳米岛,从而增加了表面积。因此,NHF 改性的 LiTiO 材料表现出显著增强的容量和倍率性能,即使在低温下也是如此。在 1 C 时,放电容量从 149 mA h g 增加到 167 mA h g,在 15 C 时,容量保持率从 17.8%增加到 52.0%。在每个低温点,NHF 改性 LiTiO 的容量保持率都大于 LiTiO。此外,F 的引入可以保护 LiTiO 材料免受与电解液和大气的副反应,提高表面稳定性,减少气态产物的释放。人们相信,具有增强电化学性能的 NHF 改性 LiTiO 是一种很有前途的锂离子电池负极材料。此外,这种简单的表面氟化策略适合大规模生产。

相似文献

1
Enhanced Rate Capability and Low-Temperature Performance of LiTiO Anode Material by Facile Surface Fluorination.通过简便的表面氟化提高 LiTiO 负极材料的倍率性能和低温性能。
ACS Appl Mater Interfaces. 2017 May 24;9(20):17145-17154. doi: 10.1021/acsami.7b03489. Epub 2017 May 11.
2
Enhanced Performance of "Flower-like" Li4Ti5O12 Motifs as Anode Materials for High-Rate Lithium-Ion Batteries.“花状”Li4Ti5O12 基序作为高倍率锂离子电池负极材料的性能增强
ChemSusChem. 2015 Oct 12;8(19):3304-13. doi: 10.1002/cssc.201500639. Epub 2015 Jul 20.
3
Comparison of LiVPO4F to Li4Ti5O12 as anode materials for lithium-ion batteries.比较 LiVPO4F 和 Li4Ti5O12 作为锂离子电池的阳极材料。
ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8615-27. doi: 10.1021/am402132u. Epub 2013 Aug 21.
4
Spherical LiTiO/NiO Composite With Enhanced Capacity and Rate Performance as Anode Material for Lithium-Ion Batteries.具有增强容量和倍率性能的球形LiTiO/NiO复合材料作为锂离子电池负极材料
Front Chem. 2020 Dec 15;8:626388. doi: 10.3389/fchem.2020.626388. eCollection 2020.
5
Li4Ti5O12/TiO2 hollow spheres composed nanoflakes with preferentially exposed Li4Ti5O12 (011) facets for high-rate lithium ion batteries.由纳米薄片组成的Li4Ti5O12/TiO2空心球,具有优先暴露的Li4Ti5O12(011)晶面,用于高倍率锂离子电池。
ACS Appl Mater Interfaces. 2014 Nov 26;6(22):19791-6. doi: 10.1021/am504931r. Epub 2014 Nov 4.
6
Enhancing Lithium Storage Performances of the LiTiO Anode by Introducing the CuVO Phase.通过引入CuVO相提高LiTiO负极的锂存储性能。
ACS Appl Mater Interfaces. 2020 Sep 2;12(35):39170-39180. doi: 10.1021/acsami.0c10603. Epub 2020 Aug 18.
7
Rapid charge-discharge property of Li4Ti5O12-TiO2 nanosheet and nanotube composites as anode material for power lithium-ion batteries.Li4Ti5O12-TiO2纳米片与纳米管复合材料作为动力锂离子电池负极材料的快速充放电性能
ACS Appl Mater Interfaces. 2014 Nov 26;6(22):20205-13. doi: 10.1021/am5057568. Epub 2014 Oct 31.
8
Facile Synthesis of Carbon-Coated Spinel LiTiO/Rutile-TiO Composites as an Improved Anode Material in Full Lithium-Ion Batteries with LiFePO@N-Doped Carbon Cathode.作为一种改进的全锂离子电池正极材料,在 LiFePO@N 掺杂碳阴极的全锂离子电池中,我们采用简便的方法合成了碳包覆尖晶石 LiTiO/Rutile-TiO 复合材料。
ACS Appl Mater Interfaces. 2017 Feb 22;9(7):6138-6143. doi: 10.1021/acsami.6b15982. Epub 2017 Feb 8.
9
Chromium-Modified Li4Ti5O12 with a Synergistic Effect of Bulk Doping, Surface Coating, and Size Reducing.具有体掺杂、表面包覆和尺寸减小协同效应的铬改性 Li4Ti5O12。
ACS Appl Mater Interfaces. 2016 Aug 24;8(33):21407-16. doi: 10.1021/acsami.6b07742. Epub 2016 Aug 9.
10
Controlling Solid-Electrolyte-Interphase Layer by Coating P-Type Semiconductor NiOx on Li4Ti5O12 for High-Energy-Density Lithium-Ion Batteries.通过在Li4Ti5O12上涂覆p型半导体NiOx来控制固体电解质界面层用于高能量密度锂离子电池
ACS Appl Mater Interfaces. 2015 Dec 23;7(50):27934-9. doi: 10.1021/acsami.5b10207. Epub 2015 Dec 11.

引用本文的文献

1
Structural Engineering of Anode Materials for Low-Temperature Lithium-Ion Batteries: Mechanisms, Strategies, and Prospects.用于低温锂离子电池的负极材料结构工程:机理、策略与展望
Nanomicro Lett. 2024 Mar 11;16(1):150. doi: 10.1007/s40820-024-01363-y.
2
Few-layer bismuth selenide cathode for low-temperature quasi-solid-state aqueous zinc metal batteries.用于低温准固态水系锌金属电池的少层硒化铋阴极
Nat Commun. 2022 Feb 8;13(1):752. doi: 10.1038/s41467-022-28380-y.
3
Polymer-templated mesoporous lithium titanate microspheres for high-performance lithium batteries.
用于高性能锂电池的聚合物模板介孔钛酸锂微球
Mater Adv. 2021 Nov 2;3(1):362-372. doi: 10.1039/d1ma00708d. eCollection 2022 Jan 4.
4
Smart Construction of Integrated CNTs/LiTiO Core/Shell Arrays with Superior High-Rate Performance for Application in Lithium-Ion Batteries.用于锂离子电池的具有卓越高倍率性能的集成碳纳米管/锂钛氧化物核壳阵列的智能构建
Adv Sci (Weinh). 2018 Jan 3;5(3):1700786. doi: 10.1002/advs.201700786. eCollection 2018 Mar.