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比较 LiVPO4F 和 Li4Ti5O12 作为锂离子电池的阳极材料。

Comparison of LiVPO4F to Li4Ti5O12 as anode materials for lithium-ion batteries.

机构信息

Faculty of Materials Science and Chemical Engineering, Ningbo University , Ningbo 315211, Zhejiang Province, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8615-27. doi: 10.1021/am402132u. Epub 2013 Aug 21.

DOI:10.1021/am402132u
PMID:23927499
Abstract

In this paper, we reported on a comparison of LiVPO4F to Li4Ti5O12 as anode materials for lithium-ion batteries. Combined with powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, galvanostatic discharge/charge tests and in situ X-ray diffraction technologies, we explore and compare the insertion/extraction mechanisms of LiVPO4F based on the V3+/V2+/V+ redox couples and Li4Ti5O12 based on the Ti4+/Ti3+ redox couple cycled in 1.0-3.0 V and 0.0-3.0 V. The electrochemical results indicate that both LiVPO4F and Li4Ti5O12 are solid electrolyte interphase free materials in 1.0-3.0 V. The insertion/extraction mechanisms of LiVPO4F and Li4Ti5O12 are similar with each other in 1.0-3.0 V as proved by in situ X-ray diffraction. It also demonstrates that both samples possess stable structure in 0.0-3.0 V. Additionally, the electrochemical performance tests of LiVPO4F and Li4Ti5O12 indicate that both samples cycled in 0.0-3.0 V exhibit much higher capacities than those cycled in 1.0-3.0 V but display worse cycle performance. The rate performance of Li4Ti5O12 far exceeds that of LiVPO4F in the same electrochemical potential window. In particular, the capacity retention of Li4Ti5O12 cycled in 1.0-3.0 V is as high as 98.2% after 20 cycles. By contrast, Li4Ti5O12 is expected to be a candidate anode material considering its high working potential, structural zero-strain property, and excellent cycle stability and rate performance.

摘要

本文报道了 LiVPO4F 和 Li4Ti5O12 作为锂离子电池的阳极材料的比较。通过粉末 X 射线衍射、扫描电子显微镜、高分辨率透射电子显微镜、恒电流放电/充电测试和原位 X 射线衍射技术,我们探索并比较了基于 V3+/V2+/V+氧化还原对的 LiVPO4F 和基于 Ti4+/Ti3+氧化还原对的 Li4Ti5O12 在 1.0-3.0 V 和 0.0-3.0 V 循环的嵌入/提取机制。电化学结果表明,在 1.0-3.0 V 下,LiVPO4F 和 Li4Ti5O12 均为无固体电解质界面材料。原位 X 射线衍射证明,LiVPO4F 和 Li4Ti5O12 在 1.0-3.0 V 下的嵌入/提取机制相似。它还表明,两个样品在 0.0-3.0 V 下都具有稳定的结构。此外,LiVPO4F 和 Li4Ti5O12 的电化学性能测试表明,两个样品在 0.0-3.0 V 下循环时的容量都比在 1.0-3.0 V 下循环时高得多,但循环性能较差。Li4Ti5O12 在相同的电化学势窗口下的倍率性能远远超过 LiVPO4F。特别是,Li4Ti5O12 在 1.0-3.0 V 下循环 20 次后的容量保持率高达 98.2%。相比之下,Li4Ti5O12 有望成为一种候选阳极材料,因为它具有高工作电位、结构零应变特性以及优异的循环稳定性和倍率性能。

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引用本文的文献

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Chemical reaction characteristics, structural transformation and electrochemical performances of new cathode LiVPOF/C synthesized by a novel one-step method for lithium ion batteries.用于锂离子电池的新型一步法合成的新型正极LiVPOF/C的化学反应特性、结构转变及电化学性能
RSC Adv. 2018 Feb 13;8(13):7044-7054. doi: 10.1039/c8ra00370j. eCollection 2018 Feb 9.
2
Effect of Environmental Temperature on the Content of Impurity LiV(PO)/C in LiVPOF/C Cathode for Lithium-ion Batteries.环境温度对锂离子电池LiVPOF/C正极中杂质LiV(PO)/C含量的影响
Front Chem. 2018 Jul 24;6:283. doi: 10.3389/fchem.2018.00283. eCollection 2018.