期刊论文详细信息
JOURNAL OF POWER SOURCES 卷:318
Enhanced charging capability of lithium metal batteries based on lithium bis(trifluoromethanesulfonyl)imide-lithium bis(oxalato) borate dual-salt electrolytes
Article
Xiang, Hongfa1,2  Shi, Pengcheng2  Bhattacharya, Priyanka1  Chen, Xilin1  Mei, Donghai3  Bowden, Mark E.4  Zheng, Jianming1  Zhang, Ji-Guang1  Xu, Wu1 
[1] Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
[2] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China
[3] Pacific NW Natl Lab, Phys & Computat Sci Directorate, Richland, WA 99354 USA
[4] Pacific NW Natl Lab, Environm & Mol Sci Lab, Richland, WA 99354 USA
关键词: Lithium metal battery;    Dual-salt electrolyte;    Lithium metal protection;    Fast chargeability;    Charge current density;    Cycling stability;   
DOI  :  10.1016/j.jpowsour.2016.04.017
来源: Elsevier
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【 摘 要 】

Rechargeable lithium (Li) metal batteries with conventional LiPF6-carbonate electrolytes have been reported to fail quickly at charging current densities of about 1.0 mA cm(-2) and above. In this work, we demonstrate the rapid charging capability of Li parallel to LiNi0.8Co0.15Al0.05O2 (NCA) cells can be enabled by a dual salt electrolyte of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and lithium bis(oxalato)borate (LiBOB) in a carbonate solvent mixture. The cells using the LiTFSI-LiBOB dual-salt electrolyte significantly outperform those using the LiPF6 electrolyte at high charging current densities. At the charging current density of 1.50 mA cm(-2), the Li parallel to INCA cells with the dual-salt electrolyte can still deliver a discharge capacity of 131 mAh g(-1) and a capacity retention of 80% after 100 cycles. The Li parallel to INCA cells with the LiPF6 electrolyte start to show fast capacity fading after the 30th cycle and only exhibit a low capacity of 25 mAh g(-1) and a low retention of 15% after 100 cycles. The reasons for the good chargeability and cycling stability of the cells using the LiTFSI-LiBOB dual-salt electrolyte can be attributed to the good film-formation ability of the electrolyte on the Li metal anode and the highly conductive nature of the sulfur-rich interphase layer. (C) 2016 Elsevier B.V. All rights reserved.

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