Improved electrolyte and its application in LiNi1/3Mn1/3Co1/3O2-Graphite full cells

被引:20
作者
Liu, Minghong [1 ]
Dai, Fang [2 ]
Ma, Zhiru
Ruthkosky, Marty [3 ]
Yang, Li [3 ]
机构
[1] Shenzhen BAK Technol Co Ltd, Shenzhen, Peoples R China
[2] Optimal CAE, Plymouth, MI USA
[3] Gen Motors Corp, Chem & Mat Syst Lab, Warren, MI 48090 USA
关键词
Lithium; NMC; Electrolyte; Additives; LiODFB; SEI; LITHIUM-ION CELLS; LI-ION; VINYLENE CARBONATE; PROPYLENE CARBONATE; BATTERY ELECTROLYTE; GRAPHITE-ELECTRODES; ETHYLENE CARBONATE; ADDITIVES; INTERFACE; BEHAVIOR;
D O I
10.1016/j.jpowsour.2014.05.109
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium oxalatodifluoroborate (LiODFB) has been synthesized and used as a novel electrolyte additive. Standard and modified electrolytes were flame-sealed in NMR tubes and stored at 60 degrees C for 3 months. Multiple nuclear NMR (H-1, B-11, C-13, F-19, P-31) studies confirmed that the modified electrolyte (2% LiODFB added) showed no signs of decomposition as that of regular electrolyte, which is possibly due to the -F of LiPF6 and oxalate of LiODFB ligand exchange effect. The high temperature stabilization mechanism of the added LiODFB was studied using quantum mechanical calculations. Electrochemical tests of LiNi1/3Mn1/3Co1/3O2 (NMC)-Graphite full-cells with and without LiODFB as the electrolyte additive were conducted. When cycling with the NMC-Graphite full-cell at elevated temperature (60 degrees C), the 100th cycle capacity retention rate of the modified electrolyte was 60%, compared to 27% with the standard electrolyte. The EIS study indicates the full-cells with LiODFB have much lower interfacial impedance than the standard cells. Theoretical calculations reveal that LiODFB generates a layer of thin and resilient SEI on the graphite surface at a higher reduction potential than ethylene carbonate (EC) due to its higher ring strain and protects graphite from the toxic Mn2+ resulting in improved electrochemical performance of NMC-Graphite based cells. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 44
页数:8
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