Nonflammable dual-salt localized high-concentration electrolyte for graphite/LiNi0.8Co0.1Mn0.1O2 lithium-ion batteries: Li plus solvation structure and interphase

被引:13
作者
Cao, Shuai [1 ]
Wen, Fanjue [1 ]
Ren, Xin [1 ]
Cao, Yuliang [2 ]
Ai, Xinping [2 ]
Xu, Fei [1 ,3 ]
机构
[1] Wuhan Univ, Sch Power & Mech Engn, Key Lab Hydraul Machinery Transients, Minist Educ, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
[3] Contemporary Amperex Technol Ltd 21C LAB, 21C Innovat Lab, Yibin 352100, Peoples R China
基金
中国国家自然科学基金;
关键词
Nonflammable electrolyte; Li plus solvation structure; Interphase compatibility; Thermodynamics; Kinetics; PHOSPHATE; STABILITY; GRAPHITE; LIPF6; SEI;
D O I
10.1016/j.jpowsour.2022.232392
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
Trimethyl phosphate (TMP) is the most promising safe solvent for lithium-ion battery (LIB) electrolyte because of the nonflammability, oxidation stability and low cost, but its application is hindered by the incompatibility with the graphite anode. Herein, a nonflammable localized high-concentration electrolyte with ordinary concentra-tion (1 mol L-1) is developed for graphite/LiNi0.8Co0.1Mn0.1O2 (Gr/NCM811) LIBs with TMP/1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropylether (TTE) binary solvents. The origin of the capacity decay is eluci-dated with a comprehensive investigation of the Li+ solvation structure and electrode/electrolyte interface. On this basis, a dual-salt strategy of lithium hexafluorophosphate (LiPF6)/lithium difluoro(oxalato)borate (LiDFOB) is employed, and a stable cycling of the Gr/NCM811 full cell is achieved with upper voltages of both 4.3 V and 4.6 V. The optimization of the nonflammable TMP/TTE electrolyte demonstrates that Li+ solvation structure and interphase are respectively the thermodynamic and kinetic factors for the side reactions of the electrolyte occurring at the electrode: the Li+ solvation structure determines the reduction and oxidation tolerances of the electrolyte in thermodynamics, while the interface determines the decomposition rate in kinetics.
引用
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页数:9
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