Tuning interface stability of nickel-rich LiNi0.9Co0.05Mn0.05O2 cathode via a novel bis(vinylsulphonyl)methane additive

被引:23
|
作者
Jiao, Tianpeng [1 ]
Liu, Gaopan [1 ]
Huang, Lin [1 ]
Zou, Yue [1 ]
Zhang, Xiaozhen [1 ]
Zheng, Jianming [1 ]
Yang, Yong [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen, Peoples R China
[2] Xiamen Univ, Collaborat Innovat Ctr Chem Energy Materials, iChEM, Xiamen, Peoples R China
关键词
Nickel-rich cathode; Electrolyte additive; Bis(vinylsulphonyl)methane; Cathode-electrolyte interface; Solvation structure; LITHIUM-ION BATTERIES; ELECTROLYTE ADDITIVES; NI-RICH; 1,3-PROPANE SULTONE; VINYLENE CARBONATE; ENERGY-DENSITY; CAPACITY; FILM; PROGRESS; SULFATE;
D O I
10.1016/j.jpowsour.2021.230917
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
By increasing the nickle content in LiNixMnyCo1-x-yO2 cathodes, the energy density and cost of lithium ion batteries (LIBs) could be further optimized. However, the structural/interfacial instability of nickel-rich cathode extremely challenges its cycling life. Here, we demonstrate a novel electrolyte additive bis(vinylsulphonyl) methane (BVSM) to enhance the cycling stability and rate capability of LiNi0.9Co0.05Mn0.05O2 (NCM90) cathode. Detailed surface characterizations prove the construction of a robust sulfur-incorporated and inorganic fluoridesenriched cathode-electrolyte interphase (CEI) film on the NCM90 surface. This BVSM-derived CEI contributes to a more reliable NCM90 cathode with suppressed interfacial side reactions, limited growth of interfacial resistance, fast electrode kinetics, less transition metal (TM) dissolution and more reversible phase transition. More importantly, first-principles calculations unravel the competitive coordination among solvents, BVSM and anions, rationalizing the CEI composition and electrochemical performance. Furthermore, the better cycling stability and stabilized average discharge voltage for graphite||NCM90 full cells are enabled by BVSM additive.
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页数:1
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