Anchoring Interfacial Nickel Cations on Single-Crystal LiNi0.8Co0.1Mn0.1O2 Cathode Surface via Controllable Electron Transfer

被引:134
作者
Han, Yongkang [1 ,2 ]
Heng, Shuai [1 ,2 ]
Wang, Yan [1 ,2 ]
Qu, Qunting [1 ,2 ]
Zheng, Honghe [1 ,2 ]
机构
[1] Soochow Univ, Coll Energy, Suzhou 215006, Jiangsu, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215006, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
NI-RICH; ELECTROCHEMICAL PROPERTIES; ION BATTERIES; LITHIUM; PERFORMANCE; PVDF; TEMPERATURE; STABILITY; CAPACITY; IMPROVE;
D O I
10.1021/acsenergylett.0c01032
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
Severe Ni dissolution and the resulting impedance rise for the single-crystal LiNi(0.8)Co(0.1)Mn(0.1)O(2 )cathode is the main challenge greatly hindering its industrial applications. Herein, we propose a novel concept of anchoring interfacial nickel cations on a single-crystal LiNi(0.8)Co(0.1)Mn(0.1)O(2 )cathode through controllable electron transfer. This strategy is realized by applying an ultrathin PMMA surface layer. Different from traditional physical coatings, electron transfer from Ni2+ to the ester group is confirmed, which contributes to anchoring the interfacial Ni cations and effectively inhibits Ni dissolution into the organic electrolyte. Meanwhile, Li diffusion on the cathode surface is significantly improved. As a result, the electrochemical performance of the LiNi0.8Co0.1Mn0.1O2 cathode with a PMMA layer is improved. A reversible capacity of 181.1 mAh g(-1) at 1C rate is obtained with enhanced rate capability and cycling stability. Moreover, the modified LiNi0.8Co0.1Mn0.1O2 is able to work well at high voltage and high temperature, especially with incorporation of polyvinylidene fluoride.
引用
收藏
页码:2421 / 2433
页数:13
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