Prelithiation Activates Li(Ni0.5Mn0.3Co0.2)O2 for High Capacity and Excellent Cycling Stability

被引:72
|
作者
Wu, Zhongzhen [1 ]
Ji, Shunping [1 ]
Zheng, Jiaxin [1 ]
Hu, Zongxiang [1 ]
Xiao, Shu [1 ]
Wei, Yi [1 ]
Zhuo, Zengqing [1 ,2 ]
Lin, Yuan [1 ]
Yang, Wanli [2 ]
Xu, Kang [3 ]
Amine, Khalil [1 ,4 ]
Pan, Feng [1 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Shenzhen 518055, Peoples R China
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[3] US Army Res Lab, Adelphi, MD 20783 USA
[4] Argonne Natl Lab, Chem Sci & Engn Div, Electrochem Technol Program, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
prelithiation; two-layer Li; Li(Ni0.5Mn0.3Co0.2)O-2; carbint nanotube (CNT); solid electrolyte interface (SEI); ATOMIC LAYER DEPOSITION; CATHODE MATERIALS; ION; ELECTRODES; NI; HYDROGENATION; FADE; CO;
D O I
10.1021/acs.nanolett.5b02246
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal oxide materials Li(NiMnyCoz)O-2 (NMC) based on layered structures are expected to replace LiFePO4 in automotive Li-ion batteries because of their higher specific capacity and operating potential. However, the actual usable capacity is much lower than the promised theoretical value [Uchaker, E.; Cao, G. Nano Today 2014 9, 499-524; Tarascon, J.-M.; Armand, M. Nature 2001 414, 359-367], in addition to the often poor cycling performance and the first-cycle Coulombic efficiency, for which Mn(II)-dissolution, its immobilization in solid electrolyte interface (SEI), oxidation of electrolytes by Ni, and other parasitic process thereat have been held responsible [Zhan, C., et al. Nat. Commun. 2013 4, 2437; Wang, L,et al. J. Solid State Electrochem. 2009 13, 1157-1164; Lin, F., et al. Nat. Commun. 2014.5, 4529]. Previously, we reported a composite Li(Ni0.5Mn0.3Co0.2)O-2 (NMC532) depolarized by the embedded carbon nanotube (CNT) and achieved capacity close to the theoretical limit [Wu, Z., et al. Nano. Lett. 2014 14, 4700-4706]; unfortunately, this high capacity failed to be maintained in long-term cycling due to the degrading contacts between the active ingredient and CNT network. On the basis of that NMC532/ CNT composite, the present work proposes a unique "prelithiation process", which brought the cathode to low potentials before regular cycling and led to an intetphase that is normally formed only on anode surfaces. The complete coverage of cathode surface by this, similar to 40 nm thick interphase effectively prevented Mn(II) dissolution and minimized the side reactions of Ni, Co, and Mn at the NMC interface during the subsequent cycling process. More importantly, such a "prelithiation" process activated a structure containing two Li layers near the surface of NMC532 particles, as verified by XRD and first principle calculation. Hence, a new cathode material of both high capacity with depolarized structure and excellent cycling performance was generated. This new structure can be incorporated in essentially all the NMC-based layered cathode materials, providing us with an effective tool to tailor-design future new cathode materials for lithium batteries.
引用
收藏
页码:5590 / 5596
页数:7
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