A New Coating Method for Alleviating Surface Degradation of LiNi0.6Co0.2Mn0.2O2 Cathode Material: Nanoscale Surface Treatment of Primary Particles

被引:495
作者
Kim, Hyejung [1 ,2 ]
Kim, Min Gyu [3 ]
Jeong, Hu Young [4 ]
Nam, Haisol [1 ,2 ]
Cho, Jaephil [1 ,2 ]
机构
[1] UNIST, Dept Energy Engn, Ulsan 689798, South Korea
[2] UNIST, Sch Energy & Chem Engn, Ulsan 689798, South Korea
[3] PAL, Beamline Res Div, Pohang 790784, South Korea
[4] UNIST, UNIST Cent Res Facil UCRF, Ulsan 689798, South Korea
关键词
LiNi0.6Co0.2Mn0.2O2; cathode; high voltage; thermal stability; primary particles; microcrack; structural degradation; ION; OXIDES; LAYER;
D O I
10.1021/acs.nanolett.5b00045
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structural degradation of Ni-rich cathode materials (LiNixM1-xO2; M = Mn, Co, and Al; x > 0.5) during cycling at both high voltage (>4.3 V) and high temperature (>50 degrees C) led to the continuous generation of microcracks in a secondary particle that consisted of aggregated micrometer-sized primary particles. These microcracks caused deterioration of the electrochemical properties by disconnecting the electrical pathway between the primary particles and creating thermal instability owing to oxygen evolution during phase transformation. Here, we report a new concept to overcome those problems of the Ni-rich cathode material via nanoscale surface treatment of the primary particles. The resultant primary particles surfaces had a higher cobalt content and a cation-mixing phase (Fm (3) over barm) with nanoscale thickness in the LiNi0.6Co0.2Mn0.2O2 cathode, leading to mitigation of the microcracks by suppressing the structural change from a layered to rock-salt phase. Furthermore, the higher oxidation state of Mn4+ at the surface minimized the oxygen evolution at high temperatures. This approach resulted in improved structural and thermal stability in the severe cycling-test environment at 60 degrees C between 3.0 and 4.45 V and at elevated temperatures, showing a rate capability that was comparable to that of the pristine sample.
引用
收藏
页码:2111 / 2119
页数:9
相关论文
共 32 条
[1]  
[Anonymous], 2010, J POWER SOURCES
[2]   Thermal behavior of Li1-yNiO2 and the decomposition mechanism [J].
Arai, H ;
Okada, S ;
Sakurai, Y ;
Yamaki, J .
SOLID STATE IONICS, 1998, 109 (3-4) :295-302
[3]   Evolutions of Li1.2Mn0.61Ni0.18Mg0.01O2 during the Initial Charge/Discharge Cycle Studied by Advanced Electron Microscopy [J].
Boulineau, Adrien ;
Simonin, Loic ;
Colin, Jean-Francois ;
Canevet, Emmanuel ;
Daniel, Lise ;
Patoux, Sebastien .
CHEMISTRY OF MATERIALS, 2012, 24 (18) :3558-3566
[4]   Hybrid density functional calculations of redox potentials and formation energies of transition metal compounds [J].
Chevrier, V. L. ;
Ong, S. P. ;
Armiento, R. ;
Chan, M. K. Y. ;
Ceder, G. .
PHYSICAL REVIEW B, 2010, 82 (07)
[5]   High-performance ZrO2-coated LiNiO2 cathode material [J].
Cho, J ;
Kim, TJ ;
Kim, YJ ;
Park, B .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (10) :A159-A161
[6]   A New Type of Protective Surface Layer for High-Capacity Ni-Based Cathode Materials: Nanoscaled Surface Pillaring Layer [J].
Cho, Yonghyun ;
Oh, Pilgun ;
Cho, Jaephil .
NANO LETTERS, 2013, 13 (03) :1145-1152
[7]   Spinel-Layered Core-Shell Cathode Materials for Li-Ion Batteries [J].
Cho, Yonghyun ;
Lee, Sanghan ;
Lee, Yongseok ;
Hong, Taeeun ;
Cho, Jaephil .
ADVANCED ENERGY MATERIALS, 2011, 1 (05) :821-828
[8]   Nanoscale Phase Separation, Cation Ordering, and Surface Chemistry in Pristine Li1.2Ni0.2Mn0.6O2 for Li-Ion Batteries [J].
Gu, Meng ;
Genc, Arda ;
Belharouak, Ilias ;
Wang, Dapeng ;
Amine, Khalil ;
Thevuthasan, Suntharampillai ;
Baer, Donald R. ;
Zhang, Ji-Guang ;
Browning, Nigel D. ;
Liu, Jun ;
Wang, Chongmin .
CHEMISTRY OF MATERIALS, 2013, 25 (11) :2319-2326
[9]   Formation of the Spinel Phase in the Layered Composite Cathode Used in Li-Ion Batteries [J].
Gu, Meng ;
Belharouak, Ilias ;
Zheng, Jianming ;
Wu, Huiming ;
Xiao, Jie ;
Genc, Arda ;
Amine, Khalil ;
Thevuthasan, Suntharampillai ;
Baer, Donald R. ;
Zhang, Ji-Guang ;
Browning, Nigel D. ;
Liu, Jun ;
Wang, Chongmin .
ACS NANO, 2013, 7 (01) :760-767
[10]  
Guo-Rong H., 2008, ELECTROCHIM ACTA, V53, P2567