Structural Stability of LiNiO2 Cycled above 4.2 V

被引:350
作者
Yoon, Chong S. [1 ]
Jun, Do-Wook [2 ]
Myung, Seung-Taek [3 ]
Sun, Yang-Kook [2 ]
机构
[1] Hanyang Univ, Dept Mat Sci & Engn, Seoul 133791, South Korea
[2] Hanyang Univ, Dept Energy Engn, Seoul 133791, South Korea
[3] Sejong Univ, Dept Nano Engn, Seoul 143747, South Korea
基金
新加坡国家研究基金会;
关键词
LITHIUM-ION BATTERIES; LAYERED CATHODE MATERIALS; SECONDARY BATTERIES; HIGH-ENERGY; CELLS; ELECTROCHEMISTRY; OPTIMIZATION; PERFORMANCE; PHASE;
D O I
10.1021/acsenergylett.7b00304
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
A spherical stoichiometric LiNiO2, particle, which was composed of compactly packed nanosized primary particles, was prepared and cycled at different cutoff voltages to explicitly demonstrate the effect of phase transitions during Li deintercalation/intercalation on the Li-ion intercalation stability of LiNiO2. The capacity retention was greatly improved by suppressing the H2 -> H3 phase transition at 4.1 V, such that 95% of the initial capacity (164 mAh g(-1)) was retained after 100 cycles when cycled at 4.1 V. At 4.2 and 4.3 V, continuous capacity loss (81% of 191 mAh g(-1) at 4.2 V and 75% of 232 mAh g(-1) at 4.3 V after 100 cycles) was observed during cycling, and these electrodes incurred extensive structural damages (micro-, hairline and nanoscale cracks observed by transmission electron microscopy) from the repeated lattice contraction and expansion accompanying the H2 -> H3 transition, in agreement with the cycling data.
引用
收藏
页码:1150 / 1155
页数:6
相关论文
共 29 条
[1]   Surface changes on LiNi0.8Co0.2O2 particles during testing of high-power lithium-ion cells [J].
Abraham, DP ;
Twesten, RD ;
Balasubramanian, M ;
Petrov, I ;
McBreen, J ;
Amine, K .
ELECTROCHEMISTRY COMMUNICATIONS, 2002, 4 (08) :620-625
[2]   Reversibility of LiNiO2 cathode [J].
Arai, H ;
Okada, S ;
Sakurai, Y ;
Yamaki, J .
SOLID STATE IONICS, 1997, 95 (3-4) :275-282
[3]   CHARACTERIZATION AND CATHODE PERFORMANCE OF LI-1-XNI1+XO2 PREPARED WITH THE EXCESS LITHIUM METHOD [J].
ARAI, H ;
OKADA, S ;
OHTSUKA, H ;
ICHIMURA, M ;
YAMAKI, J .
SOLID STATE IONICS, 1995, 80 (3-4) :261-269
[4]   An electrochemical investigation into the lithium insertion properties of LixNiO2 (0<=x<=1) [J].
Barker, J ;
Koksbang, R ;
Saidi, MY .
SOLID STATE IONICS, 1996, 89 (1-2) :25-35
[5]   Structural characterisation of the highly deintercalated LixNi1.02O2 phases (with x ≤ 0.30) [J].
Croguennec, L ;
Pouillerie, C ;
Mansour, AN ;
Delmas, C .
JOURNAL OF MATERIALS CHEMISTRY, 2001, 11 (01) :131-141
[6]   STRUCTURE AND ELECTROCHEMISTRY OF LI1+/-YNIO2 AND A NEW LI2NIO2 PHASE WITH THE NI(OH)2 STRUCTURE [J].
DAHN, JR ;
VONSACKEN, U ;
MICHAL, CA .
SOLID STATE IONICS, 1990, 44 (1-2) :87-97
[7]   PHASE RELATIONSHIP AND LITHIUM DEINTERCALATION IN LITHIUM NICKEL OXIDES [J].
KANNO, R ;
KUBO, H ;
KAWAMOTO, Y ;
KAMIYAMA, T ;
IZUMI, F ;
TAKEDA, Y ;
TAKANO, M .
JOURNAL OF SOLID STATE CHEMISTRY, 1994, 110 (02) :216-225
[8]   Anisotropic Lattice Strain and Mechanical Degradation of High- and Low-Nickel NCM Cathode Materials for Li-Ion Batteries [J].
Kondrakov, Aleksandr O. ;
Schmidt, Alexander ;
Xu, Jin ;
Gesswein, Holger ;
Moenig, Reiner ;
Hartmann, Pascal ;
Sommer, Heino ;
Brezesinski, Torsten ;
Janek, Juergen .
JOURNAL OF PHYSICAL CHEMISTRY C, 2017, 121 (06) :3286-3294
[9]   High-energy-density lithium-ion battery using a carbon-nanotube-Si composite anode and a compositionally graded Li[Ni0.85Co0.05Mn0.10]O2 cathode [J].
Lee, Joo Hyeong ;
Yoon, Chong S. ;
Hwang, Jang-Yeon ;
Kim, Sung-Jin ;
Maglia, Filippo ;
Lamp, Peter ;
Myung, Seung-Taek ;
Sun, Yang-Kook .
ENERGY & ENVIRONMENTAL SCIENCE, 2016, 9 (06) :2152-2158
[10]   Synthetic optimization of Li[Ni1/3Co1/3Mn1/3]O2 via co-precipitation [J].
Lee, MH ;
Kang, Y ;
Myung, ST ;
Sun, YK .
ELECTROCHIMICA ACTA, 2004, 50 (04) :939-948