Electrochemical characterization of zirconium-doped LiNi0.8Co0.2O2 cathode materials and investigations on deterioration mechanism

被引:56
作者
Oh, SH [1 ]
Lee, SM [1 ]
Cho, WI [1 ]
Cho, BW [1 ]
机构
[1] Korea Inst Sci & Technol, Econano Res Ctr, Seoul 136791, South Korea
关键词
zirconium doping; LiNi0.8CO0.2O2; degradation mode; cation mixing; impedance growth;
D O I
10.1016/j.electacta.2005.10.023
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical performance and the degradation mode of the zirconium doped cathode material, LiNi0.8Co0.18Zr0.02O2 were investigated and compared with the pristine cathode, LiNi0.8CO0.2O2. The cyclic performance of the doped cathode was superior to the pristine cathode, especially under the high voltage cutoff, although its rate capability remained unimproved. The trend in the graphs of the differential capacity showed that the impedance growth of the cell made of the pristine cathode was much faster than the doped. From the results of the XRD pattern changes between before and after the galvanostatic cycling, less cation mixing and more ordered hexagonal structure were observed for the doped cathode. The impedance spectra showed that the charge transfer resistance for the pristine cathode grew significantly with cycling, while that for the doped cathode increased just moderately. Considerable decrease in the impedance was observed when the new lithium was substituted with the cycled anode, which implied that the interfacial impedance growth on the anode accounted for about 20% of the total impedance measured. It is concluded that the fading mode for LiNi0.8CO0.2O2 is mainly due to the cation mixing, partially contributed by the impedance growth on the anode and by doping the pristine cathode with Zr, cation mixing can be efficiently suppressed. (c) 2005 Elsevier Ltd. All rights reserved.
引用
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页码:3637 / 3644
页数:8
相关论文
共 29 条
[1]  
[Anonymous], 2000, ENERGY STORAGE SYSTE
[2]   The study of surface phenomena related to electrochemical lithium intercalation into LixMOy host materials (M = Ni, Mn) [J].
Aurbach, D ;
Gamolsky, K ;
Markovsky, B ;
Salitra, G ;
Gofer, Y ;
Heider, U ;
Oesten, R ;
Schmidt, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (04) :1322-1331
[3]   THE USE OF ACETATES AS PRECURSORS FOR THE LOW-TEMPERATURE SYNTHESIS OF LIMN2O4 AND LICOO2 INTERCALATION COMPOUNDS [J].
BARBOUX, P ;
TARASCON, JM ;
SHOKOOHI, FK .
JOURNAL OF SOLID STATE CHEMISTRY, 1991, 94 (01) :185-196
[4]   Methods to obtain excellent capacity retention in LiCoO2 cycled to 4.5 V [J].
Chen, ZH ;
Dahn, JR .
ELECTROCHIMICA ACTA, 2004, 49 (07) :1079-1090
[5]   LiNi0.74Co0.26-xMgxO2 cathode material for a Li-ion cell [J].
Cho, J .
CHEMISTRY OF MATERIALS, 2000, 12 (10) :3089-3094
[6]   Effect of preparation methods of LiNi1-xCoxO2 cathode materials on their chemical structure and electrode performance [J].
Cho, J ;
Kim, G ;
Lim, HS .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (10) :3571-3576
[7]   Preparation and electrochemical/thermal properties of LiNi0.74Co0.26O2 cathode material [J].
Cho, JP ;
Park, B .
JOURNAL OF POWER SOURCES, 2001, 92 (1-2) :35-39
[8]   Electrochemical properties and thermal stability of LiaNi1-xCoxO2 cathode materials [J].
Cho, JP ;
Jung, HS ;
Park, YC ;
Kim, GB ;
Lim, HS .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (01) :15-20
[9]   A study of the electrochemical lithium intercalation behavior of porous LiNiO2 electrodes prepared by solid-state reaction and sol-gel methods [J].
Choi, YM ;
Pyun, SI ;
Moon, SI ;
Hyung, YE .
JOURNAL OF POWER SOURCES, 1998, 72 (01) :83-90
[10]   THERMAL-STABILITY OF LIXCOO2, LIXNIO2 AND LAMBDA-MNO2 AND CONSEQUENCES FOR THE SAFETY OF LI-ION CELLS [J].
DAHN, JR ;
FULLER, EW ;
OBROVAC, M ;
VONSACKEN, U .
SOLID STATE IONICS, 1994, 69 (3-4) :265-270