Electrochemical studies on LiCoO2 surface coated with Y3Al5O12 for lithium-ion cells

被引:26
作者
Chen, Jin-Ming [2 ]
Cho, Yung-Da [1 ]
Hsiao, Chiao-Ling [1 ]
Fey, George Ting-Kuo [1 ]
机构
[1] Natl Cent Univ, Dept Chem & Mat Engn, Chungli 320, Taiwan
[2] Ind Technol Res Inst, Mat Chem Labs, Hsinchu 310, Taiwan
关键词
Cathodes; Coated LiCoO2; Cycle stability; Lithium-ion battery; Sol-gel; YAG; SOL-GEL PRECURSOR; GARNET YAG FIBERS; THERMAL-STABILITY; CATHODE MATERIALS; CARBOXYLATE-ALUMOXANES; INTERCALATION CATHODE; ENHANCED CYCLABILITY; 4.5; V; BATTERIES; OXIDES;
D O I
10.1016/j.jpowsour.2008.09.049
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
Synthesized yttrium aluminum garnet (YAG) sol was coated on the surface of the LiCoO2 cathode particles by an in situ sol-gel process, followed by calcination at 923 K for 10 h in air. Based on XRD, TEM, and ESCA data, a compact YAG kernel with an average thickness of similar to 20nm was formed on the surface of the core LiCoO2 particles, which ranged from similar to 90 to 120 nm in size. The charge-discharge cycling studies for the coated materials suggest that 0.3 wt.% YAG-coated LiCoO2 heated at 923 K for 10 h in air. delivered a discharge capacity of 167 mAh g(-1) and a cycle stability of about 164 cycles with a fading rate of 0.2 mAh cycle(-1) at a 0.2C-rate between 2.75 and 4.40V vs. Li/Li+. The differential capacity plots revealed that impedance growth was slower for YAG surface treated LiCoO2, when cells were charged at 4.40V. DSC results exemplified that the exothermic peak at similar to 468 K corresponded to the release of much less oxygen and greater thermal-stability. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:279 / 287
页数:9
相关论文
共 43 条
  • [1] Cobalt dissolution in LiCoO2-based non-aqueous rechargeable batteries
    Amatucci, GG
    Tarascon, JM
    Klein, LC
    [J]. SOLID STATE IONICS, 1996, 83 (1-2) : 167 - 173
  • [2] Common electroanalytical behavior of Li intercalation processes into graphite and transition metal oxides
    Aurbach, D
    Levi, MD
    Levi, E
    Teller, H
    Markovsky, B
    Salitra, G
    Heider, U
    Heider, L
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (09) : 3024 - 3034
  • [3] On the capacity fading of LiCoO2 intercalation electrodes:: the effect of cycling, storage, temperature, and surface film forming additives
    Aurbach, D
    Markovsky, B
    Rodkin, A
    Levi, E
    Cohen, YS
    Kim, HJ
    Schmidt, M
    [J]. ELECTROCHIMICA ACTA, 2002, 47 (27) : 4291 - 4306
  • [4] An analysis of rechargeable lithium-ion batteries after prolonged cycling
    Aurbach, D
    Markovsky, B
    Rodkin, A
    Cojocaru, M
    Levi, E
    Kim, HJ
    [J]. ELECTROCHIMICA ACTA, 2002, 47 (12) : 1899 - 1911
  • [5] Changes in the resistance of electrolyte solutions during contact with lithium electrodes at open circuit potential that reflect the Li surface chemistry
    Aurbach, D
    Schechter, A
    [J]. ELECTROCHIMICA ACTA, 2001, 46 (15) : 2395 - 2400
  • [6] AURBACH D, 1999, J POWER SOURCES, V95, P81
  • [7] Thermal stability of LixCoO2 cathode for lithium ion battery
    Baba, Y
    Okada, S
    Yamaki, J
    [J]. SOLID STATE IONICS, 2002, 148 (3-4) : 311 - 316
  • [8] Methods to obtain excellent capacity retention in LiCoO2 cycled to 4.5 V
    Chen, ZH
    Dahn, JR
    [J]. ELECTROCHIMICA ACTA, 2004, 49 (07) : 1079 - 1090
  • [9] Effect of a ZrO2 coating on the structure and electrochemistry of LixCoO2 when cycled to 4.5 V
    Chen, ZH
    Dahn, JR
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (10) : A213 - A216
  • [10] Comparison of Al2O3- and AlPO4-coated LiCoO2 cathode materials for a Li-ion cell
    Cho, J
    Kim, TG
    Kim, C
    Lee, JG
    Kim, YW
    Park, B
    [J]. JOURNAL OF POWER SOURCES, 2005, 146 (1-2) : 58 - 64