Origin of capacity fading in nano-sized Co3O4 electrodes:: Electrochemical impedance spectroscopy study

被引:63
作者
Kang, Jin-Gu [1 ]
Ko, Young-Dae [1 ]
Park, Jae-Gwan [1 ]
Kim, Dong-Wan [1 ]
机构
[1] Korea Inst Sci & Technol, Nanomat Res Ctr, Nanosci Res Div, Seoul 136791, South Korea
来源
NANOSCALE RESEARCH LETTERS | 2008年 / 3卷 / 10期
关键词
nano-sized Co3O4; Li-ion batteries; capacity fading; electrochemical impedance spectroscopy; charge transfer reaction;
D O I
10.1007/s11671-008-9176-7
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Transition metal oxides have been suggested as innovative, high-energy electrode materials for lithium-ion batteries because their electrochemical conversion reactions can transfer two to six electrons. However, nano-sized transition metal oxides, especially Co3O4, exhibit drastic capacity decay during discharge/charge cycling, which hinders their practical use in lithium-ion batteries. Herein, we prepared nano-sized Co3O4 with high crystallinity using a simple citrate-gel method and used electrochemical impedance spectroscopy method to examine the origin for the drastic capacity fading observed in the nano-sized Co3O4 anode system. During cycling, AC impedance responses were collected at the first discharged state and at every subsequent tenth discharged state until the 100th cycle. By examining the separable relaxation time of each electrochemical reaction and the goodness-of-fit results, a direct relation between the charge transfer process and cycling performance was clearly observed.
引用
收藏
页码:390 / 394
页数:5
相关论文
共 25 条
[1]   Nanostructured materials for advanced energy conversion and storage devices [J].
Aricò, AS ;
Bruce, P ;
Scrosati, B ;
Tarascon, JM ;
Van Schalkwijk, W .
NATURE MATERIALS, 2005, 4 (05) :366-377
[2]   Electrochemical deposition of porous Co3O4 nanostructured thin film for lithium-ion battery [J].
Chou, Shu-Lei ;
Wang, Jia-Zhao ;
Liu, Hua-Kun ;
Dou, Shi-Xue .
JOURNAL OF POWER SOURCES, 2008, 182 (01) :359-364
[3]  
Débart A, 2001, J ELECTROCHEM SOC, V148, pA1266, DOI 10.1149/1.1409971
[4]   An update on the reactivity of nanoparticles Co-based compounds towards Li [J].
Grugeon, S ;
Laruelle, S ;
Dupont, L ;
Tarascon, JM .
SOLID STATE SCIENCES, 2003, 5 (06) :895-904
[5]   Particle size effects on the electrochemical performance of copper oxides toward lithium [J].
Grugeon, S ;
Laruelle, S ;
Herrera-Urbina, R ;
Dupont, L ;
Poizot, P ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (04) :A285-A292
[6]   Nanomaterials for lithium ion batteries [J].
Jiang, Chunhai ;
Hosono, Eiji ;
Zhou, Haoshen .
NANO TODAY, 2006, 1 (04) :28-33
[7]   Lithium ion phase-transfer reaction at the interface between the lithium manganese oxide electrode and the nonaqueous electrolyte [J].
Kobayashi, S ;
Uchimoto, Y .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (27) :13322-13326
[8]   Combined XRD, EXAFS, and Mossbauer studies of the reduction by lithium of α-Fe2O3 with various particle sizes [J].
Larcher, D ;
Bonnin, D ;
Cortes, R ;
Rivals, I ;
Personnaz, L ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (12) :A1643-A1650
[9]   Effect of particle size on lithium intercalation into α-Fe2O3 [J].
Larcher, D ;
Masquelier, C ;
Bonnin, D ;
Chabre, Y ;
Masson, V ;
Leriche, JB ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (01) :A133-A139
[10]   The electrochemical reduction of Co3O4 in a lithium cell [J].
Larcher, D ;
Sudant, G ;
Leriche, JB ;
Chabre, Y ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (03) :A234-A241