Kinetics of Li-ion transfer reaction at LiMn2O4, LiCoO2, and LiFePO4 cathodes

被引:31
作者
Swiderska-Mocek, Agnieszka [1 ]
Lewandowski, Andrzej [1 ]
机构
[1] Poznan Univ Tech, Fac Chem Technol, PL-60965 Poznan, Poland
关键词
LiMn2O4; LiCoO2; LiFePO4; cathodes; Graphite anode; Impedance; Kinetic parameters; Lithium-ion battery; LITHIUM-ION; GRAPHITE/ELECTROLYTE INTERFACE; SOLVATION SHEATH; ELECTROLYTES; PERFORMANCE; INSERTION; BEHAVIOR; LIXCOO2;
D O I
10.1007/s10008-016-3499-6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Kinetics of LiFePO4, LiMn2O4, and LiCoO2 cathodes operating in 1 M LIPF6 solution in a mixture of ethylene carbonate and dimethyl carbonate was deduced from impedance spectra taken at different temperatures. The most striking difference of electrochemical impedance spectroscopy (EIS) curves is the impedance magnitude: tens of ohms in the case of LiFePO4, hundreds of ohms for LiMn2O4, and thousands of ohms for LiCoO2. Charge transfer resistances (R (ct)) for lithiation/delitiation processes estimated from the deconvolution procedure were 6.0 Omega (LiFePO4), 55.4 Omega (LiCoO2), and 88.5 Omega (LiMn2O4), respectively. Exchange current density for all the three tested cathodes was found to be comparable (0.55-1 center dot 10(-2) mAcm(-2), T = 298 K). Corresponding activation energies for the charge transfer process, , differed considerably: 66.3, 48.9, and 17.0 kJmol(-1) for LiMn2O4, LiCoO2, and LiFePO4, respectively. Consequently, temperature variation may have a substantial influence on exchange current densities (j (o)) in the case of LiMn2O4 and LiCoO2 cathodes.
引用
收藏
页码:1365 / 1372
页数:8
相关论文
共 32 条
[1]   Solvated Li-ion transfer at interface between graphite and electrolyte [J].
Abe, T ;
Fukuda, H ;
Iriyama, Y ;
Ogumi, Z .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (08) :A1120-A1123
[2]   Enhancement of the Li+ ion transfer reaction at the LiCoO2 interface by 1,3,5-trifluorobenzene [J].
Baek, Byeongjin ;
Jung, Cheolsoo .
ELECTROCHIMICA ACTA, 2010, 55 (09) :3307-3311
[3]   La0.6Sr0.4CoO3-δ modified LiFePO4/C composite cathodes with improved electrochemical performances [J].
Cao, Jianmei ;
Qu, Yang ;
Guo, Ruisong .
ELECTROCHIMICA ACTA, 2012, 67 :152-158
[4]   Preparation of orthorhornbic LiMnO2 material via the sol-gel process [J].
Guo, ZP ;
Konstantinov, K ;
Wang, GX ;
Liu, HK ;
Dou, SX .
JOURNAL OF POWER SOURCES, 2003, 119 :221-225
[5]   Interfacial resistance of the LiFePO4-C/PEO-LiTFSI composite electrode for dry-polymer lithium-ion batteries [J].
Hanai, K. ;
Ueno, M. ;
Imanishi, N. ;
Hirano, A. ;
Yamamoto, O. ;
Takeda, Y. .
JOURNAL OF POWER SOURCES, 2011, 196 (16) :6756-6761
[6]   Electrolytes, SEI and Charge Discharge Kinetics of Li-ion Batteries [J].
Jow, T. R. ;
Allen, J. L. ;
Marx, M. ;
Nechev, K. ;
Deveney, B. ;
Rickman, S. .
RECHARGEABLE LITHIUM-ION BATTERIES, 2010, 25 (36) :3-12
[7]   Revisiting the electrochemical impedance behaviour of the LiFePO4/C cathode [J].
Ju, Hua ;
Wu, Jun ;
Xu, Yanhui .
JOURNAL OF CHEMICAL SCIENCES, 2013, 125 (03) :687-693
[8]   Enhanced electrochemical performance of surface modified LiCoO2 for all-solid-state lithium batteries [J].
Kim, Junghoon ;
Kim, Minjeong ;
Noh, Sungwoo ;
Lee, Giho ;
Shin, Dongwook .
CERAMICS INTERNATIONAL, 2016, 42 (02) :2140-2146
[9]   A study of electrochemical kinetics of lithium ion in organic electrolytes [J].
Lee, SI ;
Jung, UH ;
Kim, YS ;
Kim, MH ;
Ahn, DJ ;
Chun, HS .
KOREAN JOURNAL OF CHEMICAL ENGINEERING, 2002, 19 (04) :638-644
[10]   Kinetics of Na|CF x and Li|CF x systems [J].
Lewandowski, Andrzej ;
Jakobczyk, Pawel .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2016, 20 (12) :3367-3373