OCV Hysteresis in Li-Ion Batteries including Two-Phase Transition Materials

被引:117
作者
Roscher, Michael A. [1 ]
Bohlen, Oliver [2 ]
Vetter, Jens [2 ]
机构
[1] Rhein Westfal TH Aachen, Inst Power Elect & Elect Drives ISEA, D-52066 Aachen, Germany
[2] BMW AG, Div Energy Storage Syst, D-80788 Munich, Germany
关键词
D O I
10.4061/2011/984320
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 [应用化学];
摘要
The relation between batteries' state of charge (SOC) and open-circuit voltage (OCV) is a specific feature of electrochemical energy storage devices. Especially NiMH batteries are well known to exhibit OCV hysteresis, and also several kinds of lithium-ion batteries show OCV hysteresis, which can be critical for reliable state estimation issues. Electrode potential hysteresis is known to result from thermodynamical entropic effects, mechanical stress, and microscopic distortions within the active electrode materials which perform a two-phase transition during lithium insertion/extraction. Hence, some Li-ion cells including two-phase transition active materials show pronounced hysteresis referring to their open-circuit voltage. This work points out how macroscopic effects, that is, diffusion limitations, superimpose the latte- mentioned microscopic mechanisms and lead to a shrinkage of OCV hysteresis, if cells are loaded with high current rates. To validate the mentioned interaction, Li-ion cells' state of charge is adjusted to 50% with various current rates, beginning from the fully charged and the discharged state, respectively. As a pronounced difference remains between the OCV after charge and discharge adjustment, obviously the hysteresis vanishes as the target SOC is adjusted with very high current rate.
引用
收藏
页数:6
相关论文
共 21 条
[1]
An electrochemical investigation into the lithium insertion properties of LixCoO2 [J].
Barker, J ;
Pynenburg, R ;
Koksbang, R ;
Saidi, MY .
ELECTROCHIMICA ACTA, 1996, 41 (15) :2481-2488
[2]
Lithium electrochemical deintercalation from O2-LiCoO2 -: Structure and physical properties [J].
Carlier, D ;
Saadoune, I ;
Ménétrier, M ;
Delmas, C .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (10) :A1310-A1320
[3]
Dreyer W, 2010, NAT MATER, V9, P448, DOI [10.1038/NMAT2730, 10.1038/nmat2730]
[4]
Ionic vs Electronic Power Limitations and Analysis of the Fraction of Wired Grains in LiFePO4 Composite Electrodes [J].
Fongy, C. ;
Gaillot, A. -C. ;
Jouanneau, S. ;
Guyomard, D. ;
Lestriez, B. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (07) :A885-A891
[5]
Goodenough J. B., 1999, US Patent, Patent No. [5910382 A, 5910382, 5, 910, 382]
[6]
Discharge model for LiFePO4 accounting for the solid solution range [J].
Kasavajjula, Uday S. ;
Wang, Chunsheng ;
Arce, Pedro E. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (11) :A866-A874
[7]
Kohlrausch F. W. G., 2009, LEITVERM OGEN ELEKTR
[8]
Study of the LiFePO4/FePO4 two-phase system by high-resolution electron energy loss spectroscopy [J].
Laffont, L. ;
Delacourt, C. ;
Gibot, P. ;
Wu, M. Yue ;
Kooyman, P. ;
Masquelier, C. ;
Tarascon, J. Marie .
CHEMISTRY OF MATERIALS, 2006, 18 (23) :5520-5529
[9]
Frumkin intercalation isotherm - a tool for the description of lithium insertion into host materials: a review [J].
Levi, MD ;
Aurbach, D .
ELECTROCHIMICA ACTA, 1999, 45 (1-2) :167-185
[10]
Meethong N., 2008, P PAC RIM M EL SOL S