A capacity fade model for lithium-ion batteries including diffusion and kinetics

被引:74
作者
Sankarasubramanian, Shrihari [2 ]
Krishnamurthy, Balaji [1 ]
机构
[1] BITS Pliani, Dept Chem Engn, Hyderabad 500078, Andhra Pradesh, India
[2] MVJ Coll Engn, Dept Chem Engn, Bangalore 560067, Karnataka, India
关键词
Lithium ion batteries; Modeling; SEI layer; Diffusion; TIN-BASED INTERMETALLICS; LI; PERFORMANCE; ELECTRODE; GRAPHITE; CALENDAR; CELLS;
D O I
10.1016/j.electacta.2012.03.063
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
A one dimensional model incorporating solvent diffusion and kinetics of solid electrolyte interphase (SEI) formation is developed to study capacity fade in lithium ion batteries. The model assumes that solvent diffuses through the SEI (solid electrolyte interphase) and undergoes a two electron reduction at the carbon SE! interface. The kinetics of the reduction reaction at the SEI-electrolyte interface and the solvent diffusivity are seen to be the most important parameters governing SE! formation. The capacity loss is seen to be a function of the thickness of the SEI layer and is seen to vary linearly over time. The rate constant governing SEI formation and solvent diffusivity are seen to follow Arrhenius type relationships. The model results are compared with and are found to be in good agreement with experimental data. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:248 / 254
页数:7
相关论文
共 27 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]
Electrochemical SPM investigation of the solid electrolyte interphase film formed on HOPG electrodes [J].
Alliata, D ;
Kötz, R ;
Novák, P ;
Siegenthaler, H .
ELECTROCHEMISTRY COMMUNICATIONS, 2000, 2 (06) :436-440
[3]
On the correlation between surface chemistry and performance of graphite negative electrodes for Li ion batteries [J].
Aurbach, D ;
Markovsky, B ;
Weissman, I ;
Levi, E ;
Ein-Eli, Y .
ELECTROCHIMICA ACTA, 1999, 45 (1-2) :67-86
[4]
Review of selected electrode-solution interactions which determine the performance of Li and Li ion batteries [J].
Aurbach, D .
JOURNAL OF POWER SOURCES, 2000, 89 (02) :206-218
[5]
New insights into the interactions between electrode materials and electrolyte solutions for advanced nonaqueous batteries [J].
Aurbach, D ;
Markovsky, B ;
Levi, MD ;
Levi, E ;
Schechter, A ;
Moshkovich, M ;
Cohen, Y .
JOURNAL OF POWER SOURCES, 1999, 81 :95-111
[6]
Aurbach D, 2002, ADVANCES IN LITHIUM-ION BATTERIES, P7, DOI 10.1007/0-306-47508-1_2
[7]
Aging mechanism in Li ion cells and calendar life predictions [J].
Broussely, M ;
Herreyre, S ;
Biensan, P ;
Kasztejna, P ;
Nechev, K ;
Staniewicz, RJ .
JOURNAL OF POWER SOURCES, 2001, 97-8 :13-21
[8]
Modeling side reactions in composite LiyMn2O4 electrodes [J].
Darling, R ;
Newman, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (03) :990-998
[9]
THE DEPENDENCE OF THE PERFORMANCE OF LI-C INTERCALATION ANODES FOR LI-ION SECONDARY BATTERIES ON THE ELECTROLYTE SOLUTION COMPOSITION [J].
EINELI, Y ;
MARKOVSKY, B ;
AURBACH, D ;
CARMELI, Y ;
YAMIN, H ;
LUSKI, S .
ELECTROCHIMICA ACTA, 1994, 39 (17) :2559-2569
[10]
Surface film formation on graphite negative electrode in lithium-ion batteries [J].
Jeong, SK ;
Inaba, M ;
Abe, T ;
Ogumi, Z .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (09) :A989-A993