Effect of porous structure and morphology of cathode on the degradation of lithium-ion batteries

被引:6
作者
Lee, Yoon Koo [1 ]
机构
[1] Hanbat Natl Univ, Dept Mech Engn, Daejeon 34158, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium-ion battery; Degradation; Random structure; SEI layer formation; Transition-metal dissolution; Geometry; SOLID-ELECTROLYTE-INTERPHASE; CAPACITY FADE MODEL; SIDE REACTIONS; IN-SITU; SPINEL DISSOLUTION; FINITE-ELEMENT; GRAPHITE; MICROSTRUCTURE; PERFORMANCE; ANODES;
D O I
10.1016/j.est.2022.104788
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
This study investigates the effect of the micromorphology of cathodes with 3D porous structures and geometries on the degradation and electrochemical performance of lithium-ion batteries. Active particle aggregates with different particle diameters and volume fractions are randomly positioned to generate a 3D structure of the cathode in simulation. A physics-based electrochemical model that describes the degradation of the separator, anode, and cathode is developed. Simulation results show that aggregates with a smaller particle radius have a larger surface area, which leads to a higher capacity with a lower concentration gradient but also severe overall degradation. However, with a larger surface area, the volume fraction of the cathode decreases faster, whereas that of the anode decreases slower because of the difference in the fundamental degradation mechanisms of both electrodes. These results indicate that a cathode with a smaller surface area and an anode with a larger surface area are preferred to minimize battery degradation. This morphological information also impacts the diffusivity, which must be carefully optimized for maximizing the capacity and minimizing the degradation. The model developed in this study is expected to be useful to understand degradation mechanisms and to optimize battery design and manufacturing.
引用
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页数:14
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共 74 条
[1]   Capacity fade mechanisms and side reactions in lithium-ion batteries [J].
Arora, P ;
White, RE ;
Doyle, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3647-3667
[2]   Mathematical modeling of the lithium deposition overcharge reaction in lithium-ion batteries using carbon-based negative electrodes [J].
Arora, P ;
Doyle, M ;
White, RE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (10) :3543-3553
[3]   THE CORRELATION BETWEEN THE SURFACE-CHEMISTRY AND THE PERFORMANCE OF LI-CARBON INTERCALATION ANODES FOR RECHARGEABLE ROCKING-CHAIR TYPE BATTERIES [J].
AURBACH, D ;
EINELI, Y ;
CHUSID, O ;
CARMELI, Y ;
BABAI, M ;
YAMIN, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (03) :603-611
[4]   On the possibility of LiH formation on Li surfaces in wet electrolyte solutions [J].
Aurbach, D ;
Weissman, I .
ELECTROCHEMISTRY COMMUNICATIONS, 1999, 1 (08) :324-331
[5]   Reaction energy for LiMn2O4 spinel dissolution in acid [J].
Benedek, R ;
Thackeray, MM .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2006, 9 (06) :A265-A267
[6]   Molecular dynamics simulations of lithium alkyl carbonates [J].
Borodin, Oleg ;
Smith, Grant D. ;
Fan, Peng .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (45) :22773-22779
[7]   Predicting and Extending the Lifetime of Li-Ion Batteries [J].
Burns, J. C. ;
Kassam, Adil ;
Sinha, N. N. ;
Downie, L. E. ;
Solnickova, Lucie ;
Way, B. M. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2013, 160 (09) :A1451-A1456
[8]   Probing the morphological influence on solid electrolyte interphase and impedance response in intercalation electrodes [J].
Chen, Chien-Fan ;
Mukherjee, Partha P. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2015, 17 (15) :9812-9827
[9]   Comparison of metal ion dissolutions from lithium ion battery cathodes [J].
Choi, W. ;
Manthiram, A. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (09) :A1760-A1764
[10]   Electrochemistry of highly ordered pyrolytic graphite surface film formation observed by atomic force microscopy [J].
Chu, AC ;
Josefowicz, JY ;
Farrington, GC .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (12) :4161-4169