Main aging mechanisms in Li ion batteries

被引:880
作者
Broussely, M
Biensan, P
Bonhomme, F
Blanchard, P
Herreyre, S
Nechev, K
Staniewicz, RJ
机构
[1] Saft, F-86060 Poitiers, France
[2] Saft, F-33000 Bordeaux, France
[3] Saft Amer, Cockeysville, MD USA
关键词
aging reactions; Li ion batteries;
D O I
10.1016/j.jpowsour.2005.03.172
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Some of the aging mechanisms occurring in Li ion batteries, either on rest or on cycling, are described from long-term storage or cycling data. Generally, the most critical part of the cell is the negative electrode/electrolyte interface. Stability of the solid electrolyte interface (SEI), more generally of the passivating layer, must be insured by proper material choice and additives. Excessive growth induces with time a capacity loss corresponding to the lithium corrosion, and a reduction of power capability of the electrode, from the active surface area degradation. In a worst case, reduction of charge rate capability may lead to local lithium plating during cycling, strongly aggravating the capacity fading. When the SEI is correctly built, with low electronic conductivity, the negative electrode stability can be very stable, as described by long-term aging (more than 4 years) at higher temperature than ambient. Vinylen carbonate is confirmed as outstanding additive. At elevated temperature, high SOC induces side reactions at the positive interface, involving electrolyte components oxidation. The results are an increase of cell impedance, and possible Slow CO2 evolution. Presence of lithium carbonate greatly enhanced the gas formation. The observed impedance increase indicates a reduction of the active surface area, in agreement with solid deposit. When properly designed with an appropriate choice of active materials and electrolyte, the Li ion system can provide a very long service. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:90 / 96
页数:7
相关论文
共 16 条
[1]   The study of surface phenomena related to electrochemical lithium intercalation into LixMOy host materials (M = Ni, Mn) [J].
Aurbach, D ;
Gamolsky, K ;
Markovsky, B ;
Salitra, G ;
Gofer, Y ;
Heider, U ;
Oesten, R ;
Schmidt, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (04) :1322-1331
[2]  
BIENSAN P, 2003, P LITHIUM BATTERY DI
[3]  
BIESAN P, 1994, Patent No. 9404889
[4]   An accelerated calendar and cycle life study of Li-ion cells [J].
Bloom, I ;
Cole, BW ;
Sohn, JJ ;
Jones, SA ;
Polzin, EG ;
Battaglia, VS ;
Henriksen, GL ;
Motloch, C ;
Richardson, R ;
Unkelhaeuser, T ;
Ingersoll, D ;
Case, HL .
JOURNAL OF POWER SOURCES, 2001, 101 (02) :238-247
[5]  
Bonhomme F., 2004, P IBA M GRAZ
[6]   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
[7]  
BROUSSELY M, 2002, ADV LITHIUM ION BATT, V13, P394
[8]  
JUNGST RG, 2000, EL SOC FALL M PHOEN
[9]  
KOSTECKI R, 2002, ELECTROCHEM SOLID ST, V5
[10]   7Li and 1H MAS NMR observation of interphase layers on lithium nickel oxide based positive electrodes of lithium-ion batteries [J].
Ménétrier, M ;
Vaysse, C ;
Croguennec, L ;
Delmas, C ;
Jordy, C ;
Bonhomme, F ;
Biensan, P .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2004, 7 (06) :A140-A143