An Analysis of Artificial and Natural Graphite in Lithium Ion Pouch Cells Using Ultra-High Precision Coulometry, Isothermal Microcalorimetry, Gas Evolution, Long Term Cycling and Pressure Measurements

被引:66
作者
Glazier, S. L. [1 ]
Li, Jing [1 ]
Louli, A. J. [1 ]
Allen, J. P. [2 ]
Dahn, J. R. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
[2] Dalhousie Univ, Dept Chem, Halifax, NS B3H 3J5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
POSITIVE ELECTRODE MATERIALS; PARASITIC HEAT-FLOW; ELECTROCHEMICAL PERFORMANCE; ANODE; STABILITY; CARBONATE; ADDITIVES; IMPACT;
D O I
10.1149/2.0421714jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Natural graphite (NG) negative electrode materials can perform poorly compared to synthetic, or artificial, graphite (AG) negative electrodes in certain lithium ion cells. LiNi0.5Mn0.3Co0.2O2(NMC532)/(AG or NG) pouch cells were tested with various loadings of an electrolyte additive blend to study the effect of the graphite type as well as the formed solid electrolyte interphase (SEI). Cells underwent testing using ultra-high precision coulometry, isothermal microcalorimetry, in-situ pressure measurements, long term cycling and in-situ gas measurements. In short term experiments NMC532/AG and NMC532/NG cells showed similar coulombic efficiencies, parasitic heat flows, and gas production with large electrolyte additive loadings, but NG cells showed worse capacity retention in long-term tests. With low additive loadings NMC532/NG cells showed lower coulombic efficiency, higher capacity fade, more parasitic heat flow, and more gas production. In-situ cell stack pressure measurements showed that NMC532/NG cells irreversibly expanded during cycling while NMC532/AG cells did not. Although these results lead one to propose a simple model for the poor performance of NMC532/NG cells, NMC622/NG and NMC622/AG cells showed very different behavior in long term tests suggesting that positive/negative interactions play a strong role in governing the behavior of graphites in Li-ion cells. (c) The Author(s) 2017. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. All rights reserved.
引用
收藏
页码:A3545 / A3555
页数:11
相关论文
共 27 条
[1]   Thermal Stability and Electrochemical Properties of Fluorine Compounds as Nonflammable Solvents for Lithium-Ion Batteries [J].
Achiha, Takashi ;
Nakajima, Tsuyoshi ;
Ohzawa, Yoshimi ;
Koh, Meiten ;
Yamauchi, Akiyoshi ;
Kagawa, Michiru ;
Aoyama, Hirokazu .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (06) :A707-A712
[2]   An Apparatus for the Study of In Situ Gas Evolution in Li-Ion Pouch Cells [J].
Aiken, C. P. ;
Xia, J. ;
Wang, David Yaohui ;
Stevens, D. A. ;
Trussler, S. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2014, 161 (10) :A1548-A1554
[3]   Special Synergy between Electrolyte Additives and Positive Electrode Surface Coating to Enhance the Performance of Li[Ni0.6Mn0.2Co0.2]O2/Graphite Cells [J].
Arumugam, Rajalakshmi Senthil ;
Ma, Lin ;
Li, Jing ;
Xia, Xin ;
Paulsen, J. M. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2016, 163 (13) :A2531-A2538
[4]   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
[5]   User-Friendly Differential Voltage Analysis Freeware for the Analysis of Degradation Mechanisms in Li-Ion Batteries [J].
Dahn, Hannah M. ;
Smith, A. J. ;
Burns, J. C. ;
Stevens, D. A. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (09) :A1405-A1409
[6]   ENTROPY OF THE INTERCALATION COMPOUND LIXMO6SE8 FROM CALORIMETRY OF ELECTROCHEMICAL-CELLS [J].
DAHN, JR ;
MCKINNON, WR ;
MURRAY, JJ ;
HAERING, RR ;
MCMILLAN, RS ;
RIVERSBOWERMAN, AH .
PHYSICAL REVIEW B, 1985, 32 (05) :3316-3318
[7]   The Impact of Electrolyte Composition on Parasitic Reactions in Lithium Ion Cells Charged to 4.7 V Determined Using Isothermal Microcalorimetry [J].
Downie, L. E. ;
Hyatt, S. R. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2016, 163 (02) :A35-A42
[8]   Determination of the Voltage Dependence of Parasitic Heat Flow in Lithium Ion Cells Using Isothermal Microcalorimetry [J].
Downie, L. E. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2014, 161 (12) :A1782-A1787
[9]   The Impact of Electrolyte Additives Determined Using Isothermal Microcalorimetry [J].
Downie, L. E. ;
Nelson, K. J. ;
Petibon, R. ;
Chevrier, V. L. ;
Dahn, J. R. .
ECS ELECTROCHEMISTRY LETTERS, 2013, 2 (10) :A106-A109
[10]   The Effect of Different Li(Ni1-x-yMnxCoy)O2 Positive Electrode Materials and Coatings on Parasitic Heat Flow as Measured by Isothermal Microcalorimetry, Ultra-High Precision Coulometry and Long Term Cycling [J].
Glazier, S. L. ;
Nelson, K. J. ;
Allen, J. P. ;
Li, J. ;
Dahn, J. R. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2017, 164 (06) :A1203-A1212