A review of the features and analyses of the solid electrolyte interphase in Li-ion batteries

被引:2561
作者
Verma, Pallavi [1 ]
Maire, Pascal [1 ]
Novak, Petr [1 ]
机构
[1] Paul Scherrer Inst, Dept Gen Energy, Electrochem Lab, Electrochem Energy Storage Sect, CH-5232 Villigen, Switzerland
基金
瑞士国家科学基金会;
关键词
Li-ion battery; Solid electrolyte interphase (SEI); Carbon (graphite); X-ray photoelectron spectroscopy (XPS); Infrared spectroscopy (FTIR); ATOMIC-FORCE MICROSCOPY; ACCELERATING RATE CALORIMETRY; GRAPHITE NEGATIVE-ELECTRODE; CARBON INTERCALATION ANODES; DIFFERENTIAL SCANNING CALORIMETRY; COMPARATIVE THERMAL-STABILITY; SURFACE-FILM FORMATION; LITHIUM METAL ANODES; IMPEDANCE SPECTROSCOPY; ELECTROCHEMICAL IMPEDANCE;
D O I
10.1016/j.electacta.2010.05.072
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The solid electrolyte interphase (SEI) is a protecting layer formed on the negative electrode of Li-ion batteries as a result of electrolyte decomposition, mainly during the first cycle. Battery performance, irreversible charge "loss", rate capability, cyclability, exfoliation of graphite and safety are highly dependent on the quality of the SEI. Therefore, understanding the actual nature and composition of SEI is of prime interest. If the chemistry of the SEI formation and the manner in which each component affects battery performance are understood, SEI could be tuned to improve battery performance. In this paper key points related to the nature, formation, and features of the SEI formed on carbon negative electrodes are discussed. SEI has been analyzed by various analytical techniques amongst which FTIR and XPS are most widely used. FTIR and XPS data of SEI and its components as published by many research groups are compiled in tables for getting a global picture of what is known about the SEL This article shall serve as a handy reference as well as a starting point for research related to SEI. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6332 / 6341
页数:10
相关论文
共 126 条
[1]   XANES study on solid electrolyte interface of Li ion battery [J].
Akai, T. ;
Ota, H. ;
Namita, H. ;
Yamaguchi, S. ;
Nomura, M. .
PHYSICA SCRIPTA, 2005, T115 :408-411
[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]   Chemical composition and morphology of the elevated temperature SEI on graphite [J].
Andersson, AM ;
Edström, K .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (10) :A1100-A1109
[4]   Electrochemically lithiated graphite characterised by photoelectron spectroscopy [J].
Andersson, AM ;
Henningson, A ;
Siegbahn, H ;
Jansson, U ;
Edström, K .
JOURNAL OF POWER SOURCES, 2003, 119 :522-527
[5]   Solid electrolyte interphase on graphite Li-ion battery anodes studied by soft X-ray spectroscopy [J].
Augustsson, A ;
Herstedt, M ;
Guo, JH ;
Edström, K ;
Zhuang, GV ;
Ross, PN ;
Rubensson, JE ;
Nordgren, J .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2004, 6 (16) :4185-4189
[6]   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
[7]   A comparative study of synthetic graphite and Li electrodes in electrolyte solutions based on ethylene carbonate dimethyl carbonate mixtures [J].
Aurbach, D ;
Markovsky, B ;
Shechter, A ;
EinEli, Y ;
Cohen, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (12) :3809-3820
[8]   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
[9]   A short review of failure mechanisms of lithium metal and lithiated graphite anodes in liquid electrolyte solutions [J].
Aurbach, D ;
Zinigrad, E ;
Cohen, Y ;
Teller, H .
SOLID STATE IONICS, 2002, 148 (3-4) :405-416
[10]   THE SURFACE-CHEMISTRY OF LITHIUM ELECTRODES IN ALKYL CARBONATE SOLUTIONS [J].
AURBACH, D ;
EINELY, Y ;
ZABAN, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (01) :L1-L3