Investigation of the Passivation Properties of the Solid Electrolyte Interphase Using a Soluble Redox Couple

被引:10
作者
Dinh-Nguyen, M. T. [1 ]
Delacourt, C. [1 ]
机构
[1] Univ Picardie Jules Verne, CNRS UMR 7314, Lab React & Chim Solides, Amiens, France
关键词
ORIENTED PYROLYTIC-GRAPHITE; LI-ION BATTERIES; OVERCHARGE PROTECTION; LITHIUM BATTERIES; SIMULATION; MECHANISMS; MODEL; CELL; REDUCTION; FERROCENE;
D O I
10.1149/2.0771605jes
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) that forms at carbonaceous anodes makes Li-ion battery a viable technology because it inhibits solvent-decomposition reactions. However, passivation is never complete and SEI "leakage" appears as the main contributor to Li-ion battery aging. There has been a great deal of experiments focusing on the chemical analysis of SEIs over the past decades. Still, a direct evaluation of their passive character has not been much regarded. In this work, SEIs formed cathodically on glassy carbon electrodes are characterized using the rotating disk electrode method and ferrocene/ferrocenium as a redox shuttle, as originally proposed in Tang and Newman [M. Tang and J. Newman, This journal, 158(5), A530-A536 (2011)]. A comprehensive model is developed that accounts for transport of soluble redox species across the diffusion layer and the porous SEI as well as charge-transfer kinetics at the modified electrode surface. From a model analysis of electrodes with SEIs formed in various conditions, values of SEI porosity and effective rate constant of ferrocenium reduction are derived and discussed. First attempts are conducted to extend the method to SEIs formed at graphite composite electrodes. Preliminary results suggest SEIs are less passivating than those on glassy carbon. (C) The Author(s) 2016. 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:A706 / A713
页数:8
相关论文
共 27 条
[1]   NORMAL-BUTYLFERROCENE FOR OVERCHARGE PROTECTION OF SECONDARY LITHIUM BATTERIES [J].
ABRAHAM, KM ;
PASQUARIELLO, DM ;
WILLSTAEDT, EB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (06) :1856-1857
[2]   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
[3]  
Aurbach D, 1999, NONAQUEOUS ELECTROCHEMISTRY, P137
[4]   CHEMICAL MODIFICATION OF ELECTRODES [J].
BARD, AJ .
JOURNAL OF CHEMICAL EDUCATION, 1983, 60 (04) :302-304
[5]   The flow due to a rotating disc. [J].
Cochran, WG .
PROCEEDINGS OF THE CAMBRIDGE PHILOSOPHICAL SOCIETY, 1934, 30 :365-375
[6]   Life Simulation of a Graphite/LiFePO4 Cell under Cycling and Storage [J].
Delacourt, C. ;
Safari, M. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (08) :A1283-A1291
[7]   A stability criterion for accurate simulation of electrochemical diffusion-kinetic phenomena at the rotating disk electrode and implications for simulation of diffusion-migration and other problems [J].
Feldberg, SW ;
Goldstein, CI ;
Rudolph, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1996, 413 (1-2) :25-36
[8]   SIMULATION AND OPTIMIZATION OF THE DUAL LITHIUM ION INSERTION CELL [J].
FULLER, TF ;
DOYLE, M ;
NEWMAN, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (01) :1-10
[9]  
GOLOVIN MN, 1992, J ELECTROCHEM SOC, V139, P5, DOI 10.1149/1.2069200
[10]   UNDERVOLTAGE DEPOSITION OF ALKALI-METAL AT CARBON ELECTRODES IN LICL-KCL EUTECTIC MELT [J].
JAMES, SD .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1975, 122 (07) :921-927