A comparative study of polyacrylic acid (PAA) and carboxymethyl cellulose (CMC) binders for Si-based electrodes

被引:148
作者
Karkar, Z. [1 ,2 ]
Guyomard, D. [2 ]
Roue, L. [1 ]
Lestriez, B. [2 ]
机构
[1] INRS, Ctr Energie Mat Telecommun, EMT, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
[2] Univ Nantes, CNRS, Inst Mat Jean Rouxel IMN, UMR 6502, F-44322 Nantes 3, France
基金
加拿大自然科学与工程研究理事会;
关键词
Li-ion batteries; Silicon-based anodes; Binder; Polyacrylic acid; Carboxymethyl cellulose; LITHIUM-ION BATTERIES; SURFACE-FILM FORMATION; HIGH-CAPACITY ANODES; NEGATIVE ELECTRODES; POLY(VINYLIDENE FLUORIDE); COMPOSITE ELECTRODES; SILICON ANODES; ELECTROCHEMICAL PERFORMANCE; GRAPHITE PARTICLES; CELL PERFORMANCE;
D O I
10.1016/j.electacta.2017.11.082
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This work is a comparative study on two well-known binder systems for silicon-based negative composite electrodes for Li-ion batteries: polyacrylic acid (PAA) and carboxymethyl cellulose/citric acid (CMC/CA). The electrode slurry rheological properties and the dry electrode morphology and physical properties are studied as a function of the binder content. The electrochemical behavior of the electrodes is also studied as a function of the active mass loading (from 1 to 4.5 mg cm(-2)). Increasing the binder content from 4 to 12 wt% improves the 1st cycle efficiency, which is clearly related to its contribution as a pre-formed artificial solid electrolyte interphase (SEI) layer. The enhancement of the mechanical strength of the composites with increasing binder content is reflected in the better cyclability of the electrodes with active mass loading higher than 1 mg cm(-2). CMC/CA is more efficient as a binder at low content while PAA is more efficient at high content, which could be related to their molecular structure. Finally, for both binders the influence of a post-processing treatment of the electrodes (called maturation) is shown to improve the electrochemical performance. This is however more significant with CMC/CA than with PAA. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:453 / 466
页数:14
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