Issue 8, 2015

On the interaction of water-soluble binders and nano silicon particles: alternative binder towards increased cycling stability at elevated temperatures

Abstract

Silicon based composites are among the most promising negative electrodes for lithium ion battery applications due to their high theoretical capacities. One major drawback of silicon based anodes are their large volume changes during lithiation and delithiation. Although many efforts have been made in view of new binder materials and improved electrolytes, the resulting battery cell suffers from severe capacity fading at ambient or elevated temperatures, respectively. The strong reactivity with the electrolyte is considered to be responsible for the reduced cycle life at elevated temperatures. In this work we introduce silicon composite anodes with a novel composition based on a gellan gum binder material that show an improved cycling performance at ambient temperature and at 60 °C. To elucidate the influence of the binder material, we investigated the structure of the silicon based composite anodes in order to understand the nature of the interaction of the gellan gum based binder polymers with the silicon particles in comparison with a common CMC binder. Also the influence of the choice of binder on the interactions at the interface between electrode surface and electrolyte were studied. A combination of powerful techniques including solid state NMR, TEM and EELS, XPS as well as FTIR were applied.

Graphical abstract: On the interaction of water-soluble binders and nano silicon particles: alternative binder towards increased cycling stability at elevated temperatures

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2014
Accepted
14 Jan 2015
First published
27 Jan 2015

Phys. Chem. Chem. Phys., 2015,17, 5632-5641

Author version available

On the interaction of water-soluble binders and nano silicon particles: alternative binder towards increased cycling stability at elevated temperatures

S. Klamor, M. Schröder, G. Brunklaus, P. Niehoff, F. Berkemeier, F. M. Schappacher and M. Winter, Phys. Chem. Chem. Phys., 2015, 17, 5632 DOI: 10.1039/C4CP04090B

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