Abstract

Thin-film electrodes, which were exposed to pure dimethyl carbonate (DMC) or to a mixture of ethylene carbonate (EC) and DMC (1:1 by volume) containing 1 M at elevated temperatures, were studied by using X-ray diffraction, current-sensing atomic force microscopy (CSAFM), cyclic voltammetry, ordinary Raman spectroscopy, and surface-enhanced Raman spectroscopy (SERS). Thin, electronically insulating surface layers were detected by CSAFM and SERS on all electrodes. The surface layer formed by exposure to DMC at 70°C was uniform and preserved the electrode structure, however, it led to complete electrode deactivation, probably due to loss of surface electronic conductivity and slower lithium-ion transport rates through the surface layer. A similar surface layer was formed when the electrodes were exposed to however, the layer formed at 70°C did not prevent decomposition and consequent electrode capacity loss. In this case, manganese dissolution was observed, accompanied by the formation of SER spectra of the surface layers suggest that they were formed as a result of DMC decomposition at the surface. The SER spectra displayed bands characteristic of Li-O-R, carbonate, and carboxyl groups. Derivatives of carbon-oxygen triple bonds or silver-carbon-oxygen groups, which are possibly a result of interactions between the surface layer and silver microparticles, were also detected. © 2001 The Electrochemical Society. All rights reserved.

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