The slow potentiodynamic method and galvanostatic measurements in 0.25 M H,SO, have appeared to bc very useful tools to determine the quantity of the lower chromium oxides built into graphite\_CrOs compounds (GIG-CrO,'s). From the charge and discharge curves it has been possible to calculate the oxi
The electrochemical preparation and properties of ionic alkali metal-and NR4-graphite intercalation compounds in organic electrolytes
β Scribed by J.O. Besenhard
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 650 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0008-6223
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β¦ Synopsis
The preparation of graphite-alkali metal-solvent or graphite-N&-solvent ternary intercalation compounds by electrochemical reduction of graphite is described. The reduction occurs stagewise and the complete formation of a defined stage can be recognized by a striking change in the potential of the graphite electrode. Under certain conditions the stoichiometry of intercalation compounds (e.g. C,K(DMSO), C,,K(DMSO), C,,Li(DME) can be calculated from the coulombs consumed by a weighed graphite electrode until a step in potential occurs. The electrochemical intercalation of alkali metals into graphite is reversible. It may be reversed with a coulombic efficiency up to practically lOO%, e.g. for C.K(DMSO). A considerable co-intercalation of alkali metal salts from the electrolyte was not observed. From a preparative point of view, a great advantage over the direct chemical reduction of graphite is that a desired degree of intercalation can be specifically prepared. A coulometric determination of the intercalated cations is possible by way of an electrochemical reoxidation. Potential measurements of electrochemically prepared intercalation compounds with a well-defined degree of intercalation represent a simple method for investigating the thermodynamics of these reactions. Furthermore, by means of dynamic electrochemical methods, such as cyclic voltammetry, information about the kinetics of intercalation reactions is obtainable.
π SIMILAR VOLUMES
Stage-n Fe&GICs (n = 2,3) prepared in the standard two-zone method were oxidized galvanostatically in H,SO,. The electrode potential vs. electric quantity curves observed during the treatment and the X-ray powder patterns of the products showed clearly the intercalation of H,SO, into FeCI,-GICs and
Ionic conductivities of the polymer electrolytes prepared from the ionomer (poly(methy1 methacrylate-co-alkali metal methacrylate)), lithium perchlorate, and ethylene carbonate as a plasticizer, were studied as a function of the ion content and the alkali-metal cation of the ionomer. It was possible