The electrochemical redox reaction of stable organic polymer materials with unpaired electrons is a relatively new and exciting area of battery research.  Specifically, stable nitroxyl radical-containing polymers have displayed excellent characteristics as the cathode-active material and have presented themselves as a low-cost and environmentally friendly alternative to the current Li-ion battery technologies. However, with the advancement of organic-radical battery technology there is a lack of fundamental understanding of the dynamics of charge transfer processes, electronic and ionic, within organic radical-containing polymers.  In order to elucidate these mechanisms further, we have conducted extensive spectroscopic and spectroelectrochemical investigations of macromolecular systems containing nitroxide radicals.

We have employed spectroelectrochemical experiments for our study of stable radical polymer systems whereby, kinetic information was determined, specifically rates of charge transfer and ion diffusion within our polymer systems. A key factor determining the success of such experiments is that the material of interest exhibits a strong absorption coefficient and allows for measurement in the concentration regime conducive for electrochemical studies (typically up to 10 mM).  For this reason, of the available stable nitroxyl radical systems, we have chosen first to study the oxidation of a nitronyl nitroxide derivative. To simulate an electrode architecture, spectroelectrochemical studies were performed in the solid state, and the efficacy of charge transfer was investigated as a function of film thickness, counter-ion size, and radical polymer composition in “neat” polymer films. The addition of semiconducting carbon nanotubes at various loadings was also explored as changes to film conductivity has significant implications for rates of ion transport.