Electrochemistry of methanofullerene films: Simultaneous cyclic voltammetry and electrochemical quartz crystal microbalance studies

• Published in: Journal of applied polymer science Vol. 100; no. 5; pp. 3634 - 3640
• Main Authors: Zhang, H., Huang, X., Fan, L. Z., Nin, B., Wu, Y. Q., Zheng, L. P., Cao, Y.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.06.2006; Wiley
• Subjects: Cross-disciplinary physics: materials science; rheology; electrochemistry; EQCM; Exact sciences and technology; Fullerenes and related materials; diamonds, graphite; Materials science; methanofullerenes; Physics; Specific materials; Substituent effect; Short chain; Films; Fullerene compounds; electrochemistry; Long chain; methanofullerenes; Experimental study; Cyclic voltammetry; Electrochemical properties; Investigation method; Medium effect; EQCM; Fullerenes; Counterions; Property structure relationship; Quartz microbalance
• ISSN: 0021-8995; 1097-4628
• DOI: 10.1002/app.23156

Electrochemical properties of eight methanofullerene films, prepared on electrodes by casting, were examined by means of cyclic voltammetry and electrochemical quartz crystal microbalance (EQCM) technique in acetonitrile solution. Compared with C60 film, the film stability with respect to dissolution is associated with the length of the alkyl chains introduced into C60 cage and is strongly dependent on the nature of the cation of the supporting electrolyte. TBA+, Li+, K+, and Na+ were selected to observe the effect of countercations on the electrochemical behavior of methanofullerene films. In TBAPF6 solution, when short chains, such as formic ether or butyl butyrate groups, were introduced into C60 cage, the film stability was less than that of C60. When the length of the alkyl chain was extended to butyl 12 alkanoate group, the film would not dissolve until the third reduction process because the long alkyl chain could inflect and encase the cations into the film. In KPF6 or NaClO4 solution, however, the solubility of the salt formed by K+ or Na+ with methanofullerene anion was higher than that formed by TBA+ with methanofullerene anion. Li+ (alkali metal) affected the behavior of the films in different ways. The possible electron‐transfer mechanisms of methanofullerene films in various supporting electrolyte solutions were presented. Furthermore, the film images observed by atomic force microscopy indicated that TBA+ and Li+ affected the behavior of the methanofullerene films in different ways. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3634–3640, 2006