INVESTIGATION OF ELECTROCHEMICAL-BEHAVIOR AND MASS-TRANSFER PROCESS OF FERROCENE SILOXANE POLYMER FILM USING QUARTZ-CRYSTAL ELECTRODE METHOD

Authors
Citation
S. Ikeda et N. Oyama, INVESTIGATION OF ELECTROCHEMICAL-BEHAVIOR AND MASS-TRANSFER PROCESS OF FERROCENE SILOXANE POLYMER FILM USING QUARTZ-CRYSTAL ELECTRODE METHOD, Analytical chemistry, 65(14), 1993, pp. 1910-1915
Citations number
36
Categorie Soggetti
Chemistry Analytical
Journal title
ISSN journal
00032700
Volume
65
Issue
14
Year of publication
1993
Pages
1910 - 1915
Database
ISI
SICI code
0003-2700(1993)65:14<1910:IOEAMP>2.0.ZU;2-9
Abstract
The electrochemical behavior of a redox-active ferrocene-modified silo xane polymer (PSF) which is capable of acting as an electron mediator for flavin enzymes was examined. By cyclic voltammetry, it was reveale d that the redox activity of PSF film was strongly affected by anionic species in the soaking solution. While a highly stable current respon se corresponding to the ferrocene/ferricinium (Fc0/Fc+) redox couple o f the film was observed in NaClO4 or NaBF4 supporting electrolyte solu tions, the current response gradually decreased by cycling of the pote ntial in an aqueous solution of NaCl, NaNO3, sodium p-toluenesulfonate , or phosphate buffer. The result of electrochemical quartz crystal mi crobalance (EQCM) measurements and dependence of the formal potential of the Fc0/Fc+ redox couple with activity of the supporting electrolyt e anion in NaClO4 aqueous solution showed that anion, cation, and solv ent move simultaneously across the polymer film/solution interface dur ing the redox reaction. A piezoelectric admittance measurement of the PSF-coated quartz crystal electrode in NaClO4 solution showed that the viscosity of the PSF film is little affected by successive redox cycl ing and by its redox state; that is, the rigidity of the film is maint ained. Whereas, in a solution of NaNO3 or phosphate buffer, significan t changes in the physical and/or chemical properties of the PSF film, which may be correlated to electrochemical inactivation, were observed .