Electropolymerization of thionine in neutral aqueous media and H2O2 biosensor based on poly(thionine)

Citation
R. Yang et al., Electropolymerization of thionine in neutral aqueous media and H2O2 biosensor based on poly(thionine), ELECTR ACT, 44(10), 1999, pp. 1585-1596
Citations number
38
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ELECTROCHIMICA ACTA
ISSN journal
00134686 → ACNP
Volume
44
Issue
10
Year of publication
1999
Pages
1585 - 1596
Database
ISI
SICI code
0013-4686(1999)44:10<1585:EOTINA>2.0.ZU;2-Z
Abstract
A novel two-step method is presented for the electropolymerization of thion ine in neutral phosphate buffer solutions containing 1 x 10(-4) M thionine on glassy carbon electrode surfaces. The formation of the PTH film is depen dent on the preanodization voltage and occurs only on a GCE surface, The pr eanodization operation is critical. During this period, a large amount of p ositive charge can be accumulated on the GCE surface and is used to create the thionine cation radical for the electropolymerization of thionine. The poly(thionine) (PTH)-modified electrode obtained in this manner has a golde n, fairly even film, which is firm and permanent. Strong treatment in an ul trasonic bath for 20 min does not affect the voltammetric redox peaks of PT H. The E-0' decreases by 55 mV/pH between pH 6 and 8 for the immobilized PT H, which is close to the expected Nernstian value of 59 mV for a two-electr on, two-proton process. The PTH-modified electrodes show linear dependence of peak current with scan rate within the range of 20 to 100 mV s(-1). A H2 O2 biosensor was fabricated by using Nafion membranes with enzyme. The cata lytic reaction towards H2O2 reduction occurring on the H2O2 sensor in the p resence of 1 mM H2O2 demonstrated that the film of PTH can effectively shut tle electrons between the redox center of HRP and the base electrode. (C) 1 999 Published by Elsevier Science Ltd. All rights reserved.