Electrode potential-dependent colorimetric response of fluorescein-modified layer-by-layer films in the presence of hydrogen peroxide

• Published in: Journal of colloid and interface science Vol. 348; no. 2; pp. 441 - 445
• Main Authors: Nagasaka, Munenari, Yoshida, Kentaro, Sato, Katsuhiko, Hoshi, Tomonori, Anzai, Jun-ichi
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.08.2010
• Subjects: Colorimetric response; Colorimetry; Electrode potential; Electrodes; Fluorescein; Fluoresceins - chemistry; Hydrogen peroxide; Hydrogen Peroxide - analysis; Hydrogen Peroxide - chemistry; Hydrogen-Ion Concentration; Layer-by-layer film; Membranes, Artificial; Polyamines - chemistry; Polystyrenes - chemistry; Spectrophotometry, Ultraviolet; Layer-by-layer film; Hydrogen peroxide; Colorimetric response; Electrode potential; Fluorescein
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2010.05.013

UV–visible absorption spectrum of fluorescein-containing LbL film depends on the electric potential applied in the presence of H 2O 2. Layer-by-layer (LbL) thin films composed of fluorescein-modified poly(allylamine) (F-PAH) and poly(styrenesulfonic acid) (PSS) were prepared on the surface of an indium–tin oxide (ITO) electrode and the electrode potential-dependent colorimetric response of the LbL films was studied in the presence of hydrogen peroxide (H 2O 2). The LbL films were prepared by an alternate deposition of F-PAH and PSS on the surface through an electrostatic force of attraction. The LbL films exhibited a UV–visible absorption band around 500 nm originating from fluorescein residues in the film and the intensity of the absorption band depended on the pH of the solution to which the LbL film is exposed. The absorbance of the film was higher at neutral pH than that in weakly acidic solutions. The intensity of the absorption band decreased when an electrode potential higher than 0.6 V was applied in the presence of H 2O 2, while virtually no response was observed at lower electrode potential. The colorimetric response was suppressed in solutions with higher buffer capacity. The results were rationalized on the basis of the changes in local pH at the vicinity of the electrode surface, which in turn was induced by electrolysis of H 2O 2 on the electrode surface. A possible application of the system for colorimetric sensing of H 2O 2 was discussed.