Electrochemistry and electrochromic properties of phenanthroline-iron(II/III) complex films
Autor: | Kazuya Kawase, Hiroshi Inaba, Mako Kitagawa, Noboru Oyama |
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Rok vydání: | 1994 |
Předmět: |
Aqueous solution
Polymers and Plastics Chemistry Supporting electrolyte Phenanthroline Organic Chemistry Inorganic chemistry Quartz crystal microbalance Condensed Matter Physics Electrochemistry Redox Metal chemistry.chemical_compound Electrochromism visual_art Materials Chemistry visual_art.visual_art_medium |
Zdroj: | Macromolecular Symposia. 80:337-351 |
ISSN: | 1022-1360 |
DOI: | 10.1002/masy.19940800123 |
Popis: | New films of the iron complexes with bis((2-hydroxyphenyl)methylaminosulfonyl)bathophenanthroline(HPBP) and bis((2-aminophenyl)methylaminosulfonyl)bathophenanthroline(APBP) ligands are prepared on the electrode surfaces by electrochemical polymerization. The resulting film-coated electrode shows a well-defined reversible voltammogram corresponding to the redox reaction of the Fe(II/III) complexes and an electrochromic change from red(absorption maximum: 540 nm) to colorless. The response rate of the color change to a potential step was found to be correlated to the apparent diffusion coefficient(Dapp) for the homogeneous charge-transport process within the film. The Dapp values estimated are (3-4) × 10−9cm2s−1 for the [Fe(APBP)3] film and(1-2) × 10−8cm2s−2 for the [Fe(HPBP)3] film, respectively, by potential-step chronoamperometric and chronocoulometric methods. The result of electrochemical quartz crystal microbalance(EQCM) measurements4) and dependence of the formal potential of the metal complex of the Fe(II/III) redox couple with activity of the supporting electrolyte anion in NaClO4 aqueous solution showed that anion, cation, and solvent move simultaneously across the polymer film/solution interface during the redox reaction. A piezoelectric admittance measurement4) of the poly[Fe(APBP)3] coated quartz crystal electrode showed that the viscosity of the film is affected by the oxidation state of iron. |
Databáze: | OpenAIRE |
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