Methyl Viologen Mediated Oxygen Reduction in Ethanol Solvent: the Electrocatalytic Reactivity of the Radical Cation

التفاصيل البيبلوغرافية
العنوان: Methyl Viologen Mediated Oxygen Reduction in Ethanol Solvent: the Electrocatalytic Reactivity of the Radical Cation
المؤلفون: Richard G. Compton, Qianqi Lin, Qian Li, Christopher Batchelor-McAuley
المصدر: Journal of Electrochemical Science and Technology. 4:71-80
بيانات النشر: The Korean Electrochemical Society, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Inorganic chemistry, chemistry.chemical_element, Rate-determining step, Electrochemistry, Photochemistry, Oxygen, Redox, Catalysis, chemistry.chemical_compound, Reaction rate constant, chemistry, Radical ion, Hydrogen peroxide
الوصف: The study of methyl viologen (MV 2+ ) mediated oxygen reduction in electrolytic ethanol media possesses potential application in the electrochemical synthesis of hydrogen peroxide mainly due to the advantages of the much increased solubility of molecular oxygen (O 2 ) and high degree of reversibility of MV 2+/•+ redox couple. The diffusion coefficients of both MV 2+ and O 2 were investigated via electrochemical tech-niques. For the first time, MV 2+ mediated O 2 reduction in electrolytic ethanol solution has been proved to be feasible on both boron-doped diamond and micro-carbon disc electrodes. The electrocatalytic response is demonstrated to be due to the radical cation, MV •+ . The homogeneous electron transfer step is suggested to be the rate determining step with a rate constant of (1 ± 0.1) × 10 5 M − 1 s − . With the aid of a simulation program describing the EC’ mechanism, by increasing the concentration ratio of MV 2+ to O 2 electrochemical catalysis can be switched from a partial to a ‘total catalysis’ regime.Keywords: Methyl viologen, mediated oxygen reduction, ethanolic solution, diffusion coefficient and concentration of oxygen, homogeneous rate constant
تدمد: 2093-8551
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::182220365fc2d0d408f5dc75d60852f4
https://doi.org/10.5229/jecst.2013.4.2.71
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....182220365fc2d0d408f5dc75d60852f4
قاعدة البيانات: OpenAIRE