کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
218700 463215 2014 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mechanism of oxygen reduction by metallocenes near liquid|liquid interfaces
ترجمه فارسی عنوان
مکانیسم کاهش اکسیژن توسط فلز کلنها در نزدیکی مایع
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• Mechanistic ORR study at a w|DCE large interface using ferrocene derivatives.
• Simulated voltammograms compared to experimental ones to determine reaction rates.
• ORR consists of H+ transfer, aq. to org., followed by two chemical steps in org.
• Pathway is related to the classical EC-mechanism and facilitated ion transfer.
• Simulated chronoamperometry used to determine diffusion and reaction layers in org.

The mechanism of the oxygen reduction reaction (ORR) at a liquid|liquid interface, employing ferrocene (Fc) derivatives – such as decamethylferrocene (DMFc) – as a lipophilic electron donor along with sulfuric acid as an aqueous proton source, was elucidated through comparison of experimentally obtained cyclic voltammograms (CVs) to simulated CVs generated through COMSOL Multiphysics software which employs the finite element method (FEM). The simulations incorporated a potential dependent proton transfer (i.e. ion transfer, IT) step from the water (w) to organic (o) phases along with two homogeneous reactions (C1C2) occurring in the organic phase – an IT-C1C2 mechanism. The reaction of DMFc with H+(o) to form DMFc-hydride (DMFc-H+) was considered the first step (reaction 1), while reaction of DMFc-H+ with oxygen to form a peroxyl radical species, HO2, and DMFc+ was deemed the second step (reaction 2). Subsequent reactions, between HO2 and either DMFc or H+, were considered to be fast and irreversible so that 2 was a ‘proton-sink’, such that further reactions were not included; in this way, the simulation was greatly simplified. The rate of 1, kcf, and 2, kchem, were determined to be 5 × 102 and 1 × 104 L mol−1 s−1, respectively, for DMFc as the electron donor. Similarly, the rates of biphasic ORR for 1,1′-dimethylferrocene (DFc) and Fc were considered equivalent in terms of this reaction mechanism; therefore, their rates were determined to be 1 × 102 and 5 × 102 L mol−1 s−1 for 1 and 2, respectively. The reactive and diffusive layer thicknesses are also discussed.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Electroanalytical Chemistry - Volume 729, 1 September 2014, Pages 43–52
نویسندگان
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