Hydrogen Peroxide Generation at Liquid|Liquid Interface under Conditions Unfavorable for Proton Transfer from Aqueous to Organic Phase
PBN-AR
Instytucja
Instytut Chemii Fizycznej Polskiej Akademii Nauk
Informacje podstawowe
Główny język publikacji
en
Czasopismo
Journal of Physical Chemistry C
ISSN
1932-7447
EISSN
1932-7455
Wydawca
AMER CHEMICAL SOC
DOI
URL
Rok publikacji
2013
Numer zeszytu
40
Strony od-do
20681-20688
Numer tomu
117
Identyfikator DOI
Liczba arkuszy
Streszczenia
Język
en
Treść
The charge transfer processes across the interface between two immiscible electrolyte solutions (ITIES) can be employed for energy storage and conversion, solvent extraction, or sensing or in life sciences. Among them are catalytic reactions, which have only been recently studied. Here H2O2 generation is studied with decamethylferrocene (DMFc) as electron donor at the interface between tetrahexylammonium perchlorate solution in 1,2-dichloroethane (1,2-DCE) and aqueous HClO4. These conditions are unfavorable for proton transfer across ITIES because of positive Galvani potential difference. Voltammetry with 1,2-DCE droplet modified electrode shows that DMFc oxidation is accompanied by ClO4– insertion into the organic phase. The reaction progress was followed by UV–vis spectroscopy, voltammetry, and scanning electrochemical microscopy (SECM). In the first and last method, horseradish peroxidase was used as catalyst. It is concluded that O2 is reduced to H2O2 at the liquid|liquid interface not only under conditions when proton transfer to organic phase is strongly favored, namely, when Galvani potential difference is negative (Angew. Chem., Int. Ed. 2008, 47, 4675−4678).
Cechy publikacji
ORIGINAL_ARTICLE
Inne
System-identifier
673924
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