An electrogenerated chemiluminescence (ECL) system by in situ coreactant production, where Ru(bpy)32+ emission is generated at a boron-doped diamond (BDD) electrode, is presented. The system takes advantage of the unique properties of BDD to promote oxidation of carbonate (CO32-) into peroxydicarbonate (C2O62-), which further reacts with water to form hydrogen peroxide (H2O2), which acts as a coreactant for Ru(bpy)32+ ECL. Investigation of the mechanism reveals that ECL emission is triggered by the reduction of H2O2 to hydroxyl radicals (OH•), which later react with the reduced Ru(bpy)3+ molecules to form excited states, followed by light emission. The ECL signal was found to increase with the concentration of CO32- therefore, with the concentration of electrogenerated H2O2, although at the same time, higher concentrations of H2O2 can quench the ECL emission, resulting in a decrease in intensity. The carbonate concentration, pH, and oxidation parameters, such as potential and time, were optimized to find the best emission conditions.

Electrogenerated Chemiluminescence by in Situ Production of Coreactant Hydrogen Peroxide in Carbonate Aqueous Solution at a Boron-Doped Diamond Electrode / Irkham; Fiorani A.; Valenti G.; Kamoshida N.; Paolucci F.; Einaga Y.. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - ELETTRONICO. - 142:3(2020), pp. 1518-1525. [10.1021/jacs.9b11842]

Electrogenerated Chemiluminescence by in Situ Production of Coreactant Hydrogen Peroxide in Carbonate Aqueous Solution at a Boron-Doped Diamond Electrode

Valenti G.;Paolucci F.;
2020

Abstract

An electrogenerated chemiluminescence (ECL) system by in situ coreactant production, where Ru(bpy)32+ emission is generated at a boron-doped diamond (BDD) electrode, is presented. The system takes advantage of the unique properties of BDD to promote oxidation of carbonate (CO32-) into peroxydicarbonate (C2O62-), which further reacts with water to form hydrogen peroxide (H2O2), which acts as a coreactant for Ru(bpy)32+ ECL. Investigation of the mechanism reveals that ECL emission is triggered by the reduction of H2O2 to hydroxyl radicals (OH•), which later react with the reduced Ru(bpy)3+ molecules to form excited states, followed by light emission. The ECL signal was found to increase with the concentration of CO32- therefore, with the concentration of electrogenerated H2O2, although at the same time, higher concentrations of H2O2 can quench the ECL emission, resulting in a decrease in intensity. The carbonate concentration, pH, and oxidation parameters, such as potential and time, were optimized to find the best emission conditions.
2020
Electrogenerated Chemiluminescence by in Situ Production of Coreactant Hydrogen Peroxide in Carbonate Aqueous Solution at a Boron-Doped Diamond Electrode / Irkham; Fiorani A.; Valenti G.; Kamoshida N.; Paolucci F.; Einaga Y.. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - ELETTRONICO. - 142:3(2020), pp. 1518-1525. [10.1021/jacs.9b11842]
Irkham; Fiorani A.; Valenti G.; Kamoshida N.; Paolucci F.; Einaga Y.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/721927
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