Interplay Between Charge Accumulation and Oxygen Reduction Catalysis in Nanostructured TiO <sub>2</sub> Electrodes Functionalized with a Molecular Catalyst

نویسندگان

چکیده

The catalytic reduction of O2 by a manganese(III) porphyrin immobilized in nanostructured semiconductive transparent TiO2 electrode is here investigated UV-Vis spectroelectrochemistry an aqueous buffered medium. Analysis the operando spectroelectrochemical data, collected for both catalyst and matrix, demonstrates coexistence two faradaic electrochemical processes, namely (i) irreversible interfacial electron transfer from to triggering O2, (ii) reversible proton-coupled leading accumulation electrons bulk. competition between these processes modulated local concentration which itself varies with rate catalysis. Indeed, when locally strongly depleted catalysis, process switches catalysis charge storage, like battery. As result, stored were observed pursue even after polarization was switched-off (i. e., under open circuit). This overlooked phenomenon that we believe important consider applications relying on metal oxide-based photoelectrodes operating media.

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ژورنال

عنوان ژورنال: ChemElectroChem

سال: 2021

ISSN: ['2196-0216']

DOI: https://doi.org/10.1002/celc.202100424