Reactivity descriptors for Cu bis-phenanthroline catalysts for the hydrogen peroxide reduction reaction

Following previous studies where the metal-centered redox potentials of MN4 complexes are proposed as a reactivity descriptor for different electrochemical reactions, in the present work we expand this idea to a series of substituted Cu(I)-phenanthrolines adsorbed on glassy carbon electrodes as cata...

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Published in:Electrochimica acta Vol. 357; p. 136881
Main Authors: Muñoz-Becerra, Karina, Báez, Daniela F., Zagal, José H., Bollo, Soledad, Toro-Labbé, Alejandro, Venegas, Ricardo, Recio, F. Javier
Format: Journal Article
Language:English
Published: Oxford Elsevier Ltd 10-10-2020
Elsevier BV
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Summary:Following previous studies where the metal-centered redox potentials of MN4 complexes are proposed as a reactivity descriptor for different electrochemical reactions, in the present work we expand this idea to a series of substituted Cu(I)-phenanthrolines adsorbed on glassy carbon electrodes as catalysts for the hydrogen peroxide reduction reaction (HPRR) in aqueous media. As the foot of the wave for HPRR on Cu-based modified electrodes is closely related to the Cu(II)/Cu(I) formal potential, we have found a linear correlation between the catalytic activity expressed as (log i)E and the E°'Cu(II)/Cu(I) redox potential of the complexes with a slope (dE°/dlogi)E close to +0.120 V dec−1, showing that the catalytic activity increases with the shift of E°'Cu(II)/Cu(I) to more positive potentials as a result of the electron-withdrawing nature of the substituents on the ligands. Moreover, the theoretical differences in the calculated chemical potentials (Δμ) of the reactive species follow a similar trend with the E°'Cu(II)/Cu(I) where a positive shift of this parameter is related with a higher Δμ and in consequence, with high catalytic activity. Furthermore, this strategy can be used for the smart design of biosensors as it was shown by the electroanalytical results. [Display omitted]
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2020.136881