Electron Spin‐Dependent Electrocatalysis for the Oxygen Reduction Reaction in a Chiro‐Self‐Assembled Iron Phthalocyanine Device

Author:

Scarpetta‐Pizo Laura1ORCID,Venegas Ricardo1ORCID,Barrías Pablo1,Muñoz‐Becerra Karina2ORCID,Vilches‐Labbé Nayareth1ORCID,Mura Francisco1ORCID,Méndez‐Torres Ana María1ORCID,Ramírez‐Tagle Rodrigo3,Toro‐Labbé Alejandro4,Hevia Samuel5,Zagal José H.1,Oñate Rubén1ORCID,Aspée Alexis1,Ponce Ingrid1ORCID

Affiliation:

1. Departamento de Ciencias del Ambiente Departamento Química de los Materiales Facultad de Química y Biología Universidad de Santiago de Chile Av. Libertador Bernardo O'Higgins 3363 Estación Central Santiago Chile

2. Centro Integrativo de Biología y Química Aplicada (CIBQA) Universidad Bernardo O'Higgins General Gana 1702 Santiago 8370854 Chile

3. Facultad de Ingeniería y Arquitectura Universidad Central de Chile Av. Sta. Isabel 1186 Santiago 8330563 Chile

4. Departamento de Química-Física Facultad de Química y de Farmacia Pontificia Universidad Católica de Chile Av. Vicuña Mackenna 4860, Macul Región Metropolitana Santiago Chile

5. Instituto de Física Centro de Investigación en Nanotecnología y Materiales Avanzados (CIEN-UC) Pontificia Universidad Católica de Chile Av. Vicuña Mackenna 4860 Santiago 6904411 Chile

Abstract

AbstractThe chiral‐induced spin selectivity effect (CISS) is a breakthrough phenomenon that has revolutionized the field of electrocatalysis. We report the first study on the electron spin‐dependent electrocatalysis for the oxygen reduction reaction, ORR, using iron phthalocyanine, FePc, a well‐known molecular catalyst for this reaction. The FePc complex belongs to the non‐precious catalysts group, whose active site, FeN4, emulates catalytic centers of biocatalysts such as Cytochrome c. This study presents an experimental platform involving FePc self‐assembled to a gold electrode surface using chiral peptides (L and D enantiomers), i.e., chiro‐self‐assembled FePc systems (CSAFePc). The chiral peptides behave as spin filters axial ligands of the FePc. One of the main findings is that the peptides′ handedness and length in CSAFePc can optimize the kinetics and thermodynamic factors governing ORR. Moreover, the D‐enantiomer promotes the highest electrocatalytic activity of FePc for ORR, shifting the onset potential up to 1.01 V vs. RHE in an alkaline medium, a potential close to the reversible potential of the O2/H2O couple. Therefore, this work has exciting implications for developing highly efficient and bioinspired catalysts, considering that, in biological organisms, biocatalysts that promote O2 reduction to water comprise L‐enantiomers.

Funder

Agencia Nacional de Investigación y Desarrollo

Departamento de Investigaciones Científicas y Tecnológicas, Universidad de Santiago de Chile

Publisher

Wiley

Subject

General Medicine

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