Browsing by Author "Vilches-Labbe, Nayareth"

Now showing 1 - 2 of 2
  • No Thumbnail Available
    Item
    Cover Picture: Electron Spin-Dependent Electrocatalysis for the Oxygen Reduction Reaction in a Chiro-Self-Assembled Iron Phthalocyanine Device (Angew. Chem. Int. Ed. 4/2024)
    (2024) Scarpetta-Pizo, Laura; Venegas, Ricardo; Barrias, Pablo; Munoz-Becerra, Karina; Vilches-Labbe, Nayareth; Mura, Francisco; Mendez-Torres, Ana Maria; Ramirez-Tagle, Rodrigo; Toro-Labbe, Alejandro; Hevia, Samuel; Zagal, Jose H.; Onate, Ruben; Aspee, Alexis; Ponce, Ingrid
  • No Thumbnail Available
    Item
    Electron Spin-Dependent Electrocatalysis for the Oxygen Reduction Reaction in a Chiro-Self-Assembled Iron Phthalocyanine Device
    (2023) Scarpetta-Pizo, Laura; Venegas, Ricardo; Barrias, Pablo; Munoz-Becerra, Karina; Vilches-Labbe, Nayareth; Mura, Francisco; Mendez-Torres, Ana Maria; Ramirez-Tagle, Rodrigo; Toro-Labbe, Alejandro; Hevia, Samuel; Zagal, Jose H.; Onate, Ruben; Aspee, Alexis; Ponce, Ingrid
    The 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.