Insights into the electronic structure of Fe penta-coordinated complexes. Spectroscopic examination and electrochemical analysis for the oxygen reduction and oxygen evolution reactions

César Zúñiga Loyola, Gabriel Abarca, Soledad Ureta-Zañartu, Carolina Aliaga, Jose H. Zagal, Moulay Tahar Sougrati, Frédéric Jaouen, Walter Orellana, Federico Tasca

Resultado de la investigación: Contribución a una revistaArtículorevisión exhaustiva

4 Citas (Scopus)

Resumen

Fe phthalocyanine was coordinated to pyridine-modified carbon nanotubes and studied as a catalyst for the oxygen reduction (ORR) and oxygen evolution reactions (OER). X-ray photoelectron spectroscopy (XPS), Mössbauer, and electron paramagnetic resonance spectroscopy (EPR) analysis supported that pyridine acts as an axial ligand to yield penta-coordinated catalytic active Fe sites. The impedance analyses show an increase in the double-layer capacitance (Cdl) value, corroborating the adsorption of the complexes to give FePc-Py-CNT. The evaluation of the electrocatalytic activity for the ORR was performed in both acid (0.1 M H2SO4) and basic (0.1 M KOH) media, while the evaluation of the OER activity was investigated only in alkaline medium. DFT studies revealed an increased length in the Fe-N binding of the pentacoordinate Fe-based site, leading to a decreased O2-Fe binding energy, explaining the higher ORR and OER activity of FePc-Py-CNT relative to FePc-CNT.

Idioma originalInglés
Páginas (desde-hasta)23802-23816
Número de páginas15
PublicaciónJournal of Materials Chemistry A
Volumen9
N.º42
DOI
EstadoPublicada - 14 nov. 2021

Áreas temáticas de ASJC Scopus

  • Química (todo)
  • Energías renovables, sostenibilidad y medio ambiente
  • Ciencia de los materiales (todo)

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