Insights into the electronic structure of Fe penta-coordinated complexes. Spectroscopic examination and electrochemical analysis for the oxygen reduction and oxygen evolution reactions. Issue 42 (1st October 2021)

• Record Type: Journal Article
• Authors: Loyola, César Zúñiga; Abarca, Gabriel; Ureta-Zañartu, Soledad; Aliaga, Carolina; Zagal, Jose H.; Sougrati, Moulay Tahar; Jaouen, Frédéric; Orellana, Walter; Tasca, Federico
• Is Part Of: Journal of materials chemistry. Volume 9:Issue 42(2021)
• Page Start: 23802
• Page End: 23816
• Publication Date: 2021-10-01
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d1ta05991b
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Fe penta-coordinated complexes are exceptionally good electrocatalysts for the oxygen reduction and evolution reactions. Spectroscopical and electrochemical studies show the reasons. Abstract : 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 ( C dl ) 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 H2 SO4 ) 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.