Nitrogen-doped mesoporous carbons containing a small amount of Fe (Fe-N-MC) are prepared from a low-cost carbon source (agarose) together with nitrogen and iron precursors. The synthesis consists in the formation of a hydrogel embedding FeCl2 or tris(1,10-phenanthroline)iron(II)dichloride (Fe(Phen)3Cl2), which after a freeze-drying treatment, is pyrolyzed at 400 °C to give a crude product, which is further graphitized at high temperature. The formation of a hydrogel assures an optimal Fe dispersion and an optimal surface area and pore network after pyrolysis, as evaluated by N2 adsorption-desorption isotherms. The final product is further activated by treatment in KOH at 750 °C or in H2SO4 at 100 °C followed by H2 reduction at 700 °C. Both treatments allow to increase the surface area and pore volume, and to expose Fe-Nx active sites, as confirmed by both XPS and Mössbauer spectroscopies. The Fe-N-MC catalytic performances towards oxygen reduction reaction are investigated by electrochemical techniques in 0.1 M HClO4, attesting that O2 is reduced following an almost 4e- pathway at very positive potentials (0.8 V vs RHE). The effect most influencing the catalytic activity is found to be the employment of Fe(Phen)3Cl2 instead of FeCl2 +1,10-phenanthroline for the generation of Fe-Nx active sites.

Platinum-free electrocatalysts for oxygen reduction reaction: Fe-Nx modified mesoporous carbon prepared from biosources

Nodari L;
2018

Abstract

Nitrogen-doped mesoporous carbons containing a small amount of Fe (Fe-N-MC) are prepared from a low-cost carbon source (agarose) together with nitrogen and iron precursors. The synthesis consists in the formation of a hydrogel embedding FeCl2 or tris(1,10-phenanthroline)iron(II)dichloride (Fe(Phen)3Cl2), which after a freeze-drying treatment, is pyrolyzed at 400 °C to give a crude product, which is further graphitized at high temperature. The formation of a hydrogel assures an optimal Fe dispersion and an optimal surface area and pore network after pyrolysis, as evaluated by N2 adsorption-desorption isotherms. The final product is further activated by treatment in KOH at 750 °C or in H2SO4 at 100 °C followed by H2 reduction at 700 °C. Both treatments allow to increase the surface area and pore volume, and to expose Fe-Nx active sites, as confirmed by both XPS and Mössbauer spectroscopies. The Fe-N-MC catalytic performances towards oxygen reduction reaction are investigated by electrochemical techniques in 0.1 M HClO4, attesting that O2 is reduced following an almost 4e- pathway at very positive potentials (0.8 V vs RHE). The effect most influencing the catalytic activity is found to be the employment of Fe(Phen)3Cl2 instead of FeCl2 +1,10-phenanthroline for the generation of Fe-Nx active sites.
2018
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
Inglese
402
434
446
https://www.sciencedirect.com/science/article/pii/S0378775318310322?via%3Dihub
Sì, ma tipo non specificato
Agarose
Iron
Nitrogen-doped
Non-PGM
Oxygen reduction reaction
Highlights o Fe-N-C catalysts were synthetized from agarose dry hydrogel and Fe(Phen)3Cl2. o The employment of a gel allowed a very homogeneous dispersion of the precursors. o Fe-Nx and Fe3C active sites were determined by both XPS and Mössbauer analyses. o Fe-N-C900C showed high mass activity and E1/2 and a quasi-four-electron ORR process.
10
info:eu-repo/semantics/article
262
Daniel, G; Foltran, E; Brandiele, R; Nodari, L; Pilot, R; Menna, E; Rizzi, Ga; Ahmed Isse, A; Durante, C; Gennaro, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/344346
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