One-Pot Synthesis of Pt–Fe for EOR: Effect of pH

Abstract The development of efficient electrocatalysts for the ethanol oxidation reaction (EOR) remains a major challenge for direct ethanol fuel cells (DEFCs) due to slow kinetics and catalyst poisoning by reaction intermediates. Herein, Pt/C and Pt–Fe/C catalysts were prepared via a one-pot polyol synthesis, and the effect of pH on Fe incorporation and catalytic performance was investigated. X-ray diffraction showed lattice contraction in Pt–Fe catalysts, confirming Fe incorporation, which was more pronounced under alkaline conditions. Electrochemical measurements demonstrated a strong dependence on both Fe addition and pH. Pt–Fe/C at pH 11.4 achieved a mass activity density of 850 A/gPt, outperforming not only Pt–Fe/C neutral and Pt/C but also the commercial Pt/C catalyst at 20 mV/s. Moreover, a lower onset potential (0.479 V) and a higher If/Ib ratio (1.9) indicate faster reaction kinetics and qualitatively suggest tolerance to adsorbed intermediates. The enhanced performance is attributed to the synergistic effect of Fe incorporation through electronic and bifunctional mechanisms.

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Publication Details

Journal
ACS Omega
Published
2026-10-19
DOI
https://doi.org/10.1021/acsomega.6c09204
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
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article

One-Pot Synthesis of Pt–Fe for EOR: Effect of pH

Giuseppina Luciani, Almerinda Di Benedetto, Maria Portarapillo, Marco Antonio Di Francia et al.
ACS Omega
Electrocatalysts for Energy Conversion
article

One-Pot Synthesis of Pt–Fe for EOR: Effect of pH

Giuseppina Luciani, Almerinda Di Benedetto, Maria Portarapillo, Marco Antonio Di Francia, Antonella Gianna Tesone
article en

Abstract

Abstract The development of efficient electrocatalysts for the ethanol oxidation reaction (EOR) remains a major challenge for direct ethanol fuel cells (DEFCs) due to slow kinetics and catalyst poisoning by reaction intermediates. Herein, Pt/C and Pt–Fe/C catalysts were prepared via a one-pot polyol synthesis, and the effect of pH on Fe incorporation and catalytic performance was investigated. X-ray diffraction showed lattice contraction in Pt–Fe catalysts, confirming Fe incorporation, which was more pronounced under alkaline conditions. Electrochemical measurements demonstrated a strong dependence on both Fe addition and pH. Pt–Fe/C at pH 11.4 achieved a mass activity density of 850 A/gPt, outperforming not only Pt–Fe/C neutral and Pt/C but also the commercial Pt/C catalyst at 20 mV/s. Moreover, a lower onset potential (0.479 V) and a higher If/Ib ratio (1.9) indicate faster reaction kinetics and qualitatively suggest tolerance to adsorbed intermediates. The enhanced performance is attributed to the synergistic effect of Fe incorporation through electronic and bifunctional mechanisms.

ACS Omega
University of Naples Federico II (IT)
Openalex Percentile: Top 34%
Electrocatalysts for Energy Conversion
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