Green synthesis of FeNi₃/FeNiOₓ nanosponges via aluminum cementation for PGM-free anion exchange membrane water electrolysis

Low-temperature anion exchange membrane water electrolyzer (AEMWE) is widely recognized as a highly promising approach for sustainable hydrogen production. Nevertheless, current membrane–electrode assemblies (MEAs) still achieve their best performance when employing platinum group metal (PGM)-based electrocatalysts, while PGM-free alternatives generally exhibit inferior activity. In this study, a straightforward and unified synthetic route is presented for the preparation of non-noble metal electrocatalysts suitable for both the hydrogen and oxygen evolution reactions (HER and OER). The resulting electrocatalysts are composed of FeNi₃/FeNiO x nanosponges and were produced by a straightforward two-step synthetic route in aqueous solution, exploiting aluminum powder as a cementation agent. The developed electrocatalyst delivers overpotentials of 97 mV for the HER and 254 mV for the OER at a current density of 10 mA cm⁻² in 1 M KOH, enabling a direct assessment of both mass-specific and geometric activities in comparison with PGM-based electrocatalysts. Beyond the initial electrochemical evaluation of the FeNi₃/FeNiO x material, the electrocatalyst was integrated into an MEA, operating as both the anode and the cathode and tested in an AEMWE. Under these conditions, the device achieved a cell voltage of 2.037 V at 1 A cm⁻² and 50 °C, without iR correction. Notably, the resulting PGM-free MEA exhibited superior performance relative to a benchmark configuration employing Pt/C at the cathode and RuO₂ at the anode, with a voltage reduction of 105 mV at 1 A cm⁻². Long-term operation was evaluated over 150 h under a discontinuous power profile to gain insight into degradation behavior relevant to industrial operation. These results highlight a simple and scalable approach to the synthesis of earth-abundant electrocatalysts enabling high-performance AEMWE.

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Journal
Electrochimica Acta
Published
2026-03-11
DOI
https://doi.org/10.1016/j.electacta.2026.148642
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
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article

Green synthesis of FeNi₃/FeNiOₓ nanosponges via aluminum cementation for PGM-free anion exchange membrane water electrolysis

Stiven Forti, Maddalena Corsini, Francesco Ruffo, Emmanuel De Gregorio et al.
Electrochimica Acta
Electrocatalysts for Energy Conversion
article

Green synthesis of FeNi₃/FeNiOₓ nanosponges via aluminum cementation for PGM-free anion exchange membrane water electrolysis

Stiven Forti, Maddalena Corsini, Francesco Ruffo, Emmanuel De Gregorio, Alessandro Tampucci, Camilla Coletti, Mohsin Muhyuddin, Antonio Rossi, Enrico Berretti, Oreste Tarallo, Carlo Santoro, Francesko Malaj, Domenico Lentini, Lorenzo Brogi, Gianluigi Baiardi, Raoul Cosenza
article en

Abstract

Low-temperature anion exchange membrane water electrolyzer (AEMWE) is widely recognized as a highly promising approach for sustainable hydrogen production. Nevertheless, current membrane–electrode assemblies (MEAs) still achieve their best performance when employing platinum group metal (PGM)-based electrocatalysts, while PGM-free alternatives generally exhibit inferior activity. In this study, a straightforward and unified synthetic route is presented for the preparation of non-noble metal electrocatalysts suitable for both the hydrogen and oxygen evolution reactions (HER and OER). The resulting electrocatalysts are composed of FeNi₃/FeNiO x nanosponges and were produced by a straightforward two-step synthetic route in aqueous solution, exploiting aluminum powder as a cementation agent. The developed electrocatalyst delivers overpotentials of 97 mV for the HER and 254 mV for the OER at a current density of 10 mA cm⁻² in 1 M KOH, enabling a direct assessment of both mass-specific and geometric activities in comparison with PGM-based electrocatalysts. Beyond the initial electrochemical evaluation of the FeNi₃/FeNiO x material, the electrocatalyst was integrated into an MEA, operating as both the anode and the cathode and tested in an AEMWE. Under these conditions, the device achieved a cell voltage of 2.037 V at 1 A cm⁻² and 50 °C, without iR correction. Notably, the resulting PGM-free MEA exhibited superior performance relative to a benchmark configuration employing Pt/C at the cathode and RuO₂ at the anode, with a voltage reduction of 105 mV at 1 A cm⁻². Long-term operation was evaluated over 150 h under a discontinuous power profile to gain insight into degradation behavior relevant to industrial operation. These results highlight a simple and scalable approach to the synthesis of earth-abundant electrocatalysts enabling high-performance AEMWE.

Electrochimica ActaVol. 560
University of Siena (IT), Scuola Normale Superiore (IT), Parthenope University of Naples (IT), Italian Institute of Technology (IT), Nello Carrara Institute of Applied Physics (IT), Institute for the Chemistry of OrganoMetallic Compounds (IT), Federico II University Hospital (IT), Center for Nanotechnology Innovation (IT), University of Milano-Bicocca (IT), University of Naples Federico II (IT)
Industry, innovation and infrastructure
Openalex Percentile: Top 29%
Electrocatalysts for Energy Conversion
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