Issue 57, 2025, Issue in Progress

Easy access to Fe2N nanomaterials from Fe nanocrystals and investigation of their electrocatalytic properties for the water electrolysis and CO2 reduction

Abstract

The nanostructured iron nitride phases, comprising only non-toxic and abundant elements, show potential in a wide range of applications, and are thus of great interest in the context of sustainable development. Especially, the nanostructured ε-FexN phase (x = 2–3) can play the role of electrocatalyst (in fuel cells or for hydrogen production), or of anode in Li-ion batteries. However, obtaining morphology and composition (x) controlled nanoparticles of this phase is challenging. Here we show that α-Fe nanoparticles produced by an organometallic approach can be nitridated by a simple exposure to an ammonia flow in mild conditions of temperature, either in the powder form or as thin layers on FTO electrodes while keeping their initial morphology. Structural and magnetic measurements, combined with chemical analysis, and spectroscopic investigations evidenced the formation of the pure ε-Fe2N phase, with a preserved nanostructure. The electrocatalytic activity of this nanomaterial has been evaluated for CO2 reduction and for the oxygen evolution reaction. These results may open new perspectives for studying the properties and reactivity of ε-Fe2N nanomaterials, and promote their use.

Graphical abstract: Easy access to Fe2N nanomaterials from Fe nanocrystals and investigation of their electrocatalytic properties for the water electrolysis and CO2 reduction

Supplementary files

Article information

Article type
Paper
Submitted
22 Oct 2025
Accepted
27 Nov 2025
First published
09 Dec 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 48862-48875

Easy access to Fe2N nanomaterials from Fe nanocrystals and investigation of their electrocatalytic properties for the water electrolysis and CO2 reduction

A. Edalat, L. Vendier, C. Amiens, M. Respaud, P. Roblin, J. Esvan, Q. T. Nguyen, D. N. Nguyen, V. T. Tran, L. T. Le, P. D. Tran and F. Dumestre, RSC Adv., 2025, 15, 48862 DOI: 10.1039/D5RA08111D

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