posted on 2025-10-18, 02:14authored byJosé Manuel Luque-Centeno, Álvaro Carmo-Delcán, Mikel Martínez-Olaizola, Celia Gómez-Sacedón, Antonio de Lucas-Consuegra, Agustín
R. González-Elipe, Francisco Yubero, José Javier Brey Sánchez, Jorge Gil-Rostra
This manuscript reports on a Ni/Fe-based bilayer catalyst
developed
to boost the oxygen evolution reaction in anion exchange membrane
water electrolyzers. The electrochemical behavior toward the oxygen
evolution reaction of several NiFe/NiFeO metal–oxide bilayer
catalysts, prepared by magnetron sputtering at oblique angle deposition
(MS-OAD) on a flat stainless-steel substrate, was assessed in a three-electrode
electrochemical cell in comparison with the behavior of both a metal
NiFe and an oxide NiFeOx single-layer catalyst. The morphology and
chemical nature of these catalysts, as prepared and after electrochemical
usage, were characterized by X-ray photoelectron spectroscopy, Raman
spectroscopy, Fourier transform infrared spectroscopy, and scanning
electron microscopy. A thorough electrochemical characterization of
the different catalyst formulations revealed a higher efficiency for
the bilayer catalysts, in terms of both activity and long-term stability,
and provided some clues to account for this superior performance in
terms of morphology and surface reactivity of each catalyst. As a
proof of concept, the best-performing bilayer configuration was then
deposited onto a stainless steel felt porous transport layer (PTL)
substrate and tested as an ionomer-free anode electrode in a membrane
electrode assembly (MEA). Results revealed that the MS-OAD catalysts
performed well when deposited on PTLs and that, under this configuration,
a bilayer catalyst anode is slightly more efficient than the NiFe
single-layer catalyst. Additionally, the possibility of scaling up
the MS-OAD procedure to large areas has been demonstrated by the preparation
of the bilayer catalysts on a 64 cm<sup>2</sup> PTL and its successful
integration and operation in a large prototype single cell.