• Minjauw, Matthias
• Detavernier, Christophe
• Blomme, Ruben
• Vereecken, Philippe
• Dendooven, Jolien
• Henderick, Lowie
• Adriaens, Mieke
• Ramesh, Rahul

Abstract

Transition metal phosphates are promising catalysts for the oxygen evolution reaction (OER) in alkaline medium. Herein, Fe-doped Ni phosphates are deposited using plasma-enhanced atomic layer deposition (PE-ALD) at 300 degrees C. A sequence of f Fe phosphate PE-ALD cycles and n Ni phosphate PE-ALD cycles is repeated x times. The Fe to Ni ratio can be controlled by the cycle ratio (f/n), while the film thickness can be controlled by the number of cycles (x times (n+f )). 30 nm films with an Fe/Ni ratio of similar to 10% and similar to 37%, respectively, are evaluated in 1.0 M KOH solution. Remarkably, a significant difference in OER activity is found when the order of the Ni and Fe phosphate PE-ALD cycles in the deposition sequence is reversed. A 20%-45% larger current density is obtained for catalysts grown with an Fe phosphate PE-ALD cycle at the end compared to the Ni phosphate-terminated flavour. We attribute this to a higher concentration of Fe centers on the surface, as a consequence of the specific PE-ALD approach. Secondly, increasing the thickness of the catalyst films up to 160 nm results in an increase of the OER current density and active surface area, suggesting that the as-deposited smooth and continuous films are converted into electrolyte-permeable structures during catalyst activation and operation. This work demonstrates the ability of PE-ALD to control both the surface and bulk composition of thin film electrocatalysts, offering valuable opportunities to understand their impact on performance.

Topics

• density
• impedance spectroscopy
• surface
• nickel
• thin film
• Oxygen
• chemical composition
• iron
• activation
• current density
• atomic layer deposition