Efficient and Highly Transparent Ultra-Thin Nickel-Iron Oxy-hydroxide Catalyst for Oxygen Evolution Prepared by Successive Ionic Layer Adsorption and Reaction

Ivan Garcia-Torregrosa, Andrey Goryachev, Jan P. Hofmann, Emiel J.M. Hensen, Bert M. Weckhuysen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

NiFeOx thin films prepared by successive ionic layer adsorption and reaction (SILAR) were deposited onto nanostructured hematite (Fe2O3) photoanodes and their effect on the current density and photo-onset potential was studied. After optimization of bath concentration, immersion times, and number of SILAR cycles, very conformal and active NiFeOx films with controlled Fe/Ni content ratios were obtained. Upon the incorporation of Fe2+ species in the NiCl2 solution bath, a cathodic shift in the overpotential required for the oxygen evolution reaction (OER) by more than 200 mV with no decrease in current density was observed after 40 SILAR cycles. We demonstrate that by fine-tuning the film composition and thickness, NiFeOx can be employed as an efficient OER catalyst with very low absorbance in the visible spectrum. By doing so, we demonstrate that this material has great potential for incorporation in semiconductor photoelectrodes for direct solar-driven water electrolysis. Being a simple water-based layer-by-layer growth method, SILAR offers promise for the synthesis of catalyst coatings in nano-structured and high surface area electrodes.

Original languageEnglish
Pages (from-to)1050-1054
Number of pages5
JournalChemPhotoChem
Volume3
Issue number10
DOIs
Publication statusPublished - 1 Oct 2019

Funding

We acknowledge financial support from the Dutch National Research School Combination Catalysis Controlled by Chemical Design (NRSC‐Catalysis) as well as from Utrecht University in the frame of a strategic alliance program on Solar Fuels with Eindhoven University of Technology (TU/e).

Keywords

  • catalysis
  • nickel-iron oxide
  • oxygen evolution
  • photoelectrochemistry
  • water splitting

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