Issue 20, 2024

Strongly facet-dependent activity of iron-doped β-nickel oxyhydroxide for the oxygen evolution reaction

Abstract

Iron (Fe)-doped β-nickel oxyhydroxide (β-NiOOH) is a highly active, noble-metal-free electrocatalyst for the oxygen evolution reaction (OER), with the latter being the bottleneck in electrochemical water splitting for sustainable hydrogen production. The mechanisms underlying how the Fe dopant modulates this host material's water electro-oxidation activity are still not entirely clear. Here, we combine hybrid density functional theory (DFT) and Hubbard-corrected DFT to investigate the OER activity of the most thermodynamically favorable (and therefore, expected to be the majority) crystallographic facets of β-NiOOH, namely (0001) and (10[1 with combining macron]0). By considering active sites involving both oxidation and reduction of the transition-metal active center during the redox cycle on these two different facets, we show that six-fold-lattice-coordinated Fe in β-NiOOH is redox inactive towards both oxidation and reduction while five-fold-lattice-coordinated Fe in β-NiOOH does exhibit redox activity. However, the determined redox activity of Fe (or lack of it) is not indicative of good (or bad) performance as a dopant on these two facets. Three of the four active sites investigated (oxo and hydroxo sites on (0001) and a hydrated site on (10[1 with combining macron]0)) exhibit only a marginal (<0.1 V) decrease or increase in the thermodynamic overpotential upon doping with Fe. Only one of the redox-active sites investigated, the hydroxo site on (10[1 with combining macron]0), exhibits a large attenuation in the thermodynamic overpotential upon doping (to ∼0.52 V from 0.86 V), although the doped overpotential is larger than that observed experimentally for Fe-doped NiOOH. Thus, although pure β-NiOOH facets containing four-, five-, or six-fold lattice-coordinated Ni sites have roughly equal OER activities, yielding similar OER onset potentials (shown in A. Govind Rajan, J. M. P. Martirez and E. A. Carter, J. Am. Chem. Soc., 2020, 142, 3600–3612), only those facets containing four-fold lattice-coordinated Fe (e.g., as shown in J. M. P. Martirez and E. A. Carter, J. Am. Chem. Soc., 2019, 141, 693–705) would be active under analogous conditions for the Fe-doped material. It follows that, while undoped β-NiOOH demonstrates a roughly facet-independent oxygen evolution activity, the activity of Fe-doped β-NiOOH strongly depends on the crystallographic facet. Our study further motivates the investigation of strategies for the selective growth of facets with low iron coordination number to enhance the water splitting activity of Fe-doped β-NiOOH.

Graphical abstract: Strongly facet-dependent activity of iron-doped β-nickel oxyhydroxide for the oxygen evolution reaction

Supplementary files

Article information

Article type
Paper
Submitted
23 1 2024
Accepted
11 4 2024
First published
12 4 2024
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2024,26, 14721-14733

Strongly facet-dependent activity of iron-doped β-nickel oxyhydroxide for the oxygen evolution reaction

A. Govind Rajan, J. M. P. Martirez and E. A. Carter, Phys. Chem. Chem. Phys., 2024, 26, 14721 DOI: 10.1039/D4CP00315B

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