Low Pt Loading onWolframite-Type NiWO<sub>4</sub> to Excel the Electrocatalytic WaterSplitting and Ammonia OxidationReaction

Hydrogen production via water-splitting or ammonia electrolysis using transition metal-based electrodes is one of the most cost-effective approaches. Herein, ca. 1–4% of Pt atoms are stuffed into a wolframite-type NiWO<sub>4</sub> lattice to improve the electrocatalytic efficiency. The co-existence of atomically dilute quantities of Pt<sup>0</sup> and Pt<sup>IV</sup> atoms in the NiWO<sub>4</sub> without altering the lattice structure is established via powder X-ray diffraction, inductively coupled plasma mass spectrometry (ICP-MS), core-level X-ray photoelectron spectroscopy, and other spectroscopic studies. While the undoped NiWO<sub>4</sub> and a physical mixture of Pt<sup>0</sup> (2 wt %) and NiWO<sub>4</sub> exhibit poor oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and ammonia oxidation reaction (AOR) activities, 3–4% Pt-enriched NiWO<sub>4</sub> depict improved electrocatalytic performances with at least 50 mV overpotential drop for both the OER and HER. The 3%Pt/NiWO<sub>4</sub> electrode showcases a long-term (for 110 h) chronoamperometric/chronopotentiometric OER and HER performance, delivering high current at a low working potential. The bifunctional behavior of the material leads to the development of a water-splitting electrolyzer, 3%Pt/NiW<b>/</b>NF(−)/(+)3%Pt/NiW/NF, achieving >90% Faradaic efficiency for H<sub>2</sub> production. The onset potential for the AOR is also cathodically shifted for 3%Pt/NiW and 4%Pt/NiW compared to the NiWO<sub>4</sub> itself. Electrokinetic study through a rotating ring-disk electrode (RRDE) experiment and the Koutecký–Levich study provides an observed rate constant (<i>k</i><sub>obs</sub>) of 1.68 × 10<sup>–3</sup> cm s<sup>–1</sup> of AOR with a 6e<sup>–</sup> count from the kinetic current region, highlighting [NO<sub>2</sub>]<sup>−</sup> as the major product. The electrolysis of 1 M NH<sub><b>3</b></sub> using 4%Pt/NiW/NF as a working electrode produces predominantly [NO<sub>2</sub>]<sup>−</sup> (FE: 53%) and [NO<sub>3</sub>]<sup>−</sup> (FE: 30%). The improved electrocatalytic activity of 3–4% Pt-enriched NiWO<sub>4</sub> can be due to the low Tafel slope and charge transfer resistance (<i>R</i><sub>ct</sub>). Pt<sup>0</sup> being electron-rich induces facile electronic conduction during electrocatalysis and enhances a better binding of the analytes such as H<sub>2</sub>O, [OH]<sup>−</sup>, and NH<sub>3</sub>. At the same time, the Pt<sup>IV</sup> centers present adjacent to the Ni<sup>II</sup> sites can polarize the electron density to stabilize Ni<sup>III</sup> species and enhance the possibility of OER and AOR. This study demonstrates the effect of hetero-metal doping to tune the electronic structure to improve the electrochemical activity. The low-Pt-doped NiWO<sub>4</sub> material is presented here as a multimodal electrocatalyst that can efficiently electrolyze water or ammonia to produce hydrogen.

Publication Details

Journal
Figshare
Published
2025-01-28
DOI
https://doi.org/10.1021/acsami.4c20564.s001
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
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article

Low Pt Loading onWolframite-Type NiWO4 to Excel the Electrocatalytic WaterSplitting and Ammonia OxidationReaction

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Ammonia Synthesis and Nitrogen Reduction
article

Low Pt Loading onWolframite-Type NiWO4 to Excel the Electrocatalytic WaterSplitting and Ammonia OxidationReaction

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Abstract

Hydrogen production via water-splitting or ammonia electrolysis using transition metal-based electrodes is one of the most cost-effective approaches. Herein, ca. 1–4% of Pt atoms are stuffed into a wolframite-type NiWO<sub>4</sub> lattice to improve the electrocatalytic efficiency. The co-existence of atomically dilute quantities of Pt<sup>0</sup> and Pt<sup>IV</sup> atoms in the NiWO<sub>4</sub> without altering the lattice structure is established via powder X-ray diffraction, inductively coupled plasma mass spectrometry (ICP-MS), core-level X-ray photoelectron spectroscopy, and other spectroscopic studies. While the undoped NiWO<sub>4</sub> and a physical mixture of Pt<sup>0</sup> (2 wt %) and NiWO<sub>4</sub> exhibit poor oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and ammonia oxidation reaction (AOR) activities, 3–4% Pt-enriched NiWO<sub>4</sub> depict improved electrocatalytic performances with at least 50 mV overpotential drop for both the OER and HER. The 3%Pt/NiWO<sub>4</sub> electrode showcases a long-term (for 110 h) chronoamperometric/chronopotentiometric OER and HER performance, delivering high current at a low working potential. The bifunctional behavior of the material leads to the development of a water-splitting electrolyzer, 3%Pt/NiW<b>/</b>NF(−)/(+)3%Pt/NiW/NF, achieving >90% Faradaic efficiency for H<sub>2</sub> production. The onset potential for the AOR is also cathodically shifted for 3%Pt/NiW and 4%Pt/NiW compared to the NiWO<sub>4</sub> itself. Electrokinetic study through a rotating ring-disk electrode (RRDE) experiment and the Koutecký–Levich study provides an observed rate constant (<i>k</i><sub>obs</sub>) of 1.68 × 10<sup>–3</sup> cm s<sup>–1</sup> of AOR with a 6e<sup>–</sup> count from the kinetic current region, highlighting [NO<sub>2</sub>]<sup>−</sup> as the major product. The electrolysis of 1 M NH<sub><b>3</b></sub> using 4%Pt/NiW/NF as a working electrode produces predominantly [NO<sub>2</sub>]<sup>−</sup> (FE: 53%) and [NO<sub>3</sub>]<sup>−</sup> (FE: 30%). The improved electrocatalytic activity of 3–4% Pt-enriched NiWO<sub>4</sub> can be due to the low Tafel slope and charge transfer resistance (<i>R</i><sub>ct</sub>). Pt<sup>0</sup> being electron-rich induces facile electronic conduction during electrocatalysis and enhances a better binding of the analytes such as H<sub>2</sub>O, [OH]<sup>−</sup>, and NH<sub>3</sub>. At the same time, the Pt<sup>IV</sup> centers present adjacent to the Ni<sup>II</sup> sites can polarize the electron density to stabilize Ni<sup>III</sup> species and enhance the possibility of OER and AOR. This study demonstrates the effect of hetero-metal doping to tune the electronic structure to improve the electrochemical activity. The low-Pt-doped NiWO<sub>4</sub> material is presented here as a multimodal electrocatalyst that can efficiently electrolyze water or ammonia to produce hydrogen.

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