Compositional Engineering of Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene-NiMoO<sub>4</sub> Hybrid Nanostructures for Enhanced Electrocatalytic Water Oxidation

A critical step in realizing the vision of green hydrogen through water splitting is to design oxygen evolution reaction (OER) catalysts that showcase a good balance of activity and stability. This work reports the compositional tuning of a NiMoO<sub>4</sub> material and then the subsequent varying of Ti<sub>3</sub>C<sub>2</sub>T <sub><i>x</i></sub> MXene with the NiMoO<sub>4</sub> hybrid nanostructures as OER catalysts in alkaline media. In this work, the optimum NiMoO<sub>4</sub> hybrid catalyst retained good stability over 24 h of chronopotentiometry on industrial relevant supports (Ni Felt) with an overpotential value of ca. 339 mV at 100 mA cm<sup>-2</sup>. Operando Raman spectroscopy revealed that catalytically active β-NiOOH species are formed during OER in NiMoO<sub>4</sub> at lower overpotentials than for pure NiO and that a higher amount of the β-NiOOH was found in the 5% MXene loading. The ICP-OES analysis showed that Mo dissolution follows a volcano trend with MXene loading (peaking at 5 wt %) before decreasing at 10 wt %. Overall, these results hold great promises for rational design strategies for MXene-supported water oxidation catalysts in alkaline electrolytes.

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Publication Details

Journal
ACS Applied Energy Materials
Published
2025-07-25
DOI
https://doi.org/10.1021/acsaem.5c01467
Citations
2
Primary Topic
MXene and MAX Phase Materials
Type
article
Field-Weighted Citation Impact
1.04

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article

Compositional Engineering of Ti3C2Tx MXene-NiMoO4 Hybrid Nanostructures for Enhanced Electrocatalytic Water Oxidation

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article

Compositional Engineering of Ti3C2Tx MXene-NiMoO4 Hybrid Nanostructures for Enhanced Electrocatalytic Water Oxidation

Kai Steffen Exner, Karuppasamy Dharmaraj, Saeed Sajjadi, Thorsten Schultz, Nigel A. Marks, Danielle Douglas-Henry, Valeria Nicolosi, Aline Alencar Emerenciano, Michelle Phillippa Browne, Norbert Koch, C. Kaplan
article en
2 citations

Abstract

A critical step in realizing the vision of green hydrogen through water splitting is to design oxygen evolution reaction (OER) catalysts that showcase a good balance of activity and stability. This work reports the compositional tuning of a NiMoO<sub>4</sub> material and then the subsequent varying of Ti<sub>3</sub>C<sub>2</sub>T <sub><i>x</i></sub> MXene with the NiMoO<sub>4</sub> hybrid nanostructures as OER catalysts in alkaline media. In this work, the optimum NiMoO<sub>4</sub> hybrid catalyst retained good stability over 24 h of chronopotentiometry on industrial relevant supports (Ni Felt) with an overpotential value of ca. 339 mV at 100 mA cm<sup>-2</sup>. Operando Raman spectroscopy revealed that catalytically active β-NiOOH species are formed during OER in NiMoO<sub>4</sub> at lower overpotentials than for pure NiO and that a higher amount of the β-NiOOH was found in the 5% MXene loading. The ICP-OES analysis showed that Mo dissolution follows a volcano trend with MXene loading (peaking at 5 wt %) before decreasing at 10 wt %. Overall, these results hold great promises for rational design strategies for MXene-supported water oxidation catalysts in alkaline electrolytes.

ACS Applied Energy MaterialsVol. 8(15)
Trinity College Dublin (IE), Helmholtz-Zentrum Berlin für Materialien und Energie (DE), Humboldt-Universität zu Berlin (DE), Advanced Materials and BioEngineering Research (IE), Trencianska Univerzita Alexandra Dubceka V Trencine (SK), Institut für Technische und Angewandte Physik (Germany) (DE), University of Duisburg-Essen (DE)
Science Foundation Ireland, Deutscher Akademischer Austauschdienst, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Helmholtz Association, Horizon 2020 Framework Programme, European Research Council
Openalex Percentile: Top 23%
MXene and MAX Phase Materials
1.04
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