Monitoring oxygen production on mass-selected iridium–tantalum oxide electrocatalysts
Creators
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Ya-Rong Zheng1
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Jerome Vernieres2
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Zhenbin Wang2
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Ke Zhang2
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Degenhart Hochfilzer2
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Kevin Krempl2
- Ting-Wei Liao2
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Francesco Presel2
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Thomas Altantzis3
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Jarmo Fatermans3
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Soren Bertelsen Scott2
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Niklas Mørch Secher2
- Choongman Moon2
- Pei Liu3
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Sara Bals3
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Sandra Van Aert3
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Ang Cao2
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Megha Anand2
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Jens K. Nørskov2
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Jakob Kibsgaard2
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Ib Chorkendorff2
- 1. Hefei University of Technology
- 2. Technical University of Denmark
- 3. University of Antwerp
Description
Development of low-cost and high-performance oxygen evolution reaction catalysts is key to implementing polymer electrolyte membrane water electrolysers for hydrogen production. Iridium-based oxides are the state-of-the-art acidic oxygen evolution reaction catalysts but still suffer from inadequate activity and stability, and iridium’s scarcity motivates the discovery of catalysts with lower iridium loadings. Here we report a mass-selected iridium–tantalum oxide catalyst prepared by a magnetron-based cluster source with considerably reduced noble-metal loadings beyond a commercial IrO2 catalyst. A sensitive electrochemistry/mass-spectrometry instrument coupled with isotope labelling was employed to investigate the oxygen production rate under dynamic operating conditions to account for the occurrence of side reactions and quantify the number of surface active sites. Iridium–tantalum oxide nanoparticles smaller than 2 nm exhibit a mass activity of 1.2 ± 0.5 kA gIr–1 and a turnover frequency of 2.3 ± 0.9 s−1 at 320 mV overpotential, which are two and four times higher than those of mass-selected IrO2, respectively. Density functional theory calculations reveal that special iridium coordinations and the lowered aqueous decomposition free energy might be responsible for the enhanced performance.
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Monitoring oxygen production on mass-selected iridium–tantalum oxide electrocatalysts-2-29.pdf
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