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February 28, 20260 citationsOpen Access

Preprint of "Surface and Bulk Reduction Kinetics of Liquid Plasma-Sprayed NiO-YSZ Layers for Solid Oxide Cells"

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MVMichael VorochtaKBKarel BouzekŠPŠárka Paušová

Key Points

  • This study investigates the reduction kinetics of NiO-YSZ layers and their dependence on feedstock chemistry.
  • Fabrication of NiO-YSZ layers using liquid plasma spraying with hybrid water-argon plasma torch.
  • Preparation of coatings with varying NiO:YSZ ratios from ethanol and water-based solutions.
  • Characterization of reduction kinetics using near-ambient pressure X-ray photoelectron spectroscopy, thermogravimetric analysis, and X-ray diffraction.
  • Ethanol-based layers achieved up to 58% porosity and finer phase intermixing compared to water-based layers.
  • Surface reduction initiated above 300 °C, with ethanol-based layers showing a 60 °C kinetic advantage.
  • Bulk reduction required near 750 °C due to mass-transfer limitations.
  • Higher total nickel content extended reduction times.

Abstract

Nickel oxide–yttria stabilized zirconia (NiO-YSZ) is the established electrode material for solid oxide cells (SOCs), where NiO reduction dictates final microstructure and electrochemical performance. In this study, NiO-YSZ layers were fabricated via liquid plasma spraying using a hybrid water–argon stabilized plasma torch (WSP H), to create porous layers without sacrificial pore forming additives. To evaluate the influence of feedstock chemistry on reduction behavior, four coatings with varying NiO:YSZ ratios were prepared from ethanol based solution-suspensions, alongside one from a water based solution. The surface and bulk reduction kinetics were systematically characterized through a combination of near-ambient pressure X-ray photoelectron spectroscopy (NAP–XPS), thermogravimetric analysis (TGA), and X-ray diffraction (XRD). Layers derived from the ethanol based feedstock exhibited higher porosity (up to 58%) and finer phase intermixing compared to the water based counterpart. The reduction behavior of the NiO-YSZ layers strongly correlated with the feedstock solvent and nickel content. Surface reduction initiated above 300 °C with porous ethanol-based layers showing a 60 °C kinetic advantage. Conversely, bulk reduction was inhibited by mass-transfer limitations, requiring temperatures near 750 °C for completion. Finally, total nickel content was identified as the primary factor controlling activation duration, with higher NiO loading extending reduction times.

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Cite This Study

Vorochta et al. (2026) studied this question.

synapsesocial.com/papers/69a287350a974eb0d3c02bb6https://doi.org/10.5281/zenodo.18787312
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Elucidating nickel oxide reduction in a Ni-YSZ solid oxide cell via in-situ X-ray nano holo-tomography2024 · 4 citations
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  3. 3Composition-Dependent Microstructural Connectivity and Mechanical Stability of NiO–YSZ Cermets in Anode-Supported Solid Oxide Fuel Cells2026 · 1 citations
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  5. 5Mechanism Analysis of the Reduction Process of the NiO-YSZ Anode of a Solid Oxide Fuel Cell by Hydrogen2024 · 3 citations