4.7 Article

Formation, Performance, and Long-Term Stability of Nanostructured Ni-YSZ Thin Film Electrodes

Journal

ACS APPLIED ENERGY MATERIALS
Volume 4, Issue 9, Pages 9046-9056

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c01332

Keywords

IT-SOFC; Ni-YSZ nanocomposite; microstructure; polymeric precursor; electrochemical impedance spectroscopy

Funding

  1. Scientific and Technological Research Council of Turkey [217 M031]

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A new method for fabricating nickel and YSZ composite anodes was utilized in this study, with the application of a pre-calcination step in the oxidized state and a CeO2 overlayer, which significantly improved the electrochemical performance and stability of the anodes.
Nickel and yttria-stabilized zirconia (YSZ) composite anodes were fabricated by a powder-free, polymeric precursor-based process, in which Ni, Y, and Zr cations are redistributed by phase separation at the nanoscale, forming YSZ and Ni(O). Transmission electron microscopy/energy-dispersive X-ray spectroscopy analyses revealed for the first-time in the literature that the nanocomposite thin film Ni-YSZ anodes had microstructures consisting of alternating Ni and YSZ nanolayers. A pre-calcination step applied in the oxidized state enhanced the interconnectivity of the Ni and YSZ phases after reduction, which improved the electrochemical performance. Electrochemical and microstructural analyses showed that performance degradation upon long-term exposure to dilute hydrogen at 600 degrees C was closely related to Ni coarsening in general. Evidently, the pre-calcination step enhanced the performance stability of the anodes by strengthening the YSZ network and thus inhibiting Ni agglomeration. In addition, the deposition of a thin, electronically conductive CeO2 overlayer on top of the Ni-YSZ anode inhibited the excessive agglomeration of Ni at the top surface. Our experiments showed that the pre-calcination of Ni-YSZ anodes in the oxidized state with a CeO2 overlayer gave the highest electrocatalytic performance, i.e., a polarization resistance of 0.72 Omega.cm(2) at 600 degrees C, in dilute hydrogen, as well as the highest long-term performance stability.

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