Počet záznamů: 1  

Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength

  1. 1.
    0504333 - ÚFM 2020 RIV CH eng J - Článek v odborném periodiku
    Masini, Alessia - Strohbach, T. - Šiška, Filip - Chlup, Zdeněk - Dlouhý, Ivo
    Electrolyte-Supported Fuel Cell: Co-Sintering Effects of Layer Deposition on Biaxial Strength.
    Materials. Roč. 12, č. 2 (2019), č. článku 306. E-ISSN 1996-1944
    GRANT EU: European Commission(XE) 642557 - CoACH; European Commission 700300 - GrInHy
    Institucionální podpora: RVO:68081723
    Klíčová slova: SOC * mechanical strength * flexural biaxial test * ball-on-3-balls test * fractography * residual stresses
    Obor OECD: Ceramics
    Impakt faktor: 3.057, rok: 2019
    Způsob publikování: Open access
    https://www.mdpi.com/1996-1944/12/2/306/htm

    The mechanical reliability of reversible solid oxide cell (SOC) components is critical for the development of highly efficient, durable, and commercially competitive devices. In particular, the mechanical integrity of the ceramic cell, also known as membrane electrolyte assembly (MEA), is fundamental as its failure would be detrimental to the performance of the whole SOC stack. In the present work, the mechanical robustness of an electrolyte-supported cell was determined via ball-on-3-balls flexural strength measurements. The main focus was to investigate the effect of the manufacturing process (i.e., layer by layer deposition and their co-sintering) on the final strength. To allow this investigation, the electrode layers were screen-printed one by one on the electrolyte support and thus sintered. Strength tests were performed after every layer deposition and the non-symmetrical layout was taken into account during mechanical testing. Obtained experimental data were evaluated with the help of Weibull statistical analysis. A loss of mechanical strength after every layer deposition was usually detected, with the final strength of the cell being significantly smaller than the initial strength of the uncoated electrolyte (σ0 ≈ 800 MPa and σ0 ≈ 1800 MPa, respectively). Fractographic analyses helped to reveal the fracture behavior changes when individual layers were deposited. It was found that the reasons behind the weakening effect can be ascribed to the presence and redistribution of residual stresses, changes in the crack initiation site, porosity of layers, and pre-crack formation in the electrode layers.
    Trvalý link: http://hdl.handle.net/11104/0296043

     
     
Počet záznamů: 1  

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