Evolution of the structure and chemical composition of the interface between multi-component silicate glasses and yttria-stabilized zirconia after 40,000 h exposure in air at 800 °C

Qianying Guo, Tianli Feng, Michael J. Lance, Kinga A. Unocic, Sokrates T. Pantelides, Edgar Lara-Curzio

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The chemical and structural stability of two commercial multicomponent silicate glasses (SCN and G6) in contact with yttria-stabilized zirconia (YSZ) was investigated after exposure times of up to 40,000 h in air at 800 °C. With exposure time, interfacial layers develop at the SCN-YSZ and G6-YSZ interfaces, which were characterized in detail using both quantitative chemical analysis and atomic-resolution imaging. At the SCN-YSZ interface, a Ca-Ba-Si-O reaction phase was found to grow by diffusion control. In G6-YSZ, Raman spectroscopy and electron microscopy revealed a disorganized interfacial reaction later between G6 and YSZ, and the occurrence of cubic to tetragonal to monoclinic phase transformations in YSZ. This microstructural evolution is discussed in terms of devitrification resistance of glass and diffusion processes at interfaces.

Original languageEnglish
Pages (from-to)1576-1584
Number of pages9
JournalJournal of the European Ceramic Society
Volume42
Issue number4
DOIs
StatePublished - Apr 2022

Funding

This work has been authored by UT-Battelle, LLC, under contract no. DE-AC05-00OR22725 with the US Department of Energy (DOE). This research work was sponsored by DOE , Office of Fossil Energy & Carbon Management , Solid Oxide Fuel Cells Core Technology Program at Oak Ridge National Laboratory (ORNL) . The authors are grateful for the support of National Energy Technology Laboratory program managers Rin Burke and Shailesh Vora. Research was supported by the Center for Nanophase Materials Sciences (CNMS) , which is sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, DOE. The FEI Talos F200X STEM was used as part of the Nuclear Science User Facilities. We acknowledge ORNL’s Fuel Cycle Materials Characterization Group for use of the Raman spectrometer. Theoretical work by T.L.F. and S.T.P. is supported in part by DOE grant DE-FG0209ER46554 and by the McMinn Endowment . Computations were performed at the National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science, User Facility funded through contract no. DE-AC02-05CH11231. The authors thank their ORNL colleagues Beth Armstrong and David Mitchell for reviewing the manuscript and Beth Armstrong, Dana McClurg, Alexis Flores-Betancourt, Christina Padilla, Andres Marquez Rossy, Dorothy W. Coffey, and Tom. S. Geer for technical support. This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government retains and the publisher, by accepting the article for publication, acknowledges that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan ( http://energy.gov/downloads/doe-public-access-plan ). This work has been authored by UT-Battelle, LLC, under contract no. DE-AC05-00OR22725 with the US Department of Energy (DOE). This research work was sponsored by DOE, Office of Fossil Energy & Carbon Management, Solid Oxide Fuel Cells Core Technology Program at Oak Ridge National Laboratory (ORNL). The authors are grateful for the support of National Energy Technology Laboratory program managers Rin Burke and Shailesh Vora. Research was supported by the Center for Nanophase Materials Sciences (CNMS), which is sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, DOE. The FEI Talos F200X STEM was used as part of the Nuclear Science User Facilities. We acknowledge ORNL's Fuel Cycle Materials Characterization Group for use of the Raman spectrometer. Theoretical work by T.L.F. and S.T.P. is supported in part by DOE grant DE-FG0209ER46554 and by the McMinn Endowment. Computations were performed at the National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science, User Facility funded through contract no. DE-AC02-05CH11231. The authors thank their ORNL colleagues Beth Armstrong and David Mitchell for reviewing the manuscript and Beth Armstrong, Dana McClurg, Alexis Flores-Betancourt, Christina Padilla, Andres Marquez Rossy, Dorothy W. Coffey, and Tom. S. Geer for technical support. This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government retains and the publisher, by accepting the article for publication, acknowledges that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).

FundersFunder number
Center for Nanophase Materials Sciences
DOE Public Access Plan
McMinn Endowment
Office of Fossil Energy & Carbon Management
Scientific User Facilities Division
U.S. Department of Energy
Office of ScienceDE-AC02-05CH11231
Basic Energy SciencesDE-FG0209ER46554
Oak Ridge National Laboratory
National Energy Technology Laboratory

    Keywords

    • Glass seals
    • Multicomponent silicate glass
    • Phase transformation
    • Solid-oxide fuel cells
    • Yttria-stabilized zirconia

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