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Exploration of a Ce0.65Zr0.25Pr0.1O2−δ-Based Electrocatalyst That Exhibits Rapid Performance Deterioration Despite Its High Oxygen Storage Capability
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    Exploration of a Ce0.65Zr0.25Pr0.1O2−δ-Based Electrocatalyst That Exhibits Rapid Performance Deterioration Despite Its High Oxygen Storage Capability
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    • Seol Hee Oh
      Seol Hee Oh
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      More by Seol Hee Oh
    • Eun Hui Park
      Eun Hui Park
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      Department of Energy Engineering, Hanyang University, Seoul 04763, Korea
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    • Hyun-Kyu Kim
      Hyun-Kyu Kim
      School of Energy Materials and Chemical Engineering, Korea University of Technology and Education, Cheonan 31253, Korea
      More by Hyun-Kyu Kim
    • Jason Kim
      Jason Kim
      Department of Convergence IT Engineering, Pohang University of Science and Technology, Pohang 37673, Korea
      More by Jason Kim
    • Hee-Sung Yoon
      Hee-Sung Yoon
      Department of Energy Engineering, Hanyang University, Seoul 04763, Korea
    • Yeong-Cheol Kim
      Yeong-Cheol Kim
      School of Energy Materials and Chemical Engineering, Korea University of Technology and Education, Cheonan 31253, Korea
    • Sun-Young Park
      Sun-Young Park
      Technology Support Center, Korea Institute of Science and Technology, Seoul 02792, Korea
    • Sungeun Yang
      Sungeun Yang
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      Division of Nanoscience & Technology, University of Science and Technology, Seoul 02792, Korea
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    • Ho-Il Ji
      Ho-Il Ji
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      Division of Nanoscience & Technology, University of Science and Technology, Seoul 02792, Korea
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    • Kyung Joong Yoon
      Kyung Joong Yoon
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
    • Ji-Won Son
      Ji-Won Son
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      Division of Nanoscience & Technology, University of Science and Technology, Seoul 02792, Korea
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    • Jong-Ho Lee*
      Jong-Ho Lee
      Energy Materials Research Center, Korea Institute of Science and Technology, Seoul 02792, Korea
      Division of Nanoscience & Technology, University of Science and Technology, Seoul 02792, Korea
      *Email: [email protected]
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    ACS Applied Energy Materials

    Cite this: ACS Appl. Energy Mater. 2022, 5, 7, 8023–8033
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    https://doi.org/10.1021/acsaem.2c00468
    Published July 14, 2022
    Copyright © 2022 American Chemical Society

    Abstract

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    Ceria–zirconia solid solution, having superior oxygen storage/release capability and carbon coking resistance, has long been used as a favorable catalyst or supporting material for various catalytic converters and membrane reactors. Recently, rare-earth-doped ceria–zirconia with an additional improvement in its ionic conductivity by doping is attracting attention as a promising electrocatalyst for solid oxide fuel cells (SOFCs). However, despite this promising prospect, the practical usefulness for fuel cell catalysts has not been verified yet. According to our electrochemical analysis on a Pr-doped CZO (PrCZO)-based anode, the electrochemical performance does not remain stable; instead, the performance rapidly deteriorates over time even though it is initially much better than that of a conventional anode. From the thorough investigations to identify the cause of the rapid deterioration of PrCZO-based anode via computational analyses using density functional theory and defect chemical analysis, it can be concluded that the fast degradation of PrCZO-based anode is mainly due to the inactive substances precipitated on the PrCZO surface caused by the inherent thermodynamic instability and enhanced phase separation kinetics under SOFC operating conditions, where more mobile cationic defects (interstitial cations) are generated and an easier pathway with a lower migration energy is available.

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsaem.2c00468.

    • Experimental setup for EIS analysis, EIS data fitted with a 4 RC equivalent circuit model, and mixing free energy of CZO and PrCZO (PDF)

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    Cited By

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    This article is cited by 2 publications.

    1. Tom L. Underwood, Susanna Vigorito, Marco Molinari, John Purton, Nigel B. Wilding, John T.S. Irvine, Stephen C. Parker. Grain-boundary-dependent segregation and phase separation in ceria–zirconia from atomistic simulation. Acta Materialia 2024, 271 , 119872. https://doi.org/10.1016/j.actamat.2024.119872
    2. Seol Hee Oh, Hyun-Kyu Kim, Jason Kim, Yeong-Cheol Kim, Sun-Young Park, Sungeun Yang, Ho-Il Ji, Kyung Joong Yoon, Ji-Won Son, Jong-Ho Lee. Experimental and theoretical study on the complete phase separation of ceria-zirconia solid solution into two end members, ceria and zirconia. Journal of Physics: Energy 2022, 4 (4) , 045004. https://doi.org/10.1088/2515-7655/ac8a76

    ACS Applied Energy Materials

    Cite this: ACS Appl. Energy Mater. 2022, 5, 7, 8023–8033
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acsaem.2c00468
    Published July 14, 2022
    Copyright © 2022 American Chemical Society

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