Facile Interfacial Reduction Suppresses Redox Chemical Expansion and Promotes the Polaronic to Ionic Transition in Mixed Conducting (Pr,Ce)O2−δ Nanoparticles

Sipei Zhang, Zhengwu Fang, Miaofang Chi, Nicola H. Perry

Research output: Contribution to journalArticlepeer-review

Abstract

Mixed ionic/electronic conductors (MIECs) are essential components of solid-state electrochemical devices, such as solid oxide fuel/electrolysis cells. For efficient performance, MIECs are typically nanostructured, to enhance the reaction kinetics. However, the effect of nanostructuring on MIEC chemo-mechanical coupling and transport properties, which also impact cell durability and efficiency, has not yet been well understood. In this work, Pr0.2Ce0.8O2−δ (PCO20) nanopowders were prepared by coprecipitation, then sintered in a modified dilatometer at three different temperatures (600, 725, and 850 °C) for microstructure evolution, resulting in three samples with different average particle sizes (23, 30, and 53 nm). The chemical strain and electronic/ionic conductivity were then measured simultaneously on stable nanostructures in four isotherms from 550 to 400 °C with steps in pO2 (1 to 10-4 atm O2). A microcrystalline bar was prepared and measured for comparison. Particle size reduction led to a monotonically decreasing isothermal redox chemical strain, confirmed by in situ high-temperature, controlled-atmosphere XRD measurements. The corresponding conductivity measurements provided defect chemical insight into the particle size-dependent chemical expansion behavior. The significant weakening of the pO2 dependence and decreased activation energy for electrical conduction with decreasing particle size indicated a decrease in the reduction enthalpy of PCO, shifting the transition from (Pr) polaronic to ionic behavior to higher pO2. STEM-EELS measurements confirmed the majority of Pr was reduced to 3+ in the nanoparticles, while Ce remained 4+. These results demonstrate suppression of deleterious chemical expansion and tailoring of the dominant charge carrier simply through controlling the particle size, providing insights for MIEC microstructural design.

Original languageEnglish
JournalACS Applied Materials and Interfaces
DOIs
StateAccepted/In press - 2024
Externally publishedYes

Funding

The authors acknowledge the funding support from the DOE Basic Energy Science Energy Frontier Research Center (MUSIC) under DE-SC0023438. S.Z. acknowledges the support of the PPG-MRL Graduate Research Assistantship program. XRD (Bruker D8 Advance), SEM (JEOL 7000F), and TEM (JEOL 2010 LAB6) analyses were carried out in part in the Materials Research Laboratory Central Research Facilities, University of Illinois. The authors also acknowledge the use of facilities and instrumentation supported by NSF through the University of Illinois Urbana\u2013Champaign Materials Research Science and Engineering Center (I-MRSEC) DMR-1720633. STEM-EELS (JEOL JEM-ARM200F (NeoARM)) was performed at the Center for Nanophase Materials Sciences (CNMS), a U.S. Department of Energy, Office of Science User Facility.

FundersFunder number
DOE Basic Energy Science Energy Frontier Research Center
National Science Foundation
University of Illinois Urbana–Champaign Materials Research Science and Engineering Center
PPG-MRL
MUSICDE-SC0023438
I-MRSECDMR-1720633

    Keywords

    • ceria
    • chemical expansion
    • chemo-mechanical coupling
    • defect chemistry
    • mixed ionic electronic conduction
    • nanoparticle
    • redox

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