4.5 Article

Electrochemical and microstructure properties of Er-doped CaZrO3

Journal

IONICS
Volume 27, Issue 8, Pages 3511-3520

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11581-021-04104-y

Keywords

Perovskite; Proton conductor; Hydrogen sensor; Electrochemical properties

Funding

  1. National Science Foundation of China [51864038, 51762036]
  2. Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region [NJYT-19-A20]
  3. Innovation Fund of Inner Mongolia University of Science and Technology [2017YQL01]
  4. Natural Science Foundation of Inner Mongolia [2017BS0504]
  5. Guide and Innovation Award Fund of Inner Mongolia Autonomous Region Science and Technology [2017CXYD-7]
  6. Scientific Research Fund of Higher Education in Inner Mongolia Autonomous Region [NJZY21381]

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In this study, a solid-state electrolyte Er-doped CaZrO3 was successfully prepared and its microstructures and electrochemical properties were investigated. Protons were identified as the predominant charge carriers in a hydrogen atmosphere at high temperatures, while the ionic electrical conductivity decreased with increasing Er2O3 doping.
To understand electrochemical properties of the rare earth-doped CaZrO3 system in more detail, a solid-state electrolyte Er-doped CaZrO3 was successfully prepared using solid-state reaction method at the temperatures of 1673 K and 1823 K for 10 h. The microstructures and electrochemical properties of these materials were systemically investigated. The results from structural analysis showed that the electrolyte has a pure perovskite phase structure. According to the H/D isotope effect, protons were determined as the dominant charge carriers in hydrogen atmosphere between 773 and 1273 K. The electrochemical impedance spectroscopy test showed that ionic electrical conductivities are approximately 1.86 x 10(-8) similar to 2.93 x 10(-4) S/cm at 773 similar to 1273 K, and ionic conductance activation energy (E-a) is in the range of 0.823-1.416 eV, Furthermore, ionic electrical conductivity decreases with increasing Er2O3 doping amount, which is completely different from that of In2O3 or other dopant-doped CaZrO3. The abnormal phenomenon is associated with the defect association introduced by incorporation of Er2O3 into CaZrO3 lattice on the basis of the DFT calculation.

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