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Proton Conductivity in Mixed B-Site Doped Perovskite Oxide BaZr[sub 0.5]In[sub 0.25]Yb[sub 0.25]O[sub 3−δ]
- Source :
- Journal of The Electrochemical Society. 157:B1819
- Publication Year :
- 2010
- Publisher :
- The Electrochemical Society, 2010.
-
Abstract
- A wet chemical route was used to prepare the oxygen deficient codoped perovskite oxide BaZr0.5In0.25Yb0.25O3−. Analysis of X-ray powder diffraction data showed that the sample belongs to the cubic crystal system with space group Pmm. Dynamic thermogravimetric (TG) analysis confirmed complete filling of oxygen vacancies (V) by protonic defects (OH) during the hydration process. The proton conductivity was investigated by impedance spectroscopy. The bulk and total conductivities of prehydrated BaZr0.5In0.25Yb0.25O3− were found to be 8.5×10−4 and 2.2×10−5 S cm−1, respectively, at 300°C. The total conductivity in the codoped perovskite oxide was higher compared to that of the respective single doped perovskite oxides with the same doping level. The bulk and grain-boundary mobility and diffusion coefficients of protons were calculated at 200°C using impedance and TG data to obtain the conductivity and proton concentration, respectively. The high bulk diffusivity (2.3×10−7 cm2 s−1) was obtained which indicates that the protons are more free to move in the heavily doped matrix compared to the lightly doped systems where trapping of protons occurs.
- Subjects :
- Materials science
Proton
Renewable Energy, Sustainability and the Environment
Doping
Inorganic chemistry
Analytical chemistry
Oxide
Conductivity
Condensed Matter Physics
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
Dielectric spectroscopy
chemistry.chemical_compound
chemistry
X-ray crystallography
Materials Chemistry
Electrochemistry
Powder diffraction
Perovskite (structure)
Subjects
Details
- ISSN :
- 00134651
- Volume :
- 157
- Database :
- OpenAIRE
- Journal :
- Journal of The Electrochemical Society
- Accession number :
- edsair.doi...........b18e059a48ecd11732a2c62368e16f1a
- Full Text :
- https://doi.org/10.1149/1.3494119