50 mol% indium substituted BaTiO3: Characterization of structure and conductivity
Paper i proceeding, 2012

BaTi0.5In0.5O3-delta was prepared by solid state reaction at 1400 degrees C. Rietveld analysis of high resolution X-ray powder diffraction data indicated phase pure as-prepared material that adopts a cubic perovskite structure with a = 4.1536(1) angstrom. Thermogravimetric analysis revealed the presence of significant levels of protons in the as-prepared material and 57% of the theoretically achievable protonation was attained on exposure to a humid environment at 185 degrees C. After hydration the cell parameter increased to 4.1623(1) angstrom. Electrical conductivity was measured both with fixed and variable frequency ac impedance methods as a function of temperature, oxygen-, water vapour- and heavy water vapour partial pressures. In the temperature range 400-800 degrees C a slight increase in the total conductivity with increasing oxygen partial pressure is encountered, characteristic of a contribution from p-type charge carriers. The effect of the water vapour pressure on conductivity below 600 degrees C is much more prominent indicative of dominant proton conduction. At 300 degrees C the total conductivity in wet O-2 was estimated to be 9.30 x 10(-5) S/cm. At T > 800 degrees C the material is a pure oxide ion conductor.

ba2in2o5-rectangle

Brownmillerite

baceo3

transport

oxides

X-ray diffraction

quantum molecular-dynamics

perovskites

Proton conductivity

Impedance

Barium titanate

temperature protonic conductors

hydrogen

bazro3

Perovskite

Författare

Seikh Mohammad Habibur Rahman

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Christopher Knee

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Istaq Ahmed

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Sten Eriksson

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

R. Haugsrud

Universitetet i Oslo

International Journal of Hydrogen Energy

0360-3199 (ISSN)

Vol. 37 9 7975-7982

7th Petite Workshop on the Defect Chemical Nature of Energy Materials
Kongsberg, Norway,

Ämneskategorier

Kemi

DOI

10.1016/j.ijhydene.2011.12.139

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Senast uppdaterat

2021-07-21