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Title: Proton transport and structural relations in hydroxyl-bearing BaTiO{sub 3} and its doped compositions synthesised by wet-chemical methods

Journal Article · · Materials Research Bulletin

Hydrothermally synthesised powders of BaTiO{sub 3} and its Fe- or Nd-doped analogues contain hydroxyl groups in the lattice substitutional to oxide ion, as confirmed from TGA/DTA, IR spectral analysis of D{sub 2}O-treated powders, EGA-MS, the contraction in lattice constant with heat treatment by XRD and surface examination by XPS. Electrical resistivity measurements were carried out on the pellets from 298 to 1000 K by ac impedance spectroscopy and dc methods in dry or moist air and 8% H{sub 2}+Ar environments. The electrical conductivity observed for unsintered pellets between 298 and 500 K, is in the range of 10{sup -3} to 10{sup -7} S/cm and can be attributed to the extrinsic hydroxyls in BaTiO{sub 3}. The acceptor-doped composition, BaTi{sub 0.9}Fe{sub 0.1}O{sub 3-{delta}}: 2{delta}(OH) exhibits higher electrical conductivity than BaTiO{sub 3} or the donor-doped Ba{sub 0.9}Nd{sub 0.1}TiO{sub 3-{delta}}: 2{delta}(OH) in moist air. The hydrothermally prepared powders heat treated below 1000 K having cubic symmetry at room temperature, possess higher proton conductivity and reabsorption capability for hydroxyls on exposure to moisture than the powders sintered at 1673 K (tetragonal symmetry). The conductivity at 298-500 K is due to the mobility of proton along O-H-O octahedra in the perovskite lattice. The conduction at 550-1000 K is a combined effect of proton as well as oxygen vacancy mobility in BaTiO{sub 3} and Ba{sub 0.9}Nd{sub 0.1}TiO{sub 3}; electron hole (Ti{sup 4+}, Ti{sup 3+}, Fe{sup 3+}, Fe{sup 2+}) participation is the additional contribution in acceptor-doped composition in this temperature range.

OSTI ID:
20888033
Journal Information:
Materials Research Bulletin, Vol. 39, Issue 3; Other Information: DOI: 10.1016/j.materresbull.2003.10.004; PII: S0025540803003039; Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English