Issue 38, 2016

Tuning the thermoelectric properties of A-site deficient SrTiO3 ceramics by vacancies and carrier concentration

Abstract

Ceramics based on Sr0.8La0.067Ti0.8Nb0.2O3−δ have been prepared by the mixed oxide route. The La1/3NbO3 component generates ∼13.4% A-site vacancies; this was fixed for all samples. Powders were sintered under air and reducing conditions at 1450 to 1700 K; products were of high density (>90% theoretical). Processing under reducing conditions led to the formation of a Ti1−xNbxO2−y second phase, core–shell structures and oxygen deficiency. X-ray diffraction (XRD) confirmed a simple cubic structure with space group Pm[3 with combining macron]m. Transmission electron microscopy revealed a high density of dislocations while analytical scanning transmission electron microscopy at atomic resolution demonstrated a uniform distribution of La, Nb and vacancies in the lattice. X-ray photoemission spectroscopy and thermogravimetry showed the oxygen deficiency (δ value) to be ∼0.08 in reduced samples with enhanced carrier concentrations ∼2 × 1021 cm−3. Both carrier concentration and carrier mobility increased with sintering time, giving a maximum figure of merit (ZT) of 0.25. Selective additional doping by La or Nb, with no additional A site vacancies, led to the creation of additional carriers and reduced electrical resistivity. Together these led to enhanced ZT values of 0.345 at 1000 K. The contributions from oxygen vacancies and charge carriers have been investigated independently.

Graphical abstract: Tuning the thermoelectric properties of A-site deficient SrTiO3 ceramics by vacancies and carrier concentration

Article information

Article type
Paper
Submitted
09 Aug 2016
Accepted
07 Sep 2016
First published
07 Sep 2016
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2016,18, 26475-26486

Tuning the thermoelectric properties of A-site deficient SrTiO3 ceramics by vacancies and carrier concentration

D. Srivastava, C. Norman, F. Azough, M. C. Schäfer, E. Guilmeau, D. Kepaptsoglou, Q. M. Ramasse, G. Nicotra and R. Freer, Phys. Chem. Chem. Phys., 2016, 18, 26475 DOI: 10.1039/C6CP05523K

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