Effect of A‐ or B‐site doping of perovskite calcium manganite on structure, resistivity, and thermoelectric properties. Issue 10 (22nd June 2017)

• Record Type: Journal Article
• Authors: Mishra, Avinna; Bhattacharjee, Sarama
• Is Part Of: Journal of the American Ceramic Society. Volume 100:Issue 10(2017)
• Page Start: 4945
• Page End: 4953
• Publication Date: 2017-06-22
• Subjects: dopant/doping -- perovskite -- resistivity -- structure -- thermoelectric properties; Ceramics -- Periodicals; 620.1405
• DOI: 10.1111/jace.15015
• Languages: English
• ISSNs: 0002-7820

Abstract

Abstract: Bismuth‐, lanthanum‐, and molybdenum‐doped calcium manganite (CaMnO3, abbreviated Mn113) are synthesized by solid‐state synthesis route from their respective oxide precursors at a same doping level ( x =0.05). Depending on the ionic sizes, trivalent dopants (Bi 3+ and La 3+ ) replace Ca 2+ (A site), while penta/hexavalent dopant Mo 5+ /Mo 6+ replaces Mn 4+ (B site) in the Mn113 structure. XRD of all three doped samples confirm formation of single phase. In all three samples, doping causes unit cell volume to expand, while volume expansion is maximum for the Mo‐Mn113. The transport behavior of the doped samples follows small polaron hopping mechanism. Resistivity of the doped samples depends not only on the carrier concentration but also on the effective bandwidth determined by the structural distortion introduced by the dopant ions. Bi‐Mn113 has highest resistivity at the both temperature end, while La‐Mn113 has the lowest. Thermopower is determined by the carrier concentration only and does not depend on dopant type, having value ~260 μV/K at 1000 K. At high (>800 K), S reaches a saturation value and becomes independent of T . La‐Mn113 is having highest figure of merit (zT) 0.19 at 1000 K.