Structural, magnetic, electrical and electrochemical properties of SrCoO2.5, Sr9Co2Mn5O21 and SrMnO3 compounds. Issue 17 (1st December 2017)

• Record Type: Journal Article
• Authors: Demirel, S.; Oz, E.; Altin, S.; Bayri, A.; Baglayan, O.; Altin, E.; Avci, S.
• Is Part Of: Ceramics international. Volume 43:Issue 17(2017)
• Page Start: 14818
• Page End: 14826
• Publication Date: 2017-12-01
• Subjects: SrCoO2.5 -- Sr9Co2Mn5O21 and SrMnO3 -- Cycling voltammogram -- Spin state; Ceramics -- Periodicals; Céramique industrielle -- Périodiques; Ceramics; Periodicals; Electronic journals; 666
• DOI: 10.1016/j.ceramint.2017.07.230
• Languages: English
• ISSNs: 0272-8842

Abstract

Abstract: SrCo1−x Mnx O3−d (0 ≤ x ≤ 1) were synthesized by conventional solid state reaction method. We found that Mn substitution hinders the decomposition of carbonate at 900 °C and increases the synthesis temperature of SrCo1−x Mnx O3−d to 1200 °C. Three different main phases emerge as the Mn content is increased; SrCoO2.5, Sr9 Co2 Mn5 O21 and SrMnO3. Structural properties of the samples were investigated by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, x-ray diffraction (XRD) and scanning electron microscopy (SEM). Valance states of the transition metal (TM) ions were estimated based on lattice parameters and ionic radii of TM ions. High temperature resistivity measurements show hysteresis upon heating and cooling and is attributed to oxygen release without any endothermic/exothermic activity. The spin configurations of Co and Mn ions in SrCoO2.5, Sr9 Co2 Mn5 O21 and SrMnO3 were estimated by Curie-Weiss fitting of χ-T curves. Electrochemical measurements show two anodic/cathodic peaks indicating two main types of oxygen sites in the unit cell.