Interactions in ternary bismuth-containing molybdate systems M2MoO4-Bi2(MoO4)3-Zr(MoO4)2 in the subsolidus region
https://doi.org/10.21285/2227-2925-2021-11-4-508-516
Abstract
A fundamental problem in materials science consists in establishing a relationship between the chemical composition, structure, and properties of materials. This issue can be solved through the study of multicomponent systems and the directed synthesis of promising compounds. Of practical interest here are active dielectrics that are based on complex oxide compounds, specifically molybdates. Among complex molybdates and tungstates, ternary caged molybdates of the following structural types are of greatest importance: nasicon, perovskite, langbeinite, etc. Due to their widely varying elemental and quantitative compositions, such molybdates are convenient models for structural and chemical design, as well as the establishment of “composition–structure– properties” genetic relationships. Bismuth-containing complex molybdate systems exhibit the formation of phases having ferro-piezoelectric, ionic, and other properties. In this work, the Rb2MoO4–Bi2(MoO4)3–Zr(MoO4)2 ter nary salt system was studied for the first time using the method of intersecting sections in the subsolidus region (450–650 ℃). To this end, quasibinary sections were identified; triangulation was performed. Ternary molybdates Rb5BiZr(MoO4)6 and Rb2BiZr2(MoO4)6,5 were formed in the system using a ceramic technology. These compounds are isostructural to the previously obtained REE molybdates (M5LnZr(MoO4)6) but contain trivalent bismuth instead of rare earth elements. The structure of Rb5BiZr(MoO4)6 was adjusted via the Rietveld refinement technique using the TOPAS 4.2 software package. The ternary molybdate crystallizes in a trigonal system, with the following unit cell parameters of the R`3c space group: a = 10.7756(2) and c = 39.0464(7) Å. According to the studies of thermal properties exhibited by M5BiZr(MoO4)6, these ternary molybdates undergo the first-order phase transition in the temperature range of 450–600 ºC. The IR and Raman spectra of M5BiZr(MoO4)6 reveal the crystallization of ternary molybdates in the R`3c space group. The conducted comparative characterization of M2MoO4–Bi2(MoO4)3–Zr(MoO4)2 phase diagrams suggests that the phase equilibria of these systems depend on the nature of molybdates of monovalent elements.
Keywords
quasibinary sections,
concentration triangles,
phase formation,
triangulation,
vibrational spectroscopy
Supporting agencies: The authors are grateful to E. V. Kovtunets structure for the refining of Rb5BiZr(MoO4)6 structure by the Rietveld method. The work was supported by the State assignment for the Baikal Institute of Nature Management SB RAS (project no. 0273-2021-0008).
About the Authors
J. G. Bazarova
Baikal Institute of Nature Management SB RAS
Russian Federation
Russian Federation
Jibzema G. Bazarova, Dr. Sci. (Chemistry), Professor, Chief Researcher
6, Sakhyanova St., Ulan-Ude, 670047
A. V. Logvinova
Baikal Institute of Nature Management SB RAS; Buryat State University named after D. Banzarov
Russian Federation
Russian Federation
Alexandra V. Logvinova, Engineer, Baikal Institute of Nature Management SB RAS, 6, Sakhyanova St., Ulan-Ude, 670047; Laboratory Assistant, Banzarov Buryat State University, 24a, Smolin St., Ulan-Ude, 670000
B. G. Bazarov
Baikal Institute of Nature Management SB RAS; Buryat State University named after D. Banzarov
Russian Federation
Russian Federation
Bair G. Bazarov, Dr. Sci. (Physics and Mathematics), Associate Professor, Leading Researcher, Baikal Institute of Nature Management SB RAS, 6, Sakhyanova St., Ulan-Ude, 670047; Associate Professor, Banzarov Buryat State University, 24a, Smolin St., Ulan-Ude, 670000
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For citations:
Bazarova J.G., Logvinova A.V., Bazarov B.G. Interactions in ternary bismuth-containing molybdate systems M2MoO4-Bi2(MoO4)3-Zr(MoO4)2 in the subsolidus region. Proceedings of Universities. Applied Chemistry and Biotechnology. 2021;11(4):508-516. (In Russ.) https://doi.org/10.21285/2227-2925-2021-11-4-508-516
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