Solid solutions in disulfide systems Re(IV)S2–Ti(IV)S2, Re(IV)S2–Mo(IV)S2, and Re(IV)S2–W(IV)S2
https://doi.org/10.32362/2410-6593-2024-19-3-258-266
EDN: KYWKWJ
Abstract
Objectives. Chalcogenides of transition elements with low oxidation states, as well as their substituted derivatives, remain a poorly studied class of chemical compounds. Rhenium disulfide has many distinctive features and great application potential as a new twodimensional semiconductor. This is due to its unusual structure and unique anisotropic properties. The presence of weak interlayer bonding and a unique distorted octahedral (1T) structure suggests the possibility of creating new phases on its basis. The aim of this work is to obtain and study phases in systems Re(IV)S2–Ti(IV)S2, Re(IV)S2–Mo(IV)S2, and Re(IV)S2–W(IV)S2.
Methods. The samples were obtained by high-temperature solid-phase ampoule synthesis in a vacuum. The study was carried out using X-ray phase analysis and X-ray photoelectron spectroscopy.
Results. The regions of existence of solid solutions, intercalates and two-phase regions in the resulting systems were established.
Diffraction patterns were obtained for the new phases and the crystal lattice parameters were calculated. Based on data relating to the binding energies of core electrons with the nucleus, the study showed the valence states of the elements after synthesis. The study also confirmed that all phases obtained as a result of synthesis contain transition elements in the oxidation state (IV).
Conclusions. Intercalated solid solutions are formed in areas rich in rhenium, while in areas close to titanium and molybdenum disulfides, intercalated phases are attained. In the ReS2–WS2 system there is a region of solid solutions, including 30, 50, and 70 mol % rhenium disulfide. Their structure is a polymorphic modification of the structure of the original components. The presence of rhenium, molybdenum, and tungsten in these phases in the oxidation state (+IV) was confirmed. The data obtained on phase formation in dichalcogenide systems can be practically used in the creation of materials with unique electronic, magnetic, and optical properties with a wide range of applications.
About the Authors
E. I. EfremovaRussian Federation
Ekaterina I. Efremova, Cand. Sci. (Chem.), Assistant Professor, A.N. Reformatskii Department of Inorganic Chemistry
86, Vernadskogo pr., Moscow, 119571
Scopus Author ID 56506855800
M. A. Lazov
Russian Federation
Mikhail A. Lazov, Cand. Sci. (Chem.), Assistant Professor, I.P. Alimarin Department of Analytical Chemistry
86, Vernadskogo pr., Moscow, 119571
Scopus Author ID 56466030700
M. R. Kobrin
Russian Federation
Mikhail R. Kobrin, Lecturer, A.N. Reformatskii Department of Inorganic Chemistry
86, Vernadskogo pr., Moscow, 119571
V. V. Fomichev
Russian Federation
Valery V. Fomichev, Dr. Sci. (Chem.), Professor, K.A. Bolshakov Department of Chemistry and Technology of Rare Elements
86, Vernadskogo pr., Moscow, 119571
Scopus Author ID 57196028937
ResearcherID P-9883-2017
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Supplementary files
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1. Survey spectrum of the ReS2 35%–WS2 65% solid solution | |
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Type | Исследовательские инструменты | |
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Indexing metadata ▾ |
- The aim of the work is to obtain and study phases in systems Re(IV)S2–Ti(IV)S2, Re(IV)S2–Mo(IV)S2 и Re(IV)S2–W(IV)S2.
- The samples were obtained by high-temperature solid-phase ampoule synthesis in a vacuum.
- The regions of existence of solid solutions, intercalates and two-phase regions in the resulting systems were established.
- Intercalated solid solutions are formed in areas rich in rhenium, while in areas close to titanium and molybdenum disulfides, intercalated phases are attained. In the ReS2–WS2 system there is a region of solid solutions, including 30, 50 and 70 mol % rhenium disulfide. Their structure is a polymorphic modification of the structure of the original components.
Review
For citations:
Efremova E.I., Lazov M.A., Kobrin M.R., Fomichev V.V. Solid solutions in disulfide systems Re(IV)S2–Ti(IV)S2, Re(IV)S2–Mo(IV)S2, and Re(IV)S2–W(IV)S2. Fine Chemical Technologies. 2024;19(3):258-266. https://doi.org/10.32362/2410-6593-2024-19-3-258-266. EDN: KYWKWJ