Lithium tritelluride
This article will address the topic of Lithium tritelluride, an issue of great relevance and relevance in today's society. Lithium tritelluride has aroused great interest and debate in different areas, from the academic field to the political and social field. This issue has great complexity and diversity of approaches, which require a deep and exhaustive analysis. Throughout this article, different perspectives will be explored, contextualizing Lithium tritelluride within its historical and cultural framework, as well as examining its influence on various aspects of daily life. It is expected that this article contributes to the understanding and reflection on Lithium tritelluride, offering a comprehensive and critical vision of this topic of great relevance today.
| Identifiers | |
|---|---|
3D model (JSmol)
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| Properties | |
| LiTe3 | |
| Molar mass | 389.74 g·mol−1 |
| Related compounds | |
Related compounds
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lithium telluride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Lithium tritelluride is an intercalary compound of lithium and tellurium with empirical formula LiTe
3. It is one of four known members of the Li-Te system, the others being the raw metals and lithium telluride (Li
2Te).
LiTe3 was first discovered in 1969 by researchers at the US Atomic Energy Commission.[1] Research into the compound has been primarily driven by the possibility of using molten tellurium salts to cool a nuclear reactor.[2][3][4]
Lithium tritelluride can be synthesized by heating a mixture of the appropriate stoichiometry. It is unstable below 304 °C; if left below that temperature, it will decompose, releasing tellurium vapor.[2][3][4]
Structurally, lithium tritelluride is composed of parallel graphene-like planes of tellurium. Atoms in these planes are aligned to form "vertical" columns of tellurium; the lithium ions then form columns running through the center of each tellurium hexagon.[5]
References
- ^ Foster, M. S.; Johnson, C. E.; Davis, K. A.; Peck, J.; Schablaske, R. (1969). (Technical report). USAEC. p. 141. ANL-7575.
{{cite tech report}}: Missing or empty|title=(help), as cited in Valentine, Cavin & Yakel 1977. - ^ a b Hitch, B.F.; Toth, L.M.; Brynestad, J. (January 1978). "The decomposition equilibrium of LiTe3". Journal of Inorganic and Nuclear Chemistry. 40 (1): 31–34. doi:10.1016/0022-1902(78)80301-7.
- ^ a b Cunningham, P. T.; Johnson, S. A.; Cairns, E. J. (1973). "Phase Equilibria in Lithium-Chalcogen Systems". Journal of the Electrochemical Society. 120 (3): 328. doi:10.1149/1.2403448.
- ^ a b Songster, J.; Pelton, A. D. (June 1992). "The li-te (lithium-tellurium) system". Journal of Phase Equilibria. 13 (3): 300–303. doi:10.1007/BF02667559. S2CID 97799347.
- ^ Valentine, D. Y.; Cavin, O. B.; Yakel, H. L. (15 May 1977). "On the crystal structure of LiTe3". Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 33 (5): 1389–1396. Bibcode:1977AcCrB..33.1389V. doi:10.1107/S0567740877006141. S2CID 98036149.