Rhenium disulfide

Rhenium disulfide

Names
IUPAC name Bis(sulfanylidene)rhenium
Other names Rhenium(IV) sulfide
Identifiers
CAS Number	12038-63-0
3D model (JSmol)	Interactive image
ChemSpider	74775
ECHA InfoCard	100.031.695
EC Number	234-878-3
PubChem CID	82864
CompTox Dashboard (EPA)	DTXSID7065201
InChI InChI=1S/Re.2S Key: USWJSZNKYVUTIE-UHFFFAOYSA-N
SMILES S=[Re]=S
Properties
Chemical formula	ReS2
Molar mass	250.337 g/mol [1]
Odor	odorless
Density	7.6 g/cm3 [1]
Solubility in water	insoluble
Structure
Crystal structure	Triclinic, aP12, space group P1, No 2 [2]
Lattice constant	a = 0.6352 nm, b = 0.6446 nm, c = 1.2779 nm α = 91.51°, β = 105.17°, γ = 118.97°
Formula units (Z)	8
Related compounds
Other anions	Rhenium(IV) oxide Rhenium diselenide Rhenium ditelluride
Other cations	Manganese diselenide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Rhenium disulfide is an inorganic compound of rhenium and sulfur with the formula ReS₂. It has a layered structure where atoms are strongly bonded within each layer. The layers are held together by weak Van der Waals bonds, and can be easily peeled off from the bulk material.

Production

ReS₂ is found in nature as the mineral rheniite. ^[3] It can be synthesized from the reaction between rhenium and sulfur at 1000 °C, or the decomposition of rhenium(VII) sulfide at 1100 °C: ^[4]

Re + 2 S → ReS₂

Re₂S₇ → 2 ReS₂ + 3 S

Nanostructured ReS₂ can usually be achieved through mechanical exfoliation, chemical vapor deposition (CVD), and chemical and liquid exfoliations. Larger crystals can be grown with the assistance of liquid carbonate flux at high pressure. It is widely used in electronic and optoelectronic device, energy storage, photocatalytic and electrocatalytic reactions. ^[5]

Properties

It is a two-dimensional (2D) group VII transition metal dichalcogenide (TMD). ReS₂ was isolated down to monolayers which is only one unit cell in thickness for the first time in 2014. ^[6] These monolayers have shown layer-independent electrical, optical, and vibrational properties much different from other TMDs.

Structure

Bulk ReS₂ has a layered structure and a platelet-like habit. Different crystal structures were proposed for ReS₂ based on single-crystal X-ray diffraction studies. While all authors agree that the lattice is triclinic, the reported cell parameters and atomic arrangements slightly differ. The earliest work ^[7] describes ReS₂ in a triclinic unit cell (sp. gr. P${\displaystyle {\bar {1}}}$, a = 0.6455 nm, b = 0.6362 nm, c = 0.6401 nm, α = 105.04°, β = 91.60°, γ = 118.97°) as a distorted variant of the CdCl₂ prototype (1T structure, trigonal space group R${\displaystyle {\bar {3}}}$m). In comparison with ideal octahedral coordination of the metal atoms in CdCl₂, the Re atoms in ReS₂ are displaced from the centers of the surrounding Se₆ octahedra and form Re₄ clusters that are linked to chains in the b direction. A later study ^[8] proposed a more accurate description of the crystal structure. It reports a different triclinic cell (sp. gr. P${\displaystyle {\bar {1}}}$, a = 0.6352 nm, b = 0.6446 nm, c = 1.2779 nm, α = 91.51°, β = 105.17°, γ = 118.97°) with the doubled c parameter and swapped a and b, α and β. There are two layers in this unit cell, related by symmetry centers, and the chains of clusters run along the a axis. Each layer form parallelogram-shaped connected clusters with Re-Re distances of ca. 0.27-0.28 nm in the cluster, and ca. 0.29 nm between clusters. There is one more structure description of ReS₂ published in ^[9] in yet another triclinic cell (sp. gr. P${\displaystyle {\bar {1}}}$, a = 0.6417 nm, b = 0.6510 nm, c = 0.6461 nm, α = 121.10°, β = 88.38°, γ = 106.47°) where only one layer is present and the centers of symmetry are in the Re layer. The current consent is that the latter work might have overlooked the doubling of the c parameter captured in. ^[8]

Natural Occurrence

Rhenium disulfide is known in nature as the very rare mineral rheniite. ^{[10] [11]}

References

1. Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.84. ISBN   1-4398-5511-0.
2. Lamfers, H.-F.; Meetsma, A; Wiegers, G.A.; de Boer, J.L. (1996). "The crystal structure of some rhenium and technetium dichalcogenides". Journal of Alloys and Compounds. 241: 34–39. doi:10.1016/0925-8388(96)02313-4.
3. Rheniite, Mindat.org , retrieved 2020-07-17
4. Brauer, Georg (1981). Handbuch der Präparativen Anorganischen Chemie. Band III (in German) (3rd ed.). Stuttgart: Ferdinand Enke. p. 1619. ISBN   3-432-87823-0.
5. Rahman, Mohammad; Davey, Kenneth; Qiao, Shi-Zhang (2017). "Advent of 2D Rhenium Disulfide (ReS2): Fundamentals to Applications" (PDF). Advanced Functional Materials. 27 (10): 1606129. doi:10.1002/adfm.201606129. hdl: 2440/103880 . S2CID   99931114.
6. Tongay, Sefaattin; Sahin, Hasan; Ko, Changhyun; Luce, Alex; Fan, Wen; Liu, Kai; Zhou, Jian; Huang, Ying-Sheng; Ho, Ching-Hwa; Yan, Jinyuan; Ogletree, D. Frank; Aloni, Shaul; Ji, Jie; Li, Shushen; Li, Jingbo; Peeters, F. M.; Wu, Junqiao (2014). "Monolayer behaviour in bulk ReS₂ due to electronic and vibrational decoupling". Nature Communications. 5: 3252. Bibcode:2014NatCo...5.3252T. doi: 10.1038/ncomms4252 . PMID   24500082.
7. Wildervanck, J.C.; Jellinek, F. (1971-05-01). "The dichalcogenides of technetium and rhenium". Journal of the Less Common Metals. 24 (1): 73–81. doi:10.1016/0022-5088(71)90168-8. ISSN   0022-5088.
8. Lamfers, H.-J.; Meetsma, A.; Wiegers, G.A.; De Boer, J.L. (1996-08-01). "The crystal structure of some rhenium and technetium dichalcogenides". Journal of Alloys and Compounds. 241 (1–2): 34–39. doi:10.1016/0925-8388(96)02313-4. ISSN   0925-8388.
9. Murray, H. H.; Kelty, S. P.; Chianelli, R. R.; Day, C. S. (September 1994). "Structure of Rhenium Disulfide". Inorganic Chemistry. 33 (19): 4418–4420. doi:10.1021/ic00097a037. ISSN   0020-1669.
10. Webmineral
11. Mindat.org