Tantalum(IV) sulfide

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Tantalum(IV) sulfide
Molybdenite-3D-balls.png
Crystal structure showing two stacked S-Ta-S sheets
Names
Other names
tantalum disulfide
Identifiers
3D model (JSmol)
ECHA InfoCard 100.032.047 Edit this at Wikidata
  • InChI=1S/2S.Ta
  • S=[Ta]=S
Properties
TaS2
Molar mass 245.078 g/mol[1]
Appearance black crystals[1]
Density 6.86 g/cm3[1]
Melting point >3000 °C [1]
Insoluble[1]
Related compounds
Other anions
Tantalum telluride
Tantalum diselenide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Tantalum(IV) sulfide is the inorganic compound with the formula TaS2. It is a layered compound with three-coordinate sulfide centres and trigonal prismatic metal centres. It is structurally similar to the more famous material molybdenum disulfide, MoS2. TaS2 is a semiconductor with d1 electron configuration. Although an obscure material otherwise, TaS2 has been the subject of numerous studies because it is a versatile host for intercalation of electron donors,[2] and because it exhibits unusual phase transitions at low temperatures.

Preparation[]

TaS2 is prepared by reaction of powdered tantalum and sulfur at ~900 °C.[3] It is purified and crystallized by chemical vapor transport using iodine as the transporting agent:[4]

TaS2 + 2 I2 ⇌ TaI4 + 2 S

Properties[]

(a): Schematic of the David star pattern in 1T-TaS2 where green atoms are S and purple are Ta. (b) and (c) are STM images taken at 6.5 K at different magnifications, before and after application of 2.8 V pulses through the STM tip. Insets show ~10 times magnified images.

Three major crystalline phases are known for TaS2: trigonal 1T with one S-Ta-S sheet per unit cell, hexagonal 2H with two S-Ta-S sheets, and rhombohedral 3R with three S-Ta-S sheets per cell; 4H and 6R phases are also observed, but less frequently. These polymorphs mostly differ by the relative arrangement of the S-Ta-S sheet rather than the sheet structure.[5]

2H-TaS2 is a superconductor with the bulk transition temperature TC = 0.5 K, which increases to 2.2 K in flakes with a thickness of a few atomic layers.[3] The bulk TC value increases up to ~8 K at 10 GPa and then saturates with increasing pressure.[6] In contrast, 1T-TaS2 starts superconducting only at ~2 GPa; as a function of pressure its TC quickly rises up to 5 K at ~4 GPa and then saturates.[7]

At ambient pressure and low temperatures 1T-TaS2 is a Mott insulator.[7] Upon heating it changes to a Triclinic charge density wave (TCDW) state at TTCDW ~ 220 K,[8][9][10] to a nearly commensurate charge density wave (NCCDW) state at TNCCDW ~ 280 K,[11] to an incommensurate CDW (ICCDW) state at TICCDW ~ 350 K,[11] and to a metallic state at TM ~ 600 K.

In the CDW state the TaS2 lattice deforms to create a periodic Star of David pattern. Application of (e.g. 50fs) optical laser pulses[12] or voltage pulses (~2–3 V) through electrodes[13] or in a scanning tunneling microscope (STM) to the CDW state causes it to drop electrical resistance and creates a "mosaic" or domain state consisting of nanometer-sized domains, where both the domains and their walls exhibit metallic conductivity. This mosaic structure is metastable and gradually disappears upon heating.[4][14][13]

Switching of the material to and from the "mosaic", or domain state, by optical or electrical pulses is used for "Charge configuration memory" (CCM) devices. The distinguishing feature of such devices is that they exhibit very efficient and fast non-thermal resistance switching at low temperatures.[15]

References[]

  1. ^ a b c d e Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.93. ISBN 1-4398-5511-0.
  2. ^ Revelli, J. F.; Disalvo, F. J. (1995). "Tantalum Disulfide (TaS2) and Its Intercalation Compounds". Inorganic Syntheses. Inorganic Syntheses. 30: 155. doi:10.1002/9780470132616.ch32.
  3. ^ a b Navarro-Moratalla, Efrén; Island, Joshua O.; Mañas-Valero, Samuel; Pinilla-Cienfuegos, Elena; Castellanos-Gomez, Andres; Quereda, Jorge; Rubio-Bollinger, Gabino; Chirolli, Luca; Silva-Guillén, Jose Angel; Agraït, Nicolás; Steele, Gary A.; Guinea, Francisco; Van Der Zant, Herre S. J.; Coronado, Eugenio (2016). "Enhanced superconductivity in atomically thin TaS2". Nature Communications. 7: 11043. arXiv:1604.05656. Bibcode:2016NatCo...711043N. doi:10.1038/ncomms11043. PMC 5512558. PMID 26984768.
  4. ^ a b Cho, Doohee; Cheon, Sangmo; Kim, Ki-Seok; Lee, Sung-Hoon; Cho, Yong-Heum; Cheong, Sang-Wook; Yeom, Han Woong (2016). "Nanoscale manipulation of the Mott insulating state coupled to charge order in 1T-TaS2". Nature Communications. 7: 10453. arXiv:1505.00690. Bibcode:2016NatCo...710453C. doi:10.1038/ncomms10453. PMC 4735893. PMID 26795073.
  5. ^ Dunnill, Charles W.; MacLaren, Ian; Gregory, Duncan H. (2010). "Superconducting tantalum disulfide nanotapes; growth, structure and stoichiometry" (PDF). Nanoscale. 2 (1): 90–7. Bibcode:2010Nanos...2...90D. doi:10.1039/B9NR00224C. PMID 20648369.
  6. ^ Freitas, D. C.; Rodière, P.; Osorio, M. R.; Navarro-Moratalla, E.; Nemes, N. M.; Tissen, V. G.; Cario, L.; Coronado, E.; García-Hernández, M.; Vieira, S.; Núñez-Regueiro, M.; Suderow, H. (2016). "Strong enhancement of superconductivity at high pressures within the charge-density-wave states of 2H−TaS2 and 2H−TaSe2". Physical Review B. 93 (18): 184512. arXiv:1603.00425. Bibcode:2016PhRvB..93r4512F. doi:10.1103/PhysRevB.93.184512. S2CID 54705510.
  7. ^ a b Sipos, B.; Kusmartseva, A. F.; Akrap, A.; Berger, H.; Forró, L.; Tutiš, E. (2008). "From Mott state to superconductivity in 1T-TaS2". Nature Materials. 7 (12): 960–5. Bibcode:2008NatMa...7..960S. doi:10.1038/nmat2318. PMID 18997775.
  8. ^ Tanda, Satoshi; Sambongi, Takashi; Tani, Toshiro; Tanaka, Shoji (1984). "X-Ray Study of Charge Density Wave Structure in 1T-TaS2". J. Phys. Soc. Jpn. 53 (2): 476. Bibcode:1984JPSJ...53..476T. doi:10.1143/JPSJ.53.476.
  9. ^ Tanda, Satoshi; Sambongi, Takashi (1985). "X-ray study of the new charge-density-wave phase in 1T-TaS2". Synthetic Metals. 11 (2): 85–100. doi:10.1016/0379-6779(85)90177-8.
  10. ^ Coleman, R. V.; Giambattista, B.; Hansma, P.K; Johnson, A.; McNairy, W.W.; Slough, C.G. (1988). "Scanning tunnelling microscopy of charge-density waves in transition metal chalcogenides". Advances in Physics. 37 (6): 559–644. doi:10.1080/00018738800101439.
  11. ^ a b Wilson, J.A.; Di Salvo, F.J.; Mahajan, S. (1975). "Charge-density waves and superlattices in the metallic layered transition metal dichalcogenides". Advances in Physics. 24 (2): 117–201. doi:10.1080/00018737500101391.
  12. ^ Stojchevska, L.; Vaskivskyi, I.; Mertelj, T.; Kusar, P.; Svetin, D.; Brazovskii, S.; Mihailovic, D. (2014). "Ultrafast Switching to a Stable Hidden Quantum State in an Electronic Crystal". Science. 344 (6180): 177–180. arXiv:1401.6786. doi:10.1126/science.1241591. ISSN 0036-8075.
  13. ^ a b Vaskivskyi, I.; Gospodaric, J.; Brazovskii, S.; Svetin, D.; Sutar, P.; Goreshnik, E.; Mihailovic, I.A.; Mertelj, T.; Mihailovic, D. (2014). "Ultrafast Switching to a Stable Hidden Quantum State in an Electronic Crystal". Science. 344 (6180): 177–180. doi:10.1126/sciadv.1500168. ISSN 0036-8075.
  14. ^ Ma, Liguo; Ye, Cun; Yu, Yijun; Lu, Xiu Fang; Niu, Xiaohai; Kim, Sejoong; Feng, Donglai; Tománek, David; Son, Young-Woo; Chen, Xian Hui; Zhang, Yuanbo (2016). "A metallic mosaic phase and the origin of Mott-insulating state in 1T-TaS2". Nature Communications. 7: 10956. arXiv:1507.01312. Bibcode:2016NatCo...710956M. doi:10.1038/ncomms10956. PMC 4792954. PMID 26961788.
  15. ^ Mihailovic, D.; Svetin, D.; Vaskivskyi, I.; Venturini, R.; Lipovsek, B.; Mraz, A. (2021). "Ultrafast non-thermal and thermal switching in charge configuration memory devices based on 1T-TaS2". Appl. Phys. Lett. 119: 013106. doi:10.1063/5.0052311.
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