Tantalum(IV) sulfide

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 golden or black crystals, depending on polytype[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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Tantalum(IV) sulfide is an inorganic compound with the formula TaS2. It is a layered compound with three-coordinate sulfide centres and trigonal prismatic or octahedral metal centres.[2] It is structurally similar to molybdenum disulfide MoS2, and numerous other transition metal dichalcogenides. Tantalum disulfide has three polymorphs 1T-TaS2, 2H-TaS2, and 3R-TaS2, representing trigonal, hexagonal, and rhombohedral respectively.

The properties of the 1T-TaS2 polytype have been described.[3][4][5]

CDW, the periodic distortion induced by the electron-phonon interaction,[6] ia manifested by formation a superlattice constitutes of clusters of 13 atoms, which is called the Star of David (SOD), where the surrounding 12 Ta atoms move slightly towards the centre of the star.[7] there are three 1T-TaS2 charge density wave phases: commensurate charge density wave (CCDW), nearly commensurate charge density wave (NCCDW), and incommensurate charge density wave (ICCDW). In the CCDW phase, the entire material is covered with the superlattice, but in the ICCDW phase, the atoms do not move. NCCDW is the phase between the two as the SOD clusters are confined within the nearly hexagonal-shaped areas. The phase transition of 1T-TaS2 could be achieved via temperature difference, as it is one of the most investigated methods to achieve phase transition of the material. In common with many other transition metal dichalcogenide (TMD) compounds, which are metallic at high temperatures, it exhibits a series of charge-density-wave (CDW) phase transitions from 550 K to 50 K. It is unusual amongst them in showing a low-temperature insulating state below 200 K, which is believed to arise from electron correlations, similar to many oxides. The insulating state is commonly attributed to a Mott state.[8] When cooling down to 550K, 1T-TaS2 transitions from metallic to ICCDW, then the material achieves NCCDW when cooling below 350K, and finally entering CCDW below 180K. However, if the temperature change is achieved by raising the temperature, another phase could appear between the CCDW phase and the NCCDW phase. The Triclinic Charge Density Wave (TCDW) is again the hybrid state between CCDW and ICCDW, the difference is that instead of forming an enclosed hexagon area, the material forms strips with different atom shifts. When 1T-TaS2 is heated at a lower temperature, the first transition is from CCDW to TCDW at 220K; Then, continue heating the material above 280K the phase of the material transits to NCCDW.[9][10] It is also superconducting under pressure or upon doping, with a familiar dome-like phase diagram as a function of dopant, or substituted isovalent element concentration.

Metastability. 1T-TaS2 is unique, not only amongst TMDs but also amongst 'quantum materials' in general, in showing a metastable metallic state at low temperatures.[11] Switching from the insulating to the metallic state can be achieved either optically or by the application of electrical pulses. The metallic state is persistentbelow ~20K, but its lifetime can be tuned by changing the temperature. The metastable state lifetime can also be tuned by strain. The electrically-induced switching between states is of current interest, because it can be used for ultrafast energy-efficient memory devices.[12]

Because of the frustrated triangular arrangement of localized electrons, the material is suspected of supporting some form of quantum spin liquid state. It has been the subject of numerous studies as a host for intercalation of electron donors.[13]

Preparation

TaS2 is prepared by reaction of powdered tantalum and sulfur at ~900 °C.[15] It is purified and crystallized by chemical vapor transport using iodine as the transporting agent:[16]

TaS2 + 2 I2 ⇌ TaI4 + 2 S

It can be easily cleaved and has a characteristic golden sheen. Upon extended exposure to air, the formation of an oxide layer causes darkening of the surface. Thin films can be prepared by chemical vapour deposition and molecular beam epitaxy.

Properties

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.[17]

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.[15] The bulk TC value increases up to ~8 K at 10 GPa and then saturates with increasing pressure.[18] 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.[8]

At ambient pressure and low temperatures 1T-TaS2 is a Mott insulator.[8] Upon heating it changes to a Triclinic charge density wave (TCDW) state at TTCDW ~ 220 K,[19][20][21] to a nearly commensurate charge density wave (NCCDW) state at TNCCDW ~ 280 K,[2] to an incommensurate CDW (ICCDW) state at TICCDW ~ 350 K,[2] and to a metallic state at TM ~ 600 K.[14]

In the CDW state the TaS2 lattice deforms to create a periodic Star of David pattern. Application of (e.g. 50fs) optical laser pulses[11] or voltage pulses (~2–3 V) through electrodes[22] 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.[16][23][22]

Memory devices and other potential applications

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.[12] Room temperature operation of a charge-density-wave oscillator and thermally-driven GHz modulation of the CDW state has been demonstrated.[24][25]

References

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