Lead tin telluride

Lead tin telluride, also referred to as PbSnTe or Pb1−xSnxTe, is a ternary alloy of lead, tin and tellurium, generally made by alloying either tin into lead telluride or lead into tin telluride. It is a IV-VI narrow band gap semiconductor material.

The band gap of Pb1−xSnxTe is tuned by varying the composition(x) in the material. SnTe can be alloyed with Pb (or PbTe with Sn) in order to tune the band gap from 0.29 eV (PbTe) to 0.18 eV (SnTe). It is important to note that unlike II-VI chalcogenides, e.g. cadmium, mercury and zinc chalcogenides, the band gap in Pb1−xSnxTe does not changes linearly between the two extremes. In contrast, as the composition (x) is increased, the band gap decreases, approaches zero in the concentration regime (0.32–0.65 corresponding to temperature 4-300 K, respectively) and further increases towards bulk band gap of SnTe.[1] Therefore, the lead tin telluride alloys have narrower band gaps than their end point counterparts making lead tin telluride an ideal candidate for mid infrared, 3–14 μm opto-electronic application.

Properties

Lead tin telluride is p-type semiconductor at 300 K. The hole concentration increases as the tin content is increased resulting in an increase in electrical conductivity. For composition range x = 0 to 0.1, electrical conductivity decreases with increase in temperature up to 500 K and increases beyond 500 K. For composition range, x ≥ 0.25, electrical conductivity decreases with increases in temperature.

The Seebeck coefficient of Pb1−xSnxTe decreases with increases in Sn content at 300 K.

For composition x > 0.25, thermal conductivity of Pb1−xSnxTe increases with increase in Sn content. Thermal conductivity values decreases with increase in temperature over the entire composition range, x > 0.

For Pb1−xSnxTe, the optimum temperature corresponding to maximum thermoelectric power factor increases with increase in composition x. The pseudo binary alloy of Lead tin telluride acts as a thermoelectric material over 400–700 K temperature range.[2]

Lead tin telluride has a positive temperature coefficient i.e. for a given composition x, band gap increases with temperature. Therefore, temperature stability has to be maintained while working with lead tin telluride based laser. However, the advantage is that the operating wavelength of the laser can simply be tuned by varying the operating temperature.

The optical absorption coefficient of lead tin telluride is typically ~750 cm−1 as compared to ~50 cm−1 for the extrinsic semiconductors such as doped silicon.[3] The higher optical coefficient value not only ensures higher sensitivity but also reduces the spacing required between individual detector elements to prevent optical cross talk making integrated circuit technology easily accessible.[4]

Application

Due to tunable narrow band gap and relatively higher operating temperature of lead tin telluride as compared to mercury cadmium telluride, it has been a material of choice for commercial applications in IR sources, band pass filters and IR detectors.[4][5][6][7] It has found applications as photovoltaic devices for sensing radiation in 8-14 μm window.[8][9]

Single Crystal Pb1−xSnxTe diode lasers have been employed for detection of gaseous pollutants like sulfur dioxide.[10][11]

Lead tin tellurides have been used in thermoelectric devices.[12]

gollark: Strange implicit conversions.
gollark: Easy to pick up maybe, but the ecosystem is a *mess* and the type system is essentially nonexistent.
gollark: Interesting.
gollark: C is also very popular, for example.
gollark: True, but that doesn't make it good.

References

  1. Dimmock, J. O.; Melngailis, I.; Strauss, A. J. (1966). "Band Structure and Laser Action in PbxSn1−xTe". Physical Review Letters. 16 (26): 1193. Bibcode:1966PhRvL..16.1193D. doi:10.1103/PhysRevLett.16.1193.
  2. Orihashi, M.; Noda, Y.; Chen, L. D.; Goto, T.; Hirai, T. (2000). "Effect of tin content on thermoelectric properties of p-type lead tin telluride". Journal of Physics and Chemistry of Solids. 61 (6): 919–923. Bibcode:2000JPCS...61..919O. doi:10.1016/S0022-3697(99)00384-4.
  3. Burstein, E.; Picus, G.; Sciar, N. (1954). "Optical and Photoconductive Properties of Silicon and Germanium". In R. G. Breckenridge (ed.). Photoconductivity Conference. New York: John Wiley & Sons. pp. 353–409.
  4. Mathur, D. P. (1975). "Recent Infrared Detector Developments for Future Remote Sensor Applications". Optical Engineering. 14 (4): 351. Bibcode:1975OptEn..14..351M. doi:10.1117/12.7971844.
  5. Yoshikawa, M.; Shinohara, K.; Ueda, R. (1977). "Continuous operation over 1500 h of a Pb Te/PBSN Te double‐heterostructure laser at 77 K". Applied Physics Letters. 31 (10): 699–701. doi:10.1063/1.89491.
  6. Kasemset, D.; Rotter, S.; Fonstad, C. G. "Pb1−xSnxTe/PbTe1−ySey lattice-matched buried heterostructure lasers with CW Single mode output". doi:10.1109/EDL.1980.25236. Cite journal requires |journal= (help)
  7. Wakefield, S. L. (1971) "Production of lead-tin-telluride material for infrared detectors". U.S. Patent 3,673,063
  8. Rolls, W.; Lee, R.; Eddington, R. J. (1970). "Preparation and properties of lead-tin telluride photodiodes". Solid-State Electronics. 13 (1): 75–78. Bibcode:1970SSEle..13...75R. doi:10.1016/0038-1101(70)90011-0.
  9. Oron, M.; Zussman, A.; Katzir, A. (1982). "Lifetime mechanisms, tunnelling currents and laser thresholds of PbSnTe diode lasers". Infrared Physics. 22 (3): 171–174. doi:10.1016/0020-0891(82)90037-9.
  10. Antcliffe, G. A. and Wrobel, J. S. (1972). "Detection of the Gaseous Pollutant Sulfur Dioxide Using Current Tunable Pb(1-x) SNM(x) Te Diode Lasers". Applied Optics. 11 (7): 1548–1552. doi:10.1364/AO.11.001548. PMID 20119184.CS1 maint: multiple names: authors list (link)
  11. Antcliffe, G. A.; Wrobel, J. S. (1972). "Detection of the Gaseous Pollutant Sulfur Dioxide Using Current Tunable Pb1-xSnMx Te Diode Lasers". Applied Optics. 11 (7): 1548–52. doi:10.1364/AO.11.001548. PMID 20119184..
  12. Hockings, Eric F and Mularz, Walter L (1961) "Lead telluride-tin telluride thermoelectric compositions and devices" U.S. Patent 3,075,031
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.