Transactions of the Indian Institute of Metals

, Volume 70, Issue 1, pp 167–174 | Cite as

Evolution of Thermoelectric β-FeSi2 Phase by Cryo Milling and Sintering

  • V. S. Poddar
  • N. B. Dhokey
  • S. P. Butee
  • N. B. Revade
  • M. M. Thombre
  • R. D. Purohit
  • Deep Prakash
Technical Paper
  • 122 Downloads

Abstract

Development of high temperature thermoelectric materials, like β-FeSi2, is the need of twenty-first century to convert waste heat energy to electrical energy. The increasing interest in bulk semiconducting iron disilicide, β-FeSi2, is due to the advantages of its high thermoelectric power, high absorption coefficient (higher than 105 cm−1 above 1.0 eV) and direct band gap of 0.85 eV. The thermoelectric material is suitable for active component applications such as in light detectors, near-infrared sources, photovoltaic application and optical fiber communication. Powders of pure electrolytic iron and silicon were mechanically alloyed in a Cryo mill for various periods viz. 4, 6 and 8 h. As-milled powders were compacted at 700 MPa and the compacts were then subjected to different heat treatment cycles under vacuum (10−5 bar). The influence of variation in process parameters like milling period and sintering conditions on phase formation was studied. Traces of β-FeSi2 phase appeared after Cryo milling for 6 h. The optimized condition to have nearly complete formation of the β-FeSi2 phase, was found to be the one in which the material was Cryo milled for 6 h which was followed by sintering of compacts at 800 °C for 6 h under vacuum.

Graphical Abstract

XRD analysis of sintered compacts

Keywords

Thermoelectric β-FeSi2 Cryo milling Sintering 

References

  1. 1.
    Makita Y, Nakayama Y, Fukuzawa Y, Wang S N, Otogawa N, Suzuki Y, Liu Z X, Osamura M, Ootsuka T, Mise T, and Tanoue H, Thin Solid Films 461 (2004) 202.CrossRefGoogle Scholar
  2. 2.
    Chi D Z, Thin Solid Films 537 (2013) 1.CrossRefGoogle Scholar
  3. 3.
    Katsuyama S, Ito M, and Nagai H, KONA 22 (2004) 186.CrossRefGoogle Scholar
  4. 4.
    Takeda M, Kuramitsu M, and Yoshio M, Thin Solid Films 461 (2004) 179.CrossRefGoogle Scholar
  5. 5.
    Rowe DM, CRC Handbook of Thermoelectrics, (1994), p 1.Google Scholar
  6. 6.
    Yue Q I U, Hong-lie S H E N, Yu-gang Y I N, and Kai-hua W U, Trans Nonferrous Metals Soc China 17 (2007) 618.Google Scholar
  7. 7.
    Alama H, and Ramakrishna S, Nano Energy 2 (2013) 190.CrossRefGoogle Scholar
  8. 8.
    Ur S C, and Kim I H, Metals Mater Int 11 (2005) 301.CrossRefGoogle Scholar
  9. 9.
    Suryanarayana C, Prog Mater Sci 46 (2001) 1.CrossRefGoogle Scholar
  10. 10.
    ASM Metals Handbook Volume 03, Binary Alloy Phase Diagrams, p 860.Google Scholar
  11. 11.
    Kiatgamolchai S, Parinyataramas J, Nilpairach S, Thueploy A, Wanichsampan J, and Min G, J Metall 12 (2006) 119.Google Scholar
  12. 12.
    Yue Q, Hong lie S, Gang Y Y, and Kai hua W U, J Nonferrous Mater China 17 (2007) 618.Google Scholar
  13. 13.
    Chi D Z, J Thin Solid Films 537 (2013) 1.CrossRefGoogle Scholar

Copyright information

© The Indian Institute of Metals - IIM 2016

Authors and Affiliations

  • V. S. Poddar
    • 1
  • N. B. Dhokey
    • 1
  • S. P. Butee
    • 1
  • N. B. Revade
    • 1
  • M. M. Thombre
    • 1
  • R. D. Purohit
    • 2
  • Deep Prakash
    • 2
  1. 1.Department of Metallurgy and Materials ScienceCollege of EngineeringPuneIndia
  2. 2.Powder Metallurgy DivisionBhabha Atomic Research CentreNavi MumbaiIndia

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