Microstructure and varistor properties of V-doped ZnO nanoparticles prepared by co-precipitation method

Article

Abstract

V-doped ZnO nanoparticles (0.5, 1, 1.5 and 2 at.% V) for varistor application have been prepared by co-precipitation method. XRD, TEM, EDS, SEM and FTIR have been employed to characterize the as-synthesized V-doped ZnO nanopowders and varistor samples. Pure and V-doped ZnO nanoparticles have a hexagonal wurtzite structure and the (002) diffraction peaks position of V-doped ZnO shift toward smaller value of diffraction angle compared with pure ZnO powders. The results confirm that the V ions were well incorporated into ZnO crystal lattice. Simultaneously, V doping also inhibited the growth of particles and the size decreased from 45.1755 to 29.5137 nm with the increase in doping concentration from 0 to 2 at.%. The microstructure of 2 at.% V-doped ZnO varistor consists mainly of ZnO grains with Zn3(VO4)2 as the minority secondary phase at 900 °C. The varistor ceramics has a sintered density of 5.55 g/cm3 corresponding to 96.2 % of its theoretical density, with breakdown voltage of 4100 V/cm and nonlinear coefficient of ~7.2.

Keywords

Breakdown Voltage Full Width Half Maximum Nonlinear Coefficient Varistor Ceramic Versus Doping 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

This work was financially supported by Changzhou Science, Technology Innovation Project, Nature Science Foundation of China (CC20140048, CC20130204, No. 51273027) and 2014 Research and Innovation Project for College Graduates of Jiangsu Province.

References

  1. 1.
    M.P. Lu, J.H. Song, M.Y. Lu, M.T. Chen et al., Nano Lett. 9, 1223–1227 (2009)CrossRefGoogle Scholar
  2. 2.
    S.Y. Chu, T.M. Yan, S.L. Chen, Ceram. Int. 26, 733–737 (2000)CrossRefGoogle Scholar
  3. 3.
    S. Suwanboon, P. Amornpitoksuk, N. Muensit, Ceram. Int. 37, 2247–2253 (2011)CrossRefGoogle Scholar
  4. 4.
    J. Fan, K. Sreekanth, Z. Xie, S. Chang, K. Rao, Prog. Mater Sci. 58, 874–985 (2013)CrossRefGoogle Scholar
  5. 5.
    Q. Zhang, C.S. Dandeneau, X. Zhou, G. Cao, Adv. Mater. 21, 1–22 (2009)Google Scholar
  6. 6.
    O. Lupan, G. Emelchenko, V. Ursaki et al., Mater. Res. Bull. 45, 1026–1032 (2010)CrossRefGoogle Scholar
  7. 7.
    M. Ohyama, H. Kozuka, T. Yoko, J. Am. Ceram. Soc. 81, 1622–1632 (1998)CrossRefGoogle Scholar
  8. 8.
    J.L. Li, G.H. Chen, C.L. Yuan, Ceram. Int. 39, 2231–2237 (2013)CrossRefGoogle Scholar
  9. 9.
    C.W. Nahm, J. Eur. Ceram. Soc. 23, 1345–1353 (2003)CrossRefGoogle Scholar
  10. 10.
    M. Matsuoka, Jpn. J. Appl. Phys. 10, 736–746 (1971)CrossRefGoogle Scholar
  11. 11.
    J. Wong, J. Appl. Phys. 51, 4453–4459 (1980)CrossRefGoogle Scholar
  12. 12.
    K. Mukae, K. Tsuda, I. Nagasawa, Jpn. J. Appl. Phys. 16, 1361–1368 (1977)CrossRefGoogle Scholar
  13. 13.
    A.B. Alles, V.L. Burdick, J. Appl. Phys. 70, 6883–6890 (1991)CrossRefGoogle Scholar
  14. 14.
    M. Matsuoka, T. Masuyama, Y. Lida, Jpn. J. Appl. Phys. 8, 1275–1276 (1969)CrossRefGoogle Scholar
  15. 15.
    H.H. Hng, K.Y. Tse, Ceram. Int. 34, 1153–1157 (2008)CrossRefGoogle Scholar
  16. 16.
    J.K. Tsai, T.B. Wu, Mater. Lett. 26, 199–203 (1996)CrossRefGoogle Scholar
  17. 17.
    H.H. Hng, K.M. Knowles, J. Am. Ceram. Soc. 83, 2455–2462 (2000)CrossRefGoogle Scholar
  18. 18.
    H.H. Hng, P.L. Chan, Mater. Chem. Phys. 75, 61–66 (2002)CrossRefGoogle Scholar
  19. 19.
    J.K. Tsai, T.B. Wu, J. Appl. Phys. 76, 4817–4822 (1994)CrossRefGoogle Scholar
  20. 20.
    H.H. Hng, P.L. Chan, Ceram. Int. 35, 409–413 (2009)CrossRefGoogle Scholar
  21. 21.
    K.P. Shinde, R.C. Pawar, B.B. Sinha et al., Ceram. Int. 40, 16799–16804 (2014)CrossRefGoogle Scholar
  22. 22.
    A. Mhamdi, A. Boukhachem, M. Madani et al., Optik 124, 3764–3770 (2013)CrossRefGoogle Scholar
  23. 23.
    J.L. Chen, D. Chen, J.J. He, S.Y. Zhang et al., Appl. Sur. Sci. 255, 9413–9419 (2009)CrossRefGoogle Scholar
  24. 24.
    J.H. Lee, B.O. Park, Thin Solid Films 426, 94–99 (2003)CrossRefGoogle Scholar
  25. 25.
    H.R. Mardani, M. Forouzani, M. Ziari, P. Biparva, Spectrochim. Acta A 141, 27–33 (2015)CrossRefGoogle Scholar
  26. 26.
    A.J. Reddy, M.K. Kokila, H. Nagabhushan et al., J. Alloys Compd. 509, 5349–5355 (2011)CrossRefGoogle Scholar
  27. 27.
    S. Senthilkumar, K. Rajendran, S. Banerjee et al., Mater. Sci. Semi. Process 11, 6–12 (2008)CrossRefGoogle Scholar
  28. 28.
    G. Murtaza, R. Ahmad, M.S. Rashid, M. Hassan et al., Curr. Appl. Phys. 14, 176–181 (2014)CrossRefGoogle Scholar
  29. 29.
    C.W. Nahm, Ceram. Int. 39, 2117–2121 (2013)CrossRefGoogle Scholar
  30. 30.
    H.H. Hng, K.M. Knowles, J. Eur. Ceram. Soc. 19, 721–726 (1999)CrossRefGoogle Scholar
  31. 31.
    D. Xung, X.N. Cheng, G.P. Zhao, J. Yang, L.Y. Shi, Ceram. Int. 37, 201–206 (2011)CrossRefGoogle Scholar
  32. 32.
    M.A. Ashraf, A.H. Bhuiyan, M.A. Hakim, M.T. Hossain, Mater. Sci. Eng. B. 176, 855–860 (2011)CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  • Zhong-Yin Zhao
    • 1
    • 2
  • Mao-Hua Wang
    • 1
    • 2
  • Han-Ping Zhang
    • 1
    • 2
  1. 1.School of Petrochemical EngineeringChangzhou UniversityChangzhouPeople’s Republic of China
  2. 2.Huaide CollegeChangzhou UniversityChangzhouPeople’s Republic of China

Personalised recommendations