Fabrication and characterizations of Zn1−xCoxO bulk ceramics prepared by solid state reaction combined with spark plasma sintering

Article

Abstract

Zn1−xCoxO (x = 0.01, 0.05 and 0.1) bulk ceramics were prepared through a two-step, solid state reaction method combined with spark plasma sintering technique. The single phase Zn1−xCoxO powders were synthesized using ZnO and Co3O4 at 935 °C in air for 3 h. The Zn1−xCoxO bulks were prepared at sintering temperature from 900 to 1,100 °C for 5 min by SPS. The relative density of Zn1−xCoxO bulk ceramics sintered at 1,100 °C is higher than 99% of the theoretical value. The Structure, composition analysis, optical absorption, Raman and XPS measurements revealed that the Co2+ substituted Zn2+ ions and was incorporated into the lattice of ZnO in both of the single phase Zn1−xCoxO powders and bulk ceramics. Room- and low-temperature magnetization measurements reveal a paramagnetic behavior and that the paramagnetic Co amount is smaller than the nominal Co concentration for all of Zn1−xCoxO samples at 4 K. The paramagnetic magnetism of bulk ceramics is apparently larger than that of powders with the same composition. The electrical properties measurements reveal that the Co concentration has a slight influence on the electrical properties of Zn1−xCoxO bulk ceramics. The carriers concentration is about 1 × 1020 cm−3 and with the Co concentration increases the resistivity slightly increases from 3.56 × 10−3 (x = 0.01) to 5.58 × 10−3 (x = 0.1) Ωcm.

Keywords

Co3O4 Spark Plasma Sinter Solid State Reaction Method Moss Green Bulk Ceramic 
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 the New Century Excellent Talents in University (NCET-10-0662).

References

  1. 1.
    S.A. Wolf, D.D. Awschalom, R.A. Buhrman, J.M. Daughton, S. von Molna’r, M.L. Roukes, A.Y. Chtchelkanova, D.M. Treger, Science 294, 1488 (2001)CrossRefGoogle Scholar
  2. 2.
    T. Dietl, H. Ohno, F. Matsukura, J. Cibert, D. Ferrand, Science 287, 1019 (2000)CrossRefGoogle Scholar
  3. 3.
    K. Sato, H. Katayama-Yoshida, Jpn. J. Appl. Phys. 39, L555 (2000)CrossRefGoogle Scholar
  4. 4.
    M. Bouloudenine, N. Viart, S. Colis, J. Kortus, A. Dinia, Appl. Phys. Lett. 87, 052501 (2005)CrossRefGoogle Scholar
  5. 5.
    X. Wang, J. Xu, B. Zhang, H. Xu, J. Wang, X. Zhang, J. Yu, Q. Li, Adv. Mater. 18, 2476 (2006)CrossRefGoogle Scholar
  6. 6.
    J. Alaria, H. Bieber, S. Colis, G. Schmerber, A. Dinia, Appl. Phys. Lett. 88, 112503 (2006)CrossRefGoogle Scholar
  7. 7.
    N. Hasuike, K. Nishio, H. Katoh, A. Suzuki, T. Isshiki, K. Kisoda, H. Harima, J. Phys. Condens. Matter 21, 064215 (2009)CrossRefGoogle Scholar
  8. 8.
    O. Toulemonde, M. Gaudon, J. Phys. D 43, 045001 (2010)CrossRefGoogle Scholar
  9. 9.
    M.M. Can, T. Firat, S. Ozcan, J. Mater. Sci. 46, 1830 (2011)CrossRefGoogle Scholar
  10. 10.
    H.J. Lee, S.Y. Jeong, C.R. Cho, C.H. Park, Appl. Phys. Lett. 81, 4020 (2002)CrossRefGoogle Scholar
  11. 11.
    K.J. Kim, Y.R. Park, Appl. Phys. Lett. 81, 1420 (2002)CrossRefGoogle Scholar
  12. 12.
    D.A. Schwartz, D.R. Gamelin, Adv. Mater. 16, 2115 (2004)CrossRefGoogle Scholar
  13. 13.
    M. Nygren, Z. Shen, Solid. State. Sci. 5, 125 (2003)CrossRefGoogle Scholar
  14. 14.
    Y. Belghazi, D. Stoeffler, S. Colis, G. Schmerber, C. Ulhaq-Bouillet, J.L. Rehspringer, A. Berrada, H. Aubriet, J. Petersen, C. Becker, D. Ruch, A. Dinia, J. Appl. Phys. 105, 113904 (2009)CrossRefGoogle Scholar
  15. 15.
    Z.L. Lu, H.S. Hsu, Y.H. Tzeng, F.M. Zhang, Y.W. Du, J.C.A. Huang, Appl. Phys. Lett. 95, 102501 (2009)CrossRefGoogle Scholar
  16. 16.
    Y.D. Kim, S.L. Cooper, M.V. Klein, B.T. Jonker, Phys. Rev. B 49, 1732 (1994)CrossRefGoogle Scholar
  17. 17.
    Y.R. Lee, A.K. Ramdas, R.L. Aggarwal, Phys. Rev. B 38, 10600 (1988)CrossRefGoogle Scholar
  18. 18.
    P. Koidl, Phys. Rev. B 15, 2493 (1977)CrossRefGoogle Scholar
  19. 19.
    T.C. Damen, S.P.S. Porto, B. Tell, Phys. Rev. 142, 570 (1966)CrossRefGoogle Scholar
  20. 20.
    J.M. Calleja, M. Cardona, Phys. Rev. B 16, 3753 (1977)CrossRefGoogle Scholar
  21. 21.
    R. Cusco, E.A. Llado, J. Ibanez, L. Artus, J. Jimenez, B. Wang, M.J. Callahan, Phys. Rev. B 75, 165202 (2007)CrossRefGoogle Scholar
  22. 22.
    C.W. Tang, C.B. Wang, S.H. Chien, Thermochim. Acta 473, 68 (2008)CrossRefGoogle Scholar
  23. 23.
    Z.W. Dong, C.F. Zhang, H. Deng, G.J. You, S.X. Qian, Mater. Chem. Phys. 99, 160 (2006)CrossRefGoogle Scholar
  24. 24.
    V.Y. Davydov, I.N. Goncharuk, A.N. Smirnov, A.E. Nikolaev, W.V. Lundin, A.S. Usikov, A.A. Klochikhin, J. Aderhold, J. Graul, O. Semchinova, H. Harima, Phys. Rev. B 65, 125203 (2002)CrossRefGoogle Scholar
  25. 25.
    X. Wang, J. Xu, X. Yu, K. Xue, J. Yu, X. Zhao, Appl. Phys. Lett. 91, 031908 (2007)CrossRefGoogle Scholar
  26. 26.
    X. Xu, C. Cao, J. Alloy. Compd. 501, 265 (2010)CrossRefGoogle Scholar
  27. 27.
    K. Samanta, P. Bhattacharya, R.S. Katiyar, W. Iwamoto, P.G. Pagliuso, C. Rettori, Phys. Rev. B 73, 245213 (2006)CrossRefGoogle Scholar
  28. 28.
    D. Chu, Y.-P. Zeng, D.L. Jiang, J. Phys. Chem. C 111, 5893 (2007)CrossRefGoogle Scholar
  29. 29.
    J.F. Moulder, W.F. Stickle, P.E. Sobol, K.D. Bomben, Handbook of X-ray Photo-electron Spectroscopy (Perkin-Elmer, Eden Praitie, MN, 1992)Google Scholar
  30. 30.
    K.R. Kittilstved, N.S. Norberg, D.R. Gamelin, Phys. Rev. Lett. 94, 147209 (2005)CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  1. 1.State Key Lab of Advanced Technology for Materials Synthesis and Processing, Wuhan University of TechnologyWuhanChina

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