Controlling the Crystallite Size of Zinc Oxide Nanorods via Chemical Bath Deposition and Post-Hydrothermal Treatment

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ZnO nanorods were deposited on ITO glass substrate via chemical bath deposition at low temperature of 90°C. The seeding solution was made by dissolving zinc nitrate tetrahydrate and methenamine in cool water (5°C). The as-synthesized ZnOs were further subjected to post-hydrothermal treatment series. The results of scanning electron microscope (SEM) studies showed that the ZnO nanorods were grown as vertically-aligned hexagonal structure, while x-ray diffraction (XRD) patterns showed a high intensity of [002] peak. The absorption spectra of the as-synthesized sample indicated a strong absorption peak near the UV region. After post-hydrothermal treatments, the absorption was slightly shifted to visible region. The ZnO nanorods sample derived from post-hydrothermal treatment at 150°C for 12 hours has the largest crystallite size of 269.402 nm and the lowest band gap energy, Eg value of 3.205 eV.

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28-32

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January 2013

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] G. Yi, C. Wang, and W. Park, Semiconductor Science and Technology 20 (2005) S22- S34.

Google Scholar

[2] S.H. Hu, Y.C. Chen, C.C. Hwang, C.H., Peng, and D.C. Gong, Journal of Alloy and Compounds 500 (2010) L17-L21.

Google Scholar

[3] G. Kenanakis, D. Vernardou, E. Koudomas, and N. Katsarakis, Journal of Crystal Growth 311 (2009) 4799-4804.

Google Scholar

[4] X. Wu, H. Chen, L. Gong, F. Qu, and Y. Zheng, Advances in Natural Sciences, Nanoscience and Nanotechnology 2 (2011) 23.

Google Scholar

[5] Lang, J., Yang, J., Li, C., Yang, L., Han, Q., Zhang, Y., Wang, D., Gao, M., and Liu, X: Crystal Res. Technology 43 (2008) 1314-1317.

Google Scholar

[6] B.D. Cullity, Elements of X-Ray Diffraction, Addison-Wesley Publishing Co. Inc, Massachusets, (1978).

Google Scholar

[7] D. Vernardou, G. Kenanakis, K. Vlachou, E. Koudoumas, G. Kiriakidis, A. Vairis and N. Katsarakis: Physica Solidi Status C 5 (2008) 3348-3352.

DOI: 10.1002/pssc.200778879

Google Scholar

[8] H. Zhang, J. Feng, J. Wang, and M. Zhang, Materials Lett. 61 (2007) 5202-5205.

Google Scholar

[9] M. Rusu, G. G. Rusu, M. Girtan, and S. Dabos Seignon, Journal of Non-Crystalline Solids, 354 (2008) 4461-4464.

DOI: 10.1016/j.jnoncrysol.2008.06.070

Google Scholar

[10] T. H. Meen, W. Water, Y. S. Chen, W. R. Chen, L. W. Ji, and C. J. Huang, IEEE Conference on Electron Devices and Solid State Circuits (EDSSC), Tainan 2 (2007) 617-620.

Google Scholar