Temperature Effect on Phase Formation of Nanocrystalline Bismuth Titanate Synthesized via Hot Injection Method

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Nanocrystalline bismuth titanate materials were synthesized via hot injection method for the first time. Bismuth nitrate and titanium butoxide were used as precursors of Bi and Ti, respectively. The synthesis method was modified to use aqueous solution as the solvent instead of non coordinating solvent which enable production of nanosized compounds at lower reaction temperature. During the synthesis process, titanium precursor was injected into mixture of bismuth nitrate and oleic acid at 130°C, leading to a rapid burst nucleation and followed by nuclei growth at room temperature. The synthesized compound was heated at various temperatures. XRD results showed formation of cubic phase bismuth titanate compound with space group of Fm3m at room temperature after the reaction. Presence of cubic phase bismuth titanate compound with space group of I23 was observed as secondary phase at 300°C. Meanwhile, a single phase cubic form, space group I23 was obtained for material synthesized at 600°C. FESEM images indicated nano particles of bismuth titanate materials were produced at lower temperatures. However, sintering effect was observed in material heated at 600°C, resulting micro-sized particles.

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Advanced Materials Research (Volumes 287-290)

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257-260

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July 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] Yao, W., Wang, H., Xu, X., & Cheng, X. Applied Catalysis A: General, Vol 243 (2003), p.185

Google Scholar

[2] Murugesan, S., Smith, Y., Subramanian, V. Journal of Physical Chemistry Letters, Vol 10 (2010), p.1631

Google Scholar

[3] Zhou, J., Zou, Z., Ray, A. K., & Zhao, X. S. Industrial & Engineering Chemistry Research, Vol. 46 (2007), p.745

Google Scholar

[4] Chehab, S., Conflant, P., Darche, M., Boivin, J., McDonald, G. Material Research Bulletin, Vol 38 (2003), p.875

Google Scholar

[5] Xie, L., Ma, J., & Zhou, Z. Material Letters Vol 60 (2006), p.284

Google Scholar

[6] Xu, S., Shangguan, W., Yuan, J., Shi, J. Journal of Material Science and Engineering B, Vol 137 (2007), p.108

Google Scholar

[7] Thanaboneekij, N., Gulari, E., Wongkasemijit, S. Powder Technology, Vol 160 (2005), p.203

Google Scholar

[8] Li, L., Protiare, M., & Reiss, P. Chemistry of Materials, Vol. 20 (2008), p.2621

Google Scholar

[9] Murray, C., Norris, D., & Bawendi, M. J. Am. Chemistry Society, Vol 115 (1993), p.8706

Google Scholar

[10] Williams, J. V., Kotov, N. A., & Savage, P. E. Industrial & Engineering Chemistry Research, Vol. 48 (2009), p.4316

Google Scholar

[11] Kim, M., Jo, V., Kim, S., & Ok, K. Bulletin Korean Chemistry Society, Vol 29 (2008), p.2273

Google Scholar

[12] Pell, J., Delak, K., & Loye, C. Chemistry of Material, Vol. 7 (1998), p.1764

Google Scholar

[13] Lee, S. L., Lee, C. K., & Sinclair, D. C. Solid State Ionics, Vol 126 (2005), p.393

Google Scholar

[14] Yao, W. F., Wang, H., Xu, X. H., Zhou, J. T., Yang, X. N., Zhang, Y. Applied Catalysis A: General, Vol. 259 (2004), p.29

Google Scholar

[15] Schoonman, J. Solid State Ionics, Vol 135 (2000), p.5

Google Scholar