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Effects of Amines on Chemical and Physical Behaviors of Viscous Precursor Sols to Indium Gallium Zinc Oxide

Published online by Cambridge University Press:  18 June 2013

Nobuko Fukuda
Affiliation:
Flexible Electronics Research Center (FLEC), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.
Shintaro Ogura
Affiliation:
Flexible Electronics Research Center (FLEC), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.
Ken-ichi Nomura
Affiliation:
Flexible Electronics Research Center (FLEC), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.
Hirobumi Ushijima
Affiliation:
Flexible Electronics Research Center (FLEC), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8565, Japan.
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Abstract

We synthesized viscous precursors to indium gallium zinc oxide (IGZO) using three kinds of alcoholamines, ethanolamine (EA), diethanolamine (DEA), and triethanolamine (TEA), by a simple process. The viscous precursors are obtained just by vigorous stirring of alcoholamine and urea in an aqueous solution containing the metal nitrates during heating at 150-160 °C. The precursor containing EA (EA-precursor) is a pale-orange suspension containing aggregates of the metal hydroxides and shows pseudoplastic flow. The precursors containing DEA (DEA-precursor) and TEA (TEA-precursor) are transparent pale-yellow and dark-orange sols, respectively. They give Newtonian flow in the lower shear rate and pseudoplastic flow in the higher shear rate. Higher concentration of metal salts leads to higher viscosity of the precursors. According to thermogravimetry-differential thermal analysis (TG-DTA) for the EA- and DEA-precursors, evaporation of alcoholamine occurs at around each boiling point and subsequently formation of metal oxides occur at around 300 °C. In the case of the TEA-precursor, formation of metal oxides occurs before pyrolysis of TEA attributed to the higher boiling point of TEA. The thin IGZO film, which is prepared by spin-coating of the diluted DEA-precursor and subsequent sintering at 450 °C for 30 min, shows 0.02 cm2 ·V-1s-1 of the mobility and 10-5 of the on/off ratio. The highly viscous DEA-precursor containing high concentration of metal ions allows patterning in an area of 100 cm2 onto a surface of a silicon wafer with screen printing.

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Articles
Copyright
Copyright © Materials Research Society 2013 

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References

REFERENCES

Garnier, F., Hajlaoui, R., Yassar, A., and Srivastava, P., Science 265, 1684 (1994).CrossRefGoogle Scholar
Rogers, J. A., Bao, Z., Baldwin, K., Dodabalapur, A., Crone, B., Raju, V. R., Kuck, V., Katz, H., Amundson, K., Ewing, J., and Drzaic, P., Proc. Natl. Acad. Sci. USA 98, 4835 (2001).CrossRefGoogle Scholar
He, Y., Chen, Z., Zheng, Y., Newman, C., Quinn, J. R., Dötz, F., Kastler, M., and Facchetti, A., Nature 457, 679 (2009).Google Scholar
Nomura, K., Ohta, H., Takagi, A., Kamiya, T., Hirano, M., and Hosono, H., Nature 432, 488 (2004).CrossRefGoogle Scholar
Park, S. K., Kim, Y-H., and Han, J-I., J. Phys. D: Appl. Phys. 42, 125102 (2009).CrossRefGoogle Scholar
Krebs, F. C., Jørgensen, M., Norrman, K., Hagemann, O., Alstrup, J., Nielsen, T. D., Fyenbo, J., Larsen, K., and Kristensen, J., Sol. Energy Mater. Solar Cells 93, 422 (2009).CrossRefGoogle Scholar
Razali, R., Zak, A. K., Majid, W. H. A., and Darroudi, M., Ceram. Int. 37, 3657 (2011).CrossRefGoogle Scholar
Ramasami, T., Wharton, R. K., and Sykes, A. G., Inorg. Chem. 14, 359 (1975).CrossRefGoogle Scholar
Goh, P. C., Yao, K., and Chen, Z., J. Phys. Chem. C 116, 15550 (2012).CrossRefGoogle Scholar