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Oxygen ion-beam irradiation of TiO2 films reduces oxygen vacancies and improves performance of dye-sensitized solar cells

Published online by Cambridge University Press:  01 April 2011

Sung-Ryong Kim*
Affiliation:
Department of Polymer Science and Engineering, Chungju National University, Chungju 380-702, Republic of Korea
Md. Khaled Parvez
Affiliation:
Department of Polymer Science and Engineering, Chungju National University, Chungju 380-702, Republic of Korea; and Synthetic Chemistry Group, Max Planck Institute for Polymer Research, D-55021 Mainz, Germany
*
a)Address all correspondence to this author. e-mail: [email protected]
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Abstract

Oxygen vacancy-related surface defects on porous TiO2 films were reduced by oxygen ion-beam treatment, and the effect of such defects on the performance of dye-sensitized solar cells was examined. An oxygen ion-beam treatment of a TiO2 film caused a significant decrease in particle agglomeration and an increase in surface area of the resulting TiO2 film. In addition, the increased hydrophilicity of the TiO2 film by the ion beam treatment led to an increase in dye adsorption. The oxygen ion beam treatment at 500 and 1000 eV caused a significant decrease in oxygen vacancies and increase in the open-circuit voltage (Voc). Oxygen ion beam–treated TiO2 film electrodes showed the maximum solar-to-electricity conversion efficiency (η%) of 8.04% compared to the 6.15% obtained from an untreated TiO2 electrode.

Type
Articles
Copyright
Copyright © Materials Research Society 2011

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References

REFERENCES

1.Barbé, C.J., Arendse, F., Comte, P., Jirousek, M., Lenzmann, F., Shklover, V., and Grätzel, M.: Nanocrystalline titanium oxide electrodes for photovoltaic applications. J. Am. Ceram. Soc. 80, 3157 (1997).CrossRefGoogle Scholar
2.Schwarzburg, K. and Willig, F.: Influence of trap filling on photocurrent transients in polycrystalline TiO2. Appl. Phys. Lett. 58, 2520 (1991).CrossRefGoogle Scholar
3.Jongh, P.E. and Vanmaekelbergh, D.: Trap-limited electronic transport in assemblies of nanometer-size TiO2 particles. Phys. Rev. Lett. 77, 3427 (1996).CrossRefGoogle Scholar
4.Gmelin Institute: Handbuch der Anorganischen Chemie—Titanium (Verlag Chemie, Germany, 1951), 41, p. 252.Google Scholar
5.Nelson, J.: Continuous-time random-walk model of electron transport in nano-crystalline TiO2 electrodes. Phys. Rev. B 59, 15374 (1999).CrossRefGoogle Scholar
6.Cronemeyer, D.C.: Infrared absorption of reduced rutile TiO2 single crystals. Phys. Rev. B 113, 1222 (1959).CrossRefGoogle Scholar
7.Weidmann, J., Dittrich, T., Konstantinova, E., Lauermann, I., Uhlendorf, I., and Koch, F.: Influence of oxygen and water related surface defects on the dye sensitized TiO2 solar cell. Sol. Energy Mater. Sol. Cells 56, 153 (1999).CrossRefGoogle Scholar
8.Takeuchi, M., Onozaki, Y., Matsumura, Y., Uchida, H., and Kuji, T.: Photoinduced hydrophilicity of TiO2 thin film modified by Ar ion beam irradiation. Nucl. Instrum. Methods Phys. Res., Sect. B 206, 259 (2003).Google Scholar
9.Narita, T., Iida, T., Ogawa, S., Mizuno, K., So, J., Kondo, A., Yoshida, N., Itoh, T., Nonomura, S., and Tanaka, Y.: Ion beam modification of TiO2 films prepared by Cat-CVD for solar cell. Thin Solid Films 516, 810 (2008).CrossRefGoogle Scholar
10.Koh, S.K., Park, S.C., Kim, S.R., Choi, W.C., Jung, H.J., and Pae, K.D.: Surface modification of polytetrafluoroethylene by Ar+ irradiation for improved adhesion to other materials. J. Appl. Polym. Sci. 64, 1913 (1997).3.0.CO;2-L>CrossRefGoogle Scholar
11.Kim, S.R., Parvez, M.K., and Chhowalla, M.: UV-reduction of graphene oxide and its application as an interfacial layer to reduce the back-transport reactions in dye-sensitized solar cells. Chem. Phys. Lett. 483, 124 (2009).CrossRefGoogle Scholar
12.Kim, Y.S., Yoon, C.H., Kim, K., and Lee, Y.: Surface modification of porous nanocrystalline TiO films for dye-sensitized solar cell application by various gas plasmas. J. Vac. Sci. Technol., A 25, 1219 (2007).CrossRefGoogle Scholar
13.Geer, F., Van, L., Fraser, D., Coburn, J.W., and Graves, D.B.: Argon and oxygen ion chemistry effects in photoresist etching. J. Vac. Sci. Technol., B 20, 1901 (2002).Google Scholar
14.Kuang, D., Uchida, S., Baker, R.H., Zakeeruddin, S.M., and Grätzel, M.: Organic dye-sensitized ionic liquid based solar cells: Remarkable enhancement in performance through molecular design of indoline sensitizers. Angew. Chem. 120, 1949 (2008).CrossRefGoogle Scholar
15.Wu, S., Han, H., Tai, Q., Zhang, J., Xu, S., Zhou, C., Yang, Y., Hu, H., Chen, B., and Zhao, X.Z.: Improvement in dye-sensitized solar cells employing TiO2 electrodes coated with Al2O3 by reactive direct current magnetron sputtering. J. Power Sources 182, 119 (2008).CrossRefGoogle Scholar
16.Park, K.H. and Dhayal, M.: High efficiency solar cell based on dye sensitized plasma treated nano-structured TiO2 films. Electrochem. Commun. 11, 75 (2009).Google Scholar
17.Kim, Y., Yoo, B.J., Vittal, R., Lee, Y.H., Park, N.G., and Kim, K.J.: Low-temperature oxygen plasma treatment of TiO2 film for enhanced performance of dye-sensitized solar cells. J. Power Sources 175, 914 (2008).Google Scholar