journal article·2003-04

Dye adsorption behavior of anatase- and rutile-type TiO2 nanoparticles modified by various heat-treatments

J. Takahashi, H. Itoh, S. Motai, S. Shimada

Journal of Materials Science· Volume 38· Issue 8
Publisher page

Abstract

TiO2 colloidal particles with a fixed crystalline phase of anatase or rutile were heat-treated under different conditions (air-heating and hydrothermal-heating) to modify their surface characters which essentially affected the adsorption behavior of a Ru-complex dye on the surfaces. Changes in the number of surface OH group (N (OH)), apparent crystallite size, pore structure were evaluated as a function of heat-treatment conditions for various TiO2 nanoparticles. The amount of a Ru-complex dye adsorbed (N (dye)) was correlated to those surface properties of TiO2 samples. N (dye) values tended to increase with increasing crystallinity for only the anatase-type TiO2 particles. However, there was no simple, common relationship between N (dye) and N (OH) for all the TiO2 nanoparticles examined. Considerable difference in N (dye) values obtained in different nanoparticles might be explained on the basis of the surface pore structures of those particles.
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Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Nanomaterials for catalytic reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (21)

Show source-provided references
1. A. Fujishima and K. Honda, Nature 238 (1972) 37.10.1038/238037a0 ↗
2. K. Hashimoto and A. Fujishima, Bull. Ceram. Soc. Jpn. 31 (1996) 815 (In Japanese).
3. B. O'Reagan and M. GrÄtzel, Nature 353 (1991) 737.10.1038/353737a0 ↗
4. G. Smestad, C. Bignozzi and R. Argazzi, Sol. Energy Mater. Sol. Cells 32 (1994) 259; G. Smestad, ibid. 32 (1994) 273.10.1016/0927-0248(94)90263-1 ↗
5. A. Kay and M. GrÄtzel, ibid. 44 (1996) 99.10.1016/0927-0248(96)00063-3 ↗
6. J. Ferber, R. Stangl and J. Luther, ibid. 53 (1998) 29.10.1016/S0927-0248(98)00005-1 ↗
7. R. Hoyle, G. Will and D. Fitzmaurice, J. Mater. Chem. 8 (1998) 2033.10.1039/a803437k ↗
8. Y. Li, J. Hagen, W. Schaffrath, P. Otschik and D. Haarer, Sol. Energy Mater. Sol. Cells 56 (1999) 167.10.1016/S0927-0248(98)00157-3 ↗
9. S. Kambe, K. Murakoshi, T. Kitamura, Y. Wada, S. Yanagida, H. Kominami and Y. Kera, ibid. 61 (2000) 427.10.1016/S0927-0248(99)00166-X ↗
10. J. Ragai and K. S. W. Sing, J. Colloid Interface Sci. 101 (1984) 369.10.1016/0021-9797(84)90047-X ↗
11. E. Santacesaria, M. Tonello, G. Storti, R. C. Pace and S. Carra, ibid. 111 (1986) 44.
12. F. Cavani, E. Foresti, F. Parrinello and F. TrifirÒ, Appl. Catal. 38 (1988) 311.10.1016/S0166-9834(00)82834-1 ↗
13. K. R. Lee, S. J. Kim, J. S. Song, J. H. Lee, Y. J. Chung and S. J. Park, J. Amer. Ceram. Soc. 85 (2002) 341.10.1111/j.1151-2916.2002.tb00094.x ↗
14. K. Murakoshi, G. Kano, Y. Wada, S. Yanagida, H. Miyazaki, M. Matsumoto and S. Murasawa, J. Electroanal. Chem. 396 (1995) 27.10.1016/0022-0728(95)04185-Q ↗
15. V. Shkover, M.-K. Nazeeruddin, S. M. Zakeeruddin, C. Barbé, A. Kay, T. Haibach, W. Steurer, R. Hermann, H.-U. Nissen and M. GrÄtzel, Chem. Mater. 9 (1997) 430.10.1021/cm950502p ↗
16. C. J. Barbé, F. Arendse, P. Comte, M. Jirousek, F. Lenzmann, V. Shklover and M. GrÄtzel, J. Amer. Ceram. Soc. 80 (1997) 3157.10.1111/j.1151-2916.1997.tb03245.x ↗
17. P. Falaras, Sol. Energy Mater. Sol. Cells 53 (1998) 163.10.1016/S0927-0248(98)00023-3 ↗
18. J. Takahashi, H. Suzuki and K. Kodaira, J. Sol-Gel Sci. Technol. 4 (1995) 15.10.1007/BF00486698 ↗
19. P. Liska, N. Vlachopoulos, M. K. Nazeeruddin, P. Comte and M. GrÄtzel, J. Amer. Chem. Soc. 110 (1988) 3686.10.1021/ja00219a068 ↗
20. M. K. Nazeeruddin, A. Kay, I. Rodicio, R. Humphry-Baker, E. MÜller, P. Liska, N. Vlachopoulos and M. GrÄtzel, ibid. 115 (1993) 6385.10.1021/ja00067a063 ↗
21. H. Itoh, S. Utamapanya, J. V. Stark, K. J. Klabunde and J. R. Schlup, Chem. Mat. 5 (1993) 71.10.1021/cm00025a015 ↗