Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-23T17:47:55.996Z Has data issue: false hasContentIssue false
  • English
  • Français

Photoluminescence Spectral Change in Self-Assembled Layered Titanate Oxide Intercalated with Eu3+

Published online by Cambridge University Press:  26 February 2011

Shintaro Ida ,
Ugur Unal ,
Kazuyoshi Izawa ,
Chikako Ogata  and
Yasumichi Matsumoto
Shintaro Ida
Affiliation:
[email protected], Kumamoto University, Department of Nano Science and Technology, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan, +81-96-342-3679
Ugur Unal
Affiliation:
[email protected], Kumamoto University, Department of Nano Science and Technology, Graduate School and Technology, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan
Kazuyoshi Izawa
Affiliation:
[email protected], Kumamoto University, Department of Nano Science and Technology, Graduate School and Technology, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan
Chikako Ogata
Affiliation:
[email protected], Kumamoto University, Department of Nano Science and Technology, Graduate School and Technology, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan
Yasumichi Matsumoto
Affiliation:
[email protected], Kumamoto University, Department of Nano Science and Technology, Graduate School and Technology, 2-39-1 Kurokami, Kumamoto, 860-8555, Japan
Get access

Abstract

Titanate layered oxide intercalated with hydrated Eu3+ was synthesized by the electrostatic self-assembly deposition (ESD) method. The emission intensity of Eu3+ decreased rapidly with time during irradiation by UV light having energy higher than the band gap energy of the host Ti1.81O4 (TiO) layer. This is presumably due to the decrease in energy transfer from the host TiO layer to Eu3+ as a result of the change in the hydration state of water molecules surrounding Eu3+, which is caused by the hole produced in the TiO valence band. When irradiation was discontinued, the emission intensity gradually recovered. The recovery time increased when the water in the interlayer is removed by heat treatment. This indicates that the state of interlayer water changes during irradiation and returns to its initial state after discontinuation of irradiation. The excitation spectra changed drastically at any given wavelength upon irradiation with UV light. A comparison of the excitation spectra before and after irradiation reveals that only the excitation peak at around the irradiation wavelength decreased upon irradiation, as in the case of spectral hole burning. The hydration state of water molecules surrounding Eu3+ presumably changes depending on the irradiation wavelength.

Keywords

layeredluminescenceself-assembly
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 988: Symposium QQ – Solid-State Chemistry of Inorganic Materials VI , 2006 , 0988-QQ03-07
Copyright
Copyright © Materials Research Society 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Bizeto, M. A., Constantino, V. R. L., Brito, H. F., J. Alloys Compd. 311, 159–168 (2000).Google Scholar
2. Conde-Gallardo, A., Garcia-Rocha, M., Hernandez-Calderon, I., Palomino-Merino, R., Appl. Phys. Lett.78, 3436–3438 (2001).Google Scholar
3. Frindell, K. L., Bartl, M. H., Popitsch, A., Stucky, G. D., Angew. Chem., Int. Ed. 41, 959–962 (2002).Google Scholar
4. Kudo, A., Kaneko, E., Microporous Mesoporous Mater. 21, 615–620 (1998).Google Scholar
5. Xin, H., Ma, R., Wang, L., Ebina, Y., Takada, K., Sasaki, T., Appl. Phys. Lett.85, 4187–4189 (2004).Google Scholar
6. Matsumoto, Y., Unal, U., Kimura, Y., Ohashi, S., Izawa, K., J. Phys. Chem. B 109, 12748–12754 (2005).Google Scholar
7. Fujita, K., Tanaka, K., Hirao, K., Soga, N., J. Opt. Soc. Am. B 15, 2700–2705 (1998).Google Scholar
8. Nogami, M., J. Non-Cryst. Solids 259, 170–175 (1999).Google Scholar
9. M, Nogami.; T, Ishikawa. Phys. Rev. B: Condens. Matter Mater. Phys. 63, 104205/1–104205/6 (2001).Google Scholar
10. Abe, R., Kondo, J. N., Hara, M., Domen, K., Supramol. Sci. 5, 229ndash;233 (1998).Google Scholar
11. Unal, U., Matsumoto, Y., Tanaka, N., Kimura, Y., Tamoto, N., J. Phys. Chem. B 107, 12680–12689 (2003).Google Scholar