Assembly of Highly Ordered Three-Dimensional Porous Structure with Nanocrystalline TiO2 Semiconductors
Source abstract
Abstract
In this paper, we report on the assembly of a highly ordered three-dimensional porous structure with nanosized crystalline TiO 2 particles by a cooperative assembly method in which the fabrication of the template and the infiltration of the voids of the template are carried out at the same time and the related experimental parameters for the assembly, including temperature, humidity, and concentrations and concentration ratio of the colloid mixture. SEM (scanning electron microscope) images and transmission spectra of these samples demonstrate that these films have a highly ordered three-dimensional structure. The Bragg law was used to calculate the diameter of the spheres of air in the porous TiO 2 structure. A good agreement between the calculated results for the diameter of the spheres of air and those measured by SEM further confirms the high quality of the films fabricated using this simple method. Additionally, based on these experimental results, a detailed mechanism of the simple method is also discussed.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photonic Crystals and Applications · Mesoporous Materials and Catalysis · TiO2 Photocatalysis and Solar Cells
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Special Research Laboratory for Optical Science, Kanagawa Academy of Science and Technology, KSP Building East 412, 3-2-1 Sakado, Takatsu-ku, Kawasaki-shi, 213-0012 Kanagawa, Japan, State Key Laboratory for Surface Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100080, China, and Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1, Hongo Bunkyo-ku, Tokyo 113-8565, Japan
References (23)
Show source-provided references
1. Barbe C. J. · J. Am. Ceram. Soc. · 1997 · 80 · 315710.1111/j.1151-2916.1997.tb03245.x ↗
2. Regan B. · Adv. Mater. · 2000 · 12 · 126310.1002/1521-4095(200009)12:17<1263::AID-ADMA1263>3.0.CO;2-T ↗
3. Park N. G. · J. Phys. Chem. B · 2000 · 104 · 898910.1021/jp994365l ↗
4. Hoyer P. · Langmuir · 1996 · 14 · 141110.1021/la9507803 ↗
5. Moriguchi I. · Chem. Mater. · 1997 · 9 · 105010.1021/cm970023l ↗
6. Lakshmi B. B. · Chem. Mater. · 1995 · 9 · 85710.1021/cm9605577 ↗
7. Hoyer P. · J. Mater. Sci. Lett. · 1996 · 15 · 122810.1007/BF00274383 ↗
8. Fujishima A. · Electrochim. Acta · 2000 · 45 · 468310.1016/S0013-4686(00)00620-4 ↗
9. Gopidas K. R. · J. Phys. Chem. · 1990 · 94 · 643510.1021/j100379a051 ↗
10. Wijnhoven J. E. G. J. · Science · 1998 · 281 · 80210.1126/science.281.5378.802 ↗
11. Rengarajan R. · Appl. Phys. Lett. · 2000 · 77 · 351710.1063/1.1320863 ↗
12. Yin J. S. · Adv. Mater. · 1999 · 11 · 46910.1002/(SICI)1521-4095(199904)11:6<469::AID-ADMA469>3.0.CO;2-2 ↗
13. Gates B. · Chem. Mater. · 1999 · 11 · 282710.1021/cm990195d ↗
14. Vlasov Y. A. · J. Adv. Mater. · 1999 · 11 · 16510.1002/(SICI)1521-4095(199902)11:2<165::AID-ADMA165>3.0.CO;2-3 ↗
15. Jiang P. · J. Am. Chem. Soc. · 1999 · 121 · 1163010.1021/ja9903476 ↗
16. Jiang P. · J. Am. Chem. Soc. · 1999 · 121 · 795110.1021/ja990338x ↗
17. Velev O. D. · Adv. Mater. · 2000 · 12 · 53110.1002/(SICI)1521-4095(200004)12:7<531::AID-ADMA531>3.0.CO;2-S ↗
18. Velev O. D. · Nature · 1999 · 401 · 54810.1038/44065 ↗
19. Subramania G. · Appl. Phys. Lett. · 1999 · 74 · 393310.1063/1.124228 ↗
20. Subramania G. · J. Adv. Mater. · 1999 · 11 · 126110.1002/(SICI)1521-4095(199910)11:15<1261::AID-ADMA1261>3.0.CO;2-A ↗
21. Jiang P. · Chem. Mater. · 1999 · 11 · 213210.1021/cm990080+ ↗
22. Meng Q. B. · Appl. Phys. Lett. · 2000 · 77 · 431310.1063/1.1332109 ↗
23. Denkov N. D. · Langmuir · 1992 · 8 · 318310.1021/la00048a054 ↗