Photocatalysis of dye-sensitized TiO2 nanoparticles with thin overcoat of Al2O3: Enhanced activity for H2 production and dechlorination of CCl4
- Authors
- Kim, W.; Tachikawa, T.; Majima, T.; Choi, W.
- Issue Date
- Jun-2009
- Publisher
- American Chemical Society
- Citation
- Journal of Physical Chemistry C, v.113, no.24, pp 10603 - 10609
- Pages
- 7
- Journal Title
- Journal of Physical Chemistry C
- Volume
- 113
- Number
- 24
- Start Page
- 10603
- End Page
- 10609
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159261
- DOI
- 10.1021/jp9008114
- ISSN
- 1932-7447
1932-7455
- Abstract
- Dye-sensitized TiO2 nanoparticles that were loaded simultaneously with Pt and Al2O3 overlayer (Al2(VTi(V Pt) were synthesized and investigated for photocatalytic activity under visible light. Introducing a thin Al2O3 overlayer (∼1 nm thick) on dye-sensitized TiO2 markedly enhanced the visible light activities for the production of hydrogen (in the presence of EDTA as an electron donor) and the dechlorination of CCl4. The Al2(V TiO2/Pt powder was characterized by HRTEM, EDX, and XPS. In agreement with the photocatalytic activity data, the photocurrent collected via electron shuttles on a Pt electrode immersed in an aqueous photocatalyst suspension under visible light was also enhanced in the presence of an Al2O 3 overlayer, which indicates an enhanced interfacial electron transfer despite the presence of an insulating surface layer. The initial H2 and chloride generation rate increased from 0.4 and 5 ΜM min on TiO2/Pt to 0.9 and 7.5 ΜM min on Al2O 3/ TiO2/Pt, respectively. The visible light activity of the sensitized photocatalytic reactions highly depended on the thickness of the alumina layer and was optimized at a low level of Al loading (Al/Ti atom ratio ∼ 0.01), above which the activity was markedly reduced with thickening of the layer. It is suggested that the alumina layer retards the charge recombination
- Files in This Item
-
Go to Link
- Appears in
Collections - 공과대학 > 화공생명공학부 > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.