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Molecular-level understanding of the photocatalytic activity difference between anatase and rutile nanoparticles

Authors
Kim, WooyulTachikawa, TakashiMoon, Gun-heeMajima, TetsuroChoi, Wonyoung
Issue Date
Dec-2014
Publisher
John Wiley and Sons Ltd
Citation
Angewandte Chemie - International Edition, v.53, no.51, pp 14036 - 14041
Pages
6
Journal Title
Angewandte Chemie - International Edition
Volume
53
Number
51
Start Page
14036
End Page
14041
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159084
DOI
10.1002/anie.201406625
ISSN
1433-7851
1521-3773
Abstract
The generation of oxidants on illuminated photocatalysts and their participation in subsequent reactions are the main basis of the widely investigated photocatalytic processes for environmental remediation and selective oxidation. Here, the generation and the subsequent diffusion of ·OH from the illuminated TiO2 surface to the solution bulk were directly observed using a single-molecule detection method and this molecular phenomenon could explain the different macroscopic behavior of anatase and rutile in photocatalysis. The mobile ·OH is generated on anatase but not on rutile. Therefore, the photocatalytic oxidation on rutile is limited to adsorbed substrates whereas that on anatase is more facile and versatile owing to the presence of mobile ·OH. The ability of anatase to generate mobile COH is proposed as a previously unrecognized key factor that explains the common observations that anatase has higher activity than rutile for many photooxidative reactions. © 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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