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Division of Energy & Environmental Technology
1. Journal Articles
Platinum-Nitrogen-Codoped TiO2 Photocatalyst: Effect of Acid Catalysts on Visible-Light Activity
Ryu, Jungho
;
Kim, Soonhyun
Division of Energy & Environmental Technology
1. Journal Articles
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Title
Platinum-Nitrogen-Codoped TiO2 Photocatalyst: Effect of Acid Catalysts on Visible-Light Activity
Issued Date
2012
Citation
Ryu, Jungho. (2012). Platinum-Nitrogen-Codoped TiO2 Photocatalyst: Effect of Acid Catalysts on Visible-Light Activity. Materials Transactions, 53(12), 2200–2204. doi: 10.2320/matertrans.M2012294
Type
Article
Author Keywords
platinum-nitrogen-codoped TiO2
;
photocatalysis
;
sol-gel
;
acid catalyst
;
visible light
Keywords
4-Chlorophenol (4-CP)
;
4-CP Degradation
;
Acetic ACID
;
ACID Catalyst
;
ARSENITE
;
Calcination
;
CATALYSTS
;
CHROMIUM
;
CLEAVAGE
;
Co-Doped
;
DEGRADATION
;
Diffuse Reflectance
;
Light
;
MECHANISMS
;
NANOPARTICLES
;
Nitric ACID
;
OXIDATION
;
Photocatalysis
;
Photoelectrons
;
Platinum-Nitrogen-Codoped TiO2
;
Sample Surface
;
Scanning Electron Microscopy
;
Scanning Electrons
;
Sol-Gel
;
Sol-Gels
;
SULFUR-DOPED TIO2
;
Surface Area
;
SUSPENSION
;
TiO
;
Titanium Dioxide
;
Transmission Electron Microscopy
;
UV-Visible
;
Visible-Light Activity
;
Visible Irradiation
;
Visible Light
;
WATER
;
X Ray Diffraction
;
X Ray Photoelectron Spectroscopy
ISSN
1345-9678
Abstract
Platinumnitrogen- codoped TiO2 (PtNTiO2) was prepared by a conventional solgel process via the addition of different acid catalysts: nitric acid (HNO3), acetic acid (HAc) and both (HNO3HAc). The PtNTiO2 samples were then characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and UVvisible diffuse reflectance analysis. The samples successfully exhibited visible-light-induced photocatalysis for the degradation of dichloroacetate (DCA) and 4-chlorophenol (4-CP). The HAc/450 sample (following the notation "added acid catalyst/calcination temperature") exhibited the highest visible activity for DCA degradation. This finding can be explained by the much stronger visible absorption of the calcined samples than the uncalcined samples and the slightly larger surface area of HAc/450 compared to other calcined TiO2 samples. However, the performance of 4-CP degradation was proportional to the PtNTiO2 sample surface area regardless of visible absorption, which could be ascribed to the fact that 4-CP degradation can occur through a surface-complex-mediated pathway under visible irradiation. © 2012 The Japan Institute of Metals.
URI
http://hdl.handle.net/20.500.11750/56390
DOI
10.2320/matertrans.M2012294
Publisher
Japan Institute of Metals
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Kim, Soonhyun
김순현
Division of Energy & Environmental Technology
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