Photocatalytic activity and hydroxyl radical formation of carbon-doped TiO2 nanocrystalline: Effect of calcination temperature

被引:171
作者
Xiao, Qi [1 ]
Ouyang, Linli [1 ]
机构
[1] Cent S Univ, Sch Resources Proc & Bioengn, Changsha 410083, Peoples R China
关键词
Carbon-doped TiO2 nanocrystalline; Hydroxyl radical; Photocatalytic activity; LIGHT; DEGRADATION; DYE;
D O I
10.1016/j.cej.2008.08.024
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon-doped TiO2 nanocrystalline was prepared by sol-gel auto-combustion method and characterized by X-ray diffraction, X-ray photoelectron spectra (XPS), Brunauer-Emmett-Teller method (BET), UV-vis diffuse reflectance spectroscopy (DRS). The analysis of (OH)-O-center dot radical formation on the sample surface under visible light irradiation was performed by fluorescence technique with using terephthalic acid, which readily reacted with (OH)-O-center dot radical to produce highly fluorescent product. 2-hydroxyterephthalic acids. It was found that the order of photocatalytic activity per unit surface area was the same as that of the formation rate of (OH)-O-center dot radicals unit surface area, namely, the greater the formation rate of (OH)-O-center dot radicals unit surface area was, the higher photocatalytic activity unit surface area was achieved, indicating that the photocatalytic activity unit surface area was positive correlation to the formation rate of (OH)-O-center dot radicals unit surface area over the catalysts. In this study, the optimum calcination temperature was 600 degrees C, at which the highest formation rate of OH radicals per unit surface area was, and thereby the highest photocatalytic activity per unit surface area was achieved. In addition, it could be found that the order of photocatalytic activity correlated very well with the amount of visible light absorption, namely, the stronger the visible light absorption, the higher the photocatalytic activity. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:248 / 253
页数:6
相关论文
共 30 条
[1]   Visible-light photocatalysis in nitrogen-doped titanium oxides [J].
Asahi, R ;
Morikawa, T ;
Ohwaki, T ;
Aoki, K ;
Taga, Y .
SCIENCE, 2001, 293 (5528) :269-271
[2]   TEREPHTHALIC ACID - A DOSIMETER FOR THE DETECTION DF HYDROXYL RADICALS IN-VITRO [J].
BARRETO, JC ;
SMITH, GS ;
STROBEL, NHP ;
MCQUILLIN, PA ;
MILLER, TA .
LIFE SCIENCES, 1994, 56 (04) :PL89-PL96
[3]   THE IDENTIFICATION AND CHARACTERIZATION OF MIXED OXIDATION-STATES AT OXIDIZED TITANIUM SURFACES BY ANALYSIS OF X-RAY PHOTOELECTRON-SPECTRA [J].
CARLEY, AF ;
CHALKER, PR ;
RIVIERE, JC ;
ROBERTS, MW .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1987, 83 :351-370
[4]   OH radical formation by ultrasound in aqueous solutions .1. The chemistry underlying the terephthalate dosimeter [J].
Fang, XW ;
Mark, G ;
vonSonntag, C .
ULTRASONICS SONOCHEMISTRY, 1996, 3 (01) :57-63
[5]   Visible-light-activated nanoparticle photocatalyst of iodine-doped titanium dioxide [J].
Hong, XT ;
Wang, ZP ;
Cai, WM ;
Lu, F ;
Zhang, J ;
Yang, YZ ;
Ma, N ;
Liu, YJ .
CHEMISTRY OF MATERIALS, 2005, 17 (06) :1548-1552
[6]   Photocatalytic degradation pathway of methylene blue in water [J].
Houas, A ;
Lachheb, H ;
Ksibi, M ;
Elaloui, E ;
Guillard, C ;
Herrmann, JM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 31 (02) :145-157
[7]   Carbon-doped anatase TiO2 powders as a visible-light sensitive photocatalyst [J].
Irie, H ;
Watanabe, Y ;
Hashimoto, K .
CHEMISTRY LETTERS, 2003, 32 (08) :772-773
[8]   Detection of active oxidative species in TiO2 photocatalysis using the fluorescence technique [J].
Ishibashi, K ;
Fujishima, A ;
Watanabe, T ;
Hashimoto, K .
ELECTROCHEMISTRY COMMUNICATIONS, 2000, 2 (03) :207-210
[9]   EFFECT OF TEMPERATURE AND LIGHT ON THE RESPONSE OF AN AQUEOUS COUMARIN DOSIMETER [J].
KHAN, HM ;
ANWAR, M ;
AHMAD, G .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-LETTERS, 1995, 200 (06) :521-527
[10]   Efficient photochemical water splitting by a chemically modified n-TiO2 2 [J].
Khan, SUM ;
Al-Shahry, M ;
Ingler, WB .
SCIENCE, 2002, 297 (5590) :2243-2245