Enhanced photocatalytic activity of TiO2-xNx loaded with copper ions under visible light irradiation

被引:130
作者
Morikawa, Takeshi [1 ]
Irokawa, Yoshihiro [1 ]
Ohwaki, Takeshi [1 ]
机构
[1] Toyota Cent Res & Dev Labs Inc, Nagakute, Aichi 4801192, Japan
关键词
photocatalysis; nitrogeri-doped TiO2; visible light; acetaldehyde; photooxidation; carbon dioxide; metal loading; copper; nitrogen doping; antibacterial; bactericidal;
D O I
10.1016/j.apcata.2006.08.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nitrogen-doped TiO2 (TiO2-x,N-x,) photocatalysts loaded with various transition metal ions, including Cu, Pt, Ni, Zn and La, were prepared using a wet impregnation method. Photocatalytic activity of the catalysts under visible light irradiation(lambda > 410 nm) for acetaldehyde oxidation was examined. As a result, it was found that photocatalytic activity over TiO2-xNx (concentration of nitrogen was found to be similar to 0.25 at.%) was markedly enhanced by Cu or Pt loading, while Ni, Zn or La loaded TiO2-xNx showed similar photodegradation rate to the bare TiO2-xNx. Among them, the enhancement effect of Cu ion was found highest. The optimum concentration of Cu was found to be 0.5 wt%, and X-ray photoelectron spectroscopy (XPS) and X-ray induced Auger electron spectroscopy (XAES) analyses suggested the presence Of Cu2O or Cu hydroxides on the catalyst surface. In terms of the long-term stability of the catalysts, it was confirmed that more than 2100 mu mol Of CO2 was produced when acetaldehyde was continuously photooxidized over 1100 mu mol of Cu loaded TiO2-xNx under visible light for 100 consecutive days (> 410 nm, 0.9 mW/cm(2), in a 1 L vessel). (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 127
页数:5
相关论文
共 53 条
[11]   FLUIDIZED-BED PHOTOCATALYTIC OXIDATION OF TRICHLOROETHYLENE IN CONTAMINATED AIRSTREAMS [J].
DIBBLE, LA ;
RAUPP, GB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1992, 26 (03) :492-495
[12]   Complete oxidation of benzene in eas phase by platinized titania photocatalysts [J].
Einaga, H ;
Futamura, S ;
Ibusuki, T .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (09) :1880-1884
[13]   Generation of active sites for CO photooxidation on TiO2 by platinum deposition [J].
Einaga, H ;
Harada, M ;
Futamura, S ;
Ibusuki, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (35) :9290-9297
[14]   Mechanism of photooxidation of trichloroethylene on TiO2: Detection of intermediates by infrared spectroscopy [J].
Fan, JF ;
Yates, JT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (19) :4686-4692
[15]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[16]  
Fujishima A., 1999, TIO2 PHOTOCATALYSIS
[17]   Direct observation of a picosecond charge separation process in photoexcited platinum-loaded TiO2 particles by femtosecond diffuse reflectance spectroscopy [J].
Furube, A ;
Asahi, T ;
Masuhara, H ;
Yamashita, H ;
Anpo, M .
CHEMICAL PHYSICS LETTERS, 2001, 336 (5-6) :424-430
[18]   Surface chemistry of titania (anatase) and titania-supported catalysts [J].
Hadjiivanov, KI ;
Klissurski, DG .
CHEMICAL SOCIETY REVIEWS, 1996, 25 (01) :61-+
[19]   Chemistry and applications of photocatalytic oxidation of thin organic films [J].
Heller, A .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (12) :503-508
[20]   EFFECT OF CHROMIUM DOPING ON THE ELECTRICAL AND CATALYTIC PROPERTIES OF POWDER TITANIA UNDER UV AND VISIBLE ILLUMINATION [J].
HERRMANN, JM ;
DISDIER, J ;
PICHAT, P .
CHEMICAL PHYSICS LETTERS, 1984, 108 (06) :618-622