Mesostructured Pt/TiO2 Nanocomposites as Highly Active Photocatalysts for the Photooxidation of Dichloroacetic Acid

被引:166
作者
Ismail, Adel A. [1 ]
Bahnemann, Detlef W. [2 ]
机构
[1] CMRDI, Adv Mat Dept, Nanostruct & Nanotechnol Div, Cairo 11421, Egypt
[2] Leibniz Univ Hannover, Inst Tech Chem, Photocatalysis & Nanotechnol Unit, D-30167 Hannover, Germany
关键词
METAL NANOPARTICLES; MESOPOROUS TIO2; WATER DETOXIFICATION; TITANIUM-DIOXIDE; THIN-FILMS; CATALYSTS; MINERALIZATION; NANOCRYSTALS; MORPHOLOGY; FRAMEWORKS;
D O I
10.1021/jp110959b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Mesoporous Pt/TiO2 nanocomposites have been synthesized by using two pathways: (1) the in-situ preparation of Pt/TiO2 nanocomposites was carried out using a one-step synthesis by dissolving the Pt and TiO2 precursors in the presence of a triblock copolymer as the structure-directing agent followed by drying, calcinations, and reduction under H-2 gas. (2) Platinum particles have been photochemically deposited onto mesoporous TiO2. The TEM images of the mesoporous Pt/TiO2 nanocomposites calcined at 450 degrees C demonstrate that the TiO2 nanoparticles with an average diameter of about 10 nm are not agglomerated and are quite uniform in size and shape. Following the photodeposition process, the Pt nanoparticles are well-dispersed and highly uniform, exhibiting diameters of similar to 3 nm; however, following the in situ preparation, the Pt particles are reaching diameters of approximately 15 nm, most likely as a result of the calcination and reduction at high temperatures. The photocatalytic activity of the newly synthesized mesoporous photocatalysts was measured and compared with that of nonporous commercial Aeroxide TiO2 P 25 and Pt/TiO2 P 25 by measuring the rate of H+ ion release during the photodegradation of dichloroacetic acid (DCA) and confirmed by measuring the concomitant total organic carbon removal. For both preparation routes the photonic efficiency of the mesoporous TiO2 photocatalysts is found to be increased by the addition of the Pt islands and to correlate with the size of the Pt particles. The mesoporous Pt/TiO2 nanocomposites showed 2 times higher activity for the photocatalytic DCA photodegradation than Aeroxide TiO2 P 25. The larger photoactivity of the mesoporous Pt/TiO2 nanocompositcs prepared by the photodeposition process is attributed to the higher dispersity and the small size of the Pt particles (3 nm). To the best of our knowledge, the measured photonic efficiency of xi = 7.95% for the photodeposited Pt/TiO2 nanocomposites is among the highest xi value reported up to now.
引用
收藏
页码:5784 / 5791
页数:8
相关论文
共 54 条
[1]
Photocatalytic activity of structured mesoporous TiO2 materials [J].
Alvaro, M ;
Aprile, C ;
Benitez, M ;
Carbonell, E ;
García, H .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (13) :6661-6665
[2]
SYNTHESIS OF HEXAGONALLY PACKED MESOPOROUS TIO2 BY A MODIFIED SOL-GEL METHOD [J].
ANTONELLI, DM ;
YING, JY .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (18) :2014-2017
[3]
Azaroff L.V., 1958, POWDER METHOD XRAY C, P255
[4]
MECHANISTIC STUDIES OF WATER DETOXIFICATION IN ILLUMINATED TIO2 SUSPENSIONS [J].
BAHNEMANN, D ;
BOCKELMANN, D ;
GOSLICH, R .
SOLAR ENERGY MATERIALS, 1991, 24 (1-4) :564-583
[5]
DETECTION OF THE INTERMEDIATES OF COLLOIDAL TIO2-CATALYZED PHOTOREACTIONS [J].
BAHNEMANN, D ;
HENGLEIN, A ;
SPANHEL, L .
FARADAY DISCUSSIONS, 1984, 78 :151-163
[6]
BAHNEMANN DW, 1993, TRACE METALS ENV, V3
[7]
Cubic mesoporous frameworks with a mixed semiconductor nanocrystalline wall structure and enhanced sensitivity to visible light [J].
Bartl, MH ;
Puls, SP ;
Tang, J ;
Lichtenegger, HC ;
Stucky, GD .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (23) :3037-3040
[8]
Using block copolymer micellar thin films as templates for the production of catalysts for carbon nanotube growth [J].
Bennett, RD ;
Xiong, GY ;
Ren, ZF ;
Cohen, RE .
CHEMISTRY OF MATERIALS, 2004, 16 (26) :5589-5595
[9]
BOCKELMANN D, 1996, FINE PARTICLES SCI T
[10]
Supported mixed metal nanoparticles as electrocatalysts in low temperature fuel cells [J].
Chan, KY ;
Ding, J ;
Ren, JW ;
Cheng, SA ;
Tsang, KY .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (04) :505-516