Efficient dual functionality of highly porous nanocomposites based on TiO2 and noble metal particles

被引:32
作者
Baia, L. [1 ]
Diamandescu, L. [2 ]
Barbu-Tudoran, L. [3 ]
Peter, A. [4 ]
Melinte, G. [1 ]
Danciu, V. [4 ]
Baia, M. [1 ]
机构
[1] Univ Babes Bolyai, Fac Phys, Cluj Napoca 400084, Romania
[2] Natl Inst Mat Phys, Bucharest 77125, Romania
[3] Univ Babes Bolyai, Fac Biol &Geol, Cluj Napoca 400006, Romania
[4] Univ Babes Bolyai, Fac Chem & Chem Engn, Cluj Napoca 400028, Romania
关键词
Photocatalysis; SERS sensor; Porous composites; TiO2; aerogel; Noble metal particles; SURFACE-ENHANCED RAMAN; PHOTOCATALYTIC ACTIVITY; CATALYTIC-ACTIVITY; NANOPARTICLES; SERS; AEROGELS; TITANIA; AU; SPECTROSCOPY; ADSORPTION;
D O I
10.1016/j.jallcom.2010.11.154
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
Porous nanocomposites based on TiO2 aerogels and Au and, respectively, Ag particles were synthesized and their dual functionality to decontaminate water, via photocatalysis, and to detect low concentrations of pollutants from water, via SERS technique, was evaluated using model pollutants. The apparent photodegradation rate constants of a standard pollutant molecule revealed a considerable improvement of the composites photocatalytic performances (even better than one order of magnitude) in comparison with the commercial product Degussa P25. The essential role of the contact between TiO2 and Au nanoparticles was demonstrated and the potential of all synthesized porous composites for photocatalytic experiments with visible light was pointed out. The lowest concentrations of contaminants adsorbed on the noble metal particles detectable by SEAS were found to depend on the composite and pollutant species type and were determined to be between 10(-3) and 5 x 10(-6) M, and 10(-8) and 10(-10) M for off and under resonant excitation, respectively. The morphological (BET, pore size distribution, TEM) and structural (Raman, XRD, diffuse reflectance) particularities of the obtained porous composites were also discussed. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2672 / 2678
页数:7
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