Understanding the superior photocatalytic activity of noble metals modified titania under UV and visible light irradiation

被引:223
作者
Bumajdad, Ali [1 ]
Madkour, Metwally [1 ]
机构
[1] Kuwait Univ, Dept Chem, Safat 13060, Kuwait
关键词
SURFACE-PLASMON EXCITATION; EXPOSED; 001; FACETS; GOLD NANOPARTICLES; HYDROGEN-PRODUCTION; H-2; PRODUCTION; PARTICLE-SIZE; ENHANCED PHOTOCATALYSIS; PT/TIO2; NANOPARTICLES; AG/TIO2; CO2; PHOTOREDUCTION;
D O I
10.1039/c3cp54411g
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
Although TiO2 is one of the most efficient photocatalysts, with the highest stability and the lowest cost, there are drawbacks that hinder its practical applications like its wide band gap and high recombination rate of the charge carriers. Consequently, many efforts were directed toward enhancing the photocatalytic activity of TiO2 and extending its response to the visible region. To head off these attempts, modification of TiO2 with noble metal nanoparticles (NMNPs) received considerable attention due to their role in accelerating the transfer of photoexcited electrons from TiO2 and also due to the surface plasmon resonance which induces the photocatalytic activity of TiO2 under visible light irradiation. This insightful perspective is devoted to the vital role of TiO2 photocatalysis and its drawbacks that urged researchers to find solutions such as modification with NMNPs. In a coherent context, we discussed here the characteristics which qualify NMNPs to possess a great enhancement effect for TiO2 photocatalysis. Also we tried to understand the reasons behind this effect by means of photoluminescence (PL) and electron paramagnetic resonance (EPR) spectra, and Density Functional Theory (DFT) calculations. Then the mechanism of action of NMNPs upon deposition on TiO2 is presented. Finally we introduced a survey of the behaviour of these noble metal NPs on TiO2 based on the particle size and the loading amount.
引用
收藏
页码:7146 / 7158
页数:13
相关论文
共 156 条
[1]   Heterogenous Catalysis Mediated by Plasmon Heating [J].
Adleman, James R. ;
Boyd, David A. ;
Goodwin, David G. ;
Psaltis, Demetri .
NANO LETTERS, 2009, 9 (12) :4417-4423
[2]   ELECTRONIC-STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS - THE PROGRAM SYSTEM TURBOMOLE [J].
AHLRICHS, R ;
BAR, M ;
HASER, M ;
HORN, H ;
KOLMEL, C .
CHEMICAL PHYSICS LETTERS, 1989, 162 (03) :165-169
[3]   Modeling the noble metal/TiO2 (110) interface with hybrid DFT functionals: A periodic electrostatic embedded cluster model study [J].
Ammal, Salai Cheettu ;
Heyden, Andreas .
JOURNAL OF CHEMICAL PHYSICS, 2010, 133 (16)
[4]  
Andrea A., 2012, J PHYS CONDENS MATT, V24
[5]   Electronic changes at the Pt(111) interface induced by the adsorption of OH species [J].
Arce, M. D. ;
Quaino, P. ;
Santos, E. .
CATALYSIS TODAY, 2013, 202 :120-127
[6]   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
[7]   Stability of Pt nanoparticles and enhanced photocatalytic performance in mesoporous Pt-(anatase/TiO2(B)) nanoarchitecture [J].
Bai, Yang ;
Li, Wei ;
Liu, Chang ;
Yang, Zhuhong ;
Feng, Xin ;
Lu, Xiaohua ;
Chan, Kwong-Yu .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (38) :7055-7061
[8]   The influence of the preparation methods on the catalytic activity of platinum and gold supported on TiO2 for CO oxidation [J].
Bamwenda, GR ;
Tsubota, S ;
Nakamura, T ;
Haruta, M .
CATALYSIS LETTERS, 1997, 44 (1-2) :83-87
[9]   PHOTOASSISTED HYDROGEN-PRODUCTION FROM A WATER-ETHANOL SOLUTION - A COMPARISON OF ACTIVITIES OF AU-TIO2 AND PT-TIO2 [J].
BAMWENDA, GR ;
TSUBOTA, S ;
NAKAMURA, T ;
HARUTA, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1995, 89 (02) :177-189
[10]   2. Photosensitized degradation of azo dyes on Fe, Ti, and Al oxides. Mechanism of charge transfer during the degradation [J].
Bandara, J ;
Mielczarski, JA ;
Kiwi, J .
LANGMUIR, 1999, 15 (22) :7680-7687