Stability of Pt nanoparticles and enhanced photocatalytic performance in mesoporous Pt-(anatase/TiO2(B)) nanoarchitecture

被引:76
作者
Bai, Yang [1 ]
Li, Wei [1 ,2 ]
Liu, Chang [1 ]
Yang, Zhuhong [1 ]
Feng, Xin [1 ]
Lu, Xiaohua [1 ]
Chan, Kwong-Yu [2 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Univ Hong Kong, Dept Chem, Hong Kong, Hong Kong, Peoples R China
关键词
SUPPORTED METAL-CLUSTERS; CATALYTIC-ACTIVITY; TITANIUM-DIOXIDE; PALLADIUM NANOPARTICLES; HYDROGEN EVOLUTION; SURFACE SCIENCE; TIO2; PLATINUM; OXIDATION; ANATASE;
D O I
10.1039/b910240j
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
A novel metal-semiconductor nanocomposite with stable metal nanoparticles and efficient photocatalytic performance has been prepared. It consists of highly dispersed similar to 2 nm platinum (Pt) nanoparticles loaded on mesoporous and bicrystalline TiO2 fibers (Pt/mb-TiO2). Due to the well organized porous Pt/TiO2 nanoarchitecture, rate of photodegradation of CHCl3 was nearly doubled compared to both P25 and Pt/P25. And in photocatalytic production of H-2 (with methanol as an electron donor), Pt/mb-TiO2 presented much more stable activity than Pt/P25. In a 20 h H-2 production, Pt nanoparticles on P25 agglomerated and grew remarkably from 2.0 +/- 0.5 nm to 4.5 +/- 2.5 nm, while Pt nanoparticles on mb-TiO2 changed slightly from 2.0 +/- 0.5 nm to 2.2 +/- 0.5 nm. Moreover, the loss ratio of Pt on P25 is 36%, which is much larger than that of 7% on mb-TiO2. The efficient charge transfer in the interfaces of Pt/TiO2(B) and TiO2(B)/anatase was discussed. We concluded that the high photocatalytic performance of Pt/mb-TiO2 can be attributed to stable Pt nanoparticles supported on the mesoporous masonry frameworks of TiO2 and efficient charge transfer in the interfaces.
引用
收藏
页码:7055 / 7061
页数:7
相关论文
共 40 条
[1]  
[Anonymous], SURF SCI REP
[2]   PHOTO-ELECTROCHEMICAL HYDROGEN EVOLUTION AND WATER-PHOTOLYZING SEMICONDUCTOR SUSPENSIONS - PROPERTIES OF PLATINUM GROUP METAL CATALYST SEMICONDUCTOR CONTACTS IN AIR AND IN HYDROGEN [J].
ASPNES, DE ;
HELLER, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (24) :4919-4929
[3]   The impact of nanoscience on heterogeneous catalysis [J].
Bell, AT .
SCIENCE, 2003, 299 (5613) :1688-1691
[4]   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
[5]   Catalytically active gold: From nanoparticles to ultrathin films [J].
Chen, Mingshu ;
Goodman, D. Wayne .
ACCOUNTS OF CHEMICAL RESEARCH, 2006, 39 (10) :739-746
[6]   Titanium dioxide nanomaterials: Synthesis, properties, modifications, and applications [J].
Chen, Xiaobo ;
Mao, Samuel S. .
CHEMICAL REVIEWS, 2007, 107 (07) :2891-2959
[7]   The surface science of titanium dioxide [J].
Diebold, U .
SURFACE SCIENCE REPORTS, 2003, 48 (5-8) :53-229
[8]   Photocatalytic water splitting over Pt-TiO2 in the presence of sacrificial reagents [J].
Galinska, A ;
Walendziewski, J .
ENERGY & FUELS, 2005, 19 (03) :1143-1147
[9]   Photoelectrochemical cells [J].
Grätzel, M .
NATURE, 2001, 414 (6861) :338-344
[10]   Long-range effects of noble metals on the photocatalytic properties of titanium dioxide [J].
Haick, H ;
Paz, Y .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (10) :2319-2326