Novel N-F-Codoped TiO2 Inverse Opal with a Hierarchical Meso-/Macroporous Structure: Synthesis, Characterization, and Photocatalysis

被引:77
作者
Xu, Jiao [1 ]
Yang, Beifang [1 ]
Wu, Ming [1 ]
Fu, Zhengping [1 ]
Lv, Yan [1 ]
Zhao, Yongxun [1 ]
机构
[1] Univ Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Anhui, Peoples R China
基金
美国国家科学基金会;
关键词
LIQUID-PHASE DEPOSITION; LIGHT-DRIVEN PHOTOCATALYSIS; TITANIUM-DIOXIDE; AMPLIFIED PHOTOCHEMISTRY; NITROGEN; SURFACE; FILMS; ENHANCEMENT; FABRICATION; POWDERS;
D O I
10.1021/jp101168y
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
We reported a new simple route to fabricate N-F-codoped titania inverse opal (IO) films with a hierarchical meso-/macroporous structure, in which the IO structure and the N-F codoping play a role as physical and chemical modifications for titania, respectively. Both modifications are simultaneously achieved via a liquid phase deposition process using a silica colloidal crystal as a template for the first time. The average size of a mesopore in the TiO2 frameworks is 3.2 nm, and that of an interpenetrating aligned macropore is adjusted in the range of 201-315 nm. The N-F-codoped TiO2 IO films exhibit 6.6-7.4 times the methylene blue visible-light photodegradation rate comparing with N-F-codoped TiO2 films without the IO structure. This high visible-light activity was mainly ascribed to a synergetic effect of the hierarchical meso-/macroporous structure and N-F codoping. Furthermore, it was found that the multiple scattering effect of the macroporous structure is more pronounced than the slow photon effect of IOs for facilitating visible-light photocatalysis in our system from the comparison with nonperiodic macroporous N-F-codoped TiO2. The repeated cycling tests revealed that samples showed stable photocatalytic activity.
引用
收藏
页码:15251 / 15259
页数:9
相关论文
共 47 条
[31]   Chemical State of Nitrogen and Visible Surface and Schottky Barrier Driven Photoactivities of N-Doped TiO2 Thin Films [J].
Romero-Gomez, P. ;
Rico, V. ;
Borras, A. ;
Barranco, A. ;
Espinos, J. P. ;
Cotrino, J. ;
Gonzalez-Elipe, A. R. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (30) :13341-13351
[32]   TITANIUM NITRIDE OXIDATION CHEMISTRY - AN X-RAY PHOTOELECTRON-SPECTROSCOPY STUDY [J].
SAHA, NC ;
TOMPKINS, HG .
JOURNAL OF APPLIED PHYSICS, 1992, 72 (07) :3072-3079
[33]   Raman Line Shapes of Optical Phonons of Different Symmetries in Anatase TiO2 Nanocrystals [J].
Sahoo, Satyaprakash ;
Arora, A. K. ;
Sridharan, V. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (39) :16927-16933
[34]   Is the band gap of pristine TiO2 narrowed by anion- and cation-doping of titanium dioxide in second-generation photocatalysts? [J].
Serpone, Nick .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (48) :24287-24293
[35]   CONTROLLED GROWTH OF MONODISPERSE SILICA SPHERES IN MICRON SIZE RANGE [J].
STOBER, W ;
FINK, A ;
BOHN, E .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1968, 26 (01) :62-&
[36]   Liquid-phase deposition of TiO2 on polystyrene latex particles functionalized by the adsorption of polyelectrolytes [J].
Strohm, H ;
Löbmann, P .
CHEMISTRY OF MATERIALS, 2005, 17 (26) :6772-6780
[37]   Copper uptake by inorganic particles - equilibrium, kinetics, and particle interactions: experimental [J].
Subramaniam, K ;
Yiacoumi, S ;
Tsouris, C .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2001, 177 (2-3) :133-146
[38]   Interactions between dissimilar surfaces in high ionic strength solutions as determined by atomic force microscopy [J].
Veeramasuneni, S ;
Yalamanchili, MR ;
Miller, JD .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1998, 131 (1-3) :77-87
[39]   COAGULATION AND ELECTROKINETIC BEHAVIOR OF TIO2 AND AL2O3 COLLOIDAL DISPERSIONS [J].
WIESE, GR ;
HEALY, TW .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1975, 51 (03) :427-433
[40]   Fabrication of 2D and 3D ordered porous ZnO films using 3D opal templates by electrodeposition [J].
Yan, HW ;
Yang, YL ;
Fu, ZP ;
Yang, BF ;
Xia, LS ;
Fu, SQ ;
Li, FQ .
ELECTROCHEMISTRY COMMUNICATIONS, 2005, 7 (11) :1117-1121