Ionic-Liquid-Assisted Synthesis of Uniform Fluorinated B/C-Codoped TiO2 Nanocrystals and Their Enhanced Visible-Light Photocatalytic Activity

被引:163
作者
Yu, Jiaguo [1 ]
Li, Qin [1 ]
Liu, Shengwei [1 ]
Jaroniec, Mietek [2 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
关键词
doping; ionic liquids; nanocrystals; photochemistry; titanium; ANATASE TIO2; PHOTOASSISTED DEGRADATION; HYDROTHERMAL SYNTHESIS; TITANIUM-DIOXIDE; DYE POLLUTANTS; H-2; PRODUCTION; RHODAMINE-B; MICROSTRUCTURES; BORON; NANOPARTICLES;
D O I
10.1002/chem.201202778
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exploiting advanced photocatalysts under visible light is of primary significance for the development of environmentally relevant photocatalytic decontamination processes. In this study, the ionic liquid (IL), 1-butyl-3-methylimidazolium tetrafluoroborate, was employed for the first time as both a structure-directing agent and a dopant for the synthesis of novel fluorinated B/C-codoped anatase TiO2 nanocrystals (TIL) through hydrothermal hydrolysis of tetrabutyl titanate. These TIL nanocrystals feature uniform crystallite and pore sizes and are stable with respect to phase transitions, crystal ripening, and pore collapse upon calcination treatment. More significantly, these nanocrystals possess abundant localized states and strong visible-light absorption in a wide range of wavelengths. Because of synergic interactions between titania and codopants, the calcined TIL samples exhibited high visible-light photocatalytic activity in the presence of oxidizing RhodamineB (RhB). In particular, 300 degrees C-calcined TIL was most photocatalytically active; its activity was much higher than that of TiO1.98N0.02 and reference samples (TW) obtained under identical conditions in the absence of ionic liquid. Furthermore, the possible photocatalytic oxidation mechanism and the active species involved in the RhB degradation photocatalyzed by the TIL samples were primarily investigated experimentally by using different scavengers. It was found that both holes and electrons, as well as their derived active species, such as .OH, contributed to the RhB degradation occurring on the fluorinated B/C-codoped TiO2 photocatalyst, in terms of both the photocatalytic reaction dynamics and the reaction pathway. The synthesis of the aforementioned novel photocatalyst and the identification of specific active species involved in the photodegradation of dyes could shed new light on the design and synthesis of semiconductor materials with enhanced photocatalytic activity towards organic pollutants.
引用
收藏
页码:2433 / 2441
页数:9
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