Photoreduction of CO2 using sol-gel derived titania and titania-supported copper catalysts

被引:493
作者
Tseng, IH [1 ]
Chang, WC [1 ]
Wu, JCS [1 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
关键词
photocatalytic reduction; carbon dioxide; titanium dioxide; sol-gel; copper;
D O I
10.1016/S0926-3373(01)00322-8
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
Carbon dioxide was photocatalytically reduced to produce methanol in an aqueous solution using 254 nm UV irradiation. Titania and Cu-loaded titania were synthesized by an improved sol-gel method using a homogeneous hydrolysis technique. The grain size of TiO2 and Cu/TiO2 were uniform and average diameters were approximately 20 nm. Photocatalytic reduction was conducted in a quartz reactor with a UV lamp irradiating at the center. XPS analysis reveals that Cu 2P(3/2) is 933.4 eV indicating primary CU2O species on the TiO2 Supports. EDX and XPS revealed that most copper clusters were on the TiO2 surface. The optimum amount of copper loading was 2.0 wt.% for the highest dispersion among catalysts. The methanol yield of 2.0 wt.% CU/TiO2 was 118 mumol/g following 6 It of UV illumination. The yield was much higher than those of sol-gel TiO2 and Degussa P25, whose yields were 4.7 and 38.2 mumol/g, respectively. The methanol yield reached a steady-state 250 mumol/g after 20 h of irradiation. Experimental results indicated that the methanol yield was significantly increased by adding NaOH. The caustic solution dissolved more CO2 than did pure water. In addition, the OH- in aqueous solution also served as a strong hole scavenger. The redistribution of the electric charge and the Schottky barrier of Cu and TiO2 facilitates electron trapping via supported Cu. The photocatalytic efficiency of Cu/TiO2 was markedly increased because of the lowering the re-combination probability for hole-electron pairs. The highest quantum and energy efficiencies achieved were 10 and 2.5%, respectively. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 48
页数:12
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