Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, PR China.
J Colloid Interface Sci. 2010 Apr 15;344(2):382-9. doi: 10.1016/j.jcis.2010.01.002. Epub 2010 Jan 11.
A thermally stable SiO(2)-doped mesoporous TiO(2) with high crystallinity was prepared by a templating method. The content of SiO(2) dopant was varied from 3% to 20%. The gels were characterized by TG-DTA analysis. And the resultant catalysts were investigated by various physicochemical techniques, such as WAXRD, Raman spectroscopy, N(2) adsorption-desorption, TEM, FT-IR, and XPS. The WAXRD, TEM, and Raman measurements suggest that the SiO(2) dopant can enhance the thermal stability of the anatase phase remarkably. Rutile phase did not present at all even at 1000 degrees C when the SiO(2) content was up to 15%. N(2) adsorption-desorption results show that the SiO(2)-doped samples have uniform pore diameters and large specific surface area, which is beneficial for photocatalytic reaction. The photocatalytic activities of the samples were evaluated by degradation of Rhodamin-6G solution under UV irradiation. The results show that the SiO(2)-doped mesoporous TiO(2) have better activity than commercial P25. Especially, the 15% SiO(2)-doped mesoporous TiO(2) exhibited much higher photocatalytic activity than P25 in a large range of calcination temperatures, even at 900 degrees C. The excellent photocatalytic activity of the samples can be attributed to the high anatase crystallinity, large specific surface area, preserved surface hydroxyl groups and mesoporous channels.
采用模板法制备了一种具有高热稳定性和高结晶度的掺硅介孔二氧化钛。SiO2 掺杂量从 3%变化到 20%。通过 TG-DTA 分析对凝胶进行了表征。并通过各种物理化学技术,如 WAXRD、拉曼光谱、N2 吸附-脱附、TEM、FT-IR 和 XPS 对所得催化剂进行了研究。WAXRD、TEM 和拉曼测量表明,SiO2 掺杂剂可以显著提高锐钛矿相的热稳定性。当 SiO2 含量高达 15%时,即使在 1000°C 下也没有出现金红石相。N2 吸附-脱附结果表明,掺硅样品具有均匀的孔径和较大的比表面积,有利于光催化反应。通过在紫外光照射下降解罗丹明 6G 溶液评价了样品的光催化活性。结果表明,掺硅介孔 TiO2 比商业 P25 具有更好的活性。特别是,在很大的煅烧温度范围内,15%SiO2 掺杂的介孔 TiO2 甚至在 900°C 时,表现出比 P25 更高的光催化活性。样品具有优异的光催化活性,可归因于高锐钛矿结晶度、大比表面积、保留的表面羟基和介孔通道。