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TiO2/SnO2复合光催化剂的耦合效应 总被引:1,自引:0,他引:1
采用改进的sol gel技术制备TiO2/SnO2耦合型半导体光催化剂,利用XRD、气相色谱 仪、粒度仪和表面光电压装置等研究了耦合型半导体光催化机理和光催化效率的影响因素, 并通过降解甲醛探讨其在空气污染治理中的作用.实验结果表明,添加20 %(mol) SnO2的复 合半导体光催化剂,其光催化效率比纯TiO2高一倍以上.据实验结果和粒子紧密堆积原理,提 出强耦合效应和弱耦合效应的光催化反应模型,并用此模型较好地解释了TiO2/SnO2复合型半 导体光催化剂的光催化效率随SnO2含量变化规律. 相似文献
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半导体复合TiO2纳米光催化剂 总被引:12,自引:0,他引:12
对近年来利用半导体复合TiO2纳米光催化剂进行了介绍。总结了复合TiO2纳米光催化剂的制备、复合物的种类、光催化机理以及影响半导体复合TiO2光催化性能的因素。 相似文献
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SnO2-TiO2复合光催化剂的制备和性能 总被引:35,自引:0,他引:35
采用均匀沉淀法在超细TiO2表面包覆SnO2,制备出SnO2-TiO2复合光催化剂,并用EDS,XRD,TEM和BET比表面积测定等手段进行了表征.以活性艳红X-3B溶液为模拟废水,考察了SnO2-TiO2的光催化活性.结果表明,复合粒子由锐钛矿型TiO2和金红石型SnO2组成;与纯TiO2相比,SnO2-TiO2的光催化活性有较大提高,SnO2最佳包覆量为18.4%.复合光催化剂活性的提高归因于不同能级半导体之间光生载流子的输运和分离. 相似文献
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在大量研究工作的基础上,设计了纳米TiO2光催化剂制备和性能研究的综合实验,包括溶胶-凝胶自蔓燃法制备纳米二氧化钛、硝基苯光催化降解、COD测定等实验内容。 相似文献
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核-壳式纳米SnO2/TiO2光催化剂的制备和性能 总被引:8,自引:0,他引:8
以纳米SnO2·nH2O胶体粒子为基质,采用活性层包覆法制备了纳米SnO2/TiO2复合光催化剂,并用R,TEM,XPS和XRD等手段进行了表征. 采用敌敌畏的光催化降解反应对所制催化剂的活性进行了评价. 结果表明,SnO2/TiO2为核-壳结构,粒径约为12 nm. SnO2/TiO2的光催化活性受TiO2含量及SnO2·nH2O乙醇溶液含水量的影响. 最佳条件为SnO2/TiO2中TiO2含量为56.45%,SnO2·nH2O乙醇溶液含水量为20%. 所制SnO2/TiO2光催化活性比纯TiO2显著提高,且光催化活性稳定,可重复使用. 相似文献
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TiO_2/SnO_2复合光催化剂的耦合效应 总被引:1,自引:0,他引:1
采用改进的 sol-gel技术制备 TiO_2/SnO_2耦合型半导体光催化剂 ,利用 XRD、气相色谱仪、粒度仪和表面光电压装置等研究了耦合型半导体光催化机理和光催化效率的影响因素 ,并通过降解甲醛探讨其在空气污染治理中的作用 .实验结果表明 ,添加 20% (mol) SnO_2的复合半导体光催化剂 ,其光催化效率比纯 TiO_2高一倍以上 .据实验结果和粒子紧密堆积原理 ,提出强耦合效应和弱耦合效应的光催化反应模型 ,并用此模型较好地解释了 TiO_2/SnO_2复合型半导体光催化剂的光催化效率随 SnO_2含量变化规律 . 相似文献
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采用共沉淀法将SnO_2组分掺入到V_2O_5-WO_3/TiO_2催化剂载体TiO_2中,并通过多种物理化学手段,考察了不同SnO_2掺入量时对催化剂结构,表面分散物种和SCR性能影响.结果表明,SnO_2掺入到TiO_2中,元素Sn与Ti以Sn—O—Ti键形式相互作用,促进锐钛矿型TiO_2向金红石型TiO_2转变.在特定条件下,VO_x与WO_x物种和SnTi氧化物之间以V—O—Ti(Sn)和W—O—Ti(Sn)键形式相互作用,提高了VO_x物种可还原能力、促进了具有更多B酸酸量四面体WOx物种和V~(5+)物种生成.VW/SnTi催化剂表面VO_x物种与WO_x物种之间的相互作用更强.因此,VW/SnTi催化剂具有更好的SCR活性. 相似文献
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ZnO/TiO2/SnO2 mixture was prepared by mixing its component solid oxides ZnO, TiO2 and SnO2 in the molar ratio of 4?1?1, followed by calcining the solid mixture at 200-1300 °C. The products and solid-state reaction process during the calcinations were characterized with powder X-ray diffraction (XRD), thermogravimetric and differential thermal analysis (TG-DTA), UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and Brunauer-Emmett-Teller measurement of specific surface area. Neither solid-state reaction nor change of crystal phase composition took place among the ZnO, TiO2 and SnO2 powders on the calcinations up to 600 °C. However, formation of the inverse spinel Zn2TiO4 and Zn2SnO4 was detected at 700-900 and 1100-1200 °C, respectively. Further increase of the calcination temperature enabled the mixture to form a single-phase solid solution Zn2Ti0.5Sn0.5O4 with an inverse spinel structure in the space group of . The ZnO/TiO2/SnO2 mixture was photocatalytically active for the degradation of methyl orange in water; its photocatalytic mass activity was 16.4 times that of SnO2, 2.0 times that of TiO2, and 0.92 times that of ZnO after calcination at 500 °C for 2 h. But, the mass activity of the mixture decreased with increasing the calcination temperature at above 700 °C because of the formation of the photoinactive Zn2TiO4, Zn2SnO4 and Zn2Ti0.5Sn0.5O4. The sample became completely inert for the photocatalysis after prolonged calcination at 1300 °C (42 h), since all of the active component oxides were reacted to form the solid solution Zn2Ti0.5Sn0.5O4 with no photocatalytic activity. 相似文献
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N 掺杂TiO2光催化剂的制备及其可见光活性研究 总被引:15,自引:0,他引:15
A visible-light-active photocatalyst was prepared by calcination of the hydrolysis product of tetrabutyl titanate with ammonia as precipitant. The photocatalyst was characterized by X-ray diffraction (XRD), UV-Vis diffuse reflection spectra (DRS), thermal gravimetric-differential thermal analysis (TG-DTA), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM). The color of the photocatalyst was yellow and could absorb light wavelength under 550 nm as measured by DRS. The catalyst calcined at higher temperature will give lower absorbance for visible light. Structures of the sample were characterized mainly to be anatase by XRD except for the sample calcined at 700 ℃ which gave mixtures of anatase and rutile. TG-DTA results showed that temperature for anatase formation was 415 ℃. XPS results showed that doped-nitrogen was presented in the sample, they are important to show visible-light absorbency. The photocatalytic activities were evaluated using methyl orange and phenol as model pollutants, the results showed that over 90% of phenol could be degraded under visible light using N/TiO2 as the catalyst after 4 hours reaction. Almost the same activity was found for the TiO2 photocatalyst calcined at different temperature under sunlight but activities were different when the treatment was under UV light. 相似文献
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Photocatalytic N2 fixation has attracted substantial attention in recent years, as it represents a green and sustainable development route toward efficiently converting N2 to NH3 for industrial applications. How to rationally design catalysts in this regard remains a challenge. Here we propose a strategy that uses plasmonic hot electrons in the highly doped TiO2 to activate the inert N2 molecules. The synthesized semiconductor catalyst Mo-doped TiO2 shows a NH3 production efficiency as high as 134 μmol·g-1·h-1 under ambient conditions, which is comparable to that achieved by the conventional plasmonic gold metal. By means of ultrafast spectroscopy we reveal that the plasmonic hot electrons in the system are responsible for the activation of N2 molecules, enabling improvement the catalytic activity of TiO2. This work opens a new avenue toward semiconductor plasmon-based photocatalytic N2 fixation. 相似文献
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C. Hauser 《Chemical physics letters》1973,18(2):205-208
The metastability of oxygen paramagnetic centres adsorbed on a metallic oxyde has been pointed out. An energetic pattern is given and the energy values are measured. Various considerations on the density of paramagnetic centres and their probable association with a defect are presented. 相似文献
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运用基于密度泛函理论的第一性原理方法,建立了SnO2以及不同比例Ru掺杂的SnO2超胞模型,在对其进行几何优化后计算了Sn1-xRuxO2(x=0,1/16,1/12,1/8,1/6,1/4,1/2)半导体的电子结构,并讨论了其晶格参数、电荷密度、能带结构和态密度(包括分态密度)等性质。结果表明,掺杂后,晶格参数随掺杂量的增加线性减小,与实验值的偏差在4%以内;掺杂后,在费米能级处可以提供更多的填充电子,使得电子跃迁至导带更容易,固溶体的导电性增强。为Sn1-xRuxO2固溶体电极材料的发展和应用提供了理论基础。 相似文献
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