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首页> 外文期刊>Surface & Coatings Technology >Preparation of cerium-doped titania macroporous films by a sol–gel spin oating using polypropylene glycol (PPG) as pore-creating agent: Effects of Ce ions, PPG and calcination on photocatalytic activity
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Preparation of cerium-doped titania macroporous films by a sol–gel spin oating using polypropylene glycol (PPG) as pore-creating agent: Effects of Ce ions, PPG and calcination on photocatalytic activity

机译:溶胶-凝胶旋涂法制备铈掺杂的二氧化钛大孔薄膜,使用聚丙二醇(PPG)作为造孔剂:Ce离子,PPG和煅烧对光催化活性的影响

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摘要

Cerium-doped titania macroporous films (CTMs) were spin-coated on glass substrates from a controlled sol– gel solution using titanium alkoxide and polypropylene glycol (PPG) as precursor and pore-creating agent, respectively. The physicochemical properties of CTMs were characterized by scanning electron microscope (SEM), thermogravimetric and differential thermal analysis (TG-DTA), X-ray photoelectron spectroscopy (XPS), X-ray diffractometry (XRD) and BET surface area analysis. The photocatalytic activity of CTMs was evaluated by degradation of methylene blue (MB). The results showed the decomposition of PPG during calcinations was responsible for the generation of macroporous structure in the films. The Ce ions, PPG and calcination respectively influenced recombination of electron–hole pairs, surface area, hydroxyl concentration and crystalline structure of films, so that one of those factors could restrict the photocatalytic activity of films. Compared with others films, CTMs-1 showed the highest photocatalytic activity with 0.5 wt.% of Ce doping concentration and 2.0 g PPG additions at calcinating temperature of 550 °C. It was mainly attributed to the effects that both the optimum concentration of Ce ions doping and high surface area could promote the photocatalytic degradation by preventing recombination of electron–hole pairs and providing more MB molecules around TiO2 and high concentration of hydroxyl.
机译:将铈掺杂的二氧化钛大孔膜(CTM)从可控的溶胶凝胶溶液中旋涂在玻璃基板上,分别使用醇钛和丙二醇(PPG)作为前体和造孔剂。通过扫描电子显微镜(SEM),热重和差热分析(​​TG-DTA),X射线光电子能谱(XPS),X射线衍射法(XRD)和BET表面积分析来表征CTM的理化性质。通过亚甲基蓝(MB)的降解来评估CTM的光催化活性。结果表明,煅烧过程中PPG的分解是导致薄膜中大孔结构产生的原因。 Ce离子,PPG和煅烧分别影响电子-空穴对的重组,表面积,羟基浓度和薄膜的晶体结构,因此这些因素之一可能会限制薄膜的光催化活性。与其他薄膜相比,CTMs-1在550°C的煅烧温度下具有0.5 wt。%的Ce掺杂浓度和2.0 g PPG添加量表现出最高的光催化活性。主要归因于这样的效果:最佳的Ce离子掺杂浓度和高表面积都可以通过阻止电子-空穴对的复合并在TiO2周围提供更多的MB分子和高浓度的羟基来促进光催化降解。

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