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Sono-dispersion of TiO2 nanoparticles over clinoptilolite used in photocatalytic hydrogen production: Effect of ultrasound irradiation during conventional synthesis methods

机译:用于光催化氢气生产的TiO2纳米粒子的超声分散方法:常规合成方法中超声辐射的影响

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Hydrogen evolution via water splitting was investigated over the sonochemically synthesized TiO2-clinoptilolite photocomposites. To this aim, a series of photocatalysts containing 10 wt% titania were prepared by impregnation and solid state dispersion (SSD) methods in the presence and absence of ultrasound irradiation. The samples were characterized by XRD, FESEM, EDX, BET, FTIR, PL and UV-vis techniques and tested for the water splitting. The characterization results indicated that ultrasound irradiation endowed the photocatalysts with uniform morphology, higher surface area and more homogenous dispersion. In addition, the analyses also exhibited less population of particle aggregates, a strong titania-support interaction and lower electron-hole pairs recombination rate. These features were more prominent when ultrasound was employed during SSD method. The TiO2/Clinoptilolite photocatalyst prepared by the ultrasound assisted SSD method (TiO2/CLT(US)), had more uniform active sites dispersion, high separation efficiency of electron-hole pairs and as a consequence, high surface density of active sites. The highest photocatalytic activity, 569.88 mu mol/g(TiO2) . h, was obtained for the TiO2/CLT(US) sample which was about 8 times more than that of P-25 as a reference sample. Furthermore, the TiO2/CLT (US) photocomposite as optimal photocatalyst showed sufficient reusability, making it a good choice for photocatalytic water splitting applications. (C) 2017 Elsevier B.V. All rights reserved.
机译:通过Sonocheochemicaly合成的TiO2-临床光化复合材料研究了通过水分裂的氢进化。为此,通过在存在和不存在超声辐射的情况下,通过浸渍和固态分散(SSD)方法制备含有10wt%二氧化钛的一系列光催化剂。样品的特征在于XRD,FESEM,EDX,BET,FTIR,PL和UV-VIS技术,并测试水分裂。表征结果表明,超声辐射赋予光催化剂,具有均匀的形态,高度表面积和更均匀的分散体。此外,分析还表现出少于颗粒聚集体的少量少,强钛载体相互作用和较低的电子 - 空穴对重组率。在SSD方法中使用超声时,这些特征更加突出。通过超声辅助SSD方法(TiO 2 / ClT(US))制备的TiO2 / Clinophitolite光催化剂具有更均匀的活性位点分散,电子 - 空穴对的高分离效率,因此具有高表面密度的活性位点。最高光催化活性,569.88 mm mol / g(TiO 2)。获得H,用于TiO2 / CLT(US)样品,其为P-25的大约8倍作为参考样品。此外,TiO2 / CLT(US)光催化剂作为最佳光催化剂表现出足够的可重用性,使其成为光催化水分裂应用的良好选择。 (c)2017 Elsevier B.v.保留所有权利。

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