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Transition metal oxides supported onto silica gel as visible light-driven photocatalysts

机译:负载在硅胶上的过渡金属氧化物作为可见光催化的光催化剂

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摘要

Supported oxides of some transition metals have been prepared via incipient wetness impregnation of a mesoporous silica. Obtained compositions have been studied using DTA-TG and XRD analysis, FTIR, Raman, UV-Vis and XPS spectroscopy as well as low-temperature nitrogen adsorption-desorption. Deposited oxides have amorphous or low-crystalline structure and exhibit electronic properties different from those for bulk oxides. Red shift of adsorption edge is observed for most supported samples compared with corresponding bulk oxides. All tested samples regardless of the band gap showed photocatalytic activity under visible irradiation in process of rhodamine B degradation. The prepared supported oxides were more active compared with bulk oxides. The dispersion of oxides on the surface of the support and the greater accessibility of dye molecules to the active sites of the surface are the main reason for this. As a result, Ag/SiO(2)and TiO2/SiO(2)samples exhibited maximal photocatalytic activity. Three mechanisms of initiation for photocatalytic process were considered.
机译:通过初始湿度浸渍的介孔二氧化硅制备一些过渡金属的负载氧化物。已经使用DTA-Tg和XRD分析,FTIR,拉曼,UV-VI和XPS光谱以及低温氮吸附 - 解吸研究得到的组合物。沉积的氧化物具有无定形或低结晶的结构,并表现出与散装氧化物不同的电子性质。与相应的散装氧化物相比,对大多数支持的样品观察到吸附边缘的红色移位。无论带隙如何在罗丹明B降解过程中显示出在可见光辐照下的光催化活性。与散装氧化物相比,制备的负载氧化物更活跃。氧化物对载体表面的分散和染料分子的更大可达性与表面活性位点的主要原因是其中的主要原因。结果,Ag / SiO(2)和TiO 2 / SiO(2)样品表现出最大的光催化活性。考虑了光催化过程的三种启动机制。

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