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Photocatalytic performance of Pr/In/Nd composite oxides synthesized by solid state reaction

机译:固相反应合成Pr / In / Nd复合氧化物的光催化性能

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Pr/In/Nd composite oxides with different Pr/In/Nd ratios were successfully prepared using a simple solid state reaction at 873 K. The composites were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area measurements, photolumi-nescence (PL) spectra and UV-vis diffuse reflection spectroscopy (UV-vis DRS). The photocatalytic activity of Pr/In/Nd composite oxides was investigated by the degradation of methyl orange (MO) in an aqueous solution under UV and visible light irradiation. It is found that compared with pure In_2O_3, the absorption intensity of the Pr/In/Nd composite oxide (Pr/In/Nd = 1:8:1) increases in the 200-800 nm light region and the absorption edge has a shift to longer wavelength. In addition, the Pr/In/Nd composite oxide (Pr/In/ Nd= 1:8:1) shows higher UV and visible light photocatalytic activities than pure In_2O_3. The remarkably enhanced photocatalytic activities could be mainly attributed to the fact that proper introduction of Pr_2O_3 and Nd2O5 increased the BET surface area of In_2O_3, improved the separation efficiency of photogenerated electrons and holes, and enhanced the absorption intensity in 200-800 nm light region. The effect of various radical scavengers on the degradation of MO showed that OH, O_2~-, h~+ and H_2O_2, especially O_2~-, jointly dominated the photodegradation process of MO under UV light irradiation.
机译:使用简单的固态反应在873 K下成功制备了具有不同Pr / In / Nd比的Pr / In / Nd复合氧化物。通过X射线衍射(XRD),Brunauer-Emmett-Teller(BET)表面对复合材料进行了表征面积测量,光致发光(PL)光谱和紫外可见漫反射光谱(UV-vis DRS)。 Pr / In / Nd复合氧化物的光催化活性是通过在紫外和可见光辐射下降解水溶液中的甲基橙(MO)来研究的。发现与纯In_2O_3相比,Pr / In / Nd复合氧化物(Pr / In / Nd = 1:8:1)在200-800 nm的光区域中的吸收强度增加,并且吸收边缘发生了偏移到更长的波长。此外,Pr / In / Nd复合氧化物(Pr / In / Nd = 1:8:1)与纯In_2O_3相比,具有更高的UV和可见光光催化活性。适当引入Pr_2O_3和Nd2O5可增加In_2O_3的BET表面积,提高光生电子和空穴的分离效率,并增强200-800 nm光区的吸收强度,这是光催化活性显着提高的原因。各种自由基清除剂对MO的降解作用表明,OH,O_2〜-,h〜+和H_2O_2,尤其是O_2〜-共同主导着紫外光照射下MO的光降解过程。

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