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Sulfur Doped Ceria Mesoporous Nanomaterial: Solid-State Synthesis, Characterization and Photocatalytic Property of Methyl Orange

机译:硫掺杂二氧化铈介孔纳米材料:甲基橙的固态合成,表征及光催化性能

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To investigate the photocatalytic performance of rare-earth metal oxide modified with nonmetal, the sulfur doped ceria (S-CeO2) mesoporous nanomaterials with high visible light-driven activity was successfully prepared by a simple solid state reaction method at low temperature using sodium benzene sulfonate as a template. The samples were characterized by X-ray powder diffraction, high resolution transmission electron microscopy/energydispersive X-ray spectroscopy, UV-vis absorption spectra, infrared spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and N2 adsorption-desorption. The doping mechanism and photo-catalytic degradation of methyl orange under visible light irradiation were discussed. The results show that the S-CeO2-SBS has cubic fluorite structure with high BET surface area of 104.3 m(2)/g and the egg-shaped morphology of mesoporous architecture. It is composed of ca. 13 nm nanoparticles by self-assembly and accumulation. The S atoms are successfully incorporated into the (111) and (200) crystal surface of CeO2 lattice as a S(IV) and S(VI) with the assistance of SBS template, respectively, and caused the generation of oxygen vacancies, structure defects and Ce(III) ions. As compared to pure CeO2, its ultraviolet visible diffuse reflectance absorption band red shifts to 500 nm with the enhancement of light absorption intensity. Under visible-light irradiation at room temperature within 80 min, the photocatalytic oxidation activity of methyl orange follows an order of S-CeO2-SBS (98.6%) S-CeO2 (68.4%) CeO2-SBS (42.2%) CeO2 (29.3%).
机译:为了研究非金属改性稀土金属氧化物的光催化性能,采用简单的固态反应方法,采用苯磺酸钠在低温下成功制备了具有高可见光驱动活性的硫掺杂二氧化铈(S-CeO2)介孔纳米材料。作为模板。通过X射线粉末衍射,高分辨率透射电子显微镜/能量分散X射线光谱,UV-可见吸收光谱,红外光谱,拉曼光谱,X射线光电子光谱和N 2吸附-脱附对样品进行表征。讨论了可见光照射下甲基橙的掺杂机理和光催化降解。结果表明,S-CeO2-SBS具有立方萤石结构,高BET表面积为104.3 m(2)/ g,具有介孔结构的蛋形形态。它由ca组成。 13 nm纳米粒子通过自组装和积累。在SBS模板的帮助下,S原子分别作为S(IV)和S(VI)成功地掺入CeO2晶格的(111)和(200)晶体表面,并导致氧空位,结构缺陷的产生和Ce(III)离子。与纯CeO2相比,随着光吸收强度的增强,其紫外可见漫反射吸收带红移至500 nm。在室温下80分钟内在可见光照射下,甲基橙的光催化氧化活性依次为S-CeO2-SBS(98.6%)> S-CeO2(68.4%)> CeO2-SBS(42.2%)> CeO2 (29.3%)。

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