首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Fabrication of composite photocatalyst g-C _3N _4-ZnO and enhancement of photocatalytic activity under visible light
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Fabrication of composite photocatalyst g-C _3N _4-ZnO and enhancement of photocatalytic activity under visible light

机译:复合光催化剂g-C_3N_4-ZnO的制备及可见光下光催化活性的增强

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The g-C _3N _4-ZnO composite photocatalysts with various weight percents of ZnO were synthsized by a simple calcination process. The photocatalysts were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), UV-vis diffuse reflection spectroscopy (UV-vis), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA). The PXRD and HR-TEM results show that the composite materials consist of hexagonal wurzite phase ZnO and g-C _3N _4. The solid-state UV-vis diffuse reflection spectra show that the absorption edge of the composite materials shifts toward the lower energy region and to longer wavelengths in comparison with pure ZnO and g-C _3N _4. Remarkably, the photocatalytic activity of g-C _3N _4-ZnO composites has been demonstrated, via photodegradation of Methyl Orange (MO) and p-nitrophenol experiments. The photocatalytic activity of g-C _3N _4-ZnO for photodegradation of Methyl Orange and p-nitrophenol under visible light irradiation was increased by over 3 and 6 times, respectively, to be much higher than that of single-phase g-C _3N _4, clearly demonstrating a synergistic effect between ZnO and g-C _3N _4. The concentrations of Zn ~(2+) in g-C _3N _4-ZnO system after a photocatalytic reaction at various reaction times were found to be much lower than those for a ZnO system under the same reaction conditions, indicating that the g-C _3N _4-ZnO composite possesses excellent long-term stability for a photocatalytic reaction in aqueous solutions. Furthermore, a synergistic photocatalysis mechanism between ZnO and g-C _3N _4 was proposed based on the photodegradation results. Such obviously improved performance of g-C _3N _4-ZnO can be ascribed mainly to the enhancement of electron-hole separations at the interface of ZnO and g-C _3N _4.
机译:通过简单的煅烧过程合成具有不同重量百分比的ZnO的g-C _3N _4-ZnO复合光催化剂。通过粉末X射线衍射(PXRD),扫描电子显微镜(SEM),高分辨率透射电子显微镜(HR-TEM),紫外可见漫反射光谱法(UV-vis),X射线光电子能谱对光催化剂进行表征(XPS)和热重分析(TGA)。 PXRD和HR-TEM结果表明,复合材料由六方纤锌矿相ZnO和g-C _3N _4组成。固态UV-vis漫反射光谱表明,与纯ZnO和g-C _3N _4相比,复合材料的吸收边缘向较低的能量区域移动并向更长的波长移动。值得注意的是,已通过甲基橙(MO)的光降解和对硝基苯酚实验证明了g-C _3N _4-ZnO复合材料的光催化活性。 gC _3N _4-ZnO在可见光照射下对甲基橙和对硝基苯酚的光催化活性分别提高了3倍和6倍以上,远高于单相gC _3N _4,这明显证明了ZnO和gC _3N _4之间的协同作用。发现在相同反应条件下,经过不同反应时间的光催化反应后,gC _3N _4-ZnO体系中的Zn〜(2+)浓度远低于ZnO体系中的Zn〜(2+)浓度,表明gC _3N _4-ZnO复合材料对水溶液中的光催化反应具有出色的长期稳定性。此外,基于光降解结果,提出了ZnO与g-C _3N _4之间的协同光催化机理。 g-C _3N _4-ZnO的这种明显改善的性能可归因于增强ZnO和g-C _3N _4的界面处的电子-空穴分离。

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