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Fabrication of coenocytic Pd@CdS nanocomposite as a visible light photocatalyst for selective transformation under mild conditions

机译:制备共胞体Pd @ CdS纳米复合材料作为可见光光催化剂,可在温和条件下进行选择性转化

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摘要

Coenocytic Pd@CdS nanocomposite has been successfully prepared via a facile wet chemistry approach. Its structure and properties have been characterized by a series of techniques, including field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), ultra-violet/visible diffuse reflectance spectroscopy (DRS), nitrogen adsorption-desorption and electron spin resonance spectroscopy (ESR). The results demonstrate that the Pd nanoparticles as multiple cores are evenly distributed inside the photoactive CdS shell, forming a coenocytic nanostructure. It is found that the concentration of precursors and the intrinsic nature of noble metal colloids play essential roles in the growth process for such noble metal@semiconductor nanocomposite. Accordingly, a possible formation mechanism for the coenocytic Pd@CdS nanocomposite is proposed. The visible light photocatalytic activity of Pd@CdS has been evaluated by selective oxidation of a range of alcohols using molecular oxygen as oxidant under mild conditions. The results show that the coenocytic Pd@CdS exhibits enhanced photocatalytic activity as compared to blank-CdS obtained by the same procedure in the absence of Pd colloid nanoparticles as seeds. The enhanced photocatalytic performance of the coenocytic Pd@CdS can be ascribed to the coupling interaction of enhanced light absorption intensity, the longer lifetime of photogenerated charge carriers and its favorable adsorptivity. It is expected that our work could provide useful information for fabricating other core-shell nanocomposites and open an avenue to utilizing them in the field of photocatalytic selective organic transformations.
机译:已经通过一种简便的湿化学方法成功地制备了亲核Pd @ CdS纳米复合材料。其结构和特性已通过一系列技术进行了表征,包括场发射扫描电子显微镜(FE-SEM),透射电子显微镜(TEM),能量色散X射线光谱仪(EDX),X射线光电子光谱仪( XPS),X射线衍射(XRD),紫外/可见漫反射光谱(DRS),氮吸附-解吸和电子自旋共振光谱(ESR)。结果表明,作为多个核的Pd纳米颗粒均匀分布在光敏CdS壳内部,形成了共胞纳米结构。发现前体的浓度和贵金属胶体的固有性质在这种贵金属@半导体纳米复合材料的生长过程中起着至关重要的作用。因此,提出了一种可能的共胞体Pd @ CdS纳米复合物的形成机理。已经通过在温和条件下使用分子氧作为氧化剂选择性氧化多种醇来评估Pd @ CdS的可见光光催化活性。结果表明,与在没有Pd胶体纳米粒子作为种子的情况下通过相同程序获得的空白-CdS相比,共细胞Pd @ CdS表现出增强的光催化活性。介孔Pd @ CdS的增强的光催化性能可以归因于增强的光吸收强度,更长的光生电荷载流子寿命及其良好的吸附性的耦合相互作用。期望我们的工作可以为制备其他核壳纳米复合材料提供有用的信息,并为在光催化选择性有机转化领域中利用它们提供一条途径。

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