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Synthesis of One-Dimensional CdS@TiO2 Core-Shell Nanocomposites Photocatalyst for Selective Redox: The Dual Role of TiO2 Shell

机译:一维CdS @ TiO2核壳纳米复合光催化剂的选择性氧化还原的合成:TiO2壳的双重作用。

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One-dimensional (1D) CdS@TiO2 core-shell nanocomposites (CSNs) have been successfully synthesized via a two-step solvothermal method. The structure and properties of 1D CdS@TiO2 core-shell nanocomposites (CdS@ TiO2 CSNs) have been characterized by a series of techniques, including X-ray diffraction (XRD), ultraviolet—visible-light (UV-vis) diffuse reflectance spectra (DRS), field-emission scanning electron microscopy (FESEM), photoluminescence spectra (PL), and electron spin resonance (ESR) spectroscopy. The results demonstrate that 1D core—shell structure is formed by coating TiO2 onto the substrate of CdS nanowires (NWs). The visible-light-driven photocatalytic activities of the as-prepared 1D CdS@TiO2 CSNs are evaluated by selective oxidation of alcohols to aldehydes under mild conditions. Compared to bare CdS NWs, an obvious enhancement of both conversion and yield is achieved over 1D CdS@TiO2 CSNs, which is ascribed to the prolonged lifetime of photogenerated charge carriers over 1D CdS@TiO2 CSNs under visible-light irradiation. Furthermore, it is disclosed that the photogenerated holes from CdS core can be stuck by the TiO2 shell, as evidenced by controlled radical scavenger experiments and efficiently selective reduction of heavy-metal ions, Cr(VI), over 1D CdS@TiO2 CSNs, which consequently leads to the fact that the reaction mechanism of photocatalytic oxidation of alcohols over 1D CdS@TiO2 CSNs is apparently different from that over 1D CdS NWs under visible-light irradiation. It is hoped that our work could not only offer useful information on the fabrication of various specific 1D core—shell nanostructures, but also open a new doorway of such 1D core—shell semiconductors as visible-light photocatalysts in the promising field of selective transformations.
机译:通过两步溶剂热法成功地合成了一维(1D)CdS @ TiO2核壳纳米复合材料(CSN)。一维CdS @ TiO2核壳纳米复合材料(CdS @ TiO2 CSNs)的结构和性能已通过一系列技术进行了表征,包括X射线衍射(XRD),紫外-可见光(UV-vis)漫反射光谱(DRS),场发射扫描电子显微镜(FESEM),光致发光光谱(PL)和电子自旋共振(ESR)光谱。结果表明,一维核-壳结构是通过将TiO2涂覆到CdS纳米线(NWs)的基底上形成的。通过在温和条件下将醇选择性氧化为醛来评估制备的一维CdS @ TiO2 CSN的可见光驱动的光催化活性。与裸露的CdS NW相比,与一维CdS @ TiO2 CSN相比,转化率和产率都有明显提高,这归因于光生电荷载流子在可见光照射下比一维CdS @ TiO2 CSN寿命更长。此外,据披露,通过受控的自由基清除剂实验和在一维CdS @ TiO2 CSNs上有效地选择性还原重金属离子Cr(VI)证明,CdS核的光生空穴可以被TiO2壳堵塞。因此导致在可见光照射下,一维CdS @ TiO2 CSNs上光催化氧化醇的反应机理明显不同于一维CdS NWs上醇的光催化氧化反应。希望我们的工作不仅能够为各种特定的一维核壳纳米结构的制造提供有用的信息,而且还能为这种一维核壳半导体作为可见光光催化剂的新型门打开新的大门,从而成为选择性转化领域的光明前景。

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