ZnS/ZnO异质结构的制备及其光催化性能
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O474 O643

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国家自然科学基金项目(面上项目,重点项目,重大项目)


The fabrication of ZnS/ZnO heterostructures and their photocatalytic activity
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The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan)

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    摘要:

    以醋酸锌,硫脲为原料,采用简单的一步溶剂热法合成了花状ZnS微球,并分别在550、600和650℃下进行高温氧化处理,获得了ZnS/ZnO异质结构半导体材料。利用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、X射线能谱仪(EDS)、表面积分析仪、拉曼光谱仪(Raman)和紫外可见吸收光谱仪(UV-vis)对材料的形貌、结构、比表面积和光学性质进行了测定,并以罗丹明B(RhB)为模型污染物考察了样品的光催化性能。结果表明:原位合成的样品为立方相ZnS微球,经过550℃高温氧化1h后,由于O原子的进入,生成少量ZnO,经过600℃高温氧化1h后形成了II型异质结构ZnS/ZnO,经过650℃高温氧化1h后,样品基本上成为ZnO。随着高温氧化温度的升高,样品的禁带宽度整体呈下降趋势。光催化结果显示,ZnS/ZnO异质结构具备最优的光催化性能,紫外光照射40分钟,RhB降解率达到98.5%。

    Abstract:

    Flower-like ZnS microspheres are synthesized by a simple one-step solvothermal method using zinc acetate and thiourea as raw materials, and then oxidized at high-temperature 550℃,600℃ and 650℃, respectively. The crystal structures, morphologies, compositions, specific surface areas and optical properties of the samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), automatic surface area analyzer, Raman spectrometer (Raman) and UV-Vis absorption spectrum. Moreover, photocatalytic activities are evaluated by degradation of RhB solution. The results show that the samples synthesized in situ are ZnS microspheres with cubic phase. After 1 hour high-temperature oxidation of the samples at 550℃, a small amount of ZnO is observed due to the penetration of oxygen atoms and type-II ZnS/ZnO heterostructures are formed after one hour oxidation at a high temperature of 600℃.When oxidation at the highest temperature of 650 ℃ for 1 hour, the samples nearly become the ZnO component. With the increasing of oxidation temperature, the energy gap decreases in overall. Finally, the photocatalytic activity presented that fabricated ZnS/ZnO heterostructures showed best photcatalytic performance.The degradation rate of RhB reached 98.5% after 40 minutes of UV irradiation.

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崔磊,董晶,杨丽娟. ZnS/ZnO异质结构的制备及其光催化性能[J].精细化工,2018,35(4):

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  • 收稿日期:2017-05-23
  • 最后修改日期:2017-08-08
  • 录用日期:2017-08-30
  • 在线发布日期: 2018-04-09
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