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Dual-sensitized modification engineering with enhanced photocatalytic degradation for organic dye

机译:具有增强的有机染料光催化降解的双敏化改性工程

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摘要

Organic pollutant is an environmentally harmful and ubiquitous aquatic pollutant with extensive production and application. In this study, a unique novel TiO_2-based dual-sensitized heterojunction photocatalyst (PbS/CdS/TiO_2) was successfully obtained by one step hydrothermal method, chemical bath deposition (CBD) method and ionic layer adsorption and reaction (SILAR) method. Scanning electron microscopy, X-ray photoelectron spectroscopy, transmission electron microscopy and energy dispersive spectrometer characterized the composition. PbS/CdS was successfully decorated on the surface of TiO_2 nanosheet array. As a stable catalyst with wide-spectrum (300-800 nm) optical response, excited electron-hole pairs of PbS/CdS/TiO_2 could apply in degrading organic pollutants. Successfully, the degradation efficiency of PbS(5 C)/CdS(30 min)/TiO_2 nanocomposites reached 99.9% under visible light, which was 5 times over pure TiO_2. This ternary heterostructured materials will be well-promising photocatalysts.
机译:有机污染物是一种环保和无处不在的水生污染物,具有广泛的生产和应用。在该研究中,通过一步水热法,化学浴沉积(CBD)方法和离子层吸附和反应(Sill)方法成功地获得了一种独特的新型TiO_2的双敏化异质结光催化剂(PBS / CDS / TiO_2)。扫描电子显微镜,X射线光电子体光谱,透射电子显微镜和能量色散光谱仪表征组合物。 PBS / CD成功装饰在TIO_2 NANOSHEN阵列的表面上。作为具有宽频谱(300-800nm)光学响应的​​稳定催化剂,可以在降解的有机污染物中施加激发的电子空穴对PBS / Cds / TiO_2。成功地,PBS(5C)/ Cds(30分钟)/ TiO_2纳米复合材料的降解效率在可见光下达到99.9%,纯TiO_2的5倍。这种三元异性结构材料将是有充分良好的光催化剂。

著录项

  • 来源
    《Journal of materials science》 |2021年第14期|19380-19389|共10页
  • 作者单位

    State Key Laboratory of Superhard Materials Jilin University Qianjin Street 2699 Changchun 130012 People's Republic of China;

    State Key Laboratory of Superhard Materials Jilin University Qianjin Street 2699 Changchun 130012 People's Republic of China;

    State Key Laboratory of Superhard Materials Jilin University Qianjin Street 2699 Changchun 130012 People's Republic of China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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