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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >A facile in-situ hydrothermal route to construct a well-aligned beta-Ag2MoO4/g-C3N4 heterojunction with enhanced visible light photodegradation: Mechanistic views
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A facile in-situ hydrothermal route to construct a well-aligned beta-Ag2MoO4/g-C3N4 heterojunction with enhanced visible light photodegradation: Mechanistic views

机译:一种容易原位的水热途径,以构建具有增强的可见光光降解的良好对齐的β-Ag2moo4 / g-C3n4异质结:机械视图

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摘要

Constructing a well-aligned heterojunction composite and realizing its photocatalysis mechanism are pivotal in controlling the charge transfer behavior and in turn improving the photocatalytic ability of a photocatalyst. Herein, we report an in situ synthesis of an efficient heterostructured beta-Ag2MoO4/g-C3N4 composite by hydrothermal method. The structural and morphological studies revealed that beta-Ag2MoO4 nanoparticles are uniformly dispersed on the surface of isolated g-C3N4 nanosheets. The photocatalytic abilities and photocatalytic mechanism of beta-Ag2MoO4/g-C3N4 composites were evaluated towards degradation of MO under visible light. The different compositions of beta-Ag2MoO4/g-C3N4 composites were studied for their photocatalytic activities in order to get optimal composition. Photocatalytic efficiency of beta-Ag2MoO4/g-C3N4 composite is much higher than that of the pristine beta-Ag2MoO4 and g-C3N4. Photocatalytic mechanism of heterostructured beta-Ag2MoO4/g-C3N4 composite was discussed in detail with the support of photoluminescence spectra and reactive species trapping experiments. Intimately contacted interfaces with well staggered band alignment of beta-Ag2MoO4/g-C3N4 composite enhance the charge separation and reduction in the probability of electron-hole pair recombination under visible light irradiation and so a significant improvement of the photocatalytic ability. The present work offers to understand the heterojunction mechanism for constructing the efficient composites with remarkable photocatalytic efficiency.
机译:在控制电荷转移行为并且依次改善光催化剂的光催化能力时,构建对准良好的异质结复合材料并实现其光催化机构是枢转的。在此,我们通过水热法向原位合成高效的异质结构β-Ag2Moo4 / G-C3N4复合材料。结构和形态学研究表明,β-ag2moo4纳米颗粒均匀地分散在分离的G-C3N4纳米晶片表面上。评估β-Ag2Moo4 / g-C3N4复合材料的光催化能力和光催化机制朝向可见光下的MO降解。研究了β-Ag2Moo4 / g-C3N4复合材料的不同组成,以获得光催化活性,以获得最佳组合物。 Beta-Ag2Moo4 / g-C3N4复合材料的光催化效率远高于原始β-Ag2moo4和G-C3N4的效率。用光致发光光谱和反应性物种诱捕实验详细讨论了异质结构β-AG2MOO4 / G-C3N4复合物的光催化机理。 β-Ag2Moo4 / G-C3N4复合材料的紧密联系接口具有良好的交错带对准,增强了可见光照射下的电子空穴对重组概率的电荷分离和降低,因此显着提高了光催化能力。本工作提供了了解具有显着光催化效率的高效复合材料的异质结机制。

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