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Enhanced visible light photocatalytic activity in BiOCl/SnO2: heterojunction of two wide band-gap semiconductors

机译:BioCl / SnO2中增强的可见光光催化活性:两个宽带间隙半导体的异质结

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摘要

A series of BiOCl/SnO2 heterojunctions exhibiting exceptional visible light photocatalytic performance have been successfully prepared using a two-step solution route. The physical and chemical properties of the as-prepared samples were characterized by a range of techniques, including X-ray diffraction (XRD), transmission electron microscopy (TEM) and high-resolution TEM (HRTEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), Brunauer-Emmett-Teller (BET), photoluminescence spectroscopy (PL), Mott-Schottcky measurement and surface photovoltage spectroscopy ( SPS). It's found that SnO2 nanoparticles with average particle size of similar to 4 nm were uniformly dispersed on the {110} facets of BiOCl nanosheets and a heterojunction was formed at the interface between SnO2 and BiOCl. A defect state referenced to oxygen vacancies and (VBiVOVBi ''')-V-'''-V-center dot center dot vacancy associates play a vital role in reducing the band gap energy of SnO2 and BiOCl, respectively. With well-defined defect chemistry and heterostructure, the conjunction of two wide band-gap semiconductors (SnO2 and BiOCl) may lead to visible light harvesting and enhanced photocatalytic performance. The photocatalytic activities of the BiOCl/SnO2 heterojunction photocatalysts were evaluated by measuring the degradation of rhodamine B (RhB) under visible light irradiation. As was expected, the BiOCl/SnO2 composites displayed highly enhanced photocatalytic activity in comparison to the individual counterpart. The PL and SPS spectra confirmed that the formation of a p-n heterojunction between BiOCl and SnO2 can markedly accelerate the separation rate and inhibit the recombination of photo-induced electro-hole pairs, thus promoting the photocatalytic activity. As a consequence of well-modulated electronic structures, defect centers and heterostructure, the photocatalytic performance of BiOCl/SnO2 heterojunctions was well regulated and optimized.
机译:使用两步溶液途径成功地制备了呈现出异类可见光光催化性能的一系列BioCl / SnO2异质功能。用X射线衍射(XRD),透射电子显微镜(TEM)和高分辨率TEM(HRTEM),能量分散光谱(EDS),包括X射线衍射(XRD),透射电子显微镜(EDS),包括X射线衍射(XRD)的物理和化学性质。 X射线光电子体光谱(XPS),UV-Vis弥射反射谱(DRS),Brunauer-Emmett-Teller(Bet),光致发光光谱(PL),Mott-Schottcky测量和表面光电谱(SPS)。发现具有平均粒度的SnO2纳米颗粒在BioCl纳米蛋白片的{110}小件上均匀地分散在SnO2和BioCl之间的界面处形成异质结。引用氧气空位的缺陷状态和(VBivovbi'')-V-'''-V中心点中心点空位助理在减少SnO2和BioCl的带隙能量方面发挥着至关重要的作用。具有定义明确的缺陷化学和异质结构,两个宽带间隙半导体(SnO2和BioCl)的结合可能导致可见光收获和增强的光催化性能。通过测量可见光照射下的罗丹明B(RHB)的降解来评价BioCl / SnO2异质结光催化剂的光催化活性。如预期的那样,与个体对应物相比,BioCl / SnO2复合材料显示出高度增强的光催化活性。 PL和SPS光谱证实,BioCl和SnO 2之间的P-N异质结的形成可以显着加速分离率并抑制光诱导的电孔对的重组,从而促进光催化活性。由于良好调制的电子结构,缺陷中心和异质结构,BioCl / SnO2异质结的光催化性能很好地调节和优化。

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  • 来源
    《RSC Advances》 |2015年第29期|共13页
  • 作者单位

    Inner Mongolia Univ Coll Chem &

    Chem Engn Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Coll Chem &

    Chem Engn Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Coll Chem &

    Chem Engn Hohhot 010021 Inner Mongolia Peoples R China;

    Inner Mongolia Univ Coll Chem &

    Chem Engn Hohhot 010021 Inner Mongolia Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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