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首页> 外文期刊>ACS Omega >Tetrahedral UMOFNs/Ag3PO4 Core–Shell Photocatalysts for Enhanced Photocatalytic Activity under Visible Light
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Tetrahedral UMOFNs/Ag3PO4 Core–Shell Photocatalysts for Enhanced Photocatalytic Activity under Visible Light

机译:四面体UMOFNs / Ag3PO4核壳型光催化剂可在可见光下增强光催化活性

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A new visible-light-responsive tetrahedral ultrathin metal–organic framework nanosheet (UMOFNs)/Ag3PO4 composite photocatalyst with a core–shell structure was readily synthesized by sonication in an organic solvent. Characterization methods for the photocatalyst included X-ray diffraction (XRD), scanning electron microscopy, transmission electron microscopy, and UV–vis diffuse reflectance spectroscopy. The XRD patterns of the composite photocatalyst before and after visible-light irradiation demonstrated that trace amounts of Ag ions in the composite photocatalyst easily transformed into Ag nanoparticles, which play a role in promoting charge separation at the interface of a heterojunction. The UMOFNs/Ag3PO4 composite photocatalyst showed higher photocatalytic activity for the photodegradation of 2-chlorophenol (2-CP) under visible-light irradiation (>420 nm) than Ag3PO4. The complete degradation of 2-CP was achieved in 7 min using the tetrahedral UMOFNs/Ag3PO4 core–shell photocatalyst, and the apparent reaction rate was approximately 26 times higher than that of pure Ag3PO4. Further, a scavenger experiment showed h+ and O2?– were the major reactive species involved in the photocatalytic reaction system. This enhanced photocatalytic activity results from the efficient separation of photoinduced electron–hole pairs and the increase of interface area between Ag3PO4, UMOFNs, and the Ag nanoparticles.
机译:通过在有机溶剂中超声处理,可以轻松合成具有核-壳结构的新型可见光响应性四面体超薄金属-有机框架纳米片(UMOFNs)/ Ag3PO4复合光催化剂。光催化剂的表征方法包括X射线衍射(XRD),扫描电子显微镜,透射电子显微镜和UV-vis漫反射光谱。可见光辐照前后复合光催化剂的XRD图谱表明,复合光催化剂中的痕量Ag离子容易转化为Ag纳米颗粒,这在促进异质结界面处的电荷分离中起着作用。 UMOFNs / Ag3PO4复合光催化剂在可见光(> 420 nm)下对2-氯苯酚(2-CP)的光降解表现出比Ag3PO4更高的光催化活性。使用四面体UMOFNs / Ag3PO4核-壳光催化剂在7分钟内即可完成2-CP的完全降解,表观反应速率比纯Ag3PO4高约26倍。此外,清除剂实验表明,h +和O2?–是光催化反应系统中涉及的主要反应物种。这种增强的光催化活性归因于光致电子-空穴对的有效分离以及Ag3PO4,UMOFN和Ag纳米颗粒之间界面面积的增加。

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