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Controlling Pt co-catalyst loading in a WO3 quantum dot and MoS2 nanosheet composite Z-scheme system for enhanced photocatalytic H-2 evolution

机译:控制WO3量子点和MOS2纳米片复合Z方案系统中的Pt助催化剂加载,用于增强的光催化H-2演化

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摘要

A solid-state Z-scheme system, with the synergistic integration of the advantages of various narrow-band semiconductors, is considered to be a potential strategy to develop efficient photocatalysts for operation under visible light illumination. However, the charge separation efficiency of these systems has always been reduced by disordered electron transfer between coupling semiconductors. In this work, we constructed a direct Z-scheme system WO3-MoS2-Pt through the loading of WO3 quantum dots onto MoS2 nanosheets and the selective depositing of a Pt co-catalyst onto MoS2. X-ray diffraction, transmission electron microscopy, atomic electron microscopy and x-ray photoelectron spectroscopy, etc were used to confirm the successful preparation of the targeted photocatalyst. This photocatalytic system showed high visible-light-driven H-2 evolution activity (802.2 mu mol.h(-1).g(-1)) and good photostability. Control experiment and mechanism analysis suggested that the remarkable performance can be attributed to the heterojunction formed WO3 and MoS2 and the vectorial electron transfer (WO3 -> MoS2 -> Pt) achieved by selectively loading the Pt co-catalyst.
机译:具有各种窄带半导体优点的固态Z方案系统,被认为是在可见光照明下开发有效光催化剂的潜在策略。然而,这些系统的电荷分离效率始终通过耦合半导体之间的无序电子转移来降低。在这项工作中,我们通过将WO3量子点加载到MOS2纳米片中的直接Z形式系统WO3-MOS2-PT,并将PT助催化剂的选择性沉积到MOS2上。 X射线衍射,透射电子显微镜,原子电子显微镜和X射线光电子谱等用于确认靶向光催化剂的成功制备。这种光催化系统显示出高可见光驱动的H-2进化活性(802.2μmol.h(-1).g(-1))和良好的光稳定性。控制实验和机理分析表明,通过选择性加载Pt催化剂,显着的性能可以归因于形成WO3和MOS2的异质结和MOS2和vO3和vo3 - > mos2 - > pt)。

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