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Nano-design of quantum dot-based photocatalysts for hydrogen generation using advanced surface molecular chemistry

机译:使用先进的表面分子化学技术的量子点基光催化剂用于制氢的纳米设计

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Efficient photocatalytic hydrogen generation in a suspension system requires a sophisticated nano-device that combines a photon absorber with effective redox catalysts. This study demonstrates an innovative molecular linking strategy for fabricating photocatalytic materials that allow effective charge separation of excited carriers, followed by efficient hydrogen evolution. The method for the sequential replacement of ligands with appropriate molecules developed in this study tethers both quantum dots (QDs), as photosensitizers, and metal nanoparticles, as hydrogen evolution catalysts, to TiO2 surfaces in a controlled manner at the nano-level. Combining hydrophobic and hydrophilic interactions on the surface, CdSe-ZnS core-shell QDs and an Au-Pt alloy were attached to TiO2 without overlapping during the synthesis. The resultant nano-photocatalysts achieved substantially high-performance visible-light-driven photocatalysis for hydrogen evolution. All syntheses were conducted at room temperature and in ambient air, providing a promising route for fabricating visible-light-responsive photocatalysts.
机译:悬浮系统中有效的光催化氢生成需要将光子吸收剂与有效氧化还原催化剂结合在一起的精密纳米装置。这项研究证明了一种新颖的分子连接策略,可用于制造光催化材料,该材料可有效分离受激载流子,然后有效释放氢。在这项研究中开发的用合适的分子顺序取代配体的方法将作为光敏剂的量子点(QD)和作为氢释放催化剂的金属纳米颗粒以可控的方式在纳米水平上束缚在TiO2表面上。 CdSe-ZnS核-壳量子点和Au-Pt合金结合了表面上的疏水和亲水相互作用,在合成过程中没有重叠。所得的纳米光催化剂实现了用于氢析出的基本上高性能的可见光驱动的光催化。所有合成均在室温和环境空气中进行,为制备可见光响应型光催化剂提供了有希望的途径。

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