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Bifunctional Au@Pt core-shell nanostructures for in situ monitoring of catalytic reactions by surface-enhanced Raman scattering spectroscopy

机译:双功能Au @ Pt核壳纳米结构,用于通过表面增强拉曼散射光谱法原位监测催化反应

摘要

Optical probes of heterogeneous catalytic reactions are of great importance for in situ determination of the catalytic activity and monitoring of the reaction process. Surface-enhanced Raman scattering (SERS) spectroscopy could be used as a sensitive optical probe for this purpose provided that plasmonic metal nanoparticles for Raman enhancement are properly integrated with catalytic metals to form a single entity. Herein we present a facile approach for synthesizing Au@Pt core-shell nanostructures with a controllable surface density of sub-5 nm Pt nanoparticles on the surface of Au nanorods. Systematic investigations on both SERS and catalytic activities of the hybrid nanostructures reveal an optimized surface coverage of Pt. More importantly, we demonstrate that, due to their dual functionalities, the hybrid nanostructures are able to track the Pt-catalysed reaction in real time by measuring the SERS signals of the reactant, intermediate and final products. This SERS-based synergy technique provides a novel approach for quantitatively studying catalytic chemical reaction processes and is suitable for many applications such as reduction and oxidation reactions in fuel cells and catalytic water splitting.
机译:非均相催化反应的光学探针对于就地确定催化活性和监测反应过程非常重要。表面增强拉曼散射(SERS)光谱可用作此目的的灵敏光学探针,前提是用于拉曼增强的等离激元金属纳米粒子与催化金属正确结合形成单个实体。在这里,我们提出了一种简便的方法来合成Au @ Pt核壳纳米结构,其在Au纳米棒的表面上具有可控制的亚5 nm Pt纳米颗粒的表面密度。对混合纳米结构的SERS和催化活性的系统研究表明,Pt具有最佳的表面覆盖率。更重要的是,我们证明了由于其双重功能,杂化纳米结构能够通过测量反应物,中间产物和最终产物的SERS信号实时跟踪Pt催化的反应。这种基于SERS的协同技术为定量研究催化化学反应过程提供了一种新颖的方法,适用于许多应用,例如燃料电池中的还原和氧化反应以及催化水分解。

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