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

  • Zhi Yong Bao
  • , Dang Yuan Lei*
  • , Ruibin Jiang
  • , Xin Liu
  • , Jiyan Dai
  • , Jianfang Wang
  • , Helen L. W. Chan
  • , Yuen Hong Tsang*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

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.
Original languageEnglish
Pages (from-to)9063-9070
JournalNanoscale
Volume6
Issue number15
Online published4 Jun 2014
DOIs
Publication statusPublished - 7 Aug 2014
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

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