Rational Design of Au@Pt Multibranched Nanostructures as Bifunctional Nanozymes

ACS Appl Mater Interfaces. 2018 Apr 18;10(15):12954-12959. doi: 10.1021/acsami.7b17945. Epub 2018 Apr 4.

Abstract

One of the current challenges in nanozyme-based nanotechnology is the utilization of multifunctionalities in one material. In this regard, Au@Pt nanoparticles (NPs) with excellent enzyme-mimicking activities due to the Pt shell and unique surface plasmon resonance features from the Au core have attracted enormous research interest. However, the unique surface plasmon resonance features from the Au core have not been widely utilized. The practical problem of the optical-damping nature of Pt hinders the research into the combination of Au@Pt NPs' enzyme-mimicking properties with their surface-enhanced Raman scattering (SERS) activities. Herein, we rationally tuned the Pt amount to achieve Au@Pt NPs with simultaneous plasmonic and enzyme-mimicking activities. The results showed that Au@Pt NPs with 2.5% Pt produced the highest Raman signal in 2 min, which benefited from the remarkably accelerated catalytic oxidation of 3,3',5,5'-tetramethylbenzidine with the decorated Pt and strong electric field retained from the Au core for SERS. This study not only demonstrates the great promise of combining bimetallic nanomaterials' multiple functionalities but also provides rational guidelines to design high-performance nanozymes for potential biomedical applications.

Keywords: Au@Pt nanoparticles; bifunctional nanozymes; core−shell structures; finite-difference time-domain (FDTD) simulation; surface-enhanced Raman scattering (SERS).

MeSH terms

  • Gold
  • Metal Nanoparticles
  • Nanostructures*
  • Platinum
  • Silver
  • Spectrum Analysis, Raman
  • Surface Plasmon Resonance

Substances

  • Silver
  • Platinum
  • Gold