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Au@Pt 多枝状纳米结构的理性设计作为双功能纳米酶。

Rational Design of Au@Pt Multibranched Nanostructures as Bifunctional Nanozymes.

出版信息

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.

摘要

基于纳米酶的纳米技术目前面临的挑战之一是如何在一种材料中利用多功能性。在这方面,由于 Pt 壳层具有优异的模拟酶活性和 Au 核独特的表面等离子体共振特性,Au@Pt 纳米颗粒(NPs)引起了极大的研究兴趣。然而,Au 核的独特表面等离子体共振特性尚未得到广泛应用。Pt 的光学阻尼性质这一实际问题阻碍了将 Au@Pt NPs 的模拟酶特性与其表面增强拉曼散射(SERS)活性相结合的研究。在此,我们通过合理地调整 Pt 的量,实现了具有等离子体和模拟酶双重活性的 Au@Pt NPs。结果表明,Pt 含量为 2.5%的 Au@Pt NPs 在 2 分钟内产生了最高的拉曼信号,这得益于 Pt 修饰的 3,3',5,5'-四甲基联苯胺的催化氧化得到了显著加速,以及 Au 核保留的强电场,这有利于 SERS。本研究不仅展示了结合双金属纳米材料的多种功能的巨大潜力,而且为设计用于潜在生物医学应用的高性能纳米酶提供了合理的指导。

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