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通过银焊接“快速”制备具有亚纳米间隙的强耦合金属纳米颗粒簇:迈向溶液组装纳米材料的有效等离子体调谐

"Flash" preparation of strongly coupled metal nanoparticle clusters with sub-nm gaps by Ag soldering: toward effective plasmonic tuning of solution-assembled nanomaterials.

作者信息

Liu Miao, Fang Lingling, Li Yulin, Gong Ming, Xu An, Deng Zhaoxiang

机构信息

CAS Key Laboratory of Soft Matter Chemistry & Collaborative Innovation Center of Suzhou Nano Science and Technology , Department of Chemistry , University of Science and Technology of China , Hefei , Anhui 230026 , China . Email:

Engineering and Materials Science Experiment Center , University of Science and Technology of China , Hefei , Anhui 230027 , China.

出版信息

Chem Sci. 2016 Aug 1;7(8):5435-5440. doi: 10.1039/c6sc01407k. Epub 2016 May 4.

Abstract

Noble metal nanoparticle oligomers are important in applications including plasmonics, catalysis, and molecular sensing. These nanostructural units featuring abundant inter-particle junctions are helpful for a physical/chemical understanding of structure-activity relationships of self-assembled metamaterials. A simple, rapid, and potentially general strategy for the preparation of monodisperse nanoparticle clusters in a homogeneous solution is highly desired for fundamental research toward liquid metamaterials and chemical/biological applications, but this is however very challenging. Here we report an Ag soldering strategy to prepare strongly coupled plasmonic (Au) and catalytic (Pt, Au@Pd (Au core with a Pd shell)) nanoparticle clusters almost instantly (<1 min) in a solution without special synthetic efforts, complicated surface decorations, or structure-directing templates. The resulting clusters are isolatable by agarose gel electrophoresis, resulting in mechanically stable products in high purity. The optical extinctions of Au nanodimers (the simplest and most basic form of a coupled structure) exhibit prominent longitudinal plasmonic coupling for nanoparticles down to 13.3 nm in diameter. Theoretical simulations attribute the strong coupling to the existence of a sub-nm gap ( 0.76 nm) between soldered particles, suggesting an ideal (stable, soluble, monodisperse, and weakly passivated) substrate for surface enhanced Raman scattering (SERS) applications.

摘要

贵金属纳米粒子低聚物在包括等离激元学、催化和分子传感等应用中很重要。这些具有丰富粒子间连接的纳米结构单元有助于从物理/化学角度理解自组装超材料的结构-活性关系。对于液体超材料的基础研究以及化学/生物应用而言,非常需要一种在均相溶液中制备单分散纳米粒子簇的简单、快速且可能通用的策略,但这极具挑战性。在此,我们报道一种银焊接策略,可在无需特殊合成操作、复杂表面修饰或结构导向模板的情况下,几乎瞬间(<1分钟)在溶液中制备出强耦合的等离激元(金)和催化(铂、金@钯(金核包裹钯壳))纳米粒子簇。所得簇可通过琼脂糖凝胶电泳分离,从而得到高纯度的机械稳定产物。金纳米二聚体(耦合结构最简单且最基本的形式)的光学消光显示,对于直径低至13.3 nm的纳米粒子,存在显著的纵向等离激元耦合。理论模拟将这种强耦合归因于焊接粒子之间存在亚纳米级间隙(0.76 nm),这表明其是用于表面增强拉曼散射(SERS)应用的理想(稳定、可溶、单分散且弱钝化)基底。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b3/6021751/e231c2c2db08/c6sc01407k-f1.jpg

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