Thiol-immobilized silver nanoparticle aggregate films for surface enhanced Raman scattering

被引:43
作者
Caro, Carlos [1 ]
Lopez-Cartes, Carlos [2 ]
Zaderenko, Paula [1 ]
Mejias, Jose A. [1 ]
机构
[1] Univ Pablo Olavide, Dept Phys Chem & Nat Syst, Seville 41013, Spain
[2] Univ Seville, CSIC, Inst Ciencias Mat Sevilla, Seville 41092, Spain
关键词
immobilized metal nanoparticle aggregates; surface enhanced Raman spectroscopy; substrates for SERS spectroscopy; silver nanoparticles; SEM; TEM; AFM;
D O I
10.1002/jrs.1957
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
We report a novel method for the fabrication of films of silver nanoparticle aggregates that are strongly attached to Si substrates (Thiol-immobilized silver nanoparticle aggregates or TISNA). The attachment is achieved by chemically modifying the surface of a Si(100) surface in order to provide SH groups covalently linked to the substrate and then aggregating silver nanoparticles on these thiol covered surfaces. The transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM) characterization show a high coverage with single nanoparticles or small clusters and a partial coverage with fractal aggregates that provide potential hot spots for surface enhanced Raman scattering (SERS). We have confirmed the SERS activity of these films by adsorbing rhodamine 6G and recording the Raman spectra at several concentrations. By using the silver-chloride stretching band as an internal standard, the adsorbate bands can be normalized in order to correct for the effects of focusing and aggregate size, which determine the number of SERS active sites in the focal area. This allows a quantitative use of SERS to be done. The adsorption-desorption of rhodamine 6G on TISNA films is reversible. These features make our TISNA films potential candidates for their use in chemical sensors based on the SERS effect. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:1162 / 1169
页数:8
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