拉曼光谱
表面增强拉曼光谱
材料科学
胶体金
纳米颗粒
结晶紫
分子
等离子体子
光谱学
纳米结构
纳米技术
自组装
化学工程
化学
拉曼散射
光电子学
光学
有机化学
医学
物理
工程类
病理
量子力学
作者
Muhammad Usman Amin,Jixiang Fang
标识
DOI:10.1021/acsanm.2c01779
摘要
In solution-based surface-enhanced Raman spectroscopy (SERS) detection, plasmonic metal nanoparticles' controllable assembly and aggregation into highly enhanced electromagnetic coupling nanostructures remains a challenge. In this study, we demonstrate a facile and rapid strategy to control the assembly of poly(styrene sulfonate) functionalized gold nano-bipyramids (PSS-Au BPs) as highly sensitive SERS substrates for solution-based SERS detection. The assembly process of the PSS-Au BPs was controlled by adding halide ions as aggregation agents under various concentrations in the presence of analytic molecules. In comparison, the citrate-capped spherical gold nanoparticles (Cit-Au NPs) were used to investigate the influence of the shape of NPs and their assembly state on SERS performance. Both in situ ultraviolet–visible (UV–vis) and Raman spectroscopy characterizations revealed that the shape of the NPs and aggregation state are critical to achieving a highly enhanced SERS property. The PSS-Au BPs, owing to the formation of tip-to-tip dimers, have a better electromagnetic enhancement capacity than Cit-Au NP aggregation states. Thus, the PSS-Au BPs display an improved lowest recorded concentration downs to the level of 5 × 10–11 M for crystal violet (CV) molecules, which is 2 or 3 orders of magnitude lower than those of the Cit-Au NPs.
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