Department of Chemistry, Seoul National University, Seoul, 151-747, South Korea.
Nat Nanotechnol. 2011 May 29;6(7):452-60. doi: 10.1038/nnano.2011.79.
An ideal surface-enhanced Raman scattering (SERS) nanostructure for sensing and imaging applications should induce a high signal enhancement, generate a reproducible and uniform response, and should be easy to synthesize. Many SERS-active nanostructures have been investigated, but they suffer from poor reproducibility of the SERS-active sites, and the wide distribution of their enhancement factor values results in an unquantifiable SERS signal. Here, we show that DNA on gold nanoparticles facilitates the formation of well-defined gold nanobridged nanogap particles (Au-NNP) that generate a highly stable and reproducible SERS signal. The uniform and hollow gap (∼1 nm) between the gold core and gold shell can be precisely loaded with a quantifiable amount of Raman dyes. SERS signals generated by Au-NNPs showed a linear dependence on probe concentration (R(2) > 0.98) and were sensitive down to 10 fM concentrations. Single-particle nano-Raman mapping analysis revealed that >90% of Au-NNPs had enhancement factors greater than 1.0 × 10(8), which is sufficient for single-molecule detection, and the values were narrowly distributed between 1.0 × 10(8) and 5.0 × 10(9).
用于传感和成像应用的理想表面增强拉曼散射 (SERS) 纳米结构应具有高信号增强、产生可重复且均匀的响应,并且易于合成。已经研究了许多 SERS 活性纳米结构,但它们存在 SERS 活性位点再现性差的问题,并且其增强因子值的广泛分布导致 SERS 信号无法量化。在这里,我们表明金纳米粒子上的 DNA 有利于形成定义良好的金纳米桥纳米间隙粒子 (Au-NNP),从而产生高度稳定和可重复的 SERS 信号。金核和金壳之间的均匀和空心间隙(约 1nm)可以精确加载可量化量的拉曼染料。Au-NNP 产生的 SERS 信号与探针浓度呈线性关系(R(2) > 0.98),并且对 10 fM 浓度的检测非常灵敏。单粒子纳米拉曼映射分析表明,超过 90%的 Au-NNP 的增强因子大于 1.0×10(8),足以进行单分子检测,且值在 1.0×10(8)到 5.0×10(9)之间呈窄分布。