Bahns John T, Guo Qiti, Montgomery Jason M, Gray Stephen K, Jaeger Heinrich M, Chen Liaohai
Biosciences Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439.
J Phys Chem C Nanomater Interfaces. 2009 Jul 2;113(26):11190-11197. doi: 10.1021/jp900764a.
Surface Enhanced Raman Spectroscopy (SERS) is a sensitive technique that can even detect single molecules. However, in many SERS applications, the strongly inhomogeneous distribution of intense local fields makes it very difficult for a quantitive assessment of the fidelity, or reproducibility of the signal, which limits the application of SERS. Herein we report the development of exceptionally high fidelity Hole-Enhanced Raman Spectroscopy (HERS) from ordered, two-dimensional hexagonal nanohole arrays. We take the fidelity f to be a measure of the percent deviation of the Raman peaks from measurement to measurement. Overall, area averaged fidelities for 12 gold array samples ranged from f ~ 2% - 15% for HERS using aqueous R6G molecules. Furthermore, intensity modulations of the enhanced Raman spectra were measured for the first time as a function of polarization angle. The best of these measurements, which focus on static laser spots on the sample, could be consistent with even higher fidelities than the area-averaged results. Nanohole arrays in silver provided supporting polarization measurements and a more complete enhanced Raman fingerprint for phenylalanine molecules. We also carried out finite-difference time-domain calculations to assist in the interpretation of the experiments, identifying the polarization dependence as possibly arising from hole-hole interactions. Our results represent a step towards making quantitative and reproducible enhanced Raman measurements possible and also open new avenues for a large scale source of highly uniform hot spots.
表面增强拉曼光谱(SERS)是一种灵敏的技术,甚至能够检测单分子。然而,在许多SERS应用中,强局部场的高度不均匀分布使得对信号保真度或可重复性进行定量评估变得非常困难,这限制了SERS的应用。在此,我们报告了由有序二维六边形纳米孔阵列发展而来的具有极高保真度的空穴增强拉曼光谱(HERS)。我们将保真度f定义为拉曼峰在每次测量之间的偏差百分比。总体而言,对于使用水性罗丹明6G(R6G)分子的HERS,12个金阵列样品的面积平均保真度范围为f约2% - 15%。此外,首次测量了增强拉曼光谱的强度调制作为偏振角的函数。这些聚焦于样品上静态激光光斑的最佳测量结果,其保真度甚至可能比面积平均结果更高。银中的纳米孔阵列提供了支持性的偏振测量,并为苯丙氨酸分子提供了更完整的增强拉曼指纹。我们还进行了时域有限差分计算,以协助解释实验结果,确定偏振依赖性可能源于孔 - 孔相互作用。我们的结果朝着实现定量且可重复的增强拉曼测量迈出了一步,也为大规模产生高度均匀热点开辟了新途径。