McMahon Jeffrey M, Henry Anne-Isabelle, Wustholz Kristin L, Natan Michael J, Freeman R Griffith, Van Duyne Richard P, Schatz George C
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113, USA.
Anal Bioanal Chem. 2009 Aug;394(7):1819-25. doi: 10.1007/s00216-009-2738-4. Epub 2009 Mar 22.
Finite element method calculations were carried out to determine extinction spectra and the electromagnetic (EM) contributions to surface-enhanced Raman spectroscopy (SERS) for 90-nm Au nanoparticle dimers modeled after experimental nanotags. The calculations revealed that the EM properties depend significantly on the junction region, specifically the distance between the nanoparticles for spacings of less than 1 nm. For extinction spectra, spacings below 1 nm lead to maxima that are strongly red-shifted from the 600-nm plasmon maximum associated with an isolated nanoparticle. This result agrees qualitatively well with experimental transmission electron microscopy images and localized surface plasmon resonance spectra that are also presented. The calculations further revealed that spacings below 0.5 nm, and especially a slight fusing of the nanoparticles to give tiny crevices, leads to EM enhancements of 10(10) or greater. Assuming a uniform coating of SERS molecules around both nanoparticles, we determined that regardless of the separation, the highest EM fields always dominate the SERS signal. In addition, we determined that for small separations less than 3% of the molecules always contribute to greater than 90% of the signal.
进行了有限元法计算,以确定仿照实验纳米标签的90纳米金纳米颗粒二聚体的消光光谱以及对表面增强拉曼光谱(SERS)的电磁(EM)贡献。计算结果表明,电磁特性显著取决于连接区域,特别是对于间距小于1纳米的纳米颗粒之间的距离。对于消光光谱,低于1纳米的间距会导致最大值,该最大值相对于与孤立纳米颗粒相关的600纳米等离子体最大值发生强烈红移。这一结果与所呈现的实验透射电子显微镜图像和局部表面等离子体共振光谱在定性上吻合良好。计算还表明,低于0.5纳米的间距,尤其是纳米颗粒轻微融合形成微小缝隙时,会导致电磁增强10的10次方或更大。假设两个纳米颗粒周围都均匀包覆有SERS分子,我们确定无论间距如何,最高的电磁场总是主导SERS信号。此外我们还确定,对于小间距,总是有不到3%的分子对超过90%的信号有贡献。