Dieringer Jon A, Lettan Robert B, Scheidt Karl A, Van Duyne Richard P
Northwestern University, Department of Chemistry, 2145 Sheridan Road, Evanston, Illinois 60208, USA.
J Am Chem Soc. 2007 Dec 26;129(51):16249-56. doi: 10.1021/ja077243c. Epub 2007 Dec 1.
The existence of single-molecule surface-enhanced Raman spectroscopy (SMSERS) is proven by employing a frequency-domain approach. This is demonstrated using two isotopologues of Rhodamine 6G that offer unique vibrational signatures. When an average of one molecule was adsorbed per silver nanoparticle, only one isotopologue was typically observed under dry N2 environment. Additionally, the distribution of vibrational frequencies hidden under the ensemble average is revealed by examining the single-molecule spectra. Correlation with transmission electron microscopy reveals that SMSERS active aggregates are composed of multiple randomly sized and shaped nanoparticles. At higher coverage and in a humid environment, adsorbate interchange was detected. Using 2D cross correlation, vibrational modes from different isotopologues were anti-correlated, indicating that the dynamic behavior was from multiple molecules competing for a single hot spot. This allows hot-spot diffusion to be directly observed without analyzing the peak intensity fluctuations.
通过采用频域方法证明了单分子表面增强拉曼光谱(SMSERS)的存在。这是通过使用两种具有独特振动特征的罗丹明6G同位素变体来证明的。当每个银纳米颗粒平均吸附一个分子时,在干燥的N2环境下通常只能观察到一种同位素变体。此外,通过检查单分子光谱揭示了隐藏在总体平均值下的振动频率分布。与透射电子显微镜的相关性表明,SMSERS活性聚集体由多个随机大小和形状的纳米颗粒组成。在更高的覆盖率和潮湿环境下,检测到吸附质交换。使用二维交叉相关性,来自不同同位素变体的振动模式呈反相关,表明动态行为来自多个分子竞争单个热点。这使得无需分析峰强度波动就能直接观察热点扩散。