Deckert V, Zeisel D, Zenobi R, Vo-Dinh T
Laboratorium für Organische Chemie, ETH Zürich, Universitätsstrasse 16, CH-8092 Zürich, Switzerland.
Anal Chem. 1998 Jul 1;70(13):2646-50. doi: 10.1021/ac971304f.
Raman chemical imaging on a scale of 100 nm is demonstrated for the first time. This is made possible by the combination of scanning near-field optical microscopy (SNOM or NSOM) and surface-enhanced Raman scattering (SERS), using brilliant cresyl blue (BCB)-labeled DNA as a sample. SERS substrates were produced by evaporating silver layers on Teflon nanospheres. The near-field SERS spectra were measured with an exposure time of 60 s and yielded good signal-to-noise ratios (25:1). The distinction between reflected light from the excitation laser and Raman scattered light allows the local sample reflectivity to be separated from the signal of the adsorbed DNA molecules. This is of general importance to correct for topographic coupling that often occurs in near-field optical imaging. The presented data show a lateral dependence of the Raman signals that points to special surface sites with particularly high SERS enhancement.
首次展示了100纳米尺度的拉曼化学成像。这是通过扫描近场光学显微镜(SNOM或NSOM)与表面增强拉曼散射(SERS)相结合实现的,使用亮甲酚蓝(BCB)标记的DNA作为样本。通过在聚四氟乙烯纳米球上蒸发银层制备SERS基底。近场SERS光谱在60秒的曝光时间下测量,获得了良好的信噪比(25:1)。激发激光的反射光与拉曼散射光之间的区别使得能够将局部样品反射率与吸附的DNA分子信号分离。这对于校正近场光学成像中经常出现的地形耦合具有普遍重要性。所呈现的数据显示了拉曼信号的横向依赖性,这指向具有特别高SERS增强的特殊表面位点。