Near-field surface enhanced Raman imaging of dye-labeled DNA with 100-nm resolution

被引:142
作者
Deckert, V
Zeisel, D
Zenobi, R
Vo-Dinh, T
机构
[1] ETH Zurich, Organ Chem Lab, CH-8092 Zurich, Switzerland
[2] Oak Ridge Natl Lab, Adv Monitoring Dev Grp, Oak Ridge, TN 37831 USA
关键词
D O I
10.1021/ac971304f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Raman chemical imaging on a scale of 100 mn 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.
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页码:2646 / 2650
页数:5
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