High-Fidelity Nano-Hole-Enhanced Raman Spectroscopy
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 th...
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Veröffentlicht in: | Journal of physical chemistry. C 2009-07, Vol.113 (26), p.11190-11197 |
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Sprache: | eng |
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Zusammenfassung: | 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, 2D 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 toward making quantitative and reproducible enhanced Raman measurements possible and also open new avenues for a large-scale source of highly uniform hot spots. |
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ISSN: | 1932-7447 1932-7455 |
DOI: | 10.1021/jp900764a |