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Rapid Ultrasensitive Single Particle Surface-Enhanced Raman Spectroscopy Using Metallic Nanopores
Author(s) -
Michael P. Cecchini,
Aeneas Wiener,
Vladimir A. Turek,
Hyangh Chon,
Sangyeop Lee,
Aleksandar P. Ivanov,
David W. McComb,
Jaebum Choo,
Tim Albrecht,
Stefan A. Maier,
Joshua B. Edel
Publication year - 2013
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/nl402108g
Subject(s) - nanopore , analyte , raman spectroscopy , surface enhanced raman spectroscopy , materials science , molecule , plasmon , surface modification , nanotechnology , colloidal gold , nanoparticle , surface plasmon resonance , membrane , analytical chemistry (journal) , chemistry , raman scattering , optoelectronics , organic chemistry , optics , biochemistry , physics
Nanopore sensors embedded within thin dielectric membranes have been gaining significant interest due to their single molecule sensitivity and compatibility of detecting a large range of analytes, from DNA and proteins, to small molecules and particles. Building on this concept we utilize a metallic Au solid-state membrane to translocate and rapidly detect single Au nanoparticles (NPs) functionalized with 589 dye molecules using surface-enhanced resonance Raman spectroscopy (SERRS). We show that, due to the plasmonic coupling between the Au metallic nanopore surface and the NP, signal intensities are enhanced when probing analyte molecules bound to the NP surface. Although not single molecule, this nanopore sensing scheme benefits from the ability of SERRS to provide rich vibrational information on the analyte, improving on current nanopore-based electrical and optical detection techniques. We show that the full vibrational spectrum of the analyte can be detected with ultrahigh spectral sensitivity and a rapid temporal resolution of 880 μs.

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