A 30 cm long solid-core photonic crystal fiber (PCF) with immobilized and discrete Ag nanoparticles was used to obtain forward-propagating surface-enhanced Raman scattering (SERS) of 2 microM Rhodamine 6G (R6G) aqueous solution filled in the cladding air channels. The intensity distributions of characteristic Raman vibrational bands of silica and R6G in PCF were mapped for the first time to our knowledge by hyperspectral Raman imaging. We show that the measured SERS intensity arises exclusively from the forward-propagating core mode as a result of evanescent-field interaction with R6G in the innermost ring of the cladding air channels.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1364/ol.34.000968 | DOI Listing |
Opt Lett
April 2009
Department of Chemical Engineering and Materials Science, Stevens Institute of Technology, Hoboken, NJ 07030, USA.
A 30 cm long solid-core photonic crystal fiber (PCF) with immobilized and discrete Ag nanoparticles was used to obtain forward-propagating surface-enhanced Raman scattering (SERS) of 2 microM Rhodamine 6G (R6G) aqueous solution filled in the cladding air channels. The intensity distributions of characteristic Raman vibrational bands of silica and R6G in PCF were mapped for the first time to our knowledge by hyperspectral Raman imaging. We show that the measured SERS intensity arises exclusively from the forward-propagating core mode as a result of evanescent-field interaction with R6G in the innermost ring of the cladding air channels.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!