Estimating the SERS-based sensing capapbilities of colloidal silver nanoparticles: A novel physical chemistry and nanotechnology laboratory experiment

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Estimating the SERS-based sensing capapbilities of colloidal silver nanoparticles: A novel physical chemistry and nanotechnology laboratory experiment

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dc.contributor Alnajjar, Khadijeh S.
dc.contributor Monahan, Jennifer L.
dc.contributor Stahler, Adam C.
dc.contributor Hunter, Nora E.
dc.contributor Weaver, Kent M.
dc.contributor Meyerhoefer, Allie J.
dc.contributor Dolson, David A.
dc.contributor Pavel, Ioana E.
dc.contributor.author Baker, Joshua
dc.coverage.temporal 2011 en_US
dc.date.accessioned 2011-06-07T14:02:23Z
dc.date.available 2011-06-07T14:02:23Z
dc.date.created 2011-04
dc.date.issued 2011-04
dc.identifier.other celebration_abstract11_baker_j
dc.identifier.uri http://hdl.handle.net/2374.WSU/4581
dc.description.abstract

Surface-enhanced Raman spectroscopy (SERS) is an embodiment of Raman spectroscopy that hat all molecular fingerprint capabilities of Raman and extremely high sensitivity. Theory predicted and experiments confirmed that exceptionally large Raman cross-section increases (i.e., single-molecule detection events) are associated with targeted molecules located in the nano-sized interstitial sites of aggregates of interacting silver nanoparticles (AgNPs). Recently, a novel laboratory experiment was successfully implemented for undergraduate and graduate students in physical chemistry and nanotechnology classes. The main scientific goal of this experiment was to demonstrate the SERS-based sensing capabilities of colloidal AgNPs by estimating the analytical (AEF) and surface (SEF) enhancement factors. AEF and SEF are the most important values for characterizing the SERS effect. Additionally, most SERS-based cutting-edge applications (e.g., cellular imaging, chemical and biological warfare agent detection, protein and DNA recognition, etc.) require an accurate determination of the magnitude of the signal enhancement (i.e., AEF and SEF). To achieve this, students synthesized a Creighton colloid and characterized its optical properties by UVVIS absorption spectrophotometry. Rhodamine 6G (R6G), a fluorescent dye, was added to the colloidal AgNPs as a test probe to determine the AgNP enhancement efficiency. Raman, SERS, and fluorescence measurements were then performed to estimate the AEF (7.4 x 10A4) and SEF (5.2 x 10A1) values. Although these factors do not correspond to singlemolecule detection events (maximum enhancement of 10A5 and 7 x 10A9 for colloids), the R6G concentration (1.0 x 10A-6 M) was three orders of magnitude less than in previous laboratory experiments and facilitated the rapid acquisition of SERS spectra with very good signal-to-noise ratio. This laboratory experiment successfully introduced students to the fundamentals of SERS spectroscopy and to concepts related to light scattering, surface chemistry and resonance effects. Furthermore, students acquired new instrumental and nanotechnology-related skills that will benefit them in technologically-demanding careers.

This presentation occurred at the Wright State University Campus-Wide Celebration of Research, Scholarship and Creative Activities on April 8, 2011

dc.language.iso en_US en_US
dc.publisher Wright State University en_US
dc.relation.ispartof Celebration of Research, Scholarship, and Creative Activities en_US
dc.rights.uri http://www.wright.edu/web/copyright.html
dc.subject Baker, Joshua D. en_US
dc.subject Alnajjar, Khadijeh S. en_US
dc.subject Monahan, Jennifer L. en_US
dc.subject Stahler, Adam C. en_US
dc.subject Hunter, Nora E. en_US
dc.subject Weaver, Kent M. en_US
dc.subject Meyerhoefer, Allie J. en_US
dc.subject Dolson, David A. en_US
dc.subject Pavel, Ioana E. en_US
dc.subject Wright State University. College of Science and Mathematics. Department of Chemistry en_US
dc.title Estimating the SERS-based sensing capapbilities of colloidal silver nanoparticles: A novel physical chemistry and nanotechnology laboratory experiment en_US
dc.type Presentation en_US
dc.permissions World
dc.publisher.digital Digital Services Department, Wright State University Libraries en_US
dc.date.digitized 2011-04
dc.publisher.OLinstitution Wright State University

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