Enhancing SERS by Means of Supramolecular Charge Transfer
- Created: Sunday, 01 March 2009
Sensors based on this method could detect chemical and biological hazards.
In a proposed method of sensing small quantities of molecules of interest, surface enhanced Raman scattering (SERS) spectroscopy would be further enhanced by means of intermolecular or supramolecular charge transfer. There is a very large potential market for sensors based on this method for rapid detection of chemical and biological hazards.
In SERS, the Raman signals (vibrational spectra) of target molecules become enhanced by factors of the order of 108 when those molecules are in the vicinities of nanostructured substrate surfaces that have been engineered to have plasmon resonances that enhance local electric fields. SERS, as reported in several prior NASA Tech Briefs articles and elsewhere, has remained a research tool and has not yet been developed into a practical technique for sensing of target molecules: this is because the short range (5 to 20 nm) of the field enhancement necessitates engineering of receptor molecules to attract target molecules to the nanostructured substrate surfaces and to enable reliable identification of the target molecules in the presence of interferants.
Intermolecular charge-transfer complexes have been used in fluorescence-, photoluminescence-, and electrochemistry-based techniques for sensing target molecules, but, until now, have not been considered for use in SERS-based sensing. The basic idea of the proposed method is to engineer receptor molecules that would be attached to nanostructured SERS substrates and that would interact with the target molecules to form receptor-target supramolecular charge-transfer complexes wherein the charge transfer could be photoexcited.
As shown schematically in the figure, a SERS substrate would be functionalized with a receptor (R) molecule that has an affinity for a target (T) molecule. The receptor molecule could be designed so that the lowest unoccupied molecular orbital (LUMO) of the target molecule would lie above the highest occupied molecular orbital (HOMO) of the target molecule by an energy difference that would correspond to one of the plasmon resonances of the SERS. Conversely, the plasmon of the SERS substrate could be tailored so that its resonance would lie in the charge-transfer energy band of the R-T complex. In addition to the aforesaid factor-of-108 SERS enhancement, there would be an additional enhancement, by a factor of the order of 103 to 106, contributed by the vibronic energy levels associated with the charge transfer.
With this further enhancement, the detection principle is a form of surface enhanced resonance Raman scattering (SERRS) spectroscopy. The resulting Raman spectrum would consist of a mixture of SERS vibrational peaks from R and T as well more intense SERRS peaks associated with R and T modes that participate in the charge transfer. These strong charge-transfer peaks would enable discrimination of important target molecules from interferants that may also be SERS-active. The sensor/molecule system as described thus far would potentially be reversible in the sense that the R-T interactions could be turned off by applying a bias voltage to electrochemically reduce T to T-. Because T- would no longer have an affinity for R, T could be easily washed away.
This work was done by Eric Wong of Caltech, Amar Flood of the Indiana University Bloomington, and Alfredo Morales of Sandia National Laboratories for NASA’s Jet Propulsion Laboratory.
In accordance with Public Law 96-517, the contractor has elected to retain title to this invention. Inquiries concerning rights for its commercial use should be addressed to:
Innovative Technology Assets Management
Mail Stop 202-233
4800 Oak Grove Drive
Pasadena, CA 91109-8099
Refer to NPO-43791, volume and number of this NASA Tech Briefs issue, and the page number.
This Brief includes a Technical Support Package (TSP).
Enhancing SERS by Means of Supramolecular Charge Transfer (reference NPO-43791) is currently available for download from the TSP library.
Please Login at the top of the page to download.