Relevant bibliographies by topics / Surface Enhanced Resonance Raman Spectroscopy

Academic literature on the topic 'Surface Enhanced Resonance Raman Spectroscopy'

Author: Grafiati
Published: 10 December 2022
Last updated: 6 September 2023

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Journal articles on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Raser, Lydia N., Stephen V. Kolaczkowski, and Therese M. Cotton. "RESONANCE RAMAN AND SURFACE-ENHANCED RESONANCE RAMAN SPECTROSCOPY OF HYPERICIN." Photochemistry and Photobiology 56, no. 2 (August 1992): 157–62. http://dx.doi.org/10.1111/j.1751-1097.1992.tb02142.x.

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Zhao, Jing, Jon A. Dieringer, Xiaoyu Zhang, George C. Schatz, and Richard P. Van Duyne. "Wavelength-Scanned Surface-Enhanced Resonance Raman Excitation Spectroscopy." Journal of Physical Chemistry C 112, no. 49 (November 14, 2008): 19302–10. http://dx.doi.org/10.1021/jp807837t.

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Virdee, H. R., and R. E. Hester. "Surface-Enhanced Raman Spectroscopy of Thionine-modified Gold Electrodes." Laser Chemistry 9, no. 4-6 (January 1, 1988): 401–16. http://dx.doi.org/10.1155/lc.9.401.

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Surface enhanced Raman (SER) and resonance Raman (SERR) techniques have been used in situ to investigate thionine-modified gold electrodes. New surface roughening procedures for gold electrodes have resulted in an order of magnitude increase in the Raman signals. As a result of this, Raman spectra from leucothionine have been observed for the first time. The surface Raman spectra of both thionine and leucothionine are essentially unchanged over the pH range from 1.3 to 7 but both show major changes at pH 10. This behaviour has been rèlated to changes in the absorption spectrum of thionine at pH 1.0 where the compound is believed to exist as thionine hydroxide. At pH 1.3 and 7 the Raman signals from thionine arise from a combination of surface enhancement and resonance enhancement processes, whereas signals from leucothionine arise solely from surface enhancement. At pH 10 surface enhancement processes give rise to Raman intensity for both thionine and leucothionine.
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Thuy, Pham Thi, Vo Cao Minh, Vo Quang Mai, Nguyen Tri Tuan, Pham Van Tuan, Hoang Ba Cuong, and Nguyen Xuan Sang. "Local Surface Plasmonic Resonance, Surface-Enhanced Raman Scattering, Photoluminescence, and Photocatalytic Activity of Hydrothermal Titanate Nanotubes Coated with Ag Nanoparticles." Journal of Nanomaterials 2021 (December 30, 2021): 1–9. http://dx.doi.org/10.1155/2021/3806691.

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In this work, we successfully fabricated homogeneous hydrothermal titanate nanotubes (TNTs) coated with Ag nanoparticles (NPs) and elucidated the role of Ag NPs on local surface plasmonic resonance, surface-enhanced Raman scattering, and the enhanced photocatalytic activity of TNT/Ag nanocomposite. The results showed that the photodegradation process reached equilibrium in just ~5 min for the TNT/Ag nanocomposite, which was much shorter than that of the TNT sample (~90 min). TEM micrographs showed that Ag NPs were well dispersed on the walls of the nanotubes. XRD patterns and Raman spectra indicated that the TNTs were in the monoclinic structure of H2Ti3O7. Furthermore, Raman active modes of the TNTs were significantly enhanced in the TNT/Ag sample, which was attributed to surface-enhanced Raman spectroscopy. The enhanced photocatalytic activity of the TNT/Ag sample was explained by UV-vis diffuse reflectance spectroscopy and photoluminescence emission spectroscopy, which showed local surface plasmonic resonance-induced visible light absorption enhancement and effective charge separation, respectively.
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McCabe, Ailie, W. Ewen Smith, Grant Thomson, David Batchelder, Richard Lacey, Geoffrey Ashcroft, and Brian F. Foulger. "Remote Detection Using Surface-Enhanced Resonance Raman Scattering." Applied Spectroscopy 56, no. 7 (July 2002): 820–26. http://dx.doi.org/10.1366/000370202760171473.

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Surface-enhanced resonance Raman scattering (SERRS) provides intense Raman signals that are shown here to be stable in a target and to be detectable at least 10 meters from the spectrometer. The results indicate that SERRS labeling of objects and their detection at a distance with a low-power laser is feasible. Rhodamine and a dye specifically designed to give good surface adhesion, [4(5′-azobenzotriazyl)-3,5-dimethoxyphenylamine] (ABT DMOPA), were adsorbed onto silver particles and the particles dispersed in poly(vinyl acetate) (PVA) and varnish. SERRS from rhodamine was not detected from colloid dispersed either in PVA or varnish, presumably due to displacement of the dye from the silver surface. ABT DMOPA gave good SERRS. Maps of the SERRS intensity of films indicated variability of 10–20% if ultrasound was applied to improve dispersion during mixing. Scattering performance was evaluated using a system with the sample held up to one meter from the probe head. The intensity of the scattering from samples kept in the dark showed little change over a period of up to one year. However, when the samples were left in direct sunlight, the scattering intensity dropped significantly over the same period but could still be determined after eight months. An optical system was designed and constructed to detect scattering at longer distances. It consisted of a probe head based on a telephoto or CCTV lens that was fiber-optically coupled to the spectrometer. Effective detection of SERRS was obtained 10 m from the spectrometer using 3.6 mW of power and a 20 s accumulation time.
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Bizzarri, Anna Rita, and Salvatore Cannistraro. "Surface-Enhanced Resonance Raman Spectroscopy Signals from Single Myoglobin Molecules." Applied Spectroscopy 56, no. 12 (December 2002): 1531–37. http://dx.doi.org/10.1366/000370202321115977.

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The extremely large cross-section available from metallic surface enhancement has been exploited to investigate the Raman spectrum of heme myoglobin adsorbed on silver colloidal nanoparticles at very low concentrations. The study has been performed on particles both in solution and immobilized onto a polymer-coated glass surface. In both the cases, we have observed striking temporal fluctuations in the surface-enhanced resonance Raman spectroscopy (SERRS) spectra collected at short times. A statistical analysis of the temporal intensity fluctuations and of the associated correlations of the Raman signals has allowed us to verify that the single molecule limit is approached. The possible connections of these fluctuations with the entanglement of the biomolecule within the local minima of its rough energy landscape is discussed.
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Kowalchyk, Will K., Kevin L. Davis, and Michael D. Morris. "Surface-enhanced resonance Raman spectroscopy of iron-dopamine complexes." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 51, no. 1 (January 1995): 145–51. http://dx.doi.org/10.1016/0584-8539(94)00153-3.

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Francioso, O., S. Sánchez-Cortés, V. Tugnoli, C. Ciavatta, and C. Gessa. "Characterization of Peat Fulvic Acid Fractions by Means of FT-IR, SERS, and 1H, 13C NMR Spectroscopy." Applied Spectroscopy 52, no. 2 (February 1998): 270–77. http://dx.doi.org/10.1366/0003702981943347.

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Fourier transform infrared (FT-IR), surface-enhanced Raman spectroscopy (SERS), and nuclear magnetic resonance (NMR) (1H and 13C) have been applied to the characterization of un fractionated and fractionated fulvic acids extracted from an Irish peat. Raman study of these compounds is possible on rough metallic surfaces, which enhance the Raman signal and quench the high fluorescence. The application of these spectroscopic techniques has provided important structural information concerning the aromaticity and the carboxylate and carbohydrate group contents in each fraction. In addition, a SERS study at different pH levels has revealed interesting interfacial behavior of these components based on electric charge and conformational changes.
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Xue, Gi, Jian Dong, and Mingsheng Zhang. "Surface-Enhanced Raman Scattering (SERS) and Surface-Enhanced Resonance Raman Scattering (SERRS) on HNO3-Roughened Copper Foil." Applied Spectroscopy 45, no. 5 (June 1991): 756–59. http://dx.doi.org/10.1366/0003702914336570.

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Yu, Xuechao, Jin Tao, Youde Shen, Guozhen Liang, Tao Liu, Yongzhe Zhang, and Qi Jie Wang. "A metal–dielectric–graphene sandwich for surface enhanced Raman spectroscopy." Nanoscale 6, no. 17 (2014): 9925–29. http://dx.doi.org/10.1039/c4nr02301c.

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The Raman intensity of Rhodamine B (RhB) is enhanced by inserting a thin high κ dielectric layer which reduces the surface plasmon damping at the gold–graphene interface. The results indicate that the Raman intensity increases sharply by plasmonic resonance enhancement while maintaining efficient fluorescence quenching with optimized dielectric layer thickness.
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Dissertations / Theses on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Cunningham, Dale. "Fundamental studies of surface enhanced resonance Raman spectroscopy." Thesis, University of Strathclyde, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438120.

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Kier, Ruth. "Flow systems for use in surface enhanced resonance raman spectroscopy." Thesis, University of Strathclyde, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249054.

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Shadi, Iqbal Tahear. "Surface enhanced resonance Raman spectroscopy of dyes : semi-quantitative trace analysis." Thesis, University of Greenwich, 2005. http://gala.gre.ac.uk/6296/.

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Herein analysis of dye molecules has been carried out by means of surface enhanced Raman spectroscopy (SERS) and/or surface enhanced resonance Raman spectroscopy (SERRS) using citrate- and/or borohydride-reduced silver colloids employing laser exciting wavelengths equal to 514.5 and/or 632.8 nm. SERS and/or SERRS spectra are reported using, as model system probes, eight dye molecules which belong to several distinct chemical structural classes. Experimental protocols were developed and subsequently modified, as required, for each dye molecule examined. Vibrational spectroscopic profiles were obtained, where possible, with respect to concentration and pH dependence. SERS and/or SERRS vibrational bands provided unique fingerprint spectra for each dye molecule. In an attempt to develop novel applications of SERRS the technique has been used, in a kinetic investigation, to monitor and analyse the synthesis of the dye indigo carmine from indigo using a silver sol as the SERRS substrate/medium. In another study it was possible to differentiate between two structurally similar anthraquinones, alizarin and purpurin, using SERRS. It was also possible to demonstrate the existence of multiple molecular species of certain dye molecules, as a function of pH e.g. nuclear fast red, metanil yellow, purpurin and alizarin. For some dye molecules e.g. alcian blue it was possible to combine the linear regions of normal (non-resonance/non-enhanced) Raman and SERS/SERRS plots, thereby extending the dynamic range available for semi-quantitative analysis. The sensitivity of the SERS/SERRS technique for semi-quantitative trace analysis of eight dye molecules has been successfully demonstrated.
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Mallinder, Benjamin. "Detection of deoxyribonucleic acid by surface enhanced resonance Raman scattering spectroscopy (SERRS)." Thesis, University of Strathclyde, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248771.

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Sheremet, E., A. G. Milekhin, R. D. Rodriguez, T. Weiss, M. Nesterov, E. E. Rodyakina, O. D. Gordan, et al. "Surface- and tip-enhanced resonant Raman scattering from CdSe nanocrystals." Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-161500.

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Surface- and tip-enhanced resonant Raman scattering (resonant SERS and TERS) by optical phonons in a monolayer of CdSe quantum dots (QDs) is demonstrated. The SERS enhancement was achieved by employing plasmonically active substrates consisting of gold arrays with varying nanocluster diameters prepared by electron-beam lithography. The magnitude of the SERS enhancement depends on the localized surface plasmon resonance (LSPR) energy, which is determined by the structural parameters. The LSPR positions as a function of nanocluster diameter were experimentally determined from spectroscopic micro-ellipsometry, and compared to numerical simulations showing good qualitative agreement. The monolayer of CdSe QDs was deposited by the Langmuir–Blodgett-based technique on the SERS substrates. By tuning the excitation energy close to the band gap of the CdSe QDs and to the LSPR energy, resonant SERS by longitudinal optical (LO) phonons of CdSe QDs was realized. A SERS enhancement factor of 2 × 103 was achieved. This allowed the detection of higher order LO modes of CdSe QDs, evidencing the high crystalline quality of QDs. The dependence of LO phonon mode intensity on the size of Au nanoclusters reveals a resonant character, suggesting that the electromagnetic mechanism of the SERS enhancement is dominant. Finally, the resonant TERS spectrum from CdSe QDs was obtained using electrochemically etched gold tips providing an enhancement on the order of 104. This is an important step towards the detection of the phonon spectrum from a single QD
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McLaughlin, Clare. "Development and evaluation of Surface Enhanced Resonance Raman Scattering (SERRS) spectroscopy for quantitative analysis." Thesis, University of Strathclyde, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366867.

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Carella, Yvonne. "Development of SERS for the determination of environmental pollutants." Thesis, University of Strathclyde, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288745.

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Balagopal, Bavishna. "Advanced methods for enhanced sensing in biomedical Raman spectroscopy." Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/6343.

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Raman spectroscopy is a powerful tool in the field of biomedicine for disease diagnosis owing to its potential to provide the molecular fingerprint of biological samples. However due to the inherent weak nature of the Raman process, there is a constant quest for enhancing the sensitivity of this technique for enhanced diagnostic efficiency. This thesis focuses on achieving this goal by integrating advanced methods with Raman spectroscopy. Firstly this thesis explores the applicability of a laser based fluorescence suppression technique – Wavelength Modulated Raman Spectroscopy (WMRS) - for suppressing the broad luminescence background which often obscure the Raman peaks. The WMRS technique was optimized for its applications in single cell studies and tissue studies for enhanced sensing without compromising the throughput. It has been demonstrated that the optimized parameter would help to chemically profile single cell within 6 s. A two fold enhancement in SNR of Raman bands was demonstrated when WMRS was implemented in fiber Raman based systems for tissue analysis. The suitability of WMRS on highly sensitive single molecule detection techniques such as Surface Enhanced Raman Spectroscopy (SERS) and Surface Enhanced Resonance Raman Spectroscopy (SERRS) was also explored. Further this optimized technique was successfully used to address an important biological problem in the field of immunology. This involved label-free identification of major immune cell subsets from human blood. Later part of this thesis explores a multimodal approach where Raman spectroscopy was combined with Optical Coherence Tomography (OCT) for enhanced diagnostic sensitivity (>10%). This approach was used to successfully discriminate between ex-vivo adenocarcinoma tissues and normal colon tissues. Finally this thesis explores the design and implementation of a specialized fiber Raman probe that is compatible with surgical environments. This probe was originally developed to be compatible with Magnetic Resonance Imaging (MRI) environment. It has the potential to be used for performing minimally invasive optical biopsy during interventional MRI procedures.
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Brown, Rachel. "The chemical modification of DNA for analysis by surface enhanced resonance Raman scattering (SERRS) spectroscopy." Thesis, University of Strathclyde, 2002. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=21166.

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The detection of specific DNA sequences is of increasing interest due to the sequencing of the human genome. This can be achieved by the use of covalently labelled oligonucleotide probes detected by sensitive analytical techniques. Surface Enhanced Resonance Raman Scattering (SERRS) spectroscopy is one such technique that provides molecularly specific information about probes at very low concentrations. The enhancement results from adsorption of a chromophore within the probe to a roughened metal surface. Specific SERRS probes were synthesised using benzotriazole as the metal complexing agent and azo dyes as the chromophore. They were coupled to the 5' end of DNA using two strategies. Firstly, coupling was achieved via an amino linker, achieved by reaction of the activated carboxylic acid derivative of the SERRS label with DNA containing a free amine at the 5'end. Secondly, the phosphoramidite of the SERRS label was synthesised and incorporated as the final monomer during the solid phase synthesis of the DNA sequence. Preliminary spectroscopic data was obtained for the labelled oligonucleotides. Ultraviolet melting studies of a DNA sequence labelled with an azobenzotriazole dye show an increase in melting temperature (TM) of 5.42 °C over the same sequence without modification, suggesting that the label confers stability to the double helix. Initial SERRS optimisation experiments allowed the optimum sample conditions to be determined for these novel oligonucleotides. SERRS spectra have been obtained for each labelled oligonucleotide with a detection limit determined at 5x 10⁻⁸ M. A potential application of the labelled oligonucleotides was investigated resulting in the first ever preparation of a SERRS labelled nanoparticle probe. This provides the basis for a specific sequence detection technique based on SERRS.
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Westley, Chloe. "Raman spectroscopy and its enhancement techniques for the direct monitoring of biotransformations." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/raman-spectroscopy-and-its-enhancement-techniques-for-the-direct-monitoring-of-biotransformations(4ff7ebac-048b-4d81-b13c-7087a2028464).html.

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Protein engineering strategies, such as directed evolution, generate large libraries of enzyme variants, typically in the range of 106-108 variants. However, the availability of rapid, robust high-throughput screening methods has often limited the impact of directed evolution in discovering enzymes with enhanced catalyst performance. Raman spectroscopy is an established analytical technique, providing molecular specific information, permitting analysis in aqueous solutions and as such is an attractive, alternative screening method for biological systems. Although an inherently weak physical phenomenon, enhanced Raman scattering techniques, such as surface enhanced Raman scattering (SERS) and ultraviolet resonance Raman (UVRR) spectroscopy, can be used to overcome the associated sensitivity issues. Herein, we successfully monitored xanthine oxidase (XO) catalysed conversions of xanthine to uric acid, before extending to hypoxanthine, using two contrasting Raman scattering enhanced approaches. Firstly, a SERS-based assay was developed utilising silver nanoparticles to measure analytes directly and quantitatively on micromolar scale, in the absence of chromogenic substrates or lengthy chromatography. Secondly, a UVRR approach was developed enabling monitoring of the XO-mediated reaction in real-time and without the need to quench the system. Significantly, both methods demonstrated over >30 fold reduction in acquisition times (when compared to conventional HPLC analysis), and offered excellent medium-term reproducibility and accuracy of results over significant time periods. Furthermore, investigations were made into developing this SERS-based assay into an enantiomeric screen using another vibrational spectroscopy approach, Raman optical activity (ROA), along with circular dichroism (CD). Successful chiral reduced nanoparticles were synthesised, with multiple characterisation techniques employed, affording enantiopure Au-cysteine and Ag-tyrosine colloids. However, it was not possible to generate consistent and reproducible SEROA responses, with these techniques ultimately being unsuccessful in analysing these chiral sensitive nanoprobes, and thus differentiating between the D- and L- forms. Finally, a novel SERS-based approach, in combination with the standard addition method (SAM), was developed for the routine analysis of uric acid (end product in XO catalysed reaction(s) and biomarker for various diseases), at clinically relevant levels in urine samples from patients. Results were highly comparable and in very good agreement with HPLC analyses, with an average < 9% difference in predictions between the two analytical approaches across all samples analysed, and a 60-fold reduction in acquisition time (when compared with HPLC). Together, the research presented in this thesis demonstrates the suitability of Raman enhanced techniques for quantitative analysis, measuring the analytes directly using a portable Raman instrument and, most importantly, offering significant reductions in acquisition times when compared to established analytical techniques.
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Books on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Prochazka, Marek. Surface-Enhanced Raman Spectroscopy. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-23992-7.

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Schlücker, Sebastian, ed. Surface Enhanced Raman Spectroscopy. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.

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Surface enhanced vibrational spectroscopy. Hoboken, NJ: Wiley, 2006.

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Fasolato, Claudia. Surface Enhanced Raman Spectroscopy for Biophysical Applications. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03556-3.

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Schlücker, Sebastian. Surface enhanced Raman spectroscopy: Analytical, biophysical and life science applications. Weinheim: Wiley-VCH, 2011.

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Biswas, Nandita. Development of a Raman Spectrometer to study surface enhanced Raman Scattering. Mumbai: Bhabha Atomic Research Centre, 2011.

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Etchegoin, Pablo G. (Pablo Gabriel), ed. Principles of surface-enhanced Raman spectroscopy: And related plasmonic effects. Amsterdam: Elsevier, 2009.

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Tsukuba Satellite Symposium on Single Molecule and Tip-Enhanced Raman Scattering (2006 Tsukuba Kenkyū Gakuen Toshi, Japan). SM-TERS 2006, Tsukuba Satellite Symposium on Single Molecule and Tip-enhanced Raman Scattering: Extended abstracts : August 17-19, 2006, AIST Tsukuba Center Auditorium, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan. Tsukuba, Japan: AIST, 2006.

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Notholt, Justus. Untersuchungen zum oberflächenverstärkten Ramaneffekt im System Silber-Pyridin. Gauting bei München: A.S. Intemann und Ch.C. Intemann, 1988.

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Baia, Monica. Raman and SERS investigations of pharmaceuticals. Berlin: Springer, 2008.

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Book chapters on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Stevenson, Ross, Karen Faulds, and Duncan Graham. "Quantitative DNA Analysis Using Surface-Enhanced Resonance Raman Scattering." In Surface Enhanced Raman Spectroscopy, 241–62. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.ch11.

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Zhou, Chengli, Emanual Margoliash, and Therese M. Cotton. "Resonance Raman and Surface-Enhanced Resonance Raman Spectroscopy of Cytochrome C Mutants." In Spectroscopy of Biological Molecules, 253–56. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_114.

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Sánchez-Cortés, S., D. Jancura, E. Kočisova, A. Tinti, P. Miškovský, and A. Bertoluzza. "Surface-Enhanced Resonance Raman Spectroscopy of Hypericin and Emodin." In Spectroscopy of Biological Molecules, 573–74. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_265.

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Hildebrandt, Peter. "Surface-Enhanced Resonance Raman Spectroscopy in Electron Transfer Studies." In Encyclopedia of Biophysics, 1–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_132-1.

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Hildebrandt, Peter. "Surface-Enhanced Resonance Raman Spectroscopy in Electron Transfer Studies." In Encyclopedia of Biophysics, 2547–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_132.

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Shadi, I. T., B. Z. Chowdhry, M. J. Snowden, and R. Withnall. "Surface Enhanced Resonance Raman Spectroscopy (SERRS) of Nuclear Fast Red." In Spectroscopy of Biological Molecules: New Directions, 677–78. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_303.

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Macdonald, I. D. G., W. E. Smith, and A. Munro. "Surface Enhanced Resonance Raman Scattering from a Soluble Cytochrome P-450." In Spectroscopy of Biological Molecules, 259–60. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_116.

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Chumanov, George, Dale Gaul, and Therese M. Cotton. "Surface-Enhanced Resonance Raman Spectroscopy of Reaction Centers Adsorbed on Silver Electrodes." In Fifth International Conference on the Spectroscopy of Biological Molecules, 297–98. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_108.

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Podtynchencko, S., I. B. Zavodnik, and S. A. Maskevich. "Surface-Enhanced Resonance Raman Spectra of Erythrocytes Adsorbed on Silver Island Films." In Fifth International Conference on the Spectroscopy of Biological Molecules, 235–36. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_85.

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Goulet, Paul J. G., Nicholas P. W. Pieczonka, and Ricardo F. Aroca. "Protein—Nanoparticle Layer-by-Layer Films as Substrates for Surface-Enhanced Resonance Raman Scattering." In New Approaches in Biomedical Spectroscopy, 152–63. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0963.ch011.

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Conference papers on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Faulds, Karen, Alexandra MacAskill, Douglas MacRae, Jennifer Dougan, Duncan Graham, P. M. Champion, and L. D. Ziegler. "DNA Sequence Detection Using Surface Enhanced Resonance Raman Spectroscopy (SERRS) in a Homogeneous Multiplexed Assay." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482837.

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Campion, Alan. "Surface Raman Spectroscopy Without Enhancement." In Microphysics of Surfaces, Beams, and Adsorbates. Washington, D.C.: Optica Publishing Group, 1985. http://dx.doi.org/10.1364/msba.1985.mc2.

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I will describe recent experiments that demonstrate our ability to observe Raman scattering from molecules adsorbed on single crystal surfaces without requiring either surface or resonance enhancement. I will discuss the details of the experimental method, relevant selection rules, information obtainable from the angular distribution of the scattered radiation and some implications of our experiments regarding the mechanism of surface-enhanced Raman scattering. To illustrate the versatility of our method, examples will include studies of molecules adsorbed on metal and semiconductor surfaces in ultrahigh vacuum, in the presence of reactive gases at high pressures and in the electrochemical environment.
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Hildebrandt, Peter. "Cytochrome c at charged interfaces studied by resonance Raman and surface-enhanced resonance Raman spectroscopy." In Moscow - DL tentative, edited by Sergei A. Akhmanov and Marina Y. Poroshina. SPIE, 1991. http://dx.doi.org/10.1117/12.57305.

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Banaee, Mohamad G., Paul Peng, Eric D. Diebold, Eric Mazur, and Kenneth B. Crozier. "Mixed Dimer Double Resonance Substrates for Surface-Enhanced Raman Spectroscopy." In Conference on Lasers and Electro-Optics. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/cleo.2010.cfa1.

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Cotton, Therese M., George D. Chumanov, Jae-Ho Kim, and Dale Gaul. "Surface-enhanced resonance Raman scattering studies of photosynthetic systems." In Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/laca.1992.mc1.

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Surface-enhanced resonance Raman scattering (SERRS) spectroscopy is a powerful new technique for the study of membrane preparations containing chromophoric molecules. Photosynthetic reaction center and light harvesting complexes have been examined. The spatial location and redox state of the various components (chlorophylls, pheophytins, and cytochromes) can be ascertained from the spectra.
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Yonzon, Chanda R., Xiaoyu Zhang, and Richard P. Van Duyne. "Localized surface plasmon resonance immunoassay and verification using surface-enhanced Raman spectroscopy." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Guozhong Cao, Younan Xia, and Paul V. Braun. SPIE, 2003. http://dx.doi.org/10.1117/12.508611.

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Avila, F., J. Soto, J. F. Arenas, J. C. Otero, P. M. Champion, and L. D. Ziegler. "Surface-Enhanced Resonant Raman Scattering Of p-Benzosemiquinone Radical Anion." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482931.

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Chumanov, George D., Therese M. Cotton, Chengli Zhou, Dale Gaul, Rafael Picorel, and Michael Seibert. "Characterization of photosynthetic reaction centers by surface-enhanced resonance Raman scattering." In Laser Spectroscopy of Biomolecules: 4th International Conference on Laser Applications in Life Sciences, edited by Jouko E. Korppi-Tommola. SPIE, 1993. http://dx.doi.org/10.1117/12.146131.

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del Rocio Balaguera, Marcia, Edwin de La Cruz Montoya, Miguel E. Castro, Luis A. Rivera-Montalvo, and Samuel P. Hernandez-Rivera. "Functionalization of nitroexplosives for surface-enhanced resonance Raman spectroscopy of silver colloids." In Defense and Security, edited by Edward M. Carapezza. SPIE, 2005. http://dx.doi.org/10.1117/12.603510.

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Yuan, W., H. P. Ho, Y. K. Suen, S. K. Kong, Chinlon Lin, Paras N. Prasad, J. Li, and Daniel H. C. Ong. "Surface-enhanced Raman spectroscopy on a surface plasmon resonance biosensor platform for gene diagnostics." In Biomedical Optics (BiOS) 2008, edited by Tuan Vo-Dinh and Joseph R. Lakowicz. SPIE, 2008. http://dx.doi.org/10.1117/12.762286.

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Reports on the topic "Surface Enhanced Resonance Raman Spectroscopy"

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Zheng, Junwei. Surface plasmon enhanced interfacial electron transfer and resonance Raman, surface-enhanced resonance Raman studies of cytochrome C mutants. Office of Scientific and Technical Information (OSTI), November 1999. http://dx.doi.org/10.2172/754842.

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Huser, T. R. Surface-Enhanced Raman Spectroscopy with High Spatial Resolution. Office of Scientific and Technical Information (OSTI), February 2003. http://dx.doi.org/10.2172/15007309.

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Lucht, Robert. Polarization Spectroscopy And Electronic- Resonance-Enhanced Coherent Anti-stokes Raman Scattering For Quantitative Concentration Measurements. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/1854342.

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Velev, Orlin D., Eric W. Kaler, and Abraham M. Lenhoff. Characterization and Optimization of Novel Nanostructured Metallic Substrates for Surface Enhanced Raman Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, December 2001. http://dx.doi.org/10.21236/ada398973.

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Alvarez, Rene, Alexander J. Burdette, Xiaomeng Wu, Christian Kotanen, Yiping Zhao, and Ralph A. Tripp. Rapid Identification of Bacterial Pathogens of Military Interest Using Surface-Enhanced Raman Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, June 2014. http://dx.doi.org/10.21236/ada605244.

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Gao, Ping, and Michael J. Weaver. Surface-Enhanced Raman Spectroscopy as a Probe or Adsorbate-Surface Bonding: Benzene and Monosubstituted Benzenes Adsorbed at Gold Electrodes. Fort Belvoir, VA: Defense Technical Information Center, August 1985. http://dx.doi.org/10.21236/ada159978.

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Sheng, Dai, and B. Gu. A New Method for In-situ Characterization of Important Actinides and Technetium Compounds via Fiberoptic Surface Enhanced Raman Spectroscopy (SERS). Office of Scientific and Technical Information (OSTI), September 2005. http://dx.doi.org/10.2172/893264.

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Dai, Sheng, and B. Gu. A New Method for In-situ Characterization of Important Actinides and Technetium Compounds via Fiberoptic Surface Enhanced Raman Spectroscopy (SERS). Office of Scientific and Technical Information (OSTI), June 2002. http://dx.doi.org/10.2172/834954.

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Dai, Sheng, and B. Gu. A New Method for In-situ Characterization of Important Actinides and Technetium Compounds via Fiberoptic Surface Enhanced Raman Spectroscopy (SERS). Office of Scientific and Technical Information (OSTI), June 2003. http://dx.doi.org/10.2172/834955.

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Dai, Sheng, and B. Gu. A New Method for In-situ Characterization of Important Actinides and Technetium Compounds via Fiberoptic Surface Enhanced Raman Spectroscopy (SERS). Office of Scientific and Technical Information (OSTI), June 2004. http://dx.doi.org/10.2172/839076.

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