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Relevant bibliographies by topics / SERS

Academic literature on the topic 'SERS'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 July 2024

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Journal articles on the topic "SERS"

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Zaracho Paniagua, Nadia Denisse, Yasmine Maluff Ladan, Liliana Noelia Talavera Stefani, Yanina Dionisia Sapper Lacy, Carolina Elizabeth Prendeski Stolaruk, and Eliane Aya Nishii Encina. "Fe de erratas de “Glaesserella parasuis: serotipos y virulencia de cepas aisladas de cerdos en Itapúa-Paraguay entre febrero del 2022 a marzo del 2023” a marzo del 2023." Investigaciones y estudios - UNA 14, no. 2 (December 28, 2023): 74. http://dx.doi.org/10.57201/ieuna2323937.

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Los autores se disculpan sinceramente por el error involuntario en la composición tipográfica en la página 87, sección Materiales y Métodos. El contenido completo de dicha sección debe ser el siguiente la inclusión se visualiza en negrita: Tipificación molecular y virulencia. Para realizar la tipificación molecular se utilizaron los cebadores descritos por Howell (2015), con modificaciones hechas por Lacouture et al. (2017). Fueron utilizadas tres mezclas de cebadores que se detallan a continuación: PM1: funB (Ser1), glyC (Ser3), wciP (Ser4), funQ (Ser7), funAB (Ser14); PM2: wzx (Ser2), funV (Ser9), gltP (Ser13), funI (Ser15) y PM3: wcwK (Ser5/12), gltI (Ser6), scdA (Ser8), funX (Ser10), amtA (Ser11). Cada reacción de PCR consistió en 12,5 μL de 2x GoTaq® G2 Colorless Master Mix (Promega); 1 mM de cada uno de los cebadores, csp de agua libre de nucleasas y 2 μL de ADN extraído, con un volumen final de 25 µL. Las condiciones de ciclado fueron las mismas descritas por Lacouture et al., (2017). Para identificar la presencia de genes relacionados a virulencia se utilizó la metodología descrita por Galofré-Mila et al., (2017) para la amplificación de genes de virulencia vtaA.

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Baumberg, Jeremy, Steven Bell, Alois Bonifacio, Rohit Chikkaraddy, Malama Chisanga, Stella Corsetti, Ines Delfino, et al. "SERS in biology/biomedical SERS: general discussion." Faraday Discussions 205 (2017): 429–56. http://dx.doi.org/10.1039/c7fd90089a.

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Ossig, Robert, Anna Kolomijeca, Yong-Hyok Kwon, Frank Hubenthal, and Heinz-Detlef Kronfeldt. "SERS signal response and SERS/SERDS spectra of fluoranthene in water on naturally grown Ag nanoparticle ensembles." Journal of Raman Spectroscopy 44, no. 5 (March 18, 2013): 717–22. http://dx.doi.org/10.1002/jrs.4270.

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Cañamares, Maria Vega, Cat Chenal, Ronald L. Birke, and John R. Lombardi. "DFT, SERS, and Single-Molecule SERS of Crystal Violet." Journal of Physical Chemistry C 112, no. 51 (December 3, 2008): 20295–300. http://dx.doi.org/10.1021/jp807807j.

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Kwon, Yong-Hyok, Kay Sowoidnich, Zucheng Wu, and Heinz-Detlef Kronfeldt. "Innovative SERS/SERDS Concept for Chemical Trace Detection in Seawater." International Journal of Offshore and Polar Engineering 27, no. 3 (September 1, 2017): 225–31. http://dx.doi.org/10.17736/ijope.2017.aj08.

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Goel, Richa, Sibashish Chakraborty, Vimarsh Awasthi, Vijayant Bhardwaj, and Satish Kumar Dubey. "Exploring the various aspects of Surface enhanced Raman spectroscopy (SERS) with focus on the recent progress: SERS-active substrate, SERS-instrumentation, SERS-application." Sensors and Actuators A: Physical 376 (October 2024): 115555. http://dx.doi.org/10.1016/j.sna.2024.115555.

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Le Ru, Eric C., and Pablo G. Etchegoin. "Quantifying SERS enhancements." MRS Bulletin 38, no. 8 (August 2013): 631–40. http://dx.doi.org/10.1557/mrs.2013.158.

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Etchegoin, Pablo G., Eric C. Le Ru, and Matthias Meyer. "SERS assertions addressed." Physics Today 61, no. 8 (August 2008): 13–14. http://dx.doi.org/10.1063/1.2970951.

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Kneipp, Katrin. "SERS assertions addressed." Physics Today 61, no. 8 (August 2008): 14–15. http://dx.doi.org/10.1063/1.4796923.

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Szuromi, P. D. "CHEMISTRY: Taming SERS." Science 307, no. 5709 (January 28, 2005): 483b. http://dx.doi.org/10.1126/science.307.5709.483b.

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Dissertations / Theses on the topic "SERS"

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Vaughan, John. "Photographic emulsions as SERS and SERRS surfaces." Thesis, University of Manchester, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528271.

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Gühlke, Marina. "Oberflächenverstärkte Hyper-Raman-Streuung (SEHRS) und oberflächenverstärkte Raman-Streuung (SERS) für analytische Anwendungen." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät, 2016. http://dx.doi.org/10.18452/17570.

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Hyper-Raman-Streuung folgt anderen Symmetrieauswahlregeln als Raman-Streuung und profitiert als nicht-linearer Zweiphotonenprozess noch mehr von verstärkten elektromagnetischen Feldern an der Oberfläche plasmonischer Nanostrukturen. Damit könnte die oberflächenverstärkte Hyper-Raman-Streuung (SEHRS) praktische Bedeutung in der Spektroskopie erlangen. Durch die Kombination von SEHRS und oberflächenverstärkter Raman-Streuung (SERS) können komplementäre Strukturinformationen erhalten werden. Diese eignen sich aufgrund der Lokalisierung der Verstärkung auf die unmittelbare Umgebung der Nanostrukturen besonders für die Charakterisierung der Wechselwirkung zwischen Molekülen und Metalloberflächen. Ziel dieser Arbeit war es, ein tieferes Verständnis des SEHRS-Effekts zu erlangen und dessen Anwendbarkeit für analytische Fragestellungen einzuschätzen. Dazu wurden SEHRS-Experimente mit Anregung bei 1064 nm und SERS-Experimente mit Anregung bei derselben Wellenlänge sowie mit Anregung bei 532 nm - für eine Detektion von SEHRS und SERS im gleichen Spektralbereich - durchgeführt. Als Beispiel für nicht-resonante Anregung wurden die vom pH-Wert abhängigen SEHRS- und SERS-Spektren von para-Mercaptobenzoesäure untersucht. Mit diesen Spektren wurde die Wechselwirkung verschiedener Silbernanostrukturen mit den Molekülen charakterisiert. Anhand von beta-Carotin wurden Einflüsse von Resonanzverstärkung im SEHRS-Experiment durch die gleichzeitige Anregung eines molekularen elektronischen Übergangs untersucht. Dabei wurde durch eine Thiolfunktionalisierung des Carotins eine intensivere Wechselwirkung mit der Silberoberfläche erzielt, sodass nicht nur resonante SEHRS- und SERS-Spektren, sondern auch nicht-resonante SERS-Spektren von Carotin erhalten werden konnten. Die Anwendbarkeit von SEHRS für hyperspektrale Kartierung in Verbindung mit Mikrospektroskopie wurde durch die Untersuchung von Verteilungen verschiedener Farbstoffe auf strukturierten plasmonischen Oberflächen demonstriert.
Hyper-Raman scattering follows different symmetry selection rules than Raman scattering and, as a non-linear two-photon process, profits even more than Raman scattering from enhanced electromagnetic fields at the surface of plasmonic nanostructures. Surface-enhanced hyper-Raman scattering (SEHRS) could thus gain practical importance for spectroscopy. The combination of SEHRS and surface-enhanced Raman scattering (SERS) offers complementary structural information. Specifically, due to the localization of the enhancement to the close proximity of the nanostructures, this information can be utilized for the characterization of the interaction between molecules and metal surfaces. The aim of this work was to increase the understanding of the SEHRS effect and to assess its applicability to answer analytical questions. For that purpose, SEHRS experiments with excitation at 1064 nm and SERS experiments with excitation at the same wavelength, as well as with excitation at 532 nm - to detect SEHRS and SERS in the same spectral region - were conducted. As an example for non-resonant excitation, pH-dependent SEHRS and SERS spectra of para-mercaptobenzoic acid were examined. Based on these spectra, the interaction of different silver nanostructures with the molecules was characterized. beta-Carotene was used to study the influence of resonance enhancement by the excitation of a molecular electronic transition during SEHRS experiments. By the thiol-functionalization of carotene, a more intense interaction with the silver surface was achieved, which enables to obtain not only resonant SEHRS and SERS but also non-resonant SERS spectra of carotene. Hyperspectral SEHRS imaging in combination with microspectroscopy was demonstrated by analyzing the distribution of different dyes on structured plasmonic surfaces.

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Speed, Jonathon. "Tailoring plasmonic substrates for SERS." Thesis, University of Southampton, 2011. https://eprints.soton.ac.uk/191315/.

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SERS is a useful spectroscopic technique that was discovered 30 years ago, and has recently seen a renaissance in research. Sphere segment void (SSV) substrates have been developed as reproducible, stable SERS substrates by electrodeposition of a metal through a colloidal template. The effect of adsorbing an organic monolayer on the surface of an SSV substrate was studied, which results in a slight shift in the plasmonic absorption. This was compared with the reduction of a diazonium salt on the surface, which results in a significant increase in plasmonic absorption, attributed to a physical sharpening of the metal structure, and in turn better defined plasmon modes. The Au surface was also modified with an ultra thin layer of Pt, and a comparison was made between oxidation-reduction cycled roughened (ORC) and SSV substrates with and without Pt. The SSV substrates were found to be more reproducible, and (after modification with a thin-layer of Pt), gave spectra more representative of bulk Pt substrates than ORC. Lastly the surface was functionalised with metallic nanoparticles (NPs), and a large increase in spectral intensity was observed. This was attributed to a strongly localised electric field between the NP and the substrate, which resulted in an additional enhancement of between 102-103 depending on the method of assembly used. Functionalisation of the NPs introduced the possibility of drug detection or studies in drug delivery using such a system.

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Cecchini, Michael Peter. "Novel detection strategies using SERS." Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/11165.

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The use of surface-enhanced Raman spectroscopy (SERS) as an analytical tool has gained increased interest in recent years due to its greater sensitivity and “fingerprinting” ability when compared to other spectroscopic techniques. This thesis discusses approaches used to detect aggregated and single metallic nanoparticles in a high throughput fashion using SERRS. This was accomplished by building a sensitive optical detection platform with high temporal resolution detectors. Initially, nanoparticle aggregates compartmentalized within microdroplets were detected. Each microdroplet can be considered an individual microreactor. Microdroplet flow rate was changed to characterize the effect on microdroplet throughput. Multiple full spectra acquisitions were taken within each microdroplet which was used to compare the different aggregate geometries within each droplet. In addition to segmented flow, single particles in a continuous flow environment are also detected and characterized. A flow based system significantly increases nanoparticle throughput through the probe volume reducing acquisition time. Using correlation spectroscopy, the size of the nanoparticle can be determined and the effect of flow rate on the nanoparticle flow time can be seen. As another detection strategy, single metallic nanoparticles are also detected optically as they translocate through a solid state nanopore. The high electric field generated at the nanopore electrophoretically drives the charged nanoparticles through the nanopore. The nanopore confines the particles to a single channel ensuring single particle detection. Besides the vibrational information that SERS is able to extract, coupling metallic nanoparticles with metallic nanoparticles creates an additional electromagnetic enhancement with increases the SERS signal.

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Ahmad, Hossam [Verfasser], Heinz-Detlef [Akademischer Betreuer] Kronfeldt, Ulrike [Akademischer Betreuer] Woggon, and Frank [Akademischer Betreuer] Hubenthal. "Gold substrates for SERS and SERS/SERDS measurements in seawater and Raman measurements through long optical fibers / Hossam Ahmad. Gutachter: Heinz-Detlef Kronfeldt ; Ulrike Woggon ; Frank Hubenthal." Berlin : Technische Universität Berlin, 2014. http://nbn-resolving.de/urn:nbn:de:kobv:83-opus4-48713.

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Ahmad, Hossam [Verfasser], Heinz-Detlef Akademischer Betreuer] Kronfeldt, Ulrike [Akademischer Betreuer] [Woggon, and Frank [Akademischer Betreuer] Hubenthal. "Gold substrates for SERS and SERS/SERDS measurements in seawater and Raman measurements through long optical fibers / Hossam Ahmad. Gutachter: Heinz-Detlef Kronfeldt ; Ulrike Woggon ; Frank Hubenthal." Berlin : Technische Universität Berlin, 2014. http://d-nb.info/1065669534/34.

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Ahmad, Hossam Verfasser], Heinz-Detlef [Akademischer Betreuer] Kronfeldt, Ulrike [Akademischer Betreuer] [Woggon, and Frank [Akademischer Betreuer] Hubenthal. "Gold substrates for SERS and SERS/SERDS measurements in seawater and Raman measurements through long optical fibers / Hossam Ahmad. Gutachter: Heinz-Detlef Kronfeldt ; Ulrike Woggon ; Frank Hubenthal." Berlin : Technische Universität Berlin, 2014. http://d-nb.info/1065669534/34.

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Han, Sungyub. "Optimization of Aggregating agents and SERS Substrates for SERS detection of Cotinine and trans 3'-hydroxycotinine." Scholar Commons, 2015. https://scholarcommons.usf.edu/etd/5499.

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This dissertation mainly focuses on applications of Surface Enhance Raman Scattering (SERS) to detect tobacco-related biomarkers with optimized experimental conditions (pH and aggregating agents) and SERS substrates (silica core and silver shell nanoparticles). Cotinine (COT) and trans 3-hydroxycotinine (3HC), metabolized from nicotine as one of main chemicals of tobacco, have been used as tobacco biomarkers because their half-life are longer than that of nicotine, which enable to monitor the tobacco exposure. The effects of aggregating agents and pH on SERS detection of COT and 3HC were investigated. Aggregating agents play an important role in SERS detection of target molecules since the strong SERS enhancements are observed from junctions of nanoparticles which can be induced by aggregating agents, and so called "hot spot". That is, the more hot spots are created among the nanoparticles by aggregating agents, the higher the SERS enhancement is. Five cationic (K+, Na+, Mg2+, Li+, Ca2+) and three anionic (Cl-, Br-, I-) aggregating agents were tested. Interestingly but not surprisingly, optimal concentrations of 11 kinds of aggregating agents for COT and 3HC detections vary dramatically within two orders of magnitude. In addition, the effect of pH conditions on SERS intensity of COT and 3HC was investigated since the protonated or deprotonated molecules induced by various ranges of pH values produces change in SERS intensity of the molecule. The highest SERS enhancement is obtained using 1.5 mM MgCl2 for COT at pH 7 and 50 mM NaBr for 3HC at pH 3. Both cations and anions strongly influence the SERS enhancement. SERS enhancement depends also significantly on the type of metallic substrates. This indicates the choice of metallic substrate is critically important to achieve strong SERS enhancement. While Ag is the most commonly used materials for SERS substrates and has been demonstrated to exhibit high enhancement. It has the disadvantage of limited selection of excited wavelengths, which prevents to apply Ag SERS substrates to biological field. Dielectric core and metallic shell structure has been theoretically studied and it has been proposed that silica core and silver shell (SiO2@Ag) nanoparticles produces higher plasmon resonance than that of silver nanoparticles and their surface plasmon are tunable by controlling shell thickness. Here, SiO2@Ag nanoparticles were successfully fabricated and their activity as substrates for surface-enhanced Raman scattering (SERS) were examined. Both the core and the shell thickness exhibit strong effect on the SERS activity. Using Rhodamin 6 G (R6G) as a probe molecule, it was observed that SERS intensities of R6G were susceptible to change in Ag shell thickness and the size of core-shell nanoparticles. The 76 nm SiO2@ 23 nm Ag shell nanoparticles shows highest SERS intensity of R6G. Moreover, 76nm SiO2@ 23 nm Ag nanoparticles have higher SERS enhancements of R6G, 4-aminothiophenol (4-ATP), and cotinine (COT) than that of both silver nanoparticles and SiO2@Ag nanoparticles of previous studies. Also, the tuneability of surface plasmon of core-shell structure is flexible by changing in the size of either core or shell. In addition, three Raman spectroscopy application in material science fields were studied: MP-11 encapsulated inside of Tb-mesoMOFs, poly(methyl methacrylate) composites of copper-4,4'-trimethylenedipyridein, and surfactant-free TiO2 surface hydroxyl groups. For the first study, the interaction between the ligands of Tb-meso MOFs and MP-11 was examined. Individual Raman bands of MP-11 and the ligands of Tb-mesoMOFs were distinguished and some of bands were shifted from the complex of MP-11@Tb-mesoMOFs. It is turned out that the interactions is involved through π•••π interactions between the heme and the conjugated triazine and benzene rings of TATB ligand. Next, Raman was used to study the interaction between poly methyl methacrylate (PMMAP) composites and copper-4,4'-trimethylenedipyridein (CU-TMDP). Copper contained in polymer materials has shown improvement performance (thermal and mechanical stability). The Raman results reveal a red-shift of vibrational peaks associated with pyridine ring of CU-TMDP when CU-TMDP is dispersed into PMMA. This interaction, a dipole-dipole interaction or London dispersion force, may produce the stability improvement of metal-containing polymer. The last application is about the effect of pH levels on the phase of TiO2 crystalline. TiO2 crystal has attractive advantage of self-cleaning property. The efficiency of self-cleaning of TiO2 is dependent on the phases (anatase, rutile, and brookite) of TiO2. Raman study revealed that the formation of the anatase phase of TiO2 is interrupted as the pH level increases.

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Polwart, Ewan. "Development of SERS active fibre sensors." Thesis, University of Strathclyde, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249014.

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Axel, Bolz. "Papierbasierte Mikrofluidik-Systeme mit SERS-Detektion." Doctoral thesis, Humboldt-Universität zu Berlin, 2019. http://dx.doi.org/10.18452/19765.

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Schnelltests sind eine weit verbreitete Analysemethode, um vor Ort schnelle analytische Aussagen treffen zu können. Ein möglicher Zugang zu Schnelltests für Analyten in geringer Konzentration könnten Messung von Oberflächenverstärkten Raman-Spektren sein. In der vorliegenden Arbeit wird insbesondere auf drei Aspekte der SERS-Messungen (= Oberflächenverstärkte Raman-Streuung) eingegangen: die Reproduzierbarkeit der SERS-Signalintensität, die Interpretation der Konzentrationskurven und die Analyse von Probengemischen. Für die Untersuchung der Reproduzierbarkeit wurden verschiedene Auftragungsmethoden und Messsysteme getestet und es wurde untersucht, wie reproduzierbar die Signalintensitäten über einen längeren Zeitraum sind. Dabei wurde festgestellt, dass die Kombination von einer homogenen Auftragung der Nanopartikelsuspensionen auf dem Papier und ein großer Durchmesser des Laser- und Detektionspunktes auf der Probe zu einer stabileren Signalintensität führen. Die bei einem Labormessaufbau eine Stabilität des Messsignals von ca. 20 % relativer Standardabweichung über einen Zeitraum von ca. 2,5 Monaten lieferte. Für die Analyse und Auswertung der Abhängigkeiten der SERS-Signalintensität von der Konzentration des Analyten wurden Konzentrationsreihen von verschiedenen Verbindungen aufgenommen. Die Messdaten konnten mit einer Langmuir-Isotherme beschrieben und mit dem Langmuir-SERS-Modell erklärt werden. Für die gemessenen Thiolverbindungen wurde zudem noch eine weitere Möglichkeit der quantitativen Analyse gefunden, die auf der Auswertung der Verschiebung von bestimmten SERS-Banden im Spektrum in Abhängigkeit von der Analytkonzentration beruht. Für die Analysen der Mehrkomponenten-Lösungen wurden die Papierbasierten Mikrofluidik-Analysesysteme (µPADs) eingesetzt. Hier konnte beobachtet werden, dass Analyten aus einer Lösung auf Grund ihrer hohen Affinität zu den Nanopartikeln abgetrennt werden können und es so möglich ist, diese zu analysieren.
Rapid tests are widely used analytical methods for obtaining analytical information immediately on site. Surface enhanced Raman scattering (SERS) is a possible detection method for compounds in diluted samples. This thesis focuses mainly on three aspects: reproducibility of SERS signal intensity, interpretation of concentration curves and analysis of sample mixtures. The signal reproducibility was investigated using different deposition methods and measurement systems and the reproducibility of measurements was tested over longer periods of time. It was found that the most stable signal intensity was obtained using a combination of homogeneous deposition of a nanoparticle suspension on paper and a detection configuration that involves large diameters of both, the laser and the detection spot on the sample. It was shown with a laboratory setup, that comparatively stable measurements are possible with a relative standard deviation of approx. 20 % over a period of approx. 2.5 months. For the analysis and interpretation of the dependence of the SERS signal intensity on the concentration of the analyte, concentration series of different compounds were measured. The measurement data could be fitted with a Langmuir isotherm and explained with the Langmuir SERS model. For the measured thiol compounds an alternative option for quantification was found: the shift of certain SERS bands in the Raman spectrum as a function of analyte concentration. For the analysis of compound mixture in solution microfluidic paper-based analytical devices (µPADs) were used. It was observed that certain analytes which have a high affinity for the nanoparticles can be separated from the solution and thereby analyzed.

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Books on the topic "SERS"

1

Vidal, Gilles. Je sers à quoi? [Bordeaux]: Castor astral, 1996.

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Metakʻse. Sers tsotsʻis mej mnatsʻ. Erevan: Zangak 97, 2009.

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Metakʻse. Sers tsotsʻis mej mnatsʻ. Erevan: Zangak 97, 2009.

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À quoi tu sers? Paris: L'École des loisirs, 2014.

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Baia, Monica, Simion Astilean, and Traian Iliescu. Raman and SERS Investigations of Pharmaceuticals. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-78283-4.

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Sers dzez nver: Erkeri zhoghovatsu : banasteghtsutʻyunner. Erevan: Heghinakayin hratarakutʻyun, 2004.

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

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Research, United States Dept of Energy Office of Energy. SERS: Science & engineering research semester for undergraduate students. [Washington, DC] (ER-80, Room 3F-061, 1000 Independence Ave., S.W., Washington 20585): U.S. Dept. of Energy, Office of Energy Research, 1992.

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United States. Dept. of Energy. Office of Energy Research. SERS: Science & engineering research semester for undergraduate students. [Washington, DC] (ER-80, Room 3F-061, 1000 Independence Ave., S.W., Washington 20585): U.S. Dept. of Energy, Office of Energy Research, 1992.

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United States. Dept. of Energy. Office of Energy Research. SERS: Science & engineering research semester for undergraduate students. [Washington, DC] (ER-80, Room 3F-061, 1000 Independence Ave., S.W., Washington 20585): U.S. Dept. of Energy, Office of Energy Research, 1992.

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Book chapters on the topic "SERS"

1

Wang, Yuling, and Erkang Wang. "Nanoparticle SERS Substrates." In Surface Enhanced Raman Spectroscopy, 39–69. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.ch2.

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Bell, Steven E. J., and Alan Stewart. "Quantitative SERS Methods." In Surface Enhanced Raman Spectroscopy, 71–86. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.ch3.

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Pînzaru, Simona Cîntă, and Ioana E. Pavel. "SERS and Pharmaceuticals." In Surface Enhanced Raman Spectroscopy, 129–54. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.ch6.

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Henkel, Thomas, Anne März, and Jürgen Popp. "SERS and Microfluidics." In Surface Enhanced Raman Spectroscopy, 173–90. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632756.ch8.

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Maher, Robert C. "SERS Hot Spots." In Raman Spectroscopy for Nanomaterials Characterization, 215–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-20620-7_10.

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Pazos-Perez, Nicolas, and Ramón A. Álvarez-Puebla. "SERS-Encoded Particles." In Raman Spectroscopy for Nanomaterials Characterization, 33–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-20620-7_2.

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Vantasin, Sanpon, and Yukihiro Ozaki. "3D SERS Imaging." In ACS Symposium Series, 95–108. Washington, DC: American Chemical Society, 2016. http://dx.doi.org/10.1021/bk-2016-1245.ch005.

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McMahon, Jeffrey Michael. "Optimal SERS Nanostructures." In Topics in Theoretical and Computational Nanoscience, 67–81. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-8249-0_5.

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Prochazka, Marek. "Bioanalytical SERS Applications." In Surface-Enhanced Raman Spectroscopy, 61–91. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23992-7_4.

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Prochazka, Marek. "Biomolecular SERS Applications." In Surface-Enhanced Raman Spectroscopy, 93–125. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23992-7_5.

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Conference papers on the topic "SERS"

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Olivio, Malini. "SERS Based Biosensors." In Asia Communications and Photonics Conference. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/acp.2012.ath3e.1.

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Olivio, Malini. "SERS Based Biosensors." In Asia Communications and Photonics Conference. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/acpc.2012.ath3e.1.

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3

chen, chang, Yi Li, Sarp Kerman, Pieter Neutens, Liesbet Lagae, Tim Stakenborg, and Pol Van Dorpe. "Nanopore fluidic SERS." In CLEO: Science and Innovations. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/cleo_si.2014.sth4h.2.

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4

Goda, Keisuke. "Unconventional SERS: From Metal/Plasmon-Free to Wearable/Flexible SERS." In 2023 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC). IEEE, 2023. http://dx.doi.org/10.1109/cleo/europe-eqec57999.2023.10231679.

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Gupta, Nitin, Rajib R. Ghosh, and Anuj Dhawan. "Nanoholes arrays as effective SERS substrates with multiple wavelength SERS response and large electromagnetic SERS enhancement factors." In Plasmonics in Biology and Medicine XVI, edited by Tuan Vo-Dinh, Ho-Pui A. Ho, and Krishanu Ray. SPIE, 2019. http://dx.doi.org/10.1117/12.2510828.

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D'Apuzzo, Fausto, Raghuvir Sengupta, Milo Overbay, Jason S. Aronoff, Anita Rogacs, and Steven J. Barcelo. "Inkjet dispense SERS (ID-SERS) for quantitative analysis and bacterial detection." In Plasmonics in Biology and Medicine XVII, edited by Tuan Vo-Dinh, Ho-Pui A. Ho, and Krishanu Ray. SPIE, 2020. http://dx.doi.org/10.1117/12.2545084.

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Mukhopadhyay, G., S. Puri, and P. Mukhopadhyay. "SERS from ellipsoidal nanoparticles." In SPIE NanoScience + Engineering, edited by Mark I. Stockman. SPIE, 2010. http://dx.doi.org/10.1117/12.865584.

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Zhao, Yiping. "Toward practical SERS sensing." In SPIE Defense, Security, and Sensing, edited by Harold Szu and Liyi Dai. SPIE, 2012. http://dx.doi.org/10.1117/12.918761.

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Mullen, Ken, and Keith Carron. "SERS Fiber Optic Probes." In Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/laca.1992.pd8.

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Abstract:

We are using Surface Enhanced Raman Scattering (SERS) to develop a fiber optic probe for monitoring groundwater contamination. Attaching a molecule to a SERS surface produces a million fold enhancement of the Raman signal. Our approach is to fabricate a SERS surface at the fiber tip and attach indicators to the silver SERS surface. The SERS surface is fabricated by roughening the end of the optical fiber with polishing paper and vacuum depositing silver over the roughened fiber tip. We irreversibly bind the indicators by modifying the acid group of the indicator with a thiol containing species. The thiol anchors the indicator to the silver surface and forms an inert, robust coating.

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Feng, Yuhua, and Hongyu Chen. "Polymer encapsulated AuNP SERS probes and ligand exchange kinetics monitored by SERS." In 2010 IEEE 3rd International Nanoelectronics Conference (INEC). IEEE, 2010. http://dx.doi.org/10.1109/inec.2010.5424869.

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Reports on the topic "SERS"

1

Haas, John, and Tom Jenkins. Portable SERS Instrument for Explosives Monitoring. Fort Belvoir, VA: Defense Technical Information Center, January 2008. http://dx.doi.org/10.21236/ada495609.

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Prokes, S. M., O. J. Glembocki, and R. W. Rendell. Highly Efficient SERS Nanowire/Ag Composites. Fort Belvoir, VA: Defense Technical Information Center, January 2007. http://dx.doi.org/10.21236/ada574478.

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Mu, Richard. Development of Focus-Free SERS Substrate Assembly. Fort Belvoir, VA: Defense Technical Information Center, January 2007. http://dx.doi.org/10.21236/ada524871.

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Williams, B. SERS internship spring 1996 abstracts and research papers. Office of Scientific and Technical Information (OSTI), July 1996. http://dx.doi.org/10.2172/496140.

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Goldman, B. SERS internship: Fall 1994 abstracts and research papers. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/50905.

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Davis, Beverly. SERS internship fall 1995 abstracts and research papers. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/527557.

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Shimoji, Yutaka. SERS Raman Sensor Based on Diameter-Modulated Sapphire Fiber. Office of Scientific and Technical Information (OSTI), August 2010. http://dx.doi.org/10.2172/984820.

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Bazan, Guillermo C. Design and Preparation of Nanoparticle Dimers for SERS Detection. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada575625.

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Sardana, Neha, Heena Sammi, and Rajesh V. Nair. Reusable SERS substrate based on interconnected metal network structure. Peeref, June 2023. http://dx.doi.org/10.54985/peeref.2306p3513910.

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Wu, Ming C. Optical Transformers with Integrated Couplers (OTIC) for Ultrahigh SERS Enhancement. Fort Belvoir, VA: Defense Technical Information Center, January 2012. http://dx.doi.org/10.21236/ada573227.

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