Relevant bibliographies by topics / (surface raman scattering) SERS

Academic literature on the topic '(surface raman scattering) SERS'

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Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "(surface raman scattering) SERS"

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Zhang, Xian, Qin Zhou, Yu Huang, Zhengcao Li, and Zhengjun Zhang. "The Nanofabrication and Application of Substrates for Surface-Enhanced Raman Scattering." International Journal of Spectroscopy 2012 (December 19, 2012): 1–7. http://dx.doi.org/10.1155/2012/350684.

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Surface-enhanced Raman scattering (SERS) was discovered in 1974 and impacted Raman spectroscopy and surface science. Although SERS has not been developed to be an applicable detection tool so far, nanotechnology has promoted its development in recent decades. The traditional SERS substrates, such as silver electrode, metal island film, and silver colloid, cannot be applied because of their enhancement factor or stability, but newly developed substrates, such as electrochemical deposition surface, Ag porous film, and surface-confined colloids, have better sensitivity and stability. Surface enhanced Raman scattering is applied in other fields such as detection of chemical pollutant, biomolecules, DNA, bacteria, and so forth. In this paper, the development of nanofabrication and application of surface-enhanced Ramans scattering substrate are discussed.
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Gühlke, Marina, Zsuzsanna Heiner, and Janina Kneipp. "Combined near-infrared excited SEHRS and SERS spectra of pH sensors using silver nanostructures." Physical Chemistry Chemical Physics 17, no. 39 (2015): 26093–100. http://dx.doi.org/10.1039/c5cp03844h.

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Combined surface-enhanced Raman scattering (SERS) and surface-enhanced hyper-Raman scattering (SEHRS) of a pH sensor, consisting of silver nanostructures and para-mercaptobenzoic acid and operating with near-IR excitation, is studied.
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Scott, B. L., and K. T. Carron. "Dynamic Surface Enhanced Raman Spectroscopy (SERS): Extracting SERS from Normal Raman Scattering." Analytical Chemistry 84, no. 20 (September 26, 2012): 8448–51. http://dx.doi.org/10.1021/ac301914a.

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Bello, J. M., and T. Vo-Dinh. "Surface-Enhanced Raman Scattering Fiber-Optic Sensor." Applied Spectroscopy 44, no. 1 (January 1990): 63–69. http://dx.doi.org/10.1366/0003702904085877.

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A fiber-optic system was developed for exciting and collecting surface-enhanced Raman scattering (SERS) signals generated from a sensing plate tip having silver-coated microparticles deposited on a glass support. Various fiber parameters, such as fiber type, fiber-substrate geometry, and other experimental parameters, were investigated to obtain the optimum conditions for the SERS fiber-optic device. In addition, analytical figures of merit relevant to the performance of the SERS fiber-optic sensor, such as SERS spectral characteristics, reproducibility, linear dynamic range, and limit of detection, were also investigated.
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Adewumi, Blessing, Martin Feldman, Debsmita Biswas, Dongmei Cao, Li Jiang, and Naga Korivi. "Low-Cost Surface Enhanced Raman Scattering for Bio-Probes." Solids 3, no. 2 (April 7, 2022): 188–202. http://dx.doi.org/10.3390/solids3020013.

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Raman Spectroscopy is a well-known method for identifying molecules by their spectroscopic “fingerprint”. In Surface Enhanced Raman Scattering (SERS), the presence of nanometallic surfaces in contact with the molecules enormously enhances the spectroscopic signal. Raman enhancing surfaces are often fabricated lithographically or chemically, but the throughput is low and the equipment is expensive. In this work a SERS layer was formed by the self-assembly of silver nanospheres from a hexane suspension onto an imprinted thermoplastic sheet (PET). In addition, the SERS layer was transferred and securely bonded to other surfaces. This is an important attribute for probes into solid specimen. Raman spectra were obtained with Rhodamine 6G (R6G) solution concentrations ranging from 1 mm to 1 nm. The methods described here produced robust and sensitive SERS surfaces with inexpensive equipment, readily available materials, and with no chemical or lithographic steps. These may be critical concerns to laboratories faced with diminishing funding resources.
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Zeiri, Leila, and Shlomo Efrima. "Surface-Enhanced Raman Scattering (SERS) of Microorganisms." Israel Journal of Chemistry 46, no. 3 (December 2006): 337–46. http://dx.doi.org/10.1560/ijc_46_3_337.

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Zeiri, Leila, and Shlomo Efrima. "Surface-Enhanced Raman Scattering (SERS) of Microorganisms." Israel Journal of Chemistry 46, no. 3 (July 1, 2006): 337–46. http://dx.doi.org/10.1560/u792-l827-5511-8520.

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Chakaja, Chaiwat, Saksorn Limwichean, Noppadon Nuntawong, Pitak Eiamchai, Sukon Kalasung, On-Uma Nimittrakoolchai, and Nongluck Houngkamhang. "Study on Detection of Carbaryl Pesticides by Using Surface-Enhance Raman Spectroscopy." Key Engineering Materials 853 (July 2020): 97–101. http://dx.doi.org/10.4028/www.scientific.net/kem.853.97.

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In this research, the Ag nanorod structure was used as surface enhanced Raman scattering (SERS) chip which provides a sensitive detection signal for trace analysis of carbaryl pesticide. Carbaryl in solid form was measured by using the standard Raman spectroscopy to investigate the spectrum. Carbaryl at various concentrations was prepared in acetonitrile and dropped on the SERS chip for measuring Raman spectrum by a portable Raman spectrometer. The measurement condition including laser power and exposure time were studied to test the performance of SERS chip for carbaryl detection. From the results, the SERS chip useful for enhancing the Raman scattering signal which was increased depending on the laser power and exposure time. Carbaryl can be detected on SERS chip couple with the portable Raman spectrometer with the limit of detection of 10-5 M.
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Pilot, Signorini, Durante, Orian, Bhamidipati, and Fabris. "A Review on Surface-Enhanced Raman Scattering." Biosensors 9, no. 2 (April 17, 2019): 57. http://dx.doi.org/10.3390/bios9020057.

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Surface-enhanced Raman scattering (SERS) has become a powerful tool in chemical, material and life sciences, owing to its intrinsic features (i.e., fingerprint recognition capabilities and high sensitivity) and to the technological advancements that have lowered the cost of the instruments and improved their sensitivity and user-friendliness. We provide an overview of the most significant aspects of SERS. First, the phenomena at the basis of the SERS amplification are described. Then, the measurement of the enhancement and the key factors that determine it (the materials, the hot spots, and the analyte-surface distance) are discussed. A section is dedicated to the analysis of the relevant factors for the choice of the excitation wavelength in a SERS experiment. Several types of substrates and fabrication methods are illustrated, along with some examples of the coupling of SERS with separation and capturing techniques. Finally, a representative selection of applications in the biomedical field, with direct and indirect protocols, is provided. We intentionally avoided using a highly technical language and, whenever possible, intuitive explanations of the involved phenomena are provided, in order to make this review suitable to scientists with different degrees of specialization in this field.
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Huang, Jinglin, Yansong Liu, Xiaoshan He, Cuilan Tang, Kai Du, and Zhibing He. "Gradient nanoporous gold: a novel surface-enhanced Raman scattering substrate." RSC Advances 7, no. 26 (2017): 15747–53. http://dx.doi.org/10.1039/c6ra28591k.

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The design and fabrication of surface-enhanced Raman scattering (SERS) substrates with high Raman enhancement, stability, homogeneity and processing compatibility is still one of the most challenging issues in SERS research.
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Dissertations / Theses on the topic "(surface raman scattering) SERS"

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Harper, Mhairi. "DNA diagnostic assays using Surface Enhanced Raman Scattering (SERS)." Thesis, University of Strathclyde, 2013. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=22401.

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DNA is the prerequisite for all biological life and its discovery has revolutionised the understanding of biomolecular interactions and disease expression. This has enabled significant improvements in patient diagnosis and medical treatment to be carried out. The advancements in technology and instrumentation have continually progressed this knowledge and continue to push the boundaries of diagnostic and clinical advancements. One effective way to achieve this is through application of dye labelled DNA sequences and metallic nanoparticle suspensions. This research details an understanding of the interaction between dye labelled oligonucleotides and silver nanoparticle surfaces, which generate strong surface enhanced Raman scattering (SERS) responses through specific hybridisation events which correlate to the presence of targeted sequences. During this study, the attraction of oligonucleotides onto metal nanoparticles was shown to be driven through the DNA nucleobases. Therefore, the increased exposure of the base groups within single stranded DNA sequences generated a higher affinity for metal surfaces which in turn produced stronger SERS responses when compared to double stranded DNA. This principle was utilised within a DNA detection assay to successfully demonstrate the presence of target DNA sequences. Two novel DNA detection assays were also investigated which utilised SERS to determine the presence of sequences relating to the methicillin resistant Staphylococcus aureus (MRSA) strain. A solution based detection method was developed through coupling a TaqMan assay with SERS. This combination enabled highly specific detection of clinically relevant sequences of MRSA to be obtained with 7 fM limits of detection achievable. The multiple detection of different genomic S. aureus strains was achieved through the molecularly specific and narrow emission spectral profiles obtained. A contrasting DNA detection strategy which relies upon the hybridisation of comple mentary sequences on a solid substrate surface was shown. Silver nanoparticles were functionalised with specific DNA sequences and a variety of SERS active molecules, enabling the selective detection of target sequences from nitrocellulose membranes. This thesis has exploited SERS to enable the specific identification of DNA sequences to be achieved via utilisation of silver nanoparticles. Through SERS, an insight into the interactions of DNA and silver nanoparticles surfaces has been gained as well as enhancing the sensitivity and specificity achievable within SERS detection assays.
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Tsoutsi, Dionysia. "Inorganic Ions Sensing by surface-enhanced Raman scattering spectroscopy." Doctoral thesis, Universitat Rovira i Virgili, 2015. http://hdl.handle.net/10803/288213.

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En aquest projecte de tesi s'ha aconseguit desenvolupar un sistema de detecció, identificació i quantificació independent d'ions inorgànics. La detecció dels ions es basa en la diferent afinitat cap a diferents lligands orgànics mitjançant l'espectroscòpia de dispersió Raman augmentada per superfícies (surface-enhanced Raman scattering, SERS). En resum, com a substrat s'utilitzaran nanopartícules de plata o microesferes nanoestructurades que es prepararan mitjançant l'adsorció de nanopartícules d'or sobre la superfície de microesferes de sílice a partir del protocol de capa per capa i el seu posterior creixement epitaxial amb plata. Aquest últim pas es realitzarà a través de protocols desenvolupats en el nostre laboratori i té com a objectiu l'obtenció de superfícies plasmòniques discretes altament eficients en SERS. Els substrats es funcionalizaran posteriorment amb lligands orgànics tiolats amb alta afinitat per ions inorgànics (el fluoròfor orgànic, amino-MQAE i la terpiridina, pztpy-DTC). Com a pas següent, es realitzarà la detecció i quantificació simultània dels ions combinant, per a la seva detecció, espectroscòpia SERS. Els canvis espectrals SERS, en la manera de vibració dels lligands organics, estan correlacionats com a funció de la concentració de cada ió amb límits de detecció comparables als de diversos mètodes analítics convencionals.
En este proyecto de tesis se ha conseguido desarrollar un sistema de detección, identificación y cuantificación independiente de iones inorgánicos. La detección de los iones se basa en su diferente afinidad hacia diferentes ligandos orgánicos a través de la espectroscopia de dispersión Raman aumentada por superficies (surface-enhanced Raman scattering, SERS). En resumen, como sustrato se utilizarán nanopartículas de plata o microesferas nanoestructuradas que se prepararán mediante la adsorción de nanopartículas de oro sobre la superficie de microesferas de sílice mediante el protocolo de capa por capa y su posterior crecimiento epitaxial con plata. Este último paso se realizará mediante protocolos desarrollados en nuestro laboratorio y tiene como objetivo la obtención de superficies plasmónicas discretas altamente eficientes en SERS. Los sustratos se funcionalizarán posteriormente con ligandos orgánicos tiolados con alta afinidad por iones inorgánicos (el fluoróforo orgánico, amino-MQAE y la terpiridina, pztpy-DTC). Como paso siguiente, se realizará la detección y cuantificación simultánea de los iones combinando para su detección espectroscopia SERS. Los cambios espectrales SERS en el modo de vibración de los ligandos orgánicos están correlacionados como función de la concentración de cada ion con límites de detección comparables a los de varios métodos analíticos convencionales.
In this research project we successfully developed a novel sensing system for the identification and quantification of inorganic ions independently by means of surface-enhanced Raman scattering (SERS) spectroscopy. The detection of the ions is based on their different affinity toward various organic ligands. In summary, we use as SERS-active substrates, either silver nanoparticles or composite nanostructured particles prepared by adsorption of gold nanoparticles on the surface of silica microbeads, using layer-by-layer assembly protocol and the subsequent epitaxial overgrowth of silver. This last step is performed using protocols developed in our laboratory and aims to the fabrication of highly plasmonic surfaces for SERS experiments. Next, the substrates are functionalized with thiolated organic ligands with high affinity toward inorganic ions (amino-MQAE, an organic fluorophore, and pztpy-DTC, a terpyridine). As a further step, the simultaneous identification and quantification of the ions, using SERS spectroscopy, is performed. Vibrational changes in the SERS spectra of the organic ligands are correlated as a function of the concentration of each ion with limits of detection comparable to those of several conventional analytical methods.
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Yan, Bo. "Rationally designed substrates for SERS biosensing." Thesis, Boston University, 2013. https://hdl.handle.net/2144/12894.

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Thesis (Ph.D.)--Boston University
The large electromagnetic field enhancement provided by nanostructured noble metal surfaces forms the foundation for a series of enabling optical analytical techniques, such as surface enhanced Raman spectroscopy (SERS), surface enhanced IR absorption spectroscopy (SEIRA), surface enhanced fluorescent microscopy (SEF), to name only a few. Critical sensing applications have, however, other substrate requirements than mere peak signal enhancement. The substrate needs to be reliable, provide reproducible signal enhancements, and be amenable to a combination with microfluidic chips or other integrated sensor platforms. These needs motivate the development of engineerable SERS substrate "chips" with defined near- and far-field responses. In this dissertation, two types of rationally designed SERS substrates - nanoparticle cluster arrays (NCAs) and SERS stamp - will be introduced and characterized. NCAs were fabricated through a newly developed template guided self-assembly fabrication approach, in which chemically synthesized nanoparticles are integrated into predefined patterns using a hybrid top-down/bottom-up approach. Since this method relies on chemically defined building blocks, it can overcome the resolution limit of conventional lithographical methods and facilitates higher structural complexity. NCAs sustain near-field interactions within individual clusters as well as between entire neighboring clusters and create a multi-scale cascaded E-field enhancement throughout the entire array. SERS stamps were generated using an oblique angle metal deposition on a lithographically defined piston. When mounted on a nanopositioning stage, the SERS stamps were enabled to contact biological surfaces with pristine nanostructured metal surfaces for a label-free spectroscopic characterization. The developed engineered substrates were applied and tested in critical sensing applications, including the ultratrace detection of explosive vapors, the rapid discrimination of bacterial pathogens, and the label-free monitoring of the enzymatic degradation of pericellular matrices of cancer cells.
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Shi, Chao. "Molecular fiber sensor probes based on surface enhanced Raman scattering (SERS) /." Diss., Digital Dissertations Database. Restricted to UC campuses, 2009. http://uclibs.org/PID/11984.

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Karabicak, Seher. "Application Of Surface-enhanced Raman Scattering (sers) Method For Genetic Analyses." Phd thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613130/index.pdf.

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Raman spectroscopy offers much better spectral selectivity but its usage has been limited by its poor sensitivity. The discovery of surface-enhanced Raman scattering (SERS) effect, which results in increased sensitivities of up to 108-fold for some compounds, has eliminated this drawback. A new SERS active substrate was developed in this study. Silver nanoparticle-doped polyvinyl alcohol (PVA) coated SERS substrate prepared through chemical and electrochemical reduction of silver particles dispersed in the polymer matrix. Performances of the substrates were evaluated with some biologically important compounds. The specific detection of DNA has gained significance in recent years since increasingly DNA sequences of different organisms are being assigned. Such sequence knowledge can be employed for identification of the genes of microorganisms or diseases. In this study, specific proteasome gene sequences were detected both label free spectrophotometric detection and SERS detection. In label free spectrophotometic detection, proteasome gene probe and complementary target gene sequence were attached to the gold nanoparticles separately. Then, the target and probe oligonucleotide-modified gold solutions were mixed for hybridization and the shift in the surface plasmon absorption band of gold nanoparticles were followed. SERS detection of specific nucleic acid sequences are mainly based on hybridization of DNA targets to complementary probe sequences, which are labelled with SERS active dyes. In this study, to show correlation between circulating proteasome levels and disease state we suggest a Raman spectroscopic technique that uses SERGen probes. This novel approach deals with specific detection of elevated or decreased levels of proteasome genes&rsquo
transcription in patients as an alternative to available enzyme activity measurement methods. First, SERGen probes were prepared using SERS active labels and specific proteasome gene sequences. Then DNA targets to complementary SERGen probe sequences were hybridized and SERS active label peak was followed.
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Faulds, Karen Jade. "Detection of drugs of abuse by surface enhanced Raman scattering (SERS)." Thesis, University of Strathclyde, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288636.

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Boddu, Naresh Kumar. "Trace analysis of biological compounds by surface enhanced Raman scattering (SERS) spectroscopy /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229542206.

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Stewart, Shona Diane. "Surface enhanced Raman scattering on electrochemically prepared silver surfaces." Thesis, Queensland University of Technology, 1999.

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Andrade, Gustavo Fernandes Souza. "Caracterização espectroscópica da tiossemicarbazona do formilferroceno (TFF) através das técnicas SERS (Surface-Enhanced Raman Scattering) e Raman ressonante." Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/46/46132/tde-13092006-164920/.

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Nesta dissertação o processo de adsorção da tiossemicarbazona do formilferroceno (TFF) em eletrodos de prata e ouro, em soluções aquosas 0,1 mol.L-1 de KCl e de acetonitrila. 0,1 mol.L-1 de NaClO4, foi caracterizado através da técnica espectroscópica SERS. Verificou-se através das variações espectrais que a adsorção da TFF ocorre através dos átomos N1 do grupo imínico e do S do grupo tiocarbonílico. Os processos faradáicos do TFF foram monitorados pela técnica SERS e de absorção no UV-visível. Os espectros SERS para potencial de -1,4 V (Ag/AgCl) sugerem a formação de um novo composto, produto de redução da TFF, o aminometilferroceno. Através da técnica de absorção no UV-visível verificou-se, neste potencial, o aparecimento no espectro de absorção de uma nova banda em 240 nm, atribuída à formação de tiouréia. A identificação deste dois produtos de redução indica que, para o composto TFF, o mecanismo geral de redução dos derivados de tiossemicarbazonas é obedecido. Nenhuma variação espectral, tanto utilizando a técnica SERS como a absorção no UV-visível, foi detectada durante o processo redox FeII/FeIII (E1/2=0,55 V). Os comportamentos de adsorção e faradáico da tiossemicarbazida (TSC), em eletrodo de prata em soluções aquosas neutra e ácida, foram estudados através da técnica SERS. Verificou-se que em meios neutro e ácido, a TSC está adsorvida na configuração cis para potenciais próximos de 0,0 V, interagindo com a superfície através do átomo de S do grupo tiocarbonílico e dos átomos de H ligados ao N1 hidrazínico, através da formação de pares iônicos com os ânions Cl- adsorvidos. Para potenciais mais negativos, os íons cloreto deixam a superfície e a TSC sofre reorientação, assumindo a conformação trans. Não foi observado através da técnica SERS nenhum processo faradáico em solução ácida para potenciais negativos, como havia sido proposto na literatura. A não redução do composto foi confirmada através da técnica de eletroforese capilar. Foi estudado o comportamento Raman ressonante da TFF, verificando-se a ocorrência de um mínimo no perfil de excitação experimental devido à interferência destrutiva das transições dos grupos tiossemicarbazona e ferrocenil. Os perfis de excitação teóricos foram calculados utilizando o método da transformada e os resultados dos ajustes obtidos indicam que existe considerável distorção dos modos do grupo ferrocenil na transição eletrônica em 312 nm, atribuída a n-p* do grupo tiossemicarbazona, caracterizando uma grande interação eletrônica entre os cromóforos da TFF. Para comparar o comportamento Raman ressonante do TFF com o do ferroceno, os espectros Raman ressonante deste composto foram obtidos. Verificou-se que o ferroceno apresenta, também, o efeito Raman anti-ressonante, mas as bandas vibracionais do ferroceno apresentam perfis distintos dos apresentados no composto TFF, indicando que a incorporação do grupo tiossemicarbazona no anel ciclopentadienil modifica a estrutura eletrônica do grupo ferrocenil.
In this dissertation, the adsorption process of the formylpyridine thiosemicarbazone (TFF) at silver and gold surfaces in aqueous and in acetonitrile solutions has been characterized by using the SERS (Surface-enhanced Raman Scattering) technique. It has been verified that TFF adsorbs through N1’ and S atoms on the metallic surfaces. The faradaic processes of TFF have been monitored through the SERS and UV-visible absorption spectroscopies. The SERS spectra at -1,4 V (Ag/AgCl) suggest aminomethylferrocene as one of the reduction products of TFF. By using the UV-visible absorption technique, it has been verified, at this potential, a new band at 240 nm in the spectrum, which indicates the presence of thiourea. The observation of these two reduction products has confirmed that the general reduction mechanism for thiosemicarbazonas works for TFF. Neither SERS nor UV-vis spectral changes have been observed during the redox process of FeII/FeIII (E1/2= 0,55 V). The adsorption and faradaic processes of thisemicarbazide (TSC) at silver electrode have also been studied by SERS technique. It has been verified that, in acidic and neutral media, the TSC is adsorbed through a cis-configuration at a potential close to 0,0 V, showing an interaction of the S atom through bond formation with the surface and through the H atoms bonded to N1 via ion pair formation with the adsorbed Cl- anions. At more negative potentials, the chloride anions leave the electrode surface and the TSC changes to trans-configuration. No faradaic process has been observed as reported in the literature. This result has been confirmed by using the capillary electrophoresis technique. The resonance Raman effect of the TFF has been studied, and the excitation profiles of the bands have been shown as minimum, which indicates an electronic interaction between the two cromophores of the TFF (thiosemicarbazone and ferrocenyl). The theoretic excitation profiles have been calculated by using the transform method, and the results of the obtained adjustment has indicated that there has been a distortion of the ferrocenyl vibrational modes for an electronic transition at 312 nm, assigned to the n-p* of thiosemicarbazone moiety. This result has indicated a great interaction between the two cromophores of TFF. In order to compare the resonance Raman behavior of the TFF with that of the ferrocene, the resonance Raman spectra of the ferrocene have been obtained. It has been verified that the two compounds present an anti-resonant Raman effect, even though the bands have presented very different excitation profiles from those observed in the TFF, which indicates that the incorporation of the thiosemicarbazone group into the ciclopentadienyl has changed the electronic structure of the ferrocenyl group.
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Boddu, Naresh K. "Trace Analysis of Biological Compounds by Surface Enhanced Raman Scattering (SERS) Spectroscopy." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229542206.

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Books on the topic "(surface raman scattering) SERS"

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

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Ozaki, Yukihiro, Katrin Kneipp, and Ricardo Aroca, eds. Frontiers of Surface-Enhanced Raman Scattering. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.

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Milton, Kerker, ed. Selected papers on surface-enhanced raman scattering. Bellingham, Wash., USA: SPIE Optical Engineering Press, 1990.

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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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Atkinson, B. M. Characterization of substrates for surface-enhanced Raman scattering. Manchester: UMIST, 1992.

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Polubotko, A. M. The dipole-quadrupole theory of surface enhanced Raman scattering. Hauppauge, N.Y: Nova Science Publishers, 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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Chemistry, Royal Society of. Surface Enhanced Raman Scattering - SERS: Faraday Discussion 205. Royal Society of Chemistry, The, 2018.

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Hayazawa, Norihiko, and Prabhat Verma. Nanoanalysis of materials using near-field Raman spectroscopy. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.10.

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This article describes the use of tip-enhanced near-field Raman spectroscopy for the characterization of materials at the nanoscale. Tip-enhanced near-field Raman spectroscopy utilizes a metal-coated sharp tip and is based on surface-enhanced Raman scattering (SERS). Instead of the large surface enhancement from the metallic surface in SERS, the sharp metal coated tip in the tip-enhanced Raman scattering (TERS) provides nanoscaled surface enhancement only from the sample molecules in the close vicinity of the tip-apex, making it a perfect technique for nanoanalysis of materials. This article focuses on near-field analysis of some semiconducting nanomaterials and some carbon nanostructures. It first considers SERS analysis of strained silicon and TERS analysis of epsilon-Si and GaN thin layers before explaining how to improve TERS sensitivity and control the polarization in detection for crystalline materials. It also discusses ways of improving the spatial resolution in TERS.
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Surface Enhanced Raman Scattering. Springer, 2012.

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Book chapters on the topic "(surface raman scattering) SERS"

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Prochazka, Marek. "Basics of Surface-Enhanced Raman Scattering (SERS)." In Surface-Enhanced Raman Spectroscopy, 21–59. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23992-7_3.

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Itoh, Tamitake. "Experimental Demonstration of Electromagnetic Mechanism of SERS and Quantitative Analysis of SERS Fluctuation Based on the Mechanism." In Frontiers of Surface-Enhanced Raman Scattering, 59–87. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch4.

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Kneipp, Janina, and Daniela Drescher. "SERS in Cells: from Concepts to Practical Applications." In Frontiers of Surface-Enhanced Raman Scattering, 285–308. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch13.

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Khetani, Altaf, Ali Momenpour, Vidhu S. Tiwari, and Hanan Anis. "Surface Enhanced Raman Scattering (SERS) Using Nanoparticles." In Silver Nanoparticle Applications, 47–70. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-11262-6_3.

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Crozier, Kenneth B., Wenqi Zhu, Yizhuo Chu, Dongxing Wang, and Mohamad Banaee. "Lithographically-Fabricated SERS Substrates: Double Resonances, Nanogaps, and Beamed Emission." In Frontiers of Surface-Enhanced Raman Scattering, 219–41. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch10.

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Kneipp, Katrin, and Harald Kneipp. "Non-resonant SERS Using the Hottest Hot Spots of Plasmonic Nanoaggregates." In Frontiers of Surface-Enhanced Raman Scattering, 19–35. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch2.

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Titus, Eric J., and Katherine A. Willets. "Applying Super-Resolution Imaging Techniques to Problems in Single-Molecule SERS." In Frontiers of Surface-Enhanced Raman Scattering, 193–217. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch9.

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Kitahama, Yasutaka, and Yukihiro Ozaki. "Analysis of Blinking SERS by a Power Law with an Exponential Function." In Frontiers of Surface-Enhanced Raman Scattering, 107–37. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch6.

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Ranjith Premasiri, W., Paul Lemler, Ying Chen, Yoseph Gebregziabher, and Lawrence D. Ziegler. "SERS Analysis of Bacteria, Human Blood, and Cancer Cells: a Metabolomic and Diagnostic Tool." In Frontiers of Surface-Enhanced Raman Scattering, 257–83. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118703601.ch12.

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Koglin, E., and J. M. Sequaris. "Surface Enhanced Raman Scattering (SERS) Spectroscopy of Guanine Derivatives." In Redox Chemistry and Interfacial Behavior of Biological Molecules, 359–67. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-9534-2_26.

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Conference papers on the topic "(surface raman scattering) SERS"

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Procházka, M. "Raman and surface-enhanced Raman scattering (SERS) biosensing." In SPIE Optics + Optoelectronics, edited by Francesco Baldini, Jiri Homola, and Robert A. Lieberman. SPIE, 2013. http://dx.doi.org/10.1117/12.2021555.

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Olivo, Malini, Dinish U.s., and Douglas Goh. "Biomedicine with Surface Enhanced Raman Scattering (SERS)." In Asia Communications and Photonics Conference. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/acp.2013.aw3j.1.

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Bantz, Kyle C., Audrey F. Guerard, Christy L. Haynes, P. M. Champion, and L. D. Ziegler. "Surface-Enhanced Raman Scattering (SERS) Detection of a Bioactive Mediator." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482303.

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Nuntawong, Noppadon, Pitak Eiamchai, Saksorn Limwichean, Mati Horprathum, Viyapol Patthanasettakul, and Pongpan Chindaudom. "Applications of surface-enhanced Raman scattering (SERS) substrate." In 2015 Asian Conference on Defence Technology (ACDT). IEEE, 2015. http://dx.doi.org/10.1109/acdt.2015.7111591.

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Chen, Ying-Ren, Waileong Chen, and Yonhua Tzeng. "Graphene for surface enhanced Raman scattering (SERS) molecular sensors." In 2017 IEEE 17th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2017. http://dx.doi.org/10.1109/nano.2017.8117453.

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Babu, Saranya, S. Srijith, and S. Resmi. "Silver nanoparticles as surface enhanced Raman scattering (SERS) substrates." In INTERNATIONAL CONFERENCE ON RECENT TRENDS IN THEORETICAL AND APPLIED PHYSICS: ICRTTAP. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0058247.

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Raju, N. Ravi Chandra, K. Jagadeesh Kumar, A. Subrahmanyam, P. M. Champion, and L. D. Ziegler. "Silver oxide (AgO) thin films for Surface Enhanced Raman Scattering (SERS) studies." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482261.

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Yang, Xuan, Bin Chen, Shaowei Chen, Jin Z. Zhang, and Claire Gu. "Portable Fiber Sensors Based on Surface-enhanced Raman Scattering (SERS)." In Frontiers in Optics. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/fio.2010.fmc5.

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Hankus, Mikella E., Gregory Gibson, Nirmala Chandrasekharan, and Brian M. Cullum. "Surface-enhanced Raman scattering (SERS): nanoimaging probes for biological analysis." In Optics East, edited by Brian M. Cullum. SPIE, 2004. http://dx.doi.org/10.1117/12.569299.

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Kruszewski, Stefan, and Janusz Mallek. "Influence of surface roughness on the surface-enhanced Raman scattering (SERS) signal." In Laser Technology: Fourth Symposium, edited by Wieslaw L. Wolinski, Zdzislaw Jankiewicz, Jerzy K. Gajda, and Bohdan K. Wolczak. SPIE, 1995. http://dx.doi.org/10.1117/12.203251.

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Reports on the topic "(surface raman scattering) SERS"

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Sharma, Shiv K., Anupam K. Misra, Ava C. Dykes, and Lori E. Kamemoto. Biomedical Applications of Micro-Raman and Surface-Enhanced Raman Scattering (SERS) Technology. Fort Belvoir, VA: Defense Technical Information Center, October 2012. http://dx.doi.org/10.21236/ada581577.

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Driskell, Jeremy Daniel. Surface-Enhanced Raman Scattering (SERS) for Detection in Immunoassays. Applications, fundamentals, and optimization. Office of Scientific and Technical Information (OSTI), August 2006. http://dx.doi.org/10.2172/892727.

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Halas, Naomi, and Joseph Jackson. Detection of Molecular and Biomolecular Species by Surface-Enhanced Raman Scattering: Nanoengineered Substrates for SERS Detection. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada426233.

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Holthoff, Ellen, and Dimitra Stratis-Cullum. A Nanosensor for Explosives Detection Based on Molecularly Imprinted Polymers (MIPs) and Surfaced-enhanced Raman Scattering (SERS). Fort Belvoir, VA: Defense Technical Information Center, March 2010. http://dx.doi.org/10.21236/ada516676.

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Shokair, Isaac R., Mark S. Johnson, Randal L. Schmitt, and Shane Sickafoose. Concept for Maritime Near-Surface Surveillance Using Water Raman Scattering. Office of Scientific and Technical Information (OSTI), October 2016. http://dx.doi.org/10.2172/1563070.

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Talley, C., F. Reboredo, J. Chan, and S. Lane. Feasibility of Single Molecule DNA Sequencing using Surface-Enhanced Raman Scattering. Office of Scientific and Technical Information (OSTI), February 2006. http://dx.doi.org/10.2172/899105.

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Park, Hye-Young. Chip-Scale Bioassays Based on Surface-Enhanced Raman Scattering: Fundamentals and Applications. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/861629.

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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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