Academic literature on the topic 'Spectro-Microscopy'
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Journal articles on the topic "Spectro-Microscopy":
Miyoshi, N., T. Yamada, T. Ogawa, and H. Kinoshita. "Bioogical Meaning for Bioimaging by FT-IR spectro-microscopy and Raman spectro-microscopy." Seibutsu Butsuri 43, supplement (2003): S118. http://dx.doi.org/10.2142/biophys.43.s118_1.
Harter, Klaus, Alfred J. Meixner, and Frank Schleifenbaum. "Spectro-Microscopy of Living Plant Cells." Molecular Plant 5, no. 1 (January 2012): 14–26. http://dx.doi.org/10.1093/mp/ssr075.
Makita, Seiji, Hiroyuki Matsuda, Yasuaki Okano, Takayuki Yano, Eiken Nakamura, Yuri Hasegawa, Satoshi Kera, Shigemasa Suga, and Fumihiko Matsui. "Contrast Inversion of Photoelectron Spectro-microscopy Image." e-Journal of Surface Science and Nanotechnology 19 (May 13, 2021): 42–47. http://dx.doi.org/10.1380/ejssnt.2021.42.
Schmidt, Th, M. Siebert, A. Pretorius, S. Gangopadhyay, S. Figge, J. I. Flege, L. Gregoratti, A. Barinov, D. Hommel, and J. Falta. "Spectro-microscopy of Si doped GaN films." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 246, no. 1 (May 2006): 79–84. http://dx.doi.org/10.1016/j.nimb.2005.12.018.
Lepert, Guillaume, Ricardo M. Gouveia, Che J. Connon, and Carl Paterson. "Assessing corneal biomechanics with Brillouin spectro-microscopy." Faraday Discussions 187 (2016): 415–28. http://dx.doi.org/10.1039/c5fd00152h.
KURATA, Hiroki, Seiji ISODA, and Takashi KOBAYASHI. "Study of Organic Crystals by Electron Spectro-Microscopy." Nihon Kessho Gakkaishi 36, no. 3 (1994): 199–203. http://dx.doi.org/10.5940/jcrsj.36.199.
Rehman, R. A., H. J. Zhang, A. Razaq, S. M. Ramay, M. Hasan, M. A. Javed, and S. Atiq. "Spectro-microscopy characterization of CoPc-Au(111) interface." Physica E: Low-dimensional Systems and Nanostructures 125 (January 2021): 114357. http://dx.doi.org/10.1016/j.physe.2020.114357.
Bode, M., A. Kubetzka, O. Pietzsch, and R. Wiesendanger. "Spin-resolved spectro-microscopy of magnetic nanowire arrays." Surface Science 514, no. 1-3 (August 2002): 135–44. http://dx.doi.org/10.1016/s0039-6028(02)01619-9.
Bohic, S., R. Tucoulou, G. Martinez-Criado, S. Labouré, M. Salomé, and P. Cloetens. "C-10 Synchrotron Based Spectro-Microscopy for Cell Biology." Powder Diffraction 24, no. 2 (June 2009): 166. http://dx.doi.org/10.1154/1.3175930.
Stohr, J., and S. Anders. "X-ray spectro-microscopy of complex materials and surfaces." IBM Journal of Research and Development 44, no. 4 (July 2000): 535–51. http://dx.doi.org/10.1147/rd.444.0535.
Dissertations / Theses on the topic "Spectro-Microscopy":
Vanacore, Giovanni Maria. "INVESTIGATION OF Ge SURFACE DIFFUSION AND SiGe NANOSTRUCTURES BY SPECTRO-MICROSCOPY TECHNIQUES." Phd thesis, Ecole Polytechnique X, 2011. http://tel.archives-ouvertes.fr/tel-00725427.
Darwish, Hamida M. B. "Characterization of different types of synthetic diamonds by luminescence and spectro-microscopy." Thesis, University of Bristol, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.435422.
Cassese, Damiano. "Design and realization of nanoelectromechanical and plasmonic devices for raman spectro-microscopy." Doctoral thesis, Università degli studi di Trieste, 2015. http://hdl.handle.net/10077/11135.
Lo sviluppo di nano-dispositivi per la misura di molecule biologiche e non biologiche è uno dei campi più importanti e in via di sviluppo della nanotecnologia. La possibilità di studiare cellule in vivo e di capirne le caratteristiche a livello molevolare ha contribuito enormemente all'avanzamento degli studi biologici negli ultimi decenni. Fra le tecniche più utilizzate, le Scanning Probe Microscopies (SPM) hanno una speciale rilevanza: sono non distruttive, con una bassa perturbazione dei sistemi studiati e permettono misure in aria e in liquido. Tali tecniche tuttavia non permettono il riconoscimento chimico, aspetto importante nello spiegare molti meccanismi cellulari. Una delle spettroscopie più utilizzate a tale scopo è il Raman, che permette il riconoscimento delle specie chimiche senza danneggiare i campioni ed è stato ampiamente utilizzato in molti studi biologici. Una combinazione di una tecnica SPM e della spettroscopia Raman è il Tip Enhanced Raman Spectroscopy (TERS): la stessa punta è usata per ricostruire le proprietà meccaniche e per illuminare localmente il campione per estrarne informazioni chimiche. Tale combinazione rende il TERS uno strumento molto potente per lo studio di strutture nanometriche. In questo lavoro di tesi abbiamo esplorato la possibilità di realizzare una punta TERS basata su un nanofilo in materiale semiconduttore cresciuto epitassialmente sulla punta di un cantilever per AFM. Il dispositivo, compatibile con le strumentazioni AFM disponibili sul mercato, ha come scopo lo sfruttamento della risonanza plasmonica creata nella particella metallica presente sulla cima del nanofilo: il segnale Raman può essere potenziato sfruttando il campo elettrico molto intenso creato in questo modo. | 910 | Abstract Nel primo capitolo si introduce le basi della tecnica AFM e vengono presentati due studi compiuti su cellule mesoteliali tramite questa microscopia. Nel secondo capitolo vengono presentati i nanofili in silicio: sono riportati i risultati ottenuti nella crescita di tali strutture, quindi vengono analizzate la citotossicità e la proliferazione di cellule su substrati di nanofili di silicio. Misure di microscpettroscopia Raman su nanofili di GaAs sono riportate nel capitolo 3: è stato studiato il cambiamento di struttura cristallina di tali nanofili dovuta a procedimenti di riscaldamenti controllati. Il capitolo 4 affronta lo studio delle proprietà SERS di nanofili di materiali e strutture diverse; sono presentati risultati sperimentali e calcoli ottenuti tramite simulazioni ad elementi finiti (FEA). Infine nel capitolo 5 presentiamo un innovativo procedimento per la fabbricazione di punte TERS a singolo nanofilo. In Appendice sono presentate brevemente le tecniche fabbricative usate durante il lavoro di tesi.
The development of nano-devices for sensing molecules, both biological and non-biological is one of the most important and thriving fields of nanotechnology. The possibility to investigate living cells and their characteristics at a molecular level contributed to the great advance of biological studies in the last decades. Among the most investigated techniques, Scanning Probe Microscopies (SPM) have a prominent position: non-destructiveness, low perturbation of the sample, possibility of measurements in air and in liquid make them perfectly suited to biological studies. These techniques however lack chemical recognition of the analysed surfaces. Many cell mechanisms can be explained only understanding the chemistry involved: the integration of a spectroscopic technique is therefore essential to have insights on the phenomena under study. One of the most investigated spectroscopy for such an integration is Raman: its interaction with molecular and crystal structures allows for chemical recognition. It has been widely used in studies of organic samples an biosensing and it provides non-destructive measurements. A smart combination of a SPM technique and Raman Spectroscopy is the so-called Tip Enhanced Raman Spectroscopy (TERS) where the same probe that is used to reconstruct the sample mechanical properties with nm resolution is also used to illuminate locally the sample to extract chemical information. The high resolution spectroscopy combined with the topography of the SPM makes TERS a powerful tool for the investigation of nanometrical features. At the present, however, no commercially available TERS probe can provide reliable and reproducible results with high Raman enhancement.8 | Abstract With this thesis work we explored the realization of a TERS probe based on a semiconductor NW grown epitaxially on the apex of an AFM cantilever. This design, compatible with the commercially available equipment, aims at the use of the plasmonic resonance created in the noble metal nanoparticle present on the top of the nanowire to greatly enhance the Raman signal. The high aspect ratio of this nanostructure can lead to high-resolution topography and spectroscopy. We will first introduce the basics of SPM and give an example of a study of cells by AFM in Chapter 1: the effect of the uptake of asbestos fibers and carbon nanotubes by mesothelial cells is reported. In Chapter 2 we briefly present the growth mechanics for Si nanowires, with a summary of the results obtained for Si NWs. A study of the citotoxicity of ZnSe and Si nanowires follows: living cells were seeded on nanowires and their proliferation, behaviour and adhesion was measured as a mean to verify the compatibility of NWs with the imaging of living cells. Chapter 3 reports Raman measurements of GaAs NWs and the change in crystal structure of these upon annealing at high temperatures. Studies of the SERS effect on semiconductor nanowires are presented in Chapter 4: the plasmonic resonance on ZnSe, Si and GaAs NWs was modelled by Finite Element Method. The absorption spectra and the Raman enhancement factor of the same wires were measured and an understanding of their SERS capability is presented. Finally we propose in Chapter 5 a novel fabrication process for the localized growth of NWs on AFM cantilevers as TERS tips. Appendix A reports a brief explenation of the fabrication processes mention along the thesis presentation.
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KANDYBA, VIKTOR. "Electronic structure of single and few layered graphene studied by angle resolved photoemission spectro-microscopy." Doctoral thesis, Università degli Studi di Trieste, 2018. http://hdl.handle.net/11368/2929830.
Ziegler, Cornelia. "Imagerie quantitative de l'assemblage de la NADPH oxydase des phagocytes en cellules vivantes par des approches FRET-FLIM." Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLS048/document.
The phagocyte NADPH oxidase (NOX2) is a key enzyme of the immune system generating superoxide anions, which are precursors for other reactive oxygen species. Any dysfunctions of NOX2 are associated with a plethora of diseases and thus detailed knowledge about its regulation is needed. This oxidase is composed of five subunits, the membrane-bound gp91phox and p22phox and the cytosolic p47phox, p67phox, and p40phox. The latter are assumed to be in a ternary complex that translocates together with the small GTPase Rac to the membranous subunits during activation.Our aim was to discover and to characterize specific interactions of the cytosolic subunits of NOX2 in live cells using a Förster Resonance Energy Transfer (FRET) based approach: Since FRET depends on the distance between two fluorophores, it can be used to reveal protein-protein interactions non-invasively by studying fluorescent protein tagged subunits. To have a rapid method on hand to reveal specific interactions, a flow cytometer based FRET approach was developed. For more detailed studies, FRET was measured by fluorescence lifetime imaging microscopy (FLIM), because it allows a direct determination of the apparent and molecular FRET efficiency, which contains both qualitative and quantitative information about the interaction and the structure of the interacting proteins. Furthermore, the FRET-FLIM approach enables an estimation of the fraction of bound donor. This information itself is important for a better understanding of the organisation and regulation of the NOX2, but it is also necessary for the calculation of the dissociation constant Kd from the FRET-FLIM data. To confirm the findings obtained by FRET-FLIM fluorescence cross correlation spectroscopy (FCCS) experiments were performed. This completely independent method is not based on distances like FRET but on the observation of the co diffusion of the fluorescently labelled samples when they move across a small observation volume inside the cells.The FRET-FLIM approach allowed us in a first step to discover heterodimeric interactions between all cytosolic subunits in live cells. Due to the good precision of the results, we were able to extract structural information about the interactions and to compare them with available structural data obtained from in vitro studies. The information from FRET-FLIM was coherent with in vitro data. We then aligned the available structures leading to the first 3D model of the cytosolic complex of the NADPH oxidase in the resting state in live cells.Additionally, the bound fraction for all heterodimeric interactions derived by FRET-FLIM is around 20 %, which is in contrast to the general belief that all cytosolic subunits are bound in complex. The first FCCS results support our findings. Therefore, we believe that the complexation of the cytosolic subunits could be involved in the regulation of the NADPH oxidase and should be investigated further. The estimated Kd derived from the FRET-FLIM approach is in the low micomolar range, which is an order of a magnitude higher than the nanomolar range of in vitro studies.In conclusion, we showed that our quantitative FRET-FLIM approach is not only able to distinguish between specific and unspecific protein-protein interactions, but gives also information about the structural organisation of the interacting proteins. The high precision of the FRET-FLIM data allow the determination of the bound fraction and an estimation of the Kd in live cells. FCCS is a complementary method, which can verify these quantitative findings. However, it cannot replace FRET-FLIM completely as it does not give any structural information.With respect to the biological outcome of this project, we can propose for the first time a 3D-model of the cytosolic complex of the NADPH oxidase covering the in vitro as well as the live cell situation. Additionally, the small bound fraction found here may raise new ideas on the regulation of this vital enzyme
Klemm, Hagen William [Verfasser], Thomas [Akademischer Betreuer] Schmidt, Hans-Joachim [Gutachter] Freund, and Frank [Gutachter] Behrendt. "Formation and properties of ultrathin silicon dioxide films on Ru(0001) : an in-situ spectro-microscopy study / Hagen William Klemm ; Gutachter: Hans-Joachim Freund, Frank Behrendt ; Betreuer: Thomas Schmidt." Berlin : Technische Universität Berlin, 2018. http://d-nb.info/1156331250/34.
Guida, Manrique Leydy Carolina. "Mécanismes contrôlant la séquestration du gadolinium, du rhénium et du sélénium dans des conditions de faible teneur en oxygène." Electronic Thesis or Diss., Université Grenoble Alpes, 2024. http://www.theses.fr/2024GRALU015.
Trace elements, despite their scarcity (less than 100 parts per million) on Earth, serve diverse purposes: some act as micronutrients, while others, known as critical metals, possess unique industrial and medical applications. In oxygen-deprived natural aquatic systems electron transfers involve biogeochemical reactions catalyzed by iron, sulfur and trace elements. Understanding their reactivity in these environments remains a challenge. My Ph.D. research focus on filling this knowledge gap concerning three specific elements (rhenium (Re), selenium (Se), and gadolinium (Gd)). They exist in various chemical aqueous species in water: monovalent anion (perrhenate, ReO4—), divalent anion (selenate, SeO42—and selenite, SeO32—) or cation (Gadolinium, Gd3+). Rhenium is a critical metal, while selenium is a bioessential element at low levels, and becomes toxic in higher concentrations. Gadolinium is a rare earth element and a critical metal as well, due to its wide use as a contrast agent in magnetic resonance imaging (MRI).These elements are most concentrated in marine sediments formed in oxygen-deprived environments. Common mineral phases include pyrite (FeS2) and magnetite (Fe3O4) depending on sulfide content in those environments, and origin (autogenic vs. detritic, e.g., from volcanic rocks) of the particles. My research, presented across four chapters, investigates surface reduction (Re(VII), Se(VI) and Se(IV)) and the sorption (Gd(III)) processes on/into magnetite and pyrite particles. Employing various analytical methods such as XAFS spectroscopy, STEM-EELS spectro microscopie and MC-ICP-MS, our study reveals distinct reactive pathways. Re(VII) reacts with sulfidic water to form Re(III, IV, V)2S7 nanoparticles, while at lower concentrations Re is reduced and incorporated into particles, in different pathways characterized by less isotopic fractionation with pyrite than with magnetite. We also show that pyrite nanoparticles reduce Se(VI) and Se(IV), down to surface Se(0) or structure Se(-I) depending on whether adsorption or co-precipitation occurs. Lastly, Gd substitutes for Fe(III) in magnetite nanoparticles up to 5% Fe substitution by Gd. We attempt to unify the affinity behaviour of these and other trace elements with anoxic Fe-bearing sediments in the light of the hard and soft acids and bases principle.The study provides new insights into the mechanisms that govern the sequestration of metals and metalloids in sedimentary settings. The significance of this research lies in its relevance to contemporary scientific and technological endeavours, particularly in understanding how processes in Fe and sulfidic systems work like trace elements, Fe and S mobility, mass balance in the global sedimentary cycles to the exploration, mining and recycling of potential repositories of metals. Furthermore, it enhances our current understanding of the use of palaeoenvironmental proxies to reconstruct the Earth's formation. Finally, this study also has implications for the treatment of nuclear waste and pollution, particularly in the management of selenium (Se) and gadolinium (Gd) contamination
Partouche, David. "Analyse de l’assemblage de peptides amyloïdes bactériens." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLX084/document.
Hfq is a pleiotropic bacterial protein that determines several phenotypic characteristics. Its main function is to facilitate responses to stresses that bacteria may encounter during environmental changes, mainly by using post-transcriptional genetic control. The protein, by its capacity to interact with RNA, in particular small non-coding RNA, enables a rapid regulation of gene expression. In addition, the protein also interacts with DNA and compacts it. From a structural point of view, the protein adopts an Sm-like fold, characterized by a toroidal oligomer formed by a continuous 30-stranded β-sheet. Besides its conserved N-terminal Sm domain, Hfq also possesses a C-terminal region (CTR) that can vary in size and sequence between bacteria. My PhD work focused on the analysis of this CTR region in Escherichia coli bacteria. Indeed, this region has the capacity to form an amyloid structure. This structural dynamic is related to the formation of self-assembled structures in vivo, in the proximity of the inner membrane and in the nucleoid.Using various physicochemical techniques (molecular microscopy, spectroscopy and infrared microscopy, circular dichroism and small angle X-ray scattering), my work consisted in characterizing the assembly of this region of Hfq, as well as the factors influencing its assembly (in particular, the presence of nucleic acids). A part of my work consisted in setting up an innovative correlative–imaging method to analyze the chemical and morphological signature of a single amyloid fibre. Finally, my work focused on the analysis of the effect of compounds that inhibit the aggregation of the amyloid structure, which could constitute a new way to develop a novel class of antibiotics
Badjeck, Vincent. "Etude par spectro-microscopie électronique d'aciers ODS non irradiés et implantés par hélium." Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLS086.
Irradiated and non-irradiated (Y-Ti-O) oxide-dispersion-strengthened (ODS) steels are investigated by scanning transmission electron microscopy coupled with electron energy-loss spectroscopy (STEM-EELS) to study their chemical structure and the effects of radiation. Analytical methods such as multivariate statistical analysis (MVA) and EELS curve-fitting are carried out to achieve elemental quantification or study the edge fine structures (ELNES). Using MVA, the spectrum-images (SI) can be separated into independent spectral responses to gain insights into the valence state of various elements such as Ti or Cr. Investigations on post-mechanical-alloyed (MA) powders show that the nanoparticle (NP) precipitation occurs only after a further high-temperature treatment (consolidation). In non-irradiated consolidated samples, medium-sized NPs (> 3-4 nm) are found to adopt a Y2Ti2O7-d defective pyrochlore structure with a (Y-Ti-O)-Cr core-shell structure with a reduced-Ti layer also depleted in Y. Cr is also shown to segregate to the grain boundaries in non-irradiated samples. The measured O/Ti ratio of 3.2 found for medium-sized NPs and the observed non-homogeneity of the inter-reticular distance d222 through the particle is interpreted as being due to defects in the particles’ structure; it is indeed confirmed that Y2Ti2O7 medium-sized NPs in ODS steels present numerous defects and are non-stoichiometric. The Ti oxidation state is shown to vary from the centre of the NPs to their periphery from Ti4+ in distorted Oh symmetry to a valency often lower than 3+. Independent component analysis (ICA) allows us to generate bonding maps and extract a Ti-Cr interfacial response. An inter-diffusion of Ti and Cr atoms is observed at this interface. The smallest NPs present a different and ill-defined structure and interface with the Fe-Cr matrix. They either consist of a highly oxygen-deficient pyrochlore structure (Y2Ti2O6+d) or an unknown YaTibOc chemical structure. The O/Ti ratio decreases from 3-3.5 to below 1 for an NP size going from 4 to 1.8 nm. A few large particles (sized from tens to hundreds of nm) present a N-Ti-O or Ti-O chemistry but represent only a small percentage of all the NPs (< 1%). To study the neutron irradiation-induced changes, a number of ODS samples were implanted with He+ ions and irradiated with Fe+ ions. After irradiation, they display a homogeneous distribution of high-pressure He bubbles and radiation-induced Cr depletion, segregation and precipitation (RID, RIS and RIP). The He bubbles are frequently trapped at the NP-matrix interface, although bubbles can exist freely in the matrix, trapped by dislocations and at grain boundaries. The He-K line (21.218 eV for free atoms) shifts to higher energy in the bubbles (ΔE = 0.5 to 4 eV); this is shown to be correlated with the He density. He quantification is carried out with three different methods: spatial difference, curve-fitting and MVA. The density and pressure values are found to reach 100 nm-3 and 8 GPa respectively, although the pressure measurement is only semi-quantitative given that the error bars can reach 30%. The curve-fitting method allows us to map the He-K energy position and intensity, yielding the density, in individual bubbles. The spectral response of individual bubbles can be separated in an SI containing many bubbles at different densities using ICA or vertex component analysis (VCA). Bubbles larger than 4 nm are shown to be under-pressurized or at equilibrium with the Fe-Cr matrix. Below 3.5 nm, the He pressure is shown to increase markedly, passing into the over-pressurised regime
VIRGA, ALESSANDRA. "Ultrafast spectro-microscopy of highly excited low dimensional materials." Doctoral thesis, 2019. http://hdl.handle.net/11573/1251453.
Book chapters on the topic "Spectro-Microscopy":
Yagi, K., Y. Tanishiro, and H. Minoda. "Spectro-microscopy by TEM-SEM." In Nanoscale Spectroscopy and Its Applications to Semiconductor Research, 11–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45850-6_2.
Ade, H., and C. H. Ko. "Scanning Spectro-Microscopy with 250 to 800 eV X-Rays." In Chemical, Structural and Electronic Analysis of Heterogeneous Surfaces on Nanometer Scale, 53–74. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5724-7_4.
"Infrared Spectro-microscopy." In Encyclopedia of Biophysics, 1048. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_101144.
Aizawa, T., A. Mitsuo, and J. Kihara. "Acoustic spectro-microscopy of Al-implanted Ni and Ni alloys." In Laser and Ion Beam Modification of Materials, 495–98. Elsevier, 1994. http://dx.doi.org/10.1016/b978-0-444-81994-9.50105-6.
Conference papers on the topic "Spectro-Microscopy":
Kovac, J., S. Günther, A. Kolmakov, L. Casalis, L. Gregoratti, D. Lonza, M. Marsi, and M. Kiskinova. "Photoemission spectro-microscopy at ELETTRA." In The fourteenth international conference on the application of accelerators in research and industry. AIP, 1997. http://dx.doi.org/10.1063/1.52553.
Sadowski, Jerzy T. "Electron spectro-microscopy of 2D materials." In Low-Dimensional Materials and Devices 2020, edited by Nobuhiko P. Kobayashi, A. Alec Talin, Albert V. Davydov, and M. Saif Islam. SPIE, 2020. http://dx.doi.org/10.1117/12.2568816.
Ideguchi, Takuro, Simon Holzner, Birgitta Bernhardt, Guy Guelachvili, Nathalie Picqué, and Theodor W. Hänsch. "Coherent anti-Stokes Raman dual-comb spectro-microscopy." In CLEO: Science and Innovations. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/cleo_si.2013.ctu3h.2.
Yi, Minwoo, Kanghee Lee, Jin-Dong Song, and Jaewook Ahn. "Sub-wavelength terahertz microscopy using spectro-temporal phase analysis." In 2011 36th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2011). IEEE, 2011. http://dx.doi.org/10.1109/irmmw-thz.2011.6105089.
Huang, Guan-Jie, Pei-Chen Lai, Ming-Wei Shen, Jia-Xuan Su, Jhan-Yu Guo, Kuo-Chuan Guo, Peng Lin, et al. "Stimulated Raman scattering spectro-microscopy using multiple-plate continuum." In Label-free Biomedical Imaging and Sensing (LBIS) 2023, edited by Natan T. Shaked and Oliver Hayden. SPIE, 2023. http://dx.doi.org/10.1117/12.2647696.
Potts, A. W. "Polycrystalline metal surfaces studied by X-ray photoelectron spectro-microscopy." In Sixth international conference on x-ray microscopy (XRM99). AIP, 2000. http://dx.doi.org/10.1063/1.1291156.
Brotosudarmo, Tatas Hardo Panintingjati, Arif Agung Wibowo, Heriyanto Heriyanto, and Marcelinus A. S. Adhiwibawa. "Single cells diatom Chaetoceros muelleri investigated by homebuilt confocal fluorescence spectro-microscopy." In Third International Seminar on Photonics, Optics, and Its Applications (ISPhOA 2018), edited by Agus M. Hatta and Aulia M. Nasution. SPIE, 2019. http://dx.doi.org/10.1117/12.2502932.
Blonskij, Ivan V., V. G. Grytz, V. F. Kozenev, V. A. Thoryk, and V. V. Semenov. "Photoacoustic spectro- and microscopy: new diagnostic methods for materials and devices for electronics." In Optical Diagnostics of Materials and Devices for Opto-, Micro-, and Quantum Electronics: International Workshop, edited by Sergei V. Svechnikov and Mikhail Y. Valakh. SPIE, 1994. http://dx.doi.org/10.1117/12.191990.
Grenci, Gianluca. "IR-live: plastic microfluidic devices for infrared spectro-microscopy of living cells ." In The 7th International Multidisciplinary Conference on Optofluidics 2017. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/optofluidics2017-04555.
Bahou, Mohammed, Li Wen, Xiande Ding, B. Didier F. Casse, Sascha P. Heussler, Pengda Gu, Caozheng Diao, et al. "Infrared Spectro/Microscopy at SSLS — Edge Effect Source in a Compact Superconducting Storage Ring." In SYNCHROTRON RADIATION INSTRUMENTATION: Ninth International Conference on Synchrotron Radiation Instrumentation. AIP, 2007. http://dx.doi.org/10.1063/1.2436133.
Reports on the topic "Spectro-Microscopy":
Laskin, Alexander, and Ryan Moffet. Spectro-Microscopy Studies of Atmospheric Particles. Office of Scientific and Technical Information (OSTI), January 2023. http://dx.doi.org/10.2172/1914321.
Ghosh, Ishita, Manushree Tanwar, Rajesh Kumar, and C. Malla Reddy. The world of exotic crystals: Raman spectro-microscopy for probing local structure. The Israel Chemical Society, March 2023. http://dx.doi.org/10.51167/acm00045.
Paesani, Francesco, and Wei Xiong. Probing the Structure and Dynamics of Fluid Mixtures in Porous Materials Through Ultrafast Vibrational Spectro-Microscopy and Many-Body Molecular Dynamics. Office of Scientific and Technical Information (OSTI), December 2022. http://dx.doi.org/10.2172/1901582.