Дисертації з теми "Ultra spectroscopy"
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1
Newstead, David A. "Photoelectron spectroscopy of ultra-thin metallic layers." Thesis, University of Leicester, 1987. http://hdl.handle.net/2381/35747.
Повний текст джерелаАнотація:
Photoelectron spectroscopy, with LEED, Auger electron spectroscopy (AES) and secondary electron emission crystal current (SEECC) measurements, has been used to investigate the electronic structure of well-characterized overlayers of Tl, Cr, Mn and Fe on Ag(100) and Fe on Cu(100). The Stranski-Krastanov growth mode has been found for Tl on Ag(100). In the chain structure observed at 70 K, there is no evidence for a Peierls distortion, in contrast to Tl chains on Cu(100). Band-mapping of the Tl 6p band has indicated the absence of an energy gap at the Fermi level, confirming the LEED result that the Peierls distortion has been suppressed. This is believed to be due to commensurability with the substrate. A study of Cr on Ag(100) has revealed epitaxial growth up to two monolayers, with a transition to bilayers before the completion of the first layer. Photoemission measurements of the Cr 3s multiplet splitting indicate an enhanced magnetic moment, which approaches the bulk value with coverage. This enhancement is thought to be a consequence of d-band narrowing, resulting from the reduced dimensionality of the overlayer. A p(1 x 1) surface alloy is initially observed when Mn is deposited on Ag(100), but with a magnetic moment smaller than the bulk Mn value; angle-resolved photoemission measurements indicate significant overlayer- substrate d-d interaction, in contrast to Cr on Ag(100). With further coverage, the magnetic moment increases and when simultaneous multilayer growth occurs on the AgMn surface, the bulk value is attained. Pseudomorphic 1ayer-by-layer growth has been identified for Fe deposited on Cu(100) and the band structure has been determined for Fe coverages of one and seven monolayers. From a comparison with calculated band structures, it is proposed that the monolayer is ferromagnetic, while the thicker fee film may be antiferromagnetic. An Fe monolayer on Ag(100) has also been shown to have ferromagnetic order.
2
Semeniuk, Jaroslaw Ivan. "Ultra violet Fourier transform spectroscopy of transition elements." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321659.
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3
Manke, Kara Jean. "Toward ultra-broadband photoacoustic spectroscopy of supercooled liquids." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98789.
Повний текст джерелаАнотація:
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2015.Cataloged from PDF version of thesis.
Includes bibliographical references (pages 163-176).
Theoretical understanding of the dramatic slow-down of structural relaxation dynamics in supercooled liquids leading to the glass transition is limited in part by the lack of data in these systems. Between the melting point and the glass transition, the viscosity of supercooled liquids can change by 16 orders of magnitude or more and few experimental techniques can access this broad a range of frequencies and time scales. Photoacoustic spectroscopy is an ideal technique for probing the dynamics of supercooled liquids because it provides direct access to mechanical relaxation. Currently, photoacoustic spectroscopy of supercooled liquids has been carried out in the range of 10 MHz to 1 GHz with impulsive stimulated light scattering (ISS) and 8 GHz to 200 GHz with picosecond ultrasonics. In this work, I present advances in photoacoustic techniques with the goal of extending the range of frequencies accessible by these methods. To achieve higher-frequency acoustic generation, experiments on semiconductor superlattices (SLs) composed of alternating layers of gallium arsenide (GaAs) and aluminum arsenide (AlAs) and multiple quantum well structures (MQW) of indium gallium nitride (InGaN) and gallium nitride (GaN) as photoacoustic transducers are presented. The results demonstrate that InGaN/GaN SLs can be employed as broadband photoacoustic transducers, generating acoustic frequencies up to 2.5 THz. A simple transient reflectivity technique for the detection and reconstruction of short (- 2 ps) acoustic strain pulses is also presented. Using a time-domain analogue of Brillouin light scattering, data on the acoustic velocity and attenuation rate of supercooled liquid DC704 at frequencies of - 6 GHz and - 12 GHz, a region which can be hard to access with both ISS and PU approaches, is shown. Finally, the slow rise or "Mountain mode" component of ISS signal from DC704, which arises from slow components of the density response at timescales from 10- 4 s to 10- 7 s is examined. Comparison with the broadband compliance spectrum of DC704 demonstrates that the slow rise signal does not directly reflect the relaxing elastic compliance, but contains contributions from other slow degrees of freedom that couple to the density.
by Kara Jean Manke.
Ph. D.
4
Dick, Susan. "Raman spectroscopy for ultra trace detection of biomolecules." Thesis, Queen's University Belfast, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.706455.
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5
Hsieh, Chaoray. "Ultra-compact holographic spectrometers for diffuse source spectroscopy." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/22533.
Повний текст джерелаАнотація:
Thesis (Ph. D.)--Electrical and Computer Engineering, Georgia Institute of Technology, 2008.Committee Chair: Adibi, Ali; Committee Member: Chang, Gee-Kung; Committee Member: Ralph, Stephen; Committee Member: Trebino, Rick; Committee Member: Verriest, Erik I.
6
Jennings, G. "Ultra-violet photoelectron spectroscopy of BCC- and FCC- iron." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306636.
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7
Monk, Stephen David. "Ultra sensitive detection of hydrocarbons using wavelength modulation spectroscopy." Thesis, University of Glasgow, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422654.
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8
Price, Richard John. "Ultra-high-resolution spectroscopy of the ISM towards Orion." Thesis, University College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252156.
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9
Kadowaki, Jennifer, Dennis Zaritsky, and R. L. Donnerstein. "Spectroscopy of Ultra-diffuse Galaxies in the Coma Cluster." IOP PUBLISHING LTD, 2017. http://hdl.handle.net/10150/623844.
Повний текст джерелаАнотація:
We present spectra of five ultra-diffuse galaxies (UDGs) in the vicinity of the Coma cluster obtained with the Multi-object Double Spectrograph on the Large Binocular Telescope. We confirm four of these as members of the cluster, quintupling the number of spectroscopically confirmed systems. Like the previously confirmed large (projected half-light radius > 4.6 kpc) UDG, DF44, the systems we targeted all have projected half-light radii > 2.9 kpc. As such, we spectroscopically confirm a population of physically large UDGs in the Coma cluster. The remaining UDG is located in the field, about 45 Mpc behind the cluster. We observe Balmer and Ca II H and K absorption lines in all of our UDG spectra. By comparing the stacked UDG spectrum against stellar population synthesis models, we conclude that, on average, these UDGs are composed of metal-poor stars ([Fe/H] less than or similar to -1.5). We also discover the first UDG with [O II] and [O III] emission lines within a clustered environment, demonstrating that not all cluster UDGs are devoid of gas and sources of ionizing radiation.
10
Reichmuth, Andreas. "Alkali metal adsorption and ultra-thin film growth." Thesis, University of Cambridge, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338308.
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11
Schambach, Philip [Verfasser]. "Tip-enhanced Raman spectroscopy in ultra-high vacuum / Philip Schambach." Berlin : Freie Universität Berlin, 2013. http://d-nb.info/104348079X/34.
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12
Von, Klitzing Wolf Dietrich Carl. "Ultra-high resolution CO₂ laser spectroscopy and transient line narrowing." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627129.
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13
Li, King Fai. "Ultra-fast spectroscopy investigation on organic molecules two photon absorption." HKBU Institutional Repository, 2008. http://repository.hkbu.edu.hk/etd_ra/911.
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14
Adato, Ronen. "Mid-infrared plasmonics for ultra-sensitive spectroscopy of biomolecular interactions." Thesis, Boston University, 2013. https://hdl.handle.net/2144/12705.
Повний текст джерелаАнотація:
Thesis (Ph.D.)--Boston University
PLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.Mid-infrared (IR) absorption spectroscopy contrasts with numerous other biosensing methods in that it can directly probe molecular structure via bond specific vibrational modes and monitor structural changes even in the absence of any mass transfer. The technique is therefore a valuable tool for a wide range of applications critical for understanding basic biological function and important aspects of e.g. disease progression and treatment. Despite these attractive features, IR absorption spectroscopy is limited as its acquired signal depends on a molecular bonds intrinsic absorption cross-section and path length (via Beers Law). Sensitivity issues therefore restrict applications to a limited set of strong bands and/or relatively thick samples. Additionally, due to the strong absorption of water in theIR, measurements in fluid are cumbersome, requiring specialized equipment and extremely high analyte concentrations. Plasmonic nano-structures supporting resonances at mid-IR wavelengths offer an attractive means with which to overcome many of these limitations. In particular, plasmonic resonances result in strongly enhanced near-field intensities confined to the surface of metallic particles, which allow one to dramatically increase the absorption signal of molecules. This concept is termed SEIRA (Surface Enhanced Infrared Absorption Spectroscopy). This thesis focuses on leveraging IR-resonant plasmonic nanostructures to enable sensitive SEIRA measurements of molecular monolayers, even in aqueous solutions. In achieving this capability, we first develop methods for utilizing nano-particle interactions in engineered arrays and demonstrate their application to the optimal enhancement of protein absorption bands. We then demonstrate multi-band antennas, capable of simultaneously probing several vibrational bands. Thirdly, we present the first demonstrated use of engineered IR antennas for real-time, in-situ IR spectroscopy measurements on a series of protein and nano-particle binding interactions. By leveraging the far-field scattering properties of plasmonic nano-antennas in addition to the associated near-field enhancement and localization, our method enables a unique chip-based spectroscopy technology that is highly compatible with modern sample preparation and handling techniques. Finally, we present a theoretical treatment of the interaction between our engineered resonances and the natural molecular ones. Our general model correctly predicts detailed absorption spectra and a number of effects dependent the experimental setup and plasmonic antenna design.
15
Syed, Azfar A. "Surface enhanced Raman spectroscopy for ultra-sensitive detection of energetic materials." Thesis, Cranfield University, 2010. http://dspace.lib.cranfield.ac.uk/handle/1826/4644.
Повний текст джерелаАнотація:
The prospect of ultra-sensitive detection of molecular species, particularly those of energetic materials, has prompted the present research initiative. The combination of metal surface nano-technology and Raman spectroscopy has given rise to ‘Surface Enhanced Raman Spectroscopy’ (SERS). This is a very sensitive technique and has proved to be capable of detecting a single molecule. SERS was demonstrated by recording Raman spectra of the sample molecules adsorbed on various specially prepared SER-active surfaces both in the form of a colloidal suspension and on the solid roughened surfaces. Using a gold colloidal suspension, pyridine has been detected down to 10-11 molar (M) concentration. A silver slab was roughened to a dimension of a nano-scale by etching in nitric acid solution to make SER-active surface. Pentaerythritol Tetranitrate (PETN) explosive was detected using this surface after its 10-2 M solution was dropped, dried and washed (of any residue) from the surface. Lithographically engineered silver structures in the form of nanoarrays having a number of silver structures of approximately 106 in a region of 0.1 mm2 have been used for SERS. The major noise contribution to the scattering from impurities in an ordinary glass substrate has been eliminated by replacing glasses as substrates with pure quartz discs. The headspace vapours from peroxide explosives, Triacetone Triperoxide (TATP) and Hexamethylene Triperoxide Diamine (HMTD), were detected at approximately 70 parts per million (ppm) and 0.3 ppm concentrations respectively using a portable commercial Raman Spectrometer. PETN was also detected from its headspace vapour at about 18 parts per trillion (ppt) in spite of it having a much lower vapour pressure. The possibility of desorption of adsorbed molecules from a nano-structured surface by laser irradiation has been demonstrated experimentally with the aim of reusability of SER-active surfaces. Also demonstrated was the enhancement in Raman intensity through resonance Raman effect spectroscopy for the future use in surface enhanced resonance Raman spectroscopy (SERRS).
16
Syed, A. A. "Surface enhanced raman spectroscopy for ultra-sensitive detection of energetic materials." Thesis, Department of Materials and Applied Science, 2010. http://dspace.lib.cranfield.ac.uk/handle/1826/4644.
Повний текст джерелаАнотація:
The prospect of ultra-sensitive detection of molecular species, particularly those of
energetic materials, has prompted the present research initiative. The combination of
metal surface nano-technology and Raman spectroscopy has given rise to ‘Surface
Enhanced Raman Spectroscopy’ (SERS). This is a very sensitive technique and has
proved to be capable of detecting a single molecule.
SERS was demonstrated by recording Raman spectra of the sample molecules adsorbed
on various specially prepared SER-active surfaces both in the form of a colloidal
suspension and on the solid roughened surfaces. Using a gold colloidal suspension,
pyridine has been detected down to 10-11 molar (M) concentration. A silver slab was
roughened to a dimension of a nano-scale by etching in nitric acid solution to make
SER-active surface. Pentaerythritol Tetranitrate (PETN) explosive was detected using
this surface after its 10-2 M solution was dropped, dried and washed (of any residue)
from the surface. Lithographically engineered silver structures in the form of nanoarrays
having a number of silver structures of approximately 106 in a region of 0.1 mm2
have been used for SERS. The major noise contribution to the scattering from
impurities in an ordinary glass substrate has been eliminated by replacing glasses as
substrates with pure quartz discs. The headspace vapours from peroxide explosives,
Triacetone Triperoxide (TATP) and Hexamethylene Triperoxide Diamine (HMTD),
were detected at approximately 70 parts per million (ppm) and 0.3 ppm concentrations
respectively using a portable commercial Raman Spectrometer. PETN was also detected
from its headspace vapour at about 18 parts per trillion (ppt) in spite of it having a much
lower vapour pressure.
The possibility of desorption of adsorbed molecules from a nano-structured surface by
laser irradiation has been demonstrated experimentally with the aim of reusability of
SER-active surfaces. Also demonstrated was the enhancement in Raman intensity
through resonance Raman effect spectroscopy for the future use in surface enhanced
resonance Raman spectroscopy (SERRS).
17
Howie, Wendy Helen. "Molecular structure and predissociation dynamics studied using absorption spectroscopy and ion imaging." Thesis, University of Bristol, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364886.
Повний текст джерела
18
Kiwanuka, Ssegawa-Ssekintu. "Supercontinuum radiation for ultra-high sensitivity liquid-phase sensing." Thesis, University of Cambridge, 2014. https://www.repository.cam.ac.uk/handle/1810/245137.
Повний текст джерелаАнотація:
The real-time detection of trace species is key to a wide range of applications such as on-line chemical process analysis, medical diagnostics, identification of environmentally toxic species and atmospheric pollutant sensing. There is a growing demand for suitable techniques that are not only sensitive, but also simple to operate, fast and versatile. Most currently available techniques, such as spectrophotometry, are neither sensitive enough nor fast enough for kinetic studies, whilst other techniques are too complex to be operated by the non-specialist. This thesis presents two techniques that have been developed for and applied to liquid-phase analysis, with supercontinuum (SC) radiation used for liquid-phase absorption for the first time. Firstly, supercontinuum cavity enhanced absorption spectroscopy (SC-CEAS) was used for the kinetic measurement of chemical species in the liquid phase using a linear optical cavity. This technique is simple to implement, robust and achieves a sensitivity of 9.1 × 10−7 cm−1 Hz−1/2 at a wavelength of 550nm for dye species dissolved in water. SC-CEAS is not calibration-free and for this purpose a second technique, a time-resolved variant called broadband cavity ring-down spectroscopy (BB-CRDS), was successfully developed. Use of a novel single-photon avalanche diode (SPAD) array enabled the simultaneous detection of ring-down events at multiple spectral positions for BB-CRDS measurements. The performance of both techniques is demonstrated through a number of applications that included the monitoring of an oscillating (Belousov-Zhabotinsky) reaction, detection of commercially important photoluminescent metal complexes (europium(III)) at trace level concentration, and the analysis of biomedical species (whole and lysed blood) and proteins (amyloids). Absorption spectra covering the entire visible wavelength range can be acquired in fractions of a second using sample volumes measuring only 1.0mL. Most alternative devices capable of achieving similar sensitivity have, up until now, been restricted to single wavelength measurements. This has limited speed and number of species that can be measured at once. The work presented here exemplifies the potential of these techniques as analytical tools for research scientists, healthcare practitioners and process engineers alike.
19
Johnson, Brian Ivins. "Preparation and Detailed X-Ray Photoelectron Spectroscopy and Spectroscopic EllipsometryAnalysis of Ultrathin Protective Coatings." BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/8119.
Повний текст джерелаАнотація:
Ultra-thin films (UTFs) are important in many applications, seen in the semiconductor industry, in chromatography, in sensing, in microfluidics, in aerospace, and in robotics. They also protect materials from corrosion, change surface energies, limit water intrusion into materials, allow material self-cleaning and self-healing, provide scratch resistance, and impart other specific chemical properties. In many cases, UTFs drastically alter surface properties and therefore their applications. It is imperative that proper and consistent characterization be performed on coatings to confirm and understand their desired properties. In Chapter two, Al oxidation under MgF2 protective layers is studied using real time X-ray photoelectron spectroscopy (XPS), and spectroscopic ellipsometry (SE). These tools allowed me to monitor Al oxidation for both short (hours) and long (months) periods of time. XPS revealed the chemical changes that took place in these materials as a function of time, and these changes were verified with SE. These studies help increase an understanding of aluminum changes under MgF2 protective layers. The third chapter demonstrates ab initio calculations guided X-ray photoelectron spectroscopy (XPS) analysis of surfaces functionalized with fluorinated silanes. This study addresses deficiencies in the literature where CF2:CF3 ratios from experimental XPS data do not match theoretical CF2:CF3 ratios. In a systematic approach, I developed semi-empirical models directed both by ab initio calculations and adjustable, empirical parameters. These models were effective in describing the raw data and exceeded fitting methods used in literature. In Chapter four, SiO2 UTFs with variable thicknesses deposited on Eagle XG® glass substrates are characterized. Challenges associated with this work consisted of similar optical functions of the film and substrate as well as backside reflections from the substrate. These obstacles were met using a multi-sample analysis (MSA), a variable angle spectroscopic ellipsometric approach, and mechanical abrasion/roughening of the substrate backside. With these approaches, I developed a model that precisely fit the data collected from all the samples and gave the correct optical function of the material along with thickness values for each film. Surface characterization represents a commitment of resources. It takes time to make measurements, and it takes time to analyze and understand the results. As presented in this work, I increase understanding of ultra-thin films at interfaces using both a multi-tool approach as well as using multiple analytical methods on data collected from each tool.
20
Zhao, Yanning. "Hertz-level ultra-stable laser and its application to high precision spectroscopy." kostenfrei kostenfrei, 2009. http://d-nb.info/1000056449/34.
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21
Patterson, Claire Siobhan. "Portable spectroscopy system for ultra-sensitive, real-time measurement of breath ethane." Thesis, University of Glasgow, 2009. http://theses.gla.ac.uk/538/.
Повний текст джерелаАнотація:
This thesis describes the development, characterisation and application of a portable spectroscopy system for ultra-sensitive, real-time detection of breath ethane. In healthcare, breath ethane is a widely accepted marker of free radical-induced cell damage and may be used to indicate changes in oxidative stress. The aim was to deliver a compact instrument capable of long-term, on-site use in a clinical environment, while also retaining the high performance previously achieved by lab-based systems at the University of Glasgow. The newly developed instrument has a sensitivity of 70 parts per trillion with a 1 Hz sampling rate. The system incorporates a cryogenicallycooled lead-salt laser and uses a second derivative wavelength modulation detection scheme. A thermally-managed closed-loop refrigeration system has eliminated the need for liquid coolants. The instrument has been field-tested to ensure target performance is sustained in a range of environments, both indoor and outdoor. It has since been used in a number of pilot clinical studies, both off-site and on-site, in which breath ethane was monitored as a marker of oxidative stress. The three main clinical areas investigated were dialysis, radiotherapy and intensive care. In the intensive care study, the instrument was modified to enable automatic breath sampling of inspired and expired gases of ventilated patients. This technique proved highly successful and the instrument then remained at the Southern General hospital, where it continued to be used as part of a wider study into breath ethane in intensive care patients. The use of the new spectroscopy system has enabled ultra-sensitive, rapid analysis of a large number of breath samples. The use of the new instrument, in particular for continual breath monitoring, has enabled the detection of short-lived fluctuations in breath ethane, yielding some interesting findings in a number of pilot clinical studies. Our results suggest that breath ethane may be used as an indicator of dynamic changes in oxidative stress. Further studies will be required to determine if such monitoring is of clinical benefit. Chapter 1 gives a general introduction to spectroscopy and some background to our project. A number of spectroscopic techniques and laser sources are discussed, along with a review of previous work in ethane detection. In chapter 2 some background theory of molecular spectroscopy is given, with a more detailed discussion of the wavelength modulation technique. Chapter 3 describes in detail the development of the portable spectroscopy system. The achieved performance and factors contributing to this performance are discussed in chapter 4. The field test of the instrument is reported on in chapter 5. In chapter 6 the application of the technology to breath analysis and the current challenges in this field are discussed. Example breath ethane measurements for healthy controls are provided. The clinical pilot studies conducted using the new system in areas of dialysis, intensive care and radiotherapy are discussed in chapters 7, 8, and 9 respectively. Chapter 10 contains the thesis summary and conclusions, with suggestions for future work.
22
Fernandes, Carolina C. "Multinuclear magnetic resonance spectroscopy in the human brain at ultra high-field." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/46607/.
Повний текст джерелаАнотація:
In this thesis, new acquisition and analysis methods are described for multinuclear magnetic resonance spectroscopy (MRS) for the quantification of brain metabolites at ultra high magnetic field strengths (7T). An analytical model was derived for the optimisation of the stimulated echo acquisition mode (STEAM) sequence timing parameters for lactate detection. The effects of the chemical shift displacement artefact on the J-modulated signal for a weakly-coupled spin system were considered in the three applied directions of field gradients and the product operator formalism was used to obtain expressions for the signal modulation in each compartment of the excited volume. The validity of this model was demonstrated experimentally in a phantom and acquisitions with optimised parameters were performed on a healthy volunteer. The spectra acquired with an echo time (TE) of 144 ms and with an optimised mixing time and TE of 288 ms showed easily detectable lactate peaks in the normal human brain. Additionally, the acquisition with the longer TE resulted in a spectrum with less lipid/macromolecular (MM) contamination. The simulations demonstrated that the proposed analytical model is suitable for correctly predicting the resulting lactate signal. With the optimised parameters, it was possible to use a simple sequence with sufficient signal-to-noise ratio (SNR) to reliably distinguish lactate from overlapping resonances in a healthy brain at ultra high-field. Estimation of metabolic changes during neuronal activation represents a challenge for in vivo MRS, especially for metabolites with low concentration and signal overlap, such as lactate. This thesis also includes work focused on the reliable quantification of lactate during a paradigm with 15 minutes of visual stimulation. The lipid and MM signals were significantly reduced by using a long TE (144 ms) sequence and the remaining MM signals in the vicinity of the lactate peak were individually fitted with simulated Lorentzian peaks, to ensure a good fit of the inverted lactate doublet. Statistically significant changes in lactate (~10%) and glutamate (~3%) levels during stimulation were detected in the visual cortex and agree with previous measurements. Furthermore, the use of a prolonged stimulation period unveiled a distinctive metabolic response pattern, which can provide further insight into brain activation mechanisms. 13C MRS combined with the infusion of labelled substrates is able to provide unique information on the relationship between neuroenergetics and brain function. However, the lack of sensitivity associated with the general complexity of 13C experiments has hampered its widespread use for research into human brain disease. In this study, a new methodology for acquisition and analysis of 13C signal is presented for the study of neuroenergetics and neurotransmission in a deep brain structure - anterior cingulate cortex - that is thought to play a major role in the processing of sensory information and can be impaired in patients with schizophrenia. In vitro testing was performed to evaluate the performance of the implemented sequence for signal localisation and polarisation transfer, both proving adequate for the intended purpose. In vivo data were acquired in four subjects, one diagnosed with early schizophrenia, with a protocol which involved 60 minutes of infusion of [1-13C]glucose. Turnover curves for the labelled products were generated from the dynamic 13C spectra with a temporal resolution of 10 minutes and were in agreement with the ones obtained from rodent experiments. Therefore, the feasibility of 13C experiments for the study of psychosis was here demonstrated, taking advantage of the increase in SNR at ultra high-field for determination of metabolic fluxes.
23
Smith, Richard. "Optical measurement of ultra fine linewidths using artificial neural networks." Thesis, University of Nottingham, 2006. http://eprints.nottingham.ac.uk/10418/.
Повний текст джерелаАнотація:
Measuring fine track widths with optical instruments has become increasingly difficult as the dimensions of the features of interest have become smaller than the traditional optical resolution limit. This has caused a move to non-optical methods such as scanning electron and atomic force microscopy techniques, or novel optical methods combined with signal processing techniques to provide measurements of these samples. This thesis presents one method to increase the measurement capabilities of an optical system. This is achieved by combining an optical profiler such as a scanning interferometer, with an artificial neural network (ANN). Once trained the ANN can calculate the object parameter for other tracks not contained in the training set. This process works extremely well; with experimental results showing that a 60nm track width can be calculated with a 2nm error using an optical system with a spot size of 2.6 microns. The technique can be extended to obtain other parameters such as height, sidewall slope and for other structures such as double tracks. Various aspects of the ANNs have been investigated, such as the training range, the size of network and the impact of noise etc. These studies show that the technique is extremely robust, and has huge potential for general usage.
24
Lehec, Henri. "Spectroscopie Rydberg et excitation du coeur isolé d'atomes d'ytterbium ultra-froids." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS566/document.
Повний текст джерелаАнотація:
Les atomes de Rydberg constituent des objets idéaux pour l’étude des systèmes physiques en interaction à longue portée. Transposer à ces atomes très excités les techniques habituelles d’imagerie et de piegeage des atomes froids offrirait de nouvelles opportunités pour le domaine de la simulation quantique. Notre approche consiste à utiliser un atome à deux électrons de valence optiquement actifs tel que l’ytterbium. En effet, les transitions optiques du coeur ionique de cet atome ouvrent la voie à de nombreuses perspectives pour la manipulation optique dans l'état de Rydberg. Lorsque l’atome est doublement excité, il peut néanmoins auto-ioniser puisque son énergie se situe au delà de la première limite d’ionisation. La possibilité de s’affranchir totalement de l’autoionisation est une question ouverte.Dans cette thèse, nous présentons en premier lieu les contributions apportées au montage de l’expérience,du refroidissement des atomes d’ytterbium sur la raie d’intercombinaison à l’excitation dans des états de Rydberg. A cause des interactions entre électrons de valence, la spectroscopie de ces états très excités est plus complexe dans l'ytterbium que dans les atomes alcalins. Une étude expérimentale couplée à une analyse par théorie du défaut quantique à plusieurs voies (MQDT) a été réalisée sur diverses séries Rydberg (s, p, d et f). Cette étude, prérequis essentiel, a permis d’améliorer la précision de plus de deux ordres de grandeur sur la spectroscopie des séries étudiées.L’excitation du coeur ionique a ensuite été mise en place sur la transition 6s1/2 → 6p1/2 . Nous avons alors étudié expérimentalement et théoriquement l’excitation du coeur isolé pour des états de Rydberg de grand moment orbital (l = 5 - 9). Cette étude a montré que l'auto-ionisation est dominée par le couplage au continuum de l'état de coeur 5d3/2. Par opposition a l'atome de baryum, pour lequel l'autoionisation chute rapidement avec le moment orbital de l'électron Rydberg, nous avons montré que cette tendance est moins marquée sur l'ytterbium. Grace à cette étude, nous pourrons déterminer les états pour lesquels la manipulation optique par laser est possibleRydberg atoms offer an ideal platform for the study of long-range interacting systems.However, usual techniques for imaging and trapping are unavailable in alkali Rydberg atoms. Our approach rely on the use of a two-optically-active-valence-electrons atom such as ytterbium. Ionic core transitions of this atom offer new perspecives for optical manipulation in the Rydberg state. However,questions remain open, especially on the possibilities of avoiding the autoionization, process which occurs when the atom is doubly excited.In this thesis, we report on the construction of the experiment, from the cooling and trapping of theatoms to the excitation in Rydberg states. Because of the interactions between valence electrons, the spectroscopy of these highly excited states is relatively complicated. An experimental study, coupled to a multi-channel quantum defect analysis (MQDT) has been done on the s,p,d and f Rydberg series. This study produced an improvement on the precision of the spectroscopy of this series by more than two orders of magnitude. We then studied the isolated core excitationon the 6s1/2 -> 6p1/2 transition for Rydberg states of large orbital quantum numbers (l=5-9). This study showed that auto-ionisation is mostly due to the coupling to the continuum of the 5d3/2 core state. In opposition to the barium atom, where auto-ionisation drops rapidly with the orbital quantum number, we have shown that ytterbium is less favourable to that extent. Thanks to this study we will be able to determine which states are good candidates for the optical manipulation
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Marble, Daniel Keith. "Fluorine K-Shell X-Ray Cross Section Measurements for ⁷Li, ¹⁰B, ¹²C, ¹⁴N, and ¹⁶O Ions on Ultra-Clean, Ultra-Thin Yf₃ Solid Target Foils." Thesis, University of North Texas, 1991. https://digital.library.unt.edu/ark:/67531/metadc332734/.
Повний текст джерелаАнотація:
In this study, procedures were developed to produce ultra-clean, ultra-thin target foils and to remove x-ray interference from electron bremsstrahlung and low energy K-shell x-rays from contaminant elements.
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Amiri-Hezaveh, A. "Photelectron spectroscopy of ultra-thin epitaxial f.c.c. magnetic films of iron and cobalt." Thesis, University of Cambridge, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233668.
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Roland, Thomas. "Ultrafast spectroscopy of new organic molecules for photovoltaic applications." Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAE009/document.
Повний текст джерелаАнотація:
Cette thèse porte sur l'étude de nouvelles molécules organiques par différentes méthodes de spectroscopie. La combinaison de techniques de fluorescence résolue en temps, d'absorption différentielle résolue en temps et de spectro-électro-chimie avec des méthodes d'analyse globale permet de déterminer la photo-dynamique des molécules étudiées.Deux familles de molécules ont été étudiées. La première est une antenne de type donneur basée sur le pigment BODIPY. La seconde consiste en une triade donneur-accepteur-donneur (DAD) ayant des propriétés d'auto-organisation. Après une première génération de mol écules dont on a montré les limitations (temps de vie de l'état transfert de charge très court, d'environ 55 ps), une seconde génération de mol écules a été développée, incluant de nombreuses variations du groupe donneur, ce qui a permis de déterminer l'impact des-dites variations. Entre autres, un temps de vie de l'état transfert de charge de plus d'une nanoseconde est observéThe topic of this thesis is the study -through different spectroscopy methods- of new organic molecules for photovoltaic applications. Combination of time resolved fuorescence, time resolved differential absorption and spectro-electro-chemistry with global analysis methods allowed to determine the photo-dynamics of the studied molecules. Two familiesof molecules have been studied. The first one is a donor-type antenna based on the BODIPY dye. The second consists in a donor-acceptor-donor (DAD) triad, with self-organizing properties. After a first generation of molecules that we proved to be limited by a short life time of its charge transfer state (about 55 ps), a second generation of molecules wasdeveloped, including several variation of the donor group, which allowed to study the impact of said variation. Among others, a charge transfer state lifetime longer than 1 nanosecond was observed
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Xu, Lei. "Development and application of ultra-sensitive fluorescence spectroscopy and microscopy for biomolecular interaction studies." Doctoral thesis, KTH, Experimentell biomolekylär fysik, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-146181.
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This thesis describes the development of sensitive and high-resolution fluorescence spectroscopic and microscopic techniques and their application to probe biomolecules and their interactions in solution, lipid membrane model systems and in cells. Paper I-IV are largely focused on methodological developments. In paper I, a new fluorescence method based on fluorescence correlation spectroscopy (FCS) for detecting single particles was realized, requiring no fluorescent labeling of the particles. The method can yield information both about the diffusion properties of the particles as well as about their volumes. In paper II, a modified fluorescence cross correlation spectroscopy procedure with well characterized instrumental calibration was developed and applied to study cis interactions between an inhibitory receptor and its Major Histocompatibility Complex class I ligand molecule, both within the same cellular membranes. The quantitative analysis brought new insights into the Nature killer cell’s self-regulating of tolerance and aggressiveness for immune responses. Paper III describes a multi-color STED (STimulated Emission Depletion) microscopy procedure, capable of imaging four different targets in the same cells at 40nm optical resolution, which was developed and successfully demonstrated on platelets. In paper IV, a modified co-localization algorithm for fluorescence images analysis was proposed, which is essentially insensitive to resolutions and molecule densities. Further, the performance of this algorithm and of using STED microscopy for co-localization analysis was evaluated using both simulated and experimentally acquired images. Papers V-VII have their main emphasis on the application side. In paper V, transient state imaging was demonstrated on live cells to image intracellular oxygen concentration and successfully differentiated different breast cancer cell lines and the different metabolic pathways they adopted to under different culturing conditions. Paper VI describes a FCS-based study of proton exchange at biological membranes, the size-dependence of the membrane proton collecting antenna effect as well as effects of external buffer solutions on the proton exchange, in a nanodisc lipid membrane model system. These findings provide insights for understanding proton transport at and across membranes of live cells, which has a central biological relevance. In paper VII, STED imaging and co-localization analysis was applied to analyze cell adhesion related protein interactions, which are believed to have an important modulating role for the proliferation, differentiation, survival and motility of the cells. The outcome of efforts taken to develop means for early cancer diagnosis are also presented. It is based on single cells extracted by fine needle aspiration and the use of multi-parameter fluorescence detection and STED imaging to detect protein interactions in the clinical samples. Taken together, detailed studies at a molecular level are critical to understand complex systems such as living organisms. It is the hope that the methodologies developed and applied in this thesis can contribute not only to the development of fundamental science, but also that they can be of benefit to mankind in the field of biomedicine, especially with an ultimate goal of developing novel techniques for cancer diagnosis.QC 20140609
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Sharshavina, Ksenia. "Nouveaux concepts de filtres spectraux ultra-sélectifs pour spectroscopie embarquée." Thesis, Toulouse 3, 2016. http://www.theses.fr/2016TOU30264/document.
Повний текст джерелаАнотація:
Les filtres spectraux à réseaux résonants, ou GMRF (Guided-Mode Resonance Filters), sont une nouvelle génération de filtres à bande étroite et constituent une alternative très prometteuse aux filtres conventionnels multicouches Fabry-Pérot. Le pic de résonance d'un GMRF peut être très fin spectralement et de longueur d'onde de centrage accordable en fonction de l'angle d'incidence. Ces propriétés sont particulièrement importantes pour la spectroscopie. Les travaux antérieurs ont permis de mettre en œuvre une structure originale comportant deux réseaux 1D croisés. Les performances de ce filtre surpassent celles des filtres conventionnels par leur réponse spectrale subnanométrique, leur accordabilité, et leur capacité à s'affranchir de l'influence de la polarisation de l'onde incidente sous incidence oblique. Le but de ce travail est d'explorer les performances ultimes de ce type de dispositif en termes de résolution et taux de réjection, par une approche mêlant théorie, technologie et caractérisation. Nous présentons des résultats expérimentaux d'un filtre en réflexion indépendant de la polarisation, accordable sur 40 nm avec 8.3nm/° d'accordabilité, ayant une réflexion de 10-3 sur une plage de 90nm en dehors de la résonance et un facteur de qualité supérieur à 5000Guided Mode Resonance Filters ( GMRF ) are a new generation of narrowband optical filters and are a very promising alternative to conventional multilayer Fabry-Perot filters. The resonance peak of GMRF can be spectrally extremely thin and with a centering wavelength tunable according to the angle of incidence of the light. These properties are particularly important for spectroscopy. Previous works have helped to implement an original structure with two 1D crossed gratings. The performance of this filter overpasses those of conventional filters in their spectral subnanometric response, tunability and their ability to overcome the influence of the polarization of the incident wave under oblique incidence. The aim of this work is to explore the final performances of such devices in terms of resolution and rejection rate, thanks to an approach combining theory, fabrication technology and characterization. We present experimental results of a polarization independent reflective filter, tunable over 40nm with a tunability of 8.3nm / °, having a reflection of 10-3 on a 90nm range outside the resonance and a quality factor over 5000
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Butcher, V. A. "Studies of some reactive intermediates in the gas-phase by ultra-violet photoelectron spectroscopy." Thesis, University of Southampton, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381210.
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Persuy, Déborah. "Nanoscopie résolue en temps : étude de la réponse spatiale et temporelle pour l'imagerie ultra-rapide." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAE016/document.
Повний текст джерелаАнотація:
Nous nous intéressons au développement ainsi qu’à la modélisation théorique de techniques de spectroscopie optique de champ lointain capables de coupler résolutions spatiale et temporelle grâce à l’utilisation de faisceaux d'excitation mis en forme spatialement. Nous établissons, théoriquement et expérimentalement, que dans une expérience de mélange de quatre ondes réalisée avec des faisceaux de Laguerre-Gauss, la charge totale du moment orbital est conservée. Nous montrons comment cette propriété peut être mise à profit pour travailler en géométrie colinéaire dans le but d’améliorer la résolution spatiale des expériences. Dans une deuxième partie, nous présentons une technique de spectroscopie « pompe-sonde » résolue spatialement que nous avons conçue et développée : l’imagerie temporelle est obtenue via la détection interférométrique des variations d’indice d’un matériau vues par une sonde étendue et consécutives à l’excitation par une impulsion pompe focalisée à la limite de diffraction. Nos modélisations démontre d’un tel montage associé à l’emploi d’une impulsion pompe modulée spatialement doit permettre, grâce au battement entre les fréquences spatiales des inhomogénéités de l’échantillon et de la modulation spatiale de l’excitation, de dépasser la limite de RayleighThis work focuses on developing and modelling far-field spectroscopic methods that couple spatial and time resolutions by using beam-shaping. In a first part, we demonstrate, theoretically and experimentally, that generating a signal in a four-wave mixing experiment performed with Laguerre-Gauss beams, implies the conservation of the total charge of the orbital momentum. We show that this specificity can be used to perform experiments with collinear beams in order to improve spatial resolution. In a second part, we present a time- and spatially-resolved pump-probe technique of our own design: time-resolved imaging is obtained by the interferometric detection of variations in the refraction index of a material, undergone by a wide probe and induced by a diffraction-limited pump-pulse. Improving such an experiment set-up with a spatially-modulated pump-pulse should enable, thanks to the beating between spatial frequencies of sample inhomogeneities and the excitation spatial-modulation, to increase spatial resolution go the Rayleigh criterion
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Lelaidier, Tony. "Organic semiconductor characterisation by scanning tunnelling microscopy and optical spectroscopy." Thesis, Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4032/document.
Повний текст джерелаАнотація:
Les propriétés électroniques et d'autoassemblage de deux composés organiques, le DHTAP et le bis-pyrène, ont été étudiées par microscopie à effet tunnel (STM), sous ultra-vide et à basse température. Les propriétés optiques ont été étudiées par spectroscopie en cavité résonnante (CRD), également sous ultravide.La croissance du DHTAP a été étudiée sur différents métaux nobles. La croissance du bis-pyrène a été étudiée sur Au(111). Dans chaque cas, les conditions de température idéales pour la formation d’une première couche organisée ont été déterminées. Différents modèles sont proposés pour les structures observées en première couche. La formation de la seconde couche moléculaire à également été étudiée.L'évolution des propriétés optiques, étudié par CRD, du bis-pyrène déposé sur du verre borosilicate combinée aux informations obtenues par STM ont permit d’associer ces modifications aux interactions des moments dipolaires de transition des molécules de la première et de la seconde couche et on également permit de déterminer le mode de croissance.Finalement, la possibilité d’induire des modifications chimique de la molécule de DHTAP, intégrée dans une couche auto-assemblée, en utilisant le courant tunnel du STM a été observé. Il s’avère que la molécule de DHTAP intégrée en première couche peut subir une double déshydrogénation pour conduire à la formation d’un composé identifié comme étant le 5,7,12,14-tetraazapentacene (TAP). En seconde couche, la formation de deux radicaux, en plus du TAP, a été observé. La molécule de TAP présente un certain intérêt du fait qu’elle n’est pas synthétisable pas les méthodes conventionnelle de chimie organiqueElectronic and self-assembling properties of two organic compound, the DHTAP and the bis-pyrene, have been studied by the means of low temperature scanning tunnelling microscopy (STM) under ultrahigh vacuum conditions. Optical properties have been studied by cavity ring-down (CRD) spectroscopy, also under ultrahigh vacuum conditions.The growth of DHTAP has been studied on different metallic substrate. The growth of bis-pyrene has been studied on Au(111). In each case, the optimal temperature conditions for the formation of a well-ordered first monolayer have been determined. The formation of second monolayers has also been studied. The evolution of the optical properties, studied by CRD, of bis-pyrene deposited on borosilicate glass combined with information obtained from STM allow us to identify these modifications as interactions between transition dipole moments of molecules in the first and in the second layer, and also determine the growth mode.Finally, the possibility to induce chemical modification of DHTAP molecules embedded in an ordered monolayer using the tunnelling current of the STM has been studied. It appears that the molecule embedded in the first ML can be doubly dehydrogenated which leads to the formation of a compound identified as 5,7,12,14-tetraazapentacene (TAP). In the second layer, the formation of two radicals in addition to the TAP has been observed. The TAP molecule is interesting because of that it cannot be synthesized using common organic chemical methods
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Gratz, Marcel, and Petrik Galvosas. "Methodical aspects of 2D NMR correlation spectroscopy under conditions of ultra high pulsed field gradients." Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-193228.
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Gratz, Marcel, and Petrik Galvosas. "Methodical aspects of 2D NMR correlation spectroscopy under conditions of ultra high pulsed field gradients." Diffusion fundamentals 6 (2007) 6, S. 1-2, 2007. https://ul.qucosa.de/id/qucosa%3A14181.
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Isaienko, Oleksandr. "Development of ultra-broadband ultrafast infrared sources and applications to nonlinear vibrational spectroscopy of interfaces." Diss., Temple University Libraries, 2011. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/141408.
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ChemistryPh.D.
Interfaces play a crucial role in the exchange of energy and matter in various physical, chemical and biological systems. A particular interest has been to study interfaces between aqueous phases and various minerals because of their importance in understanding geochemical phenomena as well as for applications such as enhanced oil recovery. The nonlinear optical technique of vibrational sum-frequency generation (SFG) spectroscopy, introduced over 20 years ago, has become a powerful tool to investigate various surfaces, in particular, mineral-water interfaces. One of the challenges of the SFG spectroscopy of aqueous surfaces is the need to tune the central frequency of relatively narrowband IR lasers through the broad range of the OH-stretch frequencies of water molecules (3000 - 4000 cm-1). We have developed a novel ultrabroadband IR laser source that generates infrared pulses in the ~2800-6000 cm-1 range (lambda~3300-1800 nm) with bandwidths Delta(nu)>1000 cm-1, and bandwidths >2000 cm-1 in the near-IR range (lambda~1000-2000 nm). Pulse front tilt of signal pulse has been corrected allowing for compression of signal pulses down to 25 fsec. Such ultrabroadband IR pulses allow us to perform SFG spectroscopy of aqueous surfaces over the entire frequency range of water molecule spectrum (extending from ~2900 cm -1 to ~3800 cm -1) simultaneously, without tuning the laser ("in one shot"). We have used this novel ultrabroadband IR source to investigate the vibrational SFG spectra of silica/water interfaces. The high signal-to-noise ratio of our spectroscopic setup has allowed us to study low-intensity features that were not studied in detail, or recognized previously in the SFG-spectroscopy investigations, including: 1) non-hydrogen bonded OH vibrations at hydrophilic silica/water interfaces; 2) combination [stretch+bend] bands of water at the silica surface appearing at ~5000-5200 cm -1. 3) Overtones of water stretching modes at silica/water interfaces. The most important conclusions from these studies are outlined below. 1. Non-hydrogen bonded hydroxyls at silica/water interface. Typically SFG-studies of mineral/water interfaces (in particular, silica/water) have focused on the most pronounced features - peaks of H-bonded hydroxyls at ~3150 and ~3450 cm -1. We have been able to systematically observe and study a weaker peak at ~3670 - 3700 cm -1. This peak becomes more pronounced as the pH of aqueous phase decreases, as well as the ionic strength increases, indicating that the hydroxyls corresponding to this spectral feature are situated in a very close proximity to the surface. Isotopic dilution experiments indicate that the 3700 cm -1 feature is not due to asymmetric OH stretches as was suggested before. Based on our results, we suggest that this spectral feature corresponds to hydroxyls of water molecules at the silica surface that cannot hydrogen bond with silanol groups because of the lower density of silanols compared to H2O. We believe this to be the first surface-specific study of non-hydrogen bonded hydroxyls at silica, a surface widely accepted as hydrophilic. 2. SFG spectroscopy of [ν(OH)+δ(HOH)] combination bands of water at silica surface. We have extended SFG spectroscopy of the interfacial hydroxyls at mineral/water surfaces into the near-IR frequency range. The studies of overtones of interfacial OH(OD) groups will provide information on the anharmonicity of such species, and thus on the energy of dissociation. In addition, the positions of the overtone frequencies of the hydroxyls are more sensitive to interactions with the environment than the fundamental stretch frequencies. Our particular focus has been to study the stretch+bend combination band nu comb nu;(OH)+delta;(HOH) of liquid water which occurs in the near-IR spectral range at ~5000-5200 cm -1. It is typically much weaker in the FTIR absorption spectra than the fundamental transitions of the OH stretches or HOH bending, similar to overtones of these modes. We have performed, what we believe to be, the first surface-specific vibrational SFG spectroscopic measurements of combination bands of water molecules at silica surfaces. SFG spectroscopy of water combination band allows access to the water bending mode (delta~1600 cm -1), which still has not been observed in sum-frequency.
Temple University--Theses
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Qian, Ximei. "Applications of third generation synchrotron radiation in vacuum ultra-violet (VUV) photoionization spectroscopy and dynamics /." For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2003. http://uclibs.org/PID/11984.
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Hensen, Matthias [Verfasser]. "Concentrating Light: Nano-devices for spectroscopy, ultra-fast current injection and coherent energy transport / Matthias Hensen." Bielefeld : Universitätsbibliothek Bielefeld, 2016. http://d-nb.info/1105645533/34.
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Markmann, Sergej [Verfasser], Nathan [Gutachter] Jukam, and Andreas D. [Gutachter] Wieck. "Ultra-fast spectroscopy of terahertz quantum cascade lasers / Sergej Markmann ; Gutachter: Nathan Jukam, Andreas D. Wieck." Bochum : Ruhr-Universität Bochum, 2016. http://d-nb.info/1121909620/34.
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Chen, Sophia Nan. "X-ray spectroscopy of buried layer foils irradiated with an ultra high intensity short pulse laser." Diss., [La Jolla] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p3352706.
Повний текст джерелаАнотація:
Thesis (Ph. D.)--University of California, San Diego, 2009.Title from first page of PDF file (viewed June 16, 2009). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 117-126).
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Palaniyappan, Sasikumar. "Relativistic rescattering and multi-electron ionization of atoms and molecules in ultra-strong laser fields." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 174 p, 2008. http://proquest.umi.com/pqdweb?did=1597616071&sid=3&Fmt=2&clientId=8331&RQT=309&VName=PQD.
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Lopez, Kolkovsky Alfredo L. "1H and 31P NMR Spectroscopy for the study of brain metabolism at Ultra High Magnetic Field from Rodents to Men." Thesis, Paris 11, 2015. http://www.theses.fr/2015PA112080/document.
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La Spectroscopie RMN (SRMN) du 1H et du 31P permet de détecter et de mesurer in vivo de façon non-invasive la concentration de composés biologiques qui sont pertinents à l’étude des aspects variés du métabolisme cérébral comme la neurotransmission (glutamate, GABA), la densité neuronale (N-acetyl-aspartate) et gliale (myo-inositol) ou le métabolisme énergétique (phosphocreatine, ATP), entre autres. Ainsi, l’analyse des profils biochimiques permet d’étudier longitudinalement l’évolution de la physiologie cérébrale en conditions pathologiques ou normales. Par ailleurs, à ultra-haut champ magnétique la SRMN bénéficie d’une sensibilité et d’une résolution spectrale accrues, maximisant l’information métabolique exploitable. Au cours de cette thèse, nous nous sommes surtout intéressés à l’étude du vieillissement cérébral normal. Une étude longitudinale en 1H et 31P a été menée in vivo à 17.2 Tesla afin de suivre les altérations métaboliques pendant 14 mois chez deux cohortes de rats Dark Agouti âgés d’un mois et 8 mois au départ de l’étude. Les concentrations ainsi que les temps de relaxation T1 et T2 de plus de 20 métabolites ont été mesurés jusqu’à l’âge de 22 mois. Nous avons notamment observé une augmentation des concentrations de myo-inositol et des macromolécules dans les 4 volumes d’intérêt (VOI) étudiés. Dans le VOI Main, comprenant principalement du cortex mais aussi du corps calleux et de l’hippocampe, ces changements métaboliques ont été accompagnés par une augmentation des niveaux de glutamine et de composés contenant de la choline (tCho). Ces observations sont cohérentes avec une possible neuro-inflammation modéré au cours du vieillissement. Aucun changement du NAA a été observé sur le Main VOI, thalamus et putamen caudé (striatum). Additionnement, une réduction des temps T2 pour le NAA total, la tCho et les macromolécules a été observée, en accord avec une altération du milieu cellulaire et une accumulation de fer dans les tissus avec l’âge. Etonnamment, nous avons observé un effet corrélé avec le nombre d’examens RMN, qui a été fortement manifesté par une augmentation significative des temps T1 de nombreux métabolites.Un deuxième axe de travail pendant cette thèse a été la mise en place des outils méthodologiques nécessaires à la réalisation des études par SRMN du 1H et du 31P à 7 Tesla chez l’homme. Des séquences d’imagerie spectroscopique 2D ont été développées pour obtenir des cartes de concentration des métabolites 31P et 1H respectivement par la sélection d’une coupe ou bien d’un voxel par écho-stimulé. Un schéma de suppression d’eau WET a été optimisé pour son application à 7 T. Des modes d’excitation et de saturation du signal extérieur (OVS) en « anneau » ont été implémentés avec la méthode de transmission parallèle pour son application en imagerie spectroscopique 1H par l’optimisation des configurations statiques d’excitation ou « shimming-B1 ». Cette approche a permis d’appliquer des champs d’excitation plus homogènes et de réduire le dépôt d’énergie chez le sujet par rapport à l’utilisation des bandes OVS classiques. Des expériences in vitro ont été menées pour démontrer leur faisabilité. Enfin, un module de saturation BISTRO a été implémenté pour l’acquisition in vivo de cartes métaboliques en 31P. L’efficacité du module BISTRO a été démontrée et ce module peut être adapté pour des expériences 31P de transfert d’aimantation, ouvrant la voie de l’étude du métabolisme énergétique cérébral chez l’homme à très haut champ magnétique1H and 31P nuclear magnetic resonance spectroscopy allows to detect and to measure in vivo and non-invasively the concentrations of biologically relevant compounds associated to metabolic processes such as neurotransmission (glutamate, GABA), neuronal and glial density (N-acetyl-aspartate, myo-inositol) and energetic metabolism (phosphocreatine, ATP) among others. Knowledge of the biochemical profile provides a mean to evaluate the metabolic state of the brain in pathological cases or in evolving physiological conditions, such as aging. Yet, the neural basis of age-related cognitive dysfunction in normal brain aging remains to be elucidated and it has been shown to develop at different rates depending on the structural region.At ultra-high magnetic fields, magnetic resonance spectroscopy (MRS) benefits from an increased signal-to-noise ratio and a higher chemical shift dispersion, resulting in an increased sensitivity and spectral resolution. To exploit these advantages, 1H and 31P longitudinal studies were carried out in vivo at 17.2 Tesla in the aging rat brain to evaluate the progressive metabolic changes within the same individuals from the ages of 1 to up to 22 months of age using two rat cohorts with 1 and 8 months of age at the beginning of the study. For the 1H MRS studies, T1 and T2 metabolite relaxation times were measured at each exam in order to control age-related variations and to calculate absolute metabolite concentrations. 1H neurochemical profiles from four volumes of interest (VOI) in the brain were studied, revealing a progressive increase in myo-inositol and macromolecule content throughout the brain. In our main VOI composed mostly of cortex but also of corpus callosum and hippocampus, increased levels of choline-containing compounds (tCho) and glutamine were also observed, suggesting a mild neuroinflammation. No changes in NAA were observed in our main VOI, the thalamus or the caudate putamen (striatum). T2 decreases were observed with age for total NAA, tCho and macromolecules. Notably, unexpected effects correlated with the number of NMR exams were observed, the most prominent effect being an increase of the T1 relaxation times of the majority of metabolites.The second axis of the work done during this thesis was to set up an experimental framework for MR spectroscopic imaging (MRSI) studies at 7 Tesla in the human brain. 2D MRSI pulse sequences were developed for the acquisition of 31P and 1H metabolite maps using either slab selection or STEAM localization, respectively. A WET water suppression scheme was numerically optimized for its application at 7 T. Static B1-shimming configurations were implemented to reduce the inhomogeneity of the excitation field in the volume of interest and to generate outer-volume suppression (OVS) “ring” modes to saturate the signal in the periphery of the head. This approach allows to reduce the energy deposition in comparison to conventional OVS bands. Experiments were done in vitro showing their feasibility. The performance of standard OVS bands was also compared to a B1-insensitive train to obliterate signal (BISTRO) scheme in vivo using a double-tuned 1H/31P phased-array coil in a single-channel configuration for transmission. The demonstrated suppression efficacy of BISTRO opens the way for its use as a frequency-selective pre-saturation module for future 31P magnetization transfer experiments for the study of brain energy metabolism at very high magnetic field
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Fondell, Mattis. "Synthesis and Characterisation of Ultra Thin Film Oxides for Energy Applications." Doctoral thesis, Uppsala universitet, Oorganisk kemi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-232948.
Повний текст джерелаАнотація:
This thesis describes studies of materials which can be exploited for hydrogen production from water and sunlight. The materials investigated are maghemite (γ-Fe2O3), magnetite (Fe3O4) and especially hematite (α-Fe2O3), which is an iron oxide with most promising properties in this field. Hematite has been deposited using Atomic Layer Deposition (ALD) - a thin-film technique facilitating layer-by-layer growth with excellent thickness control and step coverage. The iron oxides were deposited using bis-cyclopentadienyl iron (Fe(Cp)2) or iron pentacarbonyl (Fe(CO)5) in combination with an O2 precursor. Since it is crucial to have good control of the deposition process, the influence of substrate, process temperature, precursor and carrier gas have been investigated systematically. By careful control of these deposition parameters, three polymorphs of iron oxide could be deposited: hematite (α-Fe2O3), maghemite (γ-Fe2O3) and magnetite (Fe3O4). The deposited materials were characterized using X-ray Diffraction, Raman and UV-VIS Spectroscopy, and Scanning Electron Microscopy. Hard X-ray Photoelectron Spectroscopy (HAXPES) was also used, since it is a non-destructive, chemically specific, surface sensitive technique – the surface sensitivity resulting from the short mean escape depth of the photoelectrons. The depth probed can be controlled by varying the excitation energy; higher photoelectron energies increasing the inelastic mean-free-path in the material. HAXPES studies of atomic diffusion from F-doped SnO2 substrates showed increased doping levels of Sn, Si and F in the deposited films. Diffusion from the substrate was detected at annealing temperatures between 550 °C and 800 °C. Films annealed in air exhibited improved photocatalytic behavior; a photocurrent of 0.23 mA/cm2 was observed for those films, while the as-deposited hematite films showed no photo-activity whatsoever. The optical properties of low-dimensional hematite were studied in a series of ultra-thin films (thicknesses in the 2-70 nm range). The absorption maxima were shifted to higher energies for films thinner than 20 nm, revealing a different electronic structure in thin films.
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Petersen, Michael. "Laser-cooling of neutral mercury and laser-spectroscopy of the 1So-3 Po optical clock transition." Paris 6, 2009. http://www.theses.fr/2009PA066096.
Повний текст джерелаАнотація:
La thèse détaille les premiers résultats expérimentaux du projet d'horloge à réseau optique de mercure neutre commencé au laboratoire SYRTE de l'Observatoire de Paris. Partant d'un laboratoire vide, le piégeage magnéto-optique du mercure a été obtenu, une source laser ultra stable pour la transition horloge a été réalisée et, pour la première fois au monde, la spectroscopie laser de la transition horloge a été faite, ce qui a permis d'améliorer de plus de 4 ordres de grandeur, la connaissance de la fréquence de cette transition. La spectroscopie de la transition horloge a été réalisée avec une source laser ultra stable à 65. 5 nm. Par comparaison avec un second système laser ultra stable similaire à 1062. 5 nm, nous avons obtenue une stabilité de 8*10^-16 à une seconde. Les résultats obtenus au cours de cette thèse démontrent la faisabilité d'une horloge à réseau optique de haute performance utilisant le mercure neutre.
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Bohlouli, Zanjani Parisa. "HIGH RESOLUTION MICROWAVE SPECTROSCOPY OF ULTRA COLD RYDBERG ATOMS AS A PROBE OF ELECTRIC AND MAGNETIC FIELDS." Thesis, University of Waterloo, 2003. http://hdl.handle.net/10012/1260.
Повний текст джерелаАнотація:
In highly excited Rydberg atoms, the excited electron is in a large, loosely bound orbit. Hence, in contrast with the ground states, the Rydberg states are very sensitive to external electric field and can be ionized in rather weak fields. The low ionization threshold of Rydberg states results in effective state-specific detection by the selective field ionization technique. In this thesis, high-resolution spectroscopy of Rydberg states of Rubidium using millimeter wave transitions and selective field ionization has been used as a probe of external electric and magnetic fields. Laser cooling and trapping techniques in a magneto-optical trap (MOT) are employed to have a high density and narrow velocity distribution for the atomic sample. In this work the magnetic field inhomogeneity inherent in a MOT is minimized and the stray electric field present at the trap region is compensated in order to have resolved spectra. The Stark line broadening of the spectra obtained in this work may be used to determine the electric field distribution in an expanding ultra-cold neutral plasma.
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Tombesi, Francesco <1982>. "An X-ray absorption line spectroscopy study of ultra-fast outflows from the innermost regions of AGNs." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2010. http://amsdottorato.unibo.it/2548/.
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Padgett, Miles John. "Techniques for ultra-high resolution saturation spectroscopy and laser stabilization in the 10#mu#m spectral region." Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305843.
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Venkateshwaran, Murali Manohar Saipavitra [Verfasser]. "Quantitative Magnetic Resonance Spectroscopy of Brain Metabolites and Macromolecules at Ultra-High Field / Saipavitra Venkateshwaran Murali Manohar." Tübingen : Universitätsbibliothek Tübingen, 2021. http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-1190509.
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Saule, Tobias [Verfasser], and Ferenc [Akademischer Betreuer] Krausz. "Cavity-enhanced high harmonic generation for multi-MHz ultra-fast photoemission spectroscopy / Tobias Saule ; Betreuer: Ferenc Krausz." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1213245672/34.
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Hughes, Juanita Maree. "A novel identification method for ultra trace detection of biomolecules using functionalised Surface Enhanced Raman Spectroscopy (SERS)." Thesis, Queensland University of Technology, 2014. https://eprints.qut.edu.au/72864/2/Juanita_Hughes_Thesis.pdf.
Повний текст джерелаАнотація:
This thesis developed a new method for measuring extremely low amounts of organic and biological molecules, using Surface enhanced Raman Spectroscopy. This method has many potential applications, e.g. medical diagnosis, public health, food provenance, antidoping, forensics and homeland security. The method development used caffeine as the small molecule example, and erythropoietin (EPO) as the large molecule. This method is much more sensitive and specific than currently used methods; rapid, simple and cost effective. The method can be used to detect target molecules in beverages and biological fluids without the usual preparation steps.
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Nilforoushan, Niloufar. "Out-of-equilibrium electron dynamics of Dirac semimetals and strongly correlated materials." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS573/document.
Повний текст джерелаАнотація:
Les matériaux quantiques ont récemment introduit en physique de la matière condensée pour unifier tous les matériaux dans lesquels les fortes corrélations électroniques gouvernent les propriétés physiques du système (e.g. les isolants de Mott) et les matériaux dont les propriétés électroniques sont déterminées par la géométrie de la fonction d’onde (e.g. matériaux de Dirac). Ces matériaux montrent des propriétés émergentes résultantes de l’intrication de différents degrés de libertés : la charge, le spin et le moment orbital, donnant lieu aux propriétés topologiques des électrons. L’étude de ces interactions et des compétitions entre les degrés de liberté pertinents nécessite l’utilisation de techniques pompe-sonde ultra-rapides. Particulièrement, les pulses laser femtosecondes interagissent uniquement avec les électrons pour les placer dans un état hors-équilibre décrit par des distributions de type non Fermi-Dirac. La dynamique subséquente implique de nombreux processus, avec un temps de relaxation relié aux constantes de couplage. De plus, dans les techniques résolues en temps, la lumière peut agir comme un paramètre externe, différent des paramètres thermodynamiques, pour explorer le diagramme de phase. Cela nous donne l’opportunité de stabiliser de nouveaux états inaccessibles par des chemins thermiques quasi-adiabatiques ou de manipuler les propriétés physiques des systèmes.Dans cette thèse, nous avons réalisé différentes expériences dans le but d’étudier les propriétés à l’équilibre et hors équilibre de deux matériaux corrélés: BaCo₁₋ₓNiₓS₂ et (V₁₋ₓMₓ)₂O₃.La première partie de ce projet a été dédiée principalement à l’étude de BaNiS₂, le précurseur métallique de la transition de Mott dans BaCo₁₋ₓNiₓS₂ . En utilisant l’ARPES, nous avons étudié la structure de bandes électroniques de BaNiS₂ dans toute la zone de Brillouin. L’expérience, combinée avec des calculs théoriques, révèle un nouveau type de cône de Dirac bidimensionel à caractère orbitalaire d et induit par les corrélations. Le croisement des bandes est protégé par les symétries particulières de la structure cristalline. Nous avons aussi mesuré la structure de bandes de l’isolant de Mott BaCoS₂ dans ses phases magnétique et non magnétiques.Dans la seconde partie, nous avons étudié la dynamique électronique hors équilibre de BaNiS₂ et (V₁₋ₓMx)₂O₃. Grâce à des mesures tr-ARPES et tr-Réflectivité, nous avons observé une renormalisation non thermique et ultra-rapide du cône de Dirac dans BaNiS₂. Ce phénomène est purement provoqué par les excitations électroniques et est stabilisé par l’intéraction entre les électrons et les phonons. De plus, en utilisant différentes techniques pompe-sonde (tr-XRD basé sur XFEL et tr-Réflectivité) nous avons aussi exploré des phases hors-équilibre du matériau prototype de Mott-Hubbard (V₁₋ₓMx)₂O₃ appartenant à différentes parties de son diagramme de phase. Nos résultats montrent une phase transitoire non thermique se développant immédiatement après la photoexcitation ultra-rapide et durant quelques picosecondes dans les phases métallique et isolantes. Cette phase transitoire est accompagné par une distorsion structural qui correspond à un durcissement du réseau et est marqué par un “blue shift” du mode phononique A₁g. Nos résultats soulignent l’importance du remplissage des orbitales aussi bien que des effets important des forts couplages électron-réseau sélectifs dans les matériaux fortement corrélésQuantum materials is a new term in condensed matter physics that unifies all materials in which strong electronic correlation governs physical properties of the system (e.g. Mott insulators) and materials whose electronic properties are determined by the geometry of the electronic wave function (e.g. Dirac materials). These materials show emergent properties– that is, properties that only appear by intricate interactions among many degrees of freedom, such as charge, spin and orbital, giving rise to topological properties of electrons. The study of these interactions and competitions between the relevant degrees of freedom demands applying ultrafast pump-probe techniques. Particularly, femtosecond laser pulses act only on the electrons and set them to an out-of-equilibrium state inexplicable by the Fermi-Dirac distribution. The ensuing dynamics involves various processes and the rate at which the relaxation occurs is related to the coupling constants. Moreover, in time-resolved pump-probe techniques light can act as an additional external parameter to change of the phase diagram – different from thermodynamic parameters. It gives us the opportunity of stabilizing new states inaccessible by quasi-adiabatic thermal pathways or eventually manipulating the physical properties of the systems.In this thesis, we performed different experiments in order to study the equilibrium and out-of-equilibrium properties of two correlated compounds: BaCo₁₋ₓNiₓS₂ and (V₁₋ₓMₓ)₂O₃.The first part of the project was mainly devoted to the study of BaNiS₂ that is the metallic precursor of the Mott transition in BaCo₁₋ₓNiₓS₂. By applying ARPES, we studied the electronic band structure of BaNiS₂ in its entire Brillouin zone. These results combined with some theoretical calculations give evidence of a novel correlation-induced and two-dimensional Dirac cone with d-orbital character. The band crossing is protected by the specific symmetries of the crystal structure. We also investigated the electronic band structure of the Mott insulator BaCoS₂ in its magnetic and nonmagnetic phases.In the second part, we studied the out-of-equilibrium electron dynamics of BaNiS₂ and (V₁₋ₓMx)₂O₃. By means of tr-ARPES and tr-reflectivity measurements, we observed an ultrafast and non-thermal renormalization of the Dirac cone in BaNiS₂ . This phenomenon is purely provoked by the electronic excitation and is stabilized by the interplay between the electrons and phonons. Moreover, by applying various pump-probe techniques (XFEL-based tr-XRD and tr-Reflectivity) we also explored the out-of-equilibrium phases of the prototype Mott-Hubbard material (V₁₋ₓMx)₂O₃ in different parts of its phase diagram. Our results show a transient non-thermal phase developing immediately after ultrafast photoexcitation and lasting few picoseconds in both metallic and insulating phases. This transient phase is followed by a structural distortion that corresponds to a lattice hardening and is marked by a “blue shift” of the A₁g phonon mode. These results underline the importance of the orbital filling as well as the strong effect of the selective electron-lattice coupling in the strongly correlated materials