A espectroscopia de ressonância ciclotrônica de íons foi usada para estudar reações de íons alcóxido, hidróxido, fluoreto, íon-radical óxido, acetileto e amideto com formiatos de alquila; o último íon reage também com N,N-dimetilformamida. Em todos os casos ocorre uma reação de descarbonilação, dando origem a um íon solvatado, que as evidências experimentais indicam ser unido por ponte de hidrogênio. Deslocamentos nucleófilos de grupos ligados ao esqueleto formílico podem ocorrer em casos adequados e em casos especiais ocorre ainda a formação de íons formiato. Os íons solvatados formados a partir de íons fluoreto e alcóxido com formiatos de alquila reagem com álcoois, podendo-se desta meneira estabelecer uma ordem de capacidade de solvatação para os álcoois alifáticos simples. A ordem estabelecida foi: CH3OH < C2H5OH < iso-C3H7OH < tert-C4H9OH. Foram determinadas constantes relativas de velocidade para as reações de vários íons negativos com formiatos de alquila, em sistemas onde se forma mais de um produto. Nos casos mais favoráveis (reações de íons fluoreto) foram calculadas constantes de velocidade absolutas para os vários canais de reação. / Ion-cyclotron resonance spectroscopy has been used to study the reactions between alkoxide, hydroxide, fluoride, O-, acetylide and amide ions with alkyl formates; the last ion reacts also with N,N-dimethylformamide. In all systems a decarbonylation occurs, giving rise to a solvated product ion, held by a hydrogen bond, as evidenced experimentally. Nucleophilic displacement of the formyl group substituents may occur in favorable cases and in a few particular systems the formation of formate ion is observed. The solvated ions formed through the reaction of fluoride or alkoxide ions with alkyl formates can react further with alcohols to establish the intrinsic clustering ability of simple aliphatic alcohols. The order of solvating ability is shown to follow the order CH3OH < C2H5OH < iso-C3H7OH < tert-C4H9OH. In systems where parallel reactions occur, relative rate constants were determined; in the most favorable cases (reactions of fluoride ions), absolute rate constants for the various reaction channels were calculated.

A espectroscopia de ressonância ciclotrônica de íons foi usada para estudar reações de íons alcóxido, hidróxido, fluoreto, íon-radical óxido, acetileto e amideto com formiatos de alquila; o último íon reage também com N,N-dimetilformamida. Em todos os casos ocorre uma reação de descarbonilação, dando origem a um íon solvatado, que as evidências experimentais indicam ser unido por ponte de hidrogênio. Deslocamentos nucleófilos de grupos ligados ao esqueleto formílico podem ocorrer em casos adequados e em casos especiais ocorre ainda a formação de íons formiato. Os íons solvatados formados a partir de íons fluoreto e alcóxido com formiatos de alquila reagem com álcoois, podendo-se desta meneira estabelecer uma ordem de capacidade de solvatação para os álcoois alifáticos simples. A ordem estabelecida foi: CH3OH < C2H5OH < iso-C3H7OH < tert-C4H9OH. Foram determinadas constantes relativas de velocidade para as reações de vários íons negativos com formiatos de alquila, em sistemas onde se forma mais de um produto. Nos casos mais favoráveis (reações de íons fluoreto) foram calculadas constantes de velocidade absolutas para os vários canais de reação. / Ion-cyclotron resonance spectroscopy has been used to study the reactions between alkoxide, hydroxide, fluoride, O-, acetylide and amide ions with alkyl formates; the last ion reacts also with N,N-dimethylformamide. In all systems a decarbonylation occurs, giving rise to a solvated product ion, held by a hydrogen bond, as evidenced experimentally. Nucleophilic displacement of the formyl group substituents may occur in favorable cases and in a few particular systems the formation of formate ion is observed. The solvated ions formed through the reaction of fluoride or alkoxide ions with alkyl formates can react further with alcohols to establish the intrinsic clustering ability of simple aliphatic alcohols. The order of solvating ability is shown to follow the order CH3OH < C2H5OH < iso-C3H7OH < tert-C4H9OH. In systems where parallel reactions occur, relative rate constants were determined; in the most favorable cases (reactions of fluoride ions), absolute rate constants for the various reaction channels were calculated.

The broad theme of the present research investigation is Ion Assisted Deposition of thin films and its effect on the properties of thin films. Though this activity has been of interest to researchers for more than a decade, the development of different types of ion sources with control over the ion flux and energy, makes it a current topic of interest. Ion assisted deposition was successful in depositing thin films of many material with desired qualities, however, there are certain class of materials whose deposition has been rather difficult. This has mainly been attributed to higher energies and low ion flux of conventional ion sources. The advent of ECR ion sources for thin film deposition has given impetus to the deposition of such materials. This is due to the low energy high-density plasma generated in this type of sources. Hitherto, these sources were widely used in PECVD techniques and only recently the importance of ECR sources in PVD techniques has been realized. This thesis is on the development of ECR plasma source for ion assisted deposition of thin films using PVD techniques. This thesis is organized into six chapters. The first chapter gives an introduction on the ion assisted growth of thin films and the importance of ECR plasma. A detailed discussion on various aspects of ECR sources has been included. The design details on the development of ECR source have been discussed in the second chapter. The performance of ECR source as analyzed by the Langmuir probe are also discussed. Variation of plasma parameters like ion density, electron temperature, plasma potential and floating potential as a function of pressure and microwave power have been studied using Langmuir probe analysis. An ion density of the order of 1011/cm3 was measured at a distance of 8 cm from the plasma source with a microwave power of 400 watts. This was comparable to the ion density reported in downstream plasma of ECR sources. The behavior of plasma parameters with variation in microwave power and pressure was explained on the basis of microwave transmission above critical ion density and the microwave power absorption. The uniformity of the plasma parameters at the substrate position (29 cm from the ECR source) was found to be ± 2% over a diameter of 12 cm, which makes the ion source suitable for ion assisted deposition. The third chapter deals with the simulation and experimental study of the ECR sputtering process. ECR sputter type sources are equipped with cylindrical targets. The sputtered flux distribution on the substrate depends on target geometry, sputtering pressure and target-substrate distance. The effect of cylindrical geometry on the distribution of sputtered flux has been simulated by Monte Carlo methods. It is found that the sputtered flux distribution at different pressures and target-substrate distances in ECR sputter type source differs from the conventional glow discharge sputtering system equipped with planar targets. The simulated results are compared with the experimental results. The simulated data agree very well with the experimental data. The deposition and characterization of the TiN thin films for diffusion barrier applications in copper metallization have been discussed in the fourth chapter. Titanium nitride films are prepared by ECR sputtering. The effect of high density ion bombardment on the morphology, orientation and resistivity of the films was studied. It was observed that films with atomic smoothness could be prepared by ECR sputtering. Also the high density ion bombardment has been found to be effective for the film growth in (100) orientation. The behavior of TiN films deposited by this method as a diffusion barrier in copper metallization has been investigated. The resistivity measurements and RBS depth profile studies showed that up to 700°C there is no diffusion of copper into silicon. This shows that ECR sputtered TiN can be used as an effective diffusion barrier in copper metallization. The fifth chapter contains investigations on the ECR assisted growth of silicon nitride films. The films are characterized for composition, morphology and chemical bonding using AES, RBS, AFM, XPS and FTIR. AFM studies revealed that ion bombardment results in the reduction of surface roughness, which indicates dense film growth. The effect of ion assistance on the optical and electrical properties is studied in detail. Films prepared with microwave power ranging from 100 to 200 watts are having bandgap and refractive index of 4.9 eV and 1.92 respectively. Interface state density of silicon nitride films prepared in the above mentioned range was found to be 5x10 10 eVcm2. These films exhibited a resistivity of 10 13 Ω, cm and critical field of 4 MV/cm. The electrical conductivity in these films has been explained on the basis of Poole and Frenkel conduction. The low value of interface state density, higher resistivity, and critical field show that good quality SiN4 films can be deposited with low energy high density ECR plasma. A detailed summary of this research investigation has been discussed in the last chapter. The thesis is concluded with a discussion on the need of focused ECR source to establish ECR assisted deposition as a versatile technique for the growth of thin films.

No description available.

Advances in science and technology during the past decade have greatly enhanced the level of the structural investigation of macromolecules – peptides and proteins. Biological mass spectrometry has become one of the most precise and sensitive techniques in peptide and protein analysis. However, increasing demands of biotechnological applications require further progress to be made. In the present thesis the development and improvement of peptide and protein characterization methods and techniques based on ion-electron and ion-photon reactions in electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry are described. The focus is on the development of the electron capture dissociation method, recently discovered by the group of professor McLafferty, into a high rate, efficient tandem mass spectrometrical technique. The rate and reliability of the electron capture dissociation technique were greatly increased by implementation of low-energy pencil electron beam injection systems based on indirectly heated dispenser cathodes. Further implementation of a hollow electron beam injection system combined, in a single experimental configuration, two rapid fragmentation techniques, high rate electron capture dissociation and infrared multiphoton dissociation. Simultaneous and consecutive irradiations of trapped ions with electrons and photons extended the possibilities for ion activation/dissociation reaction schemes and lead to improved peptide and protein characterization. Using these improvements, high rate electron capture dissociation was employed in time-limited experiments, such as liquid chromatography–tandem mass spectrometry and capillary electrophoresis-tandem mass spectrometry. The analytical applications of the developed techniques have been demonstrated in top-down sequencing of peptides and proteins up to 29 kDa, improved sequencing of peptides with multiple disulfide bridges and secondary fragmentation (w-ion formation), as well as extended characterization of peptide mixtures separated by liquid chromatography and capillary electrophoresis. For instance, the dissociation of peptides resulting from enzymatic digestion of proteins provided complementary structural information on peptides and proteins, as well as their post-translational modifications.

No description available.

Neste trabalho estudamos os efeitos polarônicos sobre um gás de elétrons quase bidimensional presente em heteroestruturas semicondutoras (heterojunções e poços quânticos de GaAs-AlGaAs) sob a ação de um campo magnético uniforme aplicado na direção perpendicular a interface, através de teoria de perturbação de segunda ordem. Calculamos a massa ciclotrônica considerando a interação elétron-fonon LO e os efeitos de blindagem e não parabolicidade da banda de condução do GaAs. Os resultados obtidos são comparados com recentes dados experimentais de ressonância ciclotronica e apresentam ótima concordância. Estudamos também a energia de ligação do estado fundamental de uma impureza hidrogenóide localizada no interior de um fio quântico retangular de GaAs envolvido por AlGaAs, como função das dimensões do fio para varias alturas das barreiras de variacional, usando várias formas para a função de onda tentativa do sistema. Consideramos também a contribuição polarônica a energia de ligação. Comparamos nossos resultados com recentes cálculos da energia de ligação, efetuados por outros autores. / In this work we study the polaronic effects on the two dimensional electron gas present in semiconductor heteroestructures (GaAs-AlGaAs heterojunctions and quantum wells) when a uniform magnetic field is applied perpendicular to the interface, using second order perturbation theory. By taking into account the effect of nonparabolicity and screening of the electron-fonon LO interaction the calculated effective mass is compared to the recent experimental date. Good agreement is found with available date. The binding energies of a hydrogenic impurity located in quantum well wires of GaAs surrounded by AlGaAs are calculated as a functions of the size of the wire for several values of the heights of the potential barriers and diferent positions of the impurity inside the wire. We follow a variational approach choosing several trial wave functions for the ground state. The polaronic contribution to the binding energy is considered. We compare our results with those previously obtained by other authors.

Black carbon (BC) is a complex mixture of polycondensed aromatic compounds produced by the incomplete combustion of biomass during events such as wildfires and the burning of fossil fuels. Black carbon was initially considered to be a refractory form of organic matter. However, recent studies have shown that BC can be quite mobile and reactive in the terrestrial environment. Black carbon can be translocated from soils and sediments in the form of dissolved BC (DBC). A global correlation between DBC and bulk dissolved organic carbon (DOC) has been established for fluvial systems where DBC comprises approximately 10% of the total DOC pool, which suggests that DBC may be a significant contributor to the global carbon cycle. The primary objective of this thesis was to further characterize DBC and elucidate some of the specific physical and chemical processes that promote its transfer to the aqueous phase and drive the DBC-DOC relationship. The molecular composition and qualitative distribution of DBC was assessed using Fourier transform ion cyclotron resonance mass spectrometry. Black carbon in both dissolved and particulate (PBC) phases was quantified by the benzenepolycarboxylic acid method. Dissolved BC was found to contain considerable amounts of nitrogen and the export of this dissolved black nitrogen was linked to watershed land use in global rivers. The riverine flux of PBC, a previously unstudied BC removal mechanism, was significantly increased by local wildfire activity. However in-stream DBC did not appear to be affected by short-term fire events. Once translocated to surface waters, DBC is susceptible to photodegradative processes. Dissolved BC in high molecular weight DOC fractions was more photoreactive than DBC associated with lower molecular weight fractions. In the coming decades, wildfire frequency is expected to increase with climate change and natural lands will continue to be altered for anthropogenic use. These processes have already been shown to significantly impact the composition of DOC and associated DBC exported to inland waters. The quality of DBC influences its stability in soil and resistance to degradation. Therefore, it is essential that we aim to fully understand DBC dynamics in natural systems in order to assess its contribution to global carbon cycling.

Tato práce se zabývá charakterizací topologického izolátoru Bi2Te3, materiálu s nevodivými stavy v objemu, ale jedním vodivým pásem na povrchu. Tento materiál je zkoumán již přes 60 let, ale i přes to není jeho objemová pásová struktura úplně objasněna, obzvláště charakter zakázaného pásu je stále předmětem diskuze. V této práci jsou prezentovány výsledky infračervené spektroskopie na Landauových hladinách v magnetickém poli až do 34 T, doplněné elipsometrickým měřením mimo magnetické pole. Výsledky těchto měření by měli pomoci vyjasnit některé vlastnosti zakázaného pásu. Pozorovaná optická odezva odpovídá polovodiči s přímým zakázaným pásem, ve kterém se nosiče náboje chovají jako Diracovské hmotné fermiony. Šířka zakázaného pásu za nízkých teplot byla určena jako Eg = (175±5) meV a samotný zakázaný pás se nachází mimo trigonální osu, tím pádem se v první Brillouinově zoně vyskytuje 6 krát nebo 12 krát.

This master’s thesis deals with the modelling of electronic properties of graphite crystal, which are measurable using a spectrometer based on high frequency electron paramagnetic resonance (HFEPR for short) located in laboratories of CEITEC BUT. This is especially the band structure of graphite and its Landau levels. The theoretical part of the thesis describes key effects and connections from quantum mechanics and definitions of important terms from solid state physics, which are used to describe the crystalline structure of graphite and its electronic properties. Furthermore, the project describes the HFEPR spectrometer and its functional principle. In the practical part of the thesis, there are numerical models of the band structure of graphite and of its Landau levels and description of the preparation of a graphite sample for measurement. At the end of the practical part there is the analysis of measurements results, namely the cyclotron resonance and Shubnikov-de Haas oscillations, thanks to which it is possible to determine physical parameters of the sample, such as effective mass of charge carriers and fundamental frequency.