Submitted by Jorge Silva (jorgelmsilva@ufrrj.br) on 2017-10-13T20:23:03Z No. of bitstreams: 1 2014 - Arnaldo Cesar Almeida Oliveira.pdf: 1706735 bytes, checksum: e15df5900be5e8087531ffa6a80e066e (MD5) / Made available in DSpace on 2017-10-13T20:23:03Z (GMT). No. of bitstreams: 1 2014 - Arnaldo Cesar Almeida Oliveira.pdf: 1706735 bytes, checksum: e15df5900be5e8087531ffa6a80e066e (MD5) Previous issue date: 2014-10-31 / CAPES / Understanding the structural properties of dislocations is essential since these defects govern the processes plastic deformation of materials. Particularly in semiconductors, these studies are important given the relevance of these materials for microelectronics. In this work, our focus will be the 90o partial dislocations in silicon. For the theoretical study of atomic-scale crystal dislocations, we use simulations based on semi-empirical quantum-mechanical methods closely linked to the tight-binding treatment, since it considers in its formulation that crystalline electronic states can be described in terms of atomic orbitals: Density Matrix Method Tight-Binding Order-N (DMTB). This method has a low computational cost which allows us to work with very large systems atoms in structures representation -including thousands of sites. In short, we describe how to produce and represent the 90o partial dislocations in Si, we consider three models for its core structure: a unreconstructed where the atoms have an almost fivefold coordination; a model reconstructed with period equal to the perfect lattice; and a model with twice period comparing with the perfect lattice. Finally, we calculate the range in energy of the system with the distance between the dislocations and the free surface of Si. / Compreender as propriedades estruturais de discord?ncias cristalinas ? fundamental uma vez que estes defeitos governam os processos de deforma??o pl?stica em materiais. Particularmente em semicondutores, esses estudos s?o importantes dada a relev?ncia desses materiais para a microeletr?nica. Neste trabalho nosso foco ser?o as discord?ncias cristalinas parciais a 90o em sil?cio. Para o estudo te?rico em escala at?mica das discord?ncias cristalinas, usamos simula??es baseadas em metodologias quanto-mec?nicas semi-emp?ricas atrav?s de um m?todo intimamente ligado ao tratamento tight-binding, uma vez que considera em sua formula??o que os estados eletr?nicos cristalinos podem ser descritos em termos de orbitais at?micos: M?todo da Matriz Densidade Tight-Binding de Ordem-N (DMTB). Este m?todo tem um custo computacional baixo o que permite que trabalhemos com sistemas muito grandes de ?tomos na representa??o das estruturas ? com milhares de s?tios inclusive. Em suma, descrevemos como produzir e representar as discord?ncias parciais a 90o em Si consideramos tr?s modelos para sua estrutura de caro?o: um n?o reconstru?do onde os ?tomos possuem uma coordena??o quase qu?ntupla; um modelo reconstru?do com per?odo igual ao per?odo da rede perfeita; e um modelo com per?odo dobrado em rela??o ao da rede perfeita. Por fim, calculamos a varia??o da energia do sistema com a dist?ncia entre as discord?ncias e a superf?cie livre do Si.

The selective infrared (IR) excitation of molecular vibrations is a powerful tool to control the photoreactivity prior to electronic excitation in the ultraviolet / visible (UV/Vis) light regime ("vibrationally mediated chemistry"). For adsorbates on surfaces it has been theoretically predicted that IR preexcitation will lead to higher UV/Vis photodesorption yields and larger cross sections for other photoreactions. In a recent experiment, IR-mediated desorption of molecular hydrogen from a Si(111) surface on which atomic hydrogen and deuterium were co-adsorbed was achieved, following a vibrational mechanism as indicated by the isotope-selectivity. In the present work, selective vibrational IR excitation of adsorbate molecules, treated as multi-dimensional oscillators on dissipative surfaces, has been simulated within the framework of open-system density matrix theory. Not only potential-mediated, inter-mode coupling poses an obstacle to selective excitation but also the coupling of the adsorbate ("system") modes to the electronic and phononic degrees of freedom of the surface ("bath") does. Vibrational relaxation thereby takes place, depending on the availabilty of energetically fitting electron-hole (e/h) pairs and/or phonons (lattice vibrations) in the surface, on time-scales ranging from milliseconds to several hundreds of femtoseconds. On metal surfaces, where the relaxation process of the adsorbate via the e/h pair mechanism dominates, vibrational lifetimes are usually shorter than on insulator or semiconductor surfaces, in the range of picoseconds, being also the timescale of the IR pulses used here. Further inhibiting factors for selectivity can be the harmonicity of a mode and weak dipole activities ("dark modes") rendering vibrational excitation with moderate field intensities difficult. In addition to simple analytical pulses, optimal control theory (OCT) has been employed here to generate a suitable electric field to populate the target state/mode maximally. The complex OCT fields were analyzed by Husimi transformation, resolving the control field in time and energy. The adsorbate/surface systems investigated were CO/Cu(100), H/Si(100) and 2H/Ru(0001). These systems proved to be suitable models to study the above mentioned effects. Further, effects of temperature, pure dephasing (elastic scattering processes), pulse duration and dimensionality (up to four degrees of freedom) were studied. It was possible to selectively excite single vibrational modes, often even state-selective. Special processes like hot-band excitation, vibrationally mediated desorption and the excitation of "dark modes" were simulated. Finally, a novel OCT algorithm in density matrix representation has been developed which allows for time-dependent target operators and thus enables to control the excitation mechanism instead of only the final state. The algorithm is based on a combination of global (iterative) and local (non-iterative) OCT schemes, such that short, globally controlled time-intervals are coupled locally in time. Its numerical performance and accuracy were tested and verified and it was successfully applied to stabilize a two-state linear-combination and to enforce a successive "ladder climbing" in a rather harmonic system, where monochromatic, analytical pulses simultaneously excited several states, leading to a population loss in the target state. / Die selektive Anregung von Molekülschwingungen mittels Infrarotlicht (IR) ist vorteilhaft, um die Wirkungsquerschnitte nachfolgender photochemischer oder photophysikalischer Prozesse zu steigern, welche durch Elektronenanregung mittels ultraviolettem (UV) bzw. sichtbarem (Vis) Licht ausgelöst werden. Für Adsorbatmoleküle auf Oberflächen wurden theoretische Vorhersagen getroffen, dass eine kombinierte (IR plus UV)-Strategie ("schwingungsvermittelte Chemie") die Ausbeute bei Photodesorption und anderen Photoreaktionen deutlich zu erhöhen vermag. Kürzlich wurde im Experiment gezeigt, dass eine rein IR-vermittelte Desorption möglich ist, welche über einen schwingungsangeregten Mechanismus erfolgt. Hierbei wurde molekularer Wasserstoff von einer Si(111)-Oberfläche desorbiert, an der atomarer Wasserstoff und atomares Deuterium gebunden waren. Eine thermische Anregung, die zum Bindungsbruch führt, konnte hierbei wegen der Isotopenselektivität ausgeschlossen werden. In der vorliegenden Arbeit wurde die selektive IR-Schwingungsanregung von Adsorbaten, die als multidimensionale Oszillatoren auf dissipativen Oberflächen behandelt wurden, mit Hilfe der Dichtematrixtheorie für offene Systeme simuliert. Nicht nur die potentialvermittelte Kopplung zwischen den einzelnen Moden ist ein Hindernis für selektive Anregung, sondern auch die Kopplung der Moden des Adsorbats ("Systems") an elektronische und phononische Freiheitsgrade des Substrats ("Bades"). Die Schwingungsrelaxation verläuft hierbei auf Zeitskalen, die von Millisekunden bis hin zu wenigen hundert Femtosekunden reichen, je nach Verfügbarkeit energetisch geeigneter Elektron-Loch-Paar-Anregungen bzw. Phononen (Gitterschwingungen) in der Oberfläche. Auf Metalloberflächen, bei denen die Schwingungrelaxation des Adsorbats zumeist von einem Elektronen-Loch-Paar-Mechanismus dominiert wird, sind die Schwingungslebensdauern normalerweise kürzer als auf Isolator- oder Halbleiteroberflächen und betragen einige Picosekunden, ebenso wie die Zeitskala der hier gewählten IR-Pulse. Weitere Faktoren, die die selektive Anregung behindern können sind die Harmonizität einer Mode und die geringe Dipolaktivität sogenannter "dunkler Moden", die eine Anregung mit moderat intensiven Feldern erschweren. Zusätzlich zu einfachen analytischen Pulsen wurden Felder mittels Optimaler Kontrolltheorie (OCT) erzeugt, um eine(n) Zielzustand/-mode maximal zu populieren. Komplexe OCT Pulse wurden mit Hilfe der Husimi-Transformation analysiert, welche das Kontrollfeld im Zeit- und Energieraum aufzulösen vermag. Die in dieser Arbeit untersuchten Adsorbat/Oberflächen-Systeme waren CO/Cu(100), H/Si(100) und 2H/Ru(0001), die sich als passende Modelle erwiesen, um oben genannte Faktoren zu untersuchen. Desweiteren wurden die Auswirkungen von Temperatur, reiner Dephasierung (elastische Streuprozesse), Dauer des IR-Pulses und Systemdimensionalit"at (Behandlung von bis zu vier Freiheitsgraden) studiert. Einzelne Schwingungsmoden konnten angeregt werden, in vielen Fällen sogar zustandsselektiv. Spezielle Prozesse wie die Anregung "heißer Banden", Desorption via alleiniger Schwingungsanregung und die Anregung "dunkler Moden" wurden simuliert. Schließlich wurde ein neuer OCT-Algorithmus in Dichtematrixdarstellung entwickelt, der es erlaubt, zeitabhängige Zieloperatoren einzuführen, um nicht nur Kontrolle über den Endzustand einer Anregung, sondern auch über den Anregungsmechanismus zu erlangen. Der Algorithmus basiert auf einer Kombination von globaler (iterativer) und lokaler (nicht-iterativer) optimaler Kontrollschemata in der Art, dass kurze, global kontrollierte Intervalle zeitlich lokal miteinander gekoppelt werden. Nach numerischen Tests wurde der Algorithmus erfolgreich angewandt, um eine Linearkombination aus zwei Zuständen zu stabilisieren, sowie um eine schrittweise "Leiteranregung" in einem harmonischen System zu forcieren, bei dem monochromatische, analytische Pulse mehrere Zustände zugleich anregen und somit einen Populationsverlust im angestrebten Zielzustand zur Folge haben.

Die Off-Axis-Elektronenholographie ist eine interferometrische Methode zur experimentellen Bestimmung von relativen Phasenschiebungen einer Elektronenwelle. Der Zugang zu diesen Phasenschiebungen ermöglicht z.B. die Bestimmung von intrinsischen elektrischen und magnetischen Feldern eines Objektes im Nanometerbereich. Für eine quantitative Interpretation der Resultate ist die Kenntnis des Rauschens der holographisch rekonstruierten Größen von hoher Bedeutung. In dieser Arbeit wird ein allgemeiner Formalismus abgeleitet, der den Rauschtransfer vom detektierten Hologramm in die rekonstruierten Amplituden- und Phasenbilder beschreibt. Anhand zielgerichteter Experimente wird dieser Formalismus unter Berücksichtigung von gemessenen Rauscheigenschaften des Detektors verifiziert. Im Zuge dessen wird eine experimentelle Methode entwickelt, die es erlaubt, durch Serienaufnahmen und Mittelungsprozeduren das Signal-zu-Rauschverhältnis in den holographischen Resultaten bei gleichbleibender Ortsauflösung erheblich zu verbessern. Daran knüpft sich eine Vielzahl von Anwendungen an, welche in dieser Arbeit in Auszügen aufgeführt werden. Die Grundlage für all diese Experimente besteht in den Welleneigenschaften des Elektrons, welche in der Interferenzfähigkeit (Kohärenz) des Elektrons zum Ausdruck kommen. Elektronen, welche unelastisch an einem Objekt streuen, verlieren diese Eigenschaft und es stellt sich die Frage, ob aus diesem Verlust zusätzliche Informationen über den Streuprozess bzw. über das Objekt selbst gewonnen werden können. Eine Größe, die neben der Intensität auch die Kohärenz der Elektronen beschreibt, ist die reduzierte Dichtematrix. Das motiviert, die Methode der Off-Axis-Elektronenholographie in der Sprache der Dichtematrizen zu formulieren und eine allgemeine Übertragungstheorie für ein holographiefähiges Transmissionselektronenmikroskop abzuleiten. Diese Theorie umfasst alle bisher bekannten Phänomene im Rahmen der Elektronenholographie und bietet darüber hinaus neue instrumentelle Ansätze zur Optimierung des Signal-zu-Rausch-Verhältnisses und zur Überwindung auflösungsbegrenzender Aberrationen. Vor diesem Hintergrund wird weiterhin die Kohärenz von Elektronen mittels energiegefilterter Off-Axis-Elektronenholographie untersucht, welche unelastisch an Siliziumoberflächen streuen und charakteristische Oberflächenplasmonen anregen. Für die Interpretation der Resultate werden zwei Modelle für die Dekohärenz des Elektrons infolge der Wechselwirkung mit einer Objektoberfläche entwickelt und unter Berücksichtigung der Aberrationen des Energiefilters mit dem Experiment verglichen. / Off-axis electron holography provides access to the relative phase shift of an electron wave and allows the experimental determination of intrinsic electric and magnetic fields within an object at nanometre scale. A quantitative interpretation of the results requires the knowledge about the noise in the reconstructed data. In this work, a general formalism is derived describing the transfer of noise from an experimental hologram into reconstructed amplitude and phase images. Concerted experiments verify this formalism under consideration of measured noise properties of the detector. In this frame, a method based on series acquisition and averaging is developed to improve significantly the signal-to-noise ratio of the reconstructed amplitude and phase images at constant spatial resolution. The usefulnes of this method is demonstrated by selected experimental examples from the materials sciences. The capability to show interference, i.e. to be coherent, is a consequence of the electron's wave nature and provides the fundament for all applications of electron holography. By inelastic interaction with the object, the electron loses coherence and the question comes up, whether this loss mechanism contains additional information about the scattering process or even about the object itself. The reduced density matrix is introduced as a suitable quantity describing both intensity and coherence of scattered electrons. That motivates to formulate off-axis electron holography in the language of density matrices and to derive a general transfer theory for this quantity in a holography-dedicated transmission electron microscope. This theory reproduces all known phenomena related to off-axis electron holography and provides new instrumental approaches to improve the signal-to-noise ratio and to overcome resolution limiting aberrations. In this context, the coherence of electrons, which are inelastically scattered by silicon surfaces and have excited characteristic surface plasmons, is investigated by energy-filtered electron holography. For the interpretation of the experimental results, two models are developed for the decoherence of the electron by interaction with an object surface and are compared to the experiment under consideration of the aberrations of the energy-filter.

No description available.

Quantum entanglement is a phenomenon which has shown great potential use in modern technical implementations, but there is still much development needed in the field. One major problem is how to measure the amount of entanglement present in a given entangled state. There are numerous different entanglement measures suggested, all satisfying some conditions being of either operational, or more abstract, mathematical nature. However, in contradiction to what one might expect, the measures show discrepancies in the ordering of entangled states. Concretely this means that with respect to one measure, a state can be more entangled than another state, but the ordering may be opposite for the same states using another measure. In this thesis we take a closer look at some of the most commonly occurring entanglement measures, and find examples of states showing inequivalent entanglement ordering for the different measures. / Kvantmekanisk sammanflätning är ett fenomen som visat stor potential för framtida tekniska tillämpningar, men för att kunna använda oss av detta krävs att vi hittar lämpliga modeller att mäta omfattningen av sammanflätningen hos ett givet tillstånd. Detta har visat sig vara en svår uppgift, då de modeller som finns idag är otillräckliga när det gäller att konsekvent avgöra till vilken grad olika tillstånd är sammanflätade. Exempelvis kan en modell visa att ett tillstånd är mer sammanflätat än ett annat, medan en annan modell kan visa på motsatsen - att det första tillståndet är mindre sammanflätat än det andra. En möljig orsak kan ligga i de olika modellernas deifnition, då vissa utgår från operativa definitioner, medan andra grundas på matematiska, abstrakta villkor. I denna uppsats tittar vi lite närmre på några av de mätmodeller som finns, och hittar exempel på tillstånd som uppvisar olika ordning av sammanflätningsgrad beroende på vilken modell som används.

No description available.

In this thesis the path integral formalism is applied to the calculation of the dynamics of dissipative quantum systems. The time evolution of a system of bilinearly coupled bosonic modes is treated using the real-time path integral technique in coherent-state representation. This method is applied to a damped harmonic oscillator within the Caldeira-Leggett model. In order to get the stationary trajectories the corresponding Lagrangian function is diagonalized and then the path integrals are evaluated by means of the stationary-phase method. The time evolution of the reduced density matrix in the basis of coherent states is given in simple analytic form for weak system-bath coupling, i.e. the so-called rotating-wave terms can be evaluated exactly but the non-rotating-wave terms only in a perturbative manner. The validity range of the rotating-wave approximation is discussed from the viewpoint of spectral equations. In addition, it is shown that systems without initial system-bath correlations can exhibit initial jumps in the population dynamics even for rather weak dissipation. Only with initial correlations the classical trajectories for the system coordinate can be recovered. The path integral formalism in a combined phase-space and coherent-state representation is applied to the problem of curve-crossing dynamics. The system of interest is described by two coupled one-dimensional harmonic potential energy surfaces interacting with a heat bath. The mapping approach is used to rewrite the Lagrangian function of the electronic part of the system. Using the Feynman-Vernon influence-functional method the bath is eliminated whereas the non-Gaussian part of the path integral is treated using the perturbation theory in the small coordinate shift between potential energy surfaces. The vibrational and the population dynamics is considered in a lowest order of the perturbation. The dynamics of a Gaussian wave packet is analyzed along a one-dimensional reaction coordinate. Also the damping rate of coherence in the electronic part of the relevant system is evaluated within the ordinary and variational perturbation theory. The analytic expressions for the rate functions are obtained in the low and high temperature regimes.

The electron transport through a molecular wire under the influence of an external laser field is studied using a reduced density matrix formalism. The full system is partitioned into the relevant part, i.e. the wire, electron reservoirs and a phonon bath. An earlier second-order perturbation theory approach of Meier and Tannor for bosonic environments which employs a numerical decomposition of the spectral density is used to describe the coupling to the phonon bath and is extended to deal with the electron transfer between the reservoirs and the molecular wire. Furthermore, from the resulting time-nonlocal (TNL) scheme a time-local (TL) approach can be determined. Both are employed to propagate the reduced density operator in time for an arbitrary time-dependent system Hamiltonian which incorporates the laser field non-perturbatively. Within the TL formulation, one can extract a current operator for the open quantum system. This enables a more general formulation of the problem which is necessary to employ an optimal control algorithm for open quantum systems in order to compute optimal control fields for time-distributed target states, e.g. current patterns. Thus, we take a fundamental step towards optimal control in molecular electronics. Numerical examples of the population dynamics, laser controlled current, TNL vs. TL and optimal control fields are presented to demonstrate the diverse applicability of the derived formalism.

Title: Optimizing quantum simulations and the DMRG method Author: Jan Brandejs Department: Department of Chemical Physics and Optics Supervisor: doc. Dr. rer. nat. Jiří Pittner, DSc., J. Heyrovský Institute of Physical Chemistry of the Czech Academy of Sciences Abstract: In this work, we explore the quantum information theoretical aspects of simulation of quantum systems on classical computers, in particular the many- electron strongly correlated wave functions. We describe a way how to reduce the amount of data required for storing the wavefunction by a lossy compression of quantum information. For this purpose, we describe the measures of quantum entanglement for the density matrix renormalization group method. We imple- ment the computation of multi-site generalization of mutual information within the DMRG method and investigate entanglement patterns of strongly correlated chemical systems. We present several ways how to optimize the ground state calculation in the DMRG method. The theoretical conclusions are supported by numerical simulations of the diborane molecule, exhibiting chemically interest- ing electronic structure, like the 3-centered 2-electron bonds. In the theoretical part, we give a brief introduction to the principles of the DMRG method. Then we explain the quantum informational...

The central problem in the modern electronic structure theory is the calculation of cor- relation energy, possibly by an approach that would account for both static and dynamic correlation in an efficient, balanced and accurate way. In this thesis, I present a collection of methods that combine the effective treatment of dynamic correlation by the coupled cluster theory with density matrix renormalization group, a well-established technique for calculations of strongly correlated systems. The connection between them is achieved via the tailored coupled clusters (TCC) ansatz, which conveniently does not impose any ad- ditional computational costs. After the successful initial assessment, we developed more efficient implementations of these methods by employing the local approaches based on pair natural orbitals. This way, we extended the range of possible applications to larger systems with thousands of basis functions. To assess the accuracy of TCC as well as its local counterparts, we performed a variety of benchmark calculations ranging from small, yet challenging systems such as the nitrogen molecule or tetramethyleneethane diradical, to larger molecules like oxo-Mn(Salen) or Fe(II)-porphyrin model. 1