<p>The following dissertation presents neutron scattering studies on three specific magnetic insulating oxide materials whose lattice is based on triangular structural motifs. Each of the three materials studied, LuCoGaO₄, Co₃V₂O₈ and Tb₂Ti₂O₇, displays an interesting disordered ground state that is reached by different mechanisms: site disorder, geometric frustration, and quantum fluctuations induced by a transverse magnetic field. The main focus of this work is the characterization of the resulting magnetic ground states and magnetic excitations within these systems.</p> <p>Chapters 3, 4 and 5 contain original work in the form of six research articles that have either been published or have been prepared for publication in peer-reviewed journals.</p> <p>Chapter 3 describes studies of the quasi two-dimensional triangular layered antiferromagnet LuCoGaO₄. This material is found to exhibit a spin glass ground state as a result of geometrical frustration and site disorder inherent in this system. Below the freezing temperature, this system exhibits static, two-dimensional correlations consistent with frozen short-range correlated regions in the plane of the bilayers that extend over roughly five unit cells. The dynamic correlations reveal typical spin glass behavior upon cooling. Furthermore, a resonant gapped spin-wave-like excitation is observed, that can be related to the anisotropy in the system. Such an excitation is relatively uncommon in spin glasses and has been studied for the first time in such detail.</p> <p>Chapter 4 is concerned with the study of the kagome staircase system Co₃V₂O₈. While prone to geometrical frustration due to its underlying kagome structural motif, this material is characterized by predominantly ferromagnetic interactions that lead to an unfrustrated, ferromagnetic ground state. In this chapter, departures from this conventional ground state by different disordering mechanisms are investigated. The first part focuses on the effects of site disorder by introducing quenched nonmagnetic impurities into the system. The growth of single crystals of (Co_1-xMg_x)₃V₂O₈ is reported. These crystals reveal that the ferromagnetic ground state is very sensitive to doping, and show that a low doping concentration of 19% leads to a suppression of the ferromagnetic ground state below 1.5 K. This could be understood as percolation problem on the quasi two-dimensional kagome lattice including site and bond percolation. The second part focuses on the influence of a transverse magnetic field on the ground state of Ising spins, introducing quantum fluctuations that lead to quantum phase transitions at ~6.25, 7 and 13 T. The observed quantum phase transitions are characterized by distinct changes in the magnetic structure and their associated spin excitation spectra.</p> <p>Chapter 5 presents studies on the pyrochlore antiferromagnet Tb₂Ti₂O₇, which is a proposed spin liquid candidate but whose actual ground state is still the topic of current debate. The ground state of Tb₂Ti₂O₇ was revisited by neutron scattering measurements, revealing a new phase in the low temperature low field phase diagram that can be described as a frozen antiferromagnetic spin ice that exhibits distinct elastic and inelastic scattering features.</p> / Doctor of Philosophy (PhD)

<p>In this thesis I present three publications about the use of<br />valence bonds to gain information about quantum spin systems.<br />Valence bonds are an essential ingredient of low energy states present<br />in many compounds.<br /><br />The first part of this thesis is dedicated to<br />two studies of the antiferromagnetic J₁-J₂ chain with<br />S=1/2. We show how automated variational calculations based on<br />valence bond states can be performed close to the Majumdar-Ghosh point<br />(MG-point). At this point, the groundstate is a product state of<br />dimers (valence bonds between nearest neighbours). In the dimerized<br />region surrounding the MG-point, we find such variational computations<br />to be reliable.<br /><br />The first publication is about<br />the entanglement properties of an impurity attached to the chain. We show<br />how to use the variational method to calculate the negativity, an<br />entanglement measure between the impurity and a distant part of the<br />chain. We find that increasing the impurity coupling and a<br />minute explicit dimerization, suppress the long-ranged entanglement<br />present in the system for small impurity coupling at the MG-point. <br /><br />The second publication is about a<br />transition from commensurate to incommensurate behaviour and how its<br />characteristics depend on the parity of the length of the chain. The<br />variational technique is used in a parameter regime inaccessible to<br />DMRG. We find that in odd chains, unlike in even chains, a very<br />intricate and interesting pattern of level crossings can be observed. <br /><br />The publication of the second part is about novel worm algorithms for<br />a popular quantum Monte Carlo method called valence bond quantum Monte<br />Carlo (VBQMC). The algorithms are based on the notion of a worm<br />moving through a decision tree. VBQMC is entirely formulated in<br />terms of valence bonds. In this thesis, I explain how the approach<br />of VBQMC can be translated to the S_z-basis. The algorithms explained<br />in the publication can be applied to this S_z-method.</p> / Doctor of Philosophy (PhD)

Spin filtering properties of novel GaNAs alloys are reported in this thesis. Spin-dependent recombination (SDR) in GaNAs via a deep paramagnetic defect center is intensively studied.  By using the optical orientation photoluminescence (PL) technique, GaNAs is shown to be able to spin filter electrons injected from GaAs, which is a useful functional property for integratition with future electronic devices.  The spin filtering ability is found to degrade in narrow GaNAs quantum well (QW) structures which is attributed to (i) acceleration of band-to-band recombination competing with the SDR process and to (ii) faster electron spin relaxation in the narrow QWs.  Ga interstitial-related defect centers have been found to be responsible for the SDR process by using the optically detected magnetic resonance (ODMR) technique. The defects are found to be the dominant grown-in defects in GaNAs, commonly formed during both MBE and MOCVD growths.  Methods to control the concentration of the Ga interstitials by varying doping, growth parameters and post-growth treatments are also examined.

This thesis presents a theoretical study of Bose-Einstein condensates in a doublering trap. In particular, we determine the ground states of the condensate in the double-ring trap that arise from the interplay of quantum tunnelling and the trap’s rotation. The trap geometry is a concentric ring system, where the inner ring is of smaller radius than the outer ring and both lie in the same two-dimensional plane. Due to the difference in radii between the inner and outer rings, the angular momentum that minimises the kinetic energy of a condensate when confined in the individual rings is different at most frequencies. This preference is in direct competition with the tunnel coupling of the rings which favours the same angular momentum states being occupied in both rings. Our calculations show that at low tunnel coupling ground state solutions exist where the expectation value of angular momentum per atom in each ring differs by approximately an integer multiple. The energy of these solutions is minimised by maintaining a uniform phase difference around most of the ring, and introducing a Josephson vortex between the inner and outer rings. A Josephson vortex is identified by a 2p step in the relative phase between the two rings, and accounts for one quantum of circulation. We discuss similarities and differences between Josephson vortices in cold-atom systems and in superconducting Josephson junctions. Josephson vortices are actuated by a sudden change in the trapping potential. After this change Josephson vortices rotate around the double-ring system at a different frequency to the rotation of the double-ring potential. Numerical studies of the dependence of the velocity on the ground state tunnel coupling and interaction strength are presented. An analytical theory of the Josephson vortex dynamics is also presented which is consistent with our numerical results.

The present thesis reports computer simulation studies of several phase transition related phenomena in a range of soft-condensed matter systems. A coherent unifying theme of the thesis is the understanding of dynamics of phase transitions through free energy calculations using recently developed efficient non-Boltzmann sampling methods. Based on the system/phenomena of interest, the thesis has been classified into four major parts: I. Isotropic-nematic (IN) phase transition in liquid crystals. II. Nucleation phenomena in gas-liquid transition with particular emphasis on the systems close to the spinodal curve. III. Collapse transition in linear hydrocarbon (n-alkane) chains for a varying range of length, solvent and temperature. IV. Crystallization of unbranched polymer chains in dilute solution, with particular emphasis on the temperature dependent crossover between the rod-like crystalline state and spherical molten globule state. The thesis has been further divided into ten chapters running through the four parts mentioned before. In the following we provide a brief chapter-wise outline of the thesis. Part I deals with the power law relaxation and glassy dynamics in thermotropic liquid crystals close to the IN transition and consists of two chapters. To start with, Chapter I.1 provides an introduction to thermotropic liquid crystals. Here we briefly introduce various liquid crystalline phases, the order parameter used to characterize the IN transition, a few well established theoretical models, and we conclude with describing the recent experimental and computer simulation studies that have motivated the work described in the next chapter. In Chapter I.2, we present our molecular dynamics simulation studies on single particle and collective orientational dynamics across the IN transition for Lebwohl Lasher model, which is a well-known lattice model for thermotropic liquid crystals. Even this simplified model without any translational degrees of freedom successfully captures the short-tointermediate time power law decay recently observed in optical heterodyne detected optical Kerr effect (OHDOKE) measurements near the IN transition. The angular velocity time correlation function also exhibits a rather pronounced power law decay near the IN boundary. In the mean squared angular displacement at comparable time scales, we observe the emergence of a sub-diffusive regime which is followed by a super-diffusive regime before the onset of the longtime diffusive behavior. We observe signature of dynamical heterogeneity through pronounced non-Gaussian behavior in the orientational motion particularly at lower temperatures. Interestingly, this behavior closely resembles what is usually observed in supercooled liquids. We obtain the free energy as a function of orientational order parameter by the use of recently developed transition matrix Monte Carlo (TMMC) method. The free energy surface is flat for the system considered here and the barrier between isotropic and nematic phases is vanishingly small for this weakly first-order transition, hence allowing for large scale, collective, and correlated orientational density fluctuations. We attribute this large scale fluctuations as the reason for the observed power law decay of the orientational time correlation functions. Part II consists of three chapters, where we focus on the age old problem of nucleation and growth, both from the perspective of thermodynamics and kinetics. We account for the rich history of the problem in the introductory Chapter II.1. In this chapter we describe various types and examples of the nucleation phenomena, and a brief account of the major theoretical approaches used so far. We begin with the most successful Classical Nucleation Theory (CNT), and then move on to more recent applications of Density Functional Theory (DFT) and other mean-field types of models. We conclude with a comparison between the experiments, theories and computational studies. In the next chapter (Chapter II.2) we attempt to elucidate the mechanism of nucleation near the gas-liquid spinodal from a microscopic point of view. Here we construct a multidimensional free energy surface of nucleation of the liquid phase from the parent supercooled and supersaturated vapor phase near the gas-liquid spinodal. In particular, we remove the Becker-Doring constraint of having only one growing cluster in the system. The free energy, as a function of the size of the largest cluster, develops a pronounced minimum at a subcritical cluster size close to the spinodal. This signifies a two step nature of the process of nucleation, where the rapid formation of subcritical nuclei is followed by further growth by slower density fluctuations on an uphill free energy surface. An alternative free energy pathway involving the participation of many subcritical clusters is envisaged near the spinodal where the growth of the nucleus is found to be promoted by a coalescence mechanism in contrast to the single particle addition assumption within CNT. The growth of the stable phase becomes progressively collective and spatially diffuse, and the significance of a “critical nucleus” is lost for deeper quenches. In this chapter we present our studies both in 3dimensional Lennard-Jones (LJ) system and Ising model (both 2and 3dimensions). Our general findings seem to be independent of the model chosen. While the previous chapter focuses on relatively well-studied 3-dimensional (3D) LJ system, in Chapter II.3 we present our studies on the characteristics of the nucleation phenomena in 2dimensional (2D) Lennard-Jones fluid. To the best of our knowledge this is the first extensive computer simulation study to check the accuracy of CNT in 2D. Using various Monte Carlo methods, we calculate the free energy barrier for nucleation, line tension, and bulk densities of equilibrium liquid and vapor phases, and also investigate the size and shape of the critical nucleus. The study is carried out at an intermediate level of supersaturation (away from the spinoidal limit). In 2D, a surprisingly large cutoff (rc ≥ 7.0σ where σ is the diameter of LJ particles) in the truncation of the LJ potential is required to obtain converged results. A lower cutoff leads to a substantial error in the values of the line tension, nucleation barrier, and characteristics of the critical cluster. Note that typically 2.5σ is sufficient for 3D LJ fluids. We observe that in 2D system CNT fails to provide a reliable estimate of the free energy barrier. While it is known to slightly overestimate the nucleation barrier in 3D, it underestimates the barrier by as much as 50% at the saturation ratio S = 1.1(defined as S = P/Pc, where Pc is the coexistence pressure) and at the reduced temperature T* = 0.427(defined as T* = KBT/ ε, where ε is the depth of the potential well). The reason for the marked inadequacy of the CNT in 2D can be attributed to the non-circular nature of the critical clusters. Although the shape becomes increasingly circular and the clusters become more compact with increase in cutoff radius, an appreciable non-circular nature remains even without any cutoff to make the simple CNT inaccurate. Part III again consists of three chapters and focuses on the conformational equilibria. Collapse transition and self-organized structures of n-alkanes in solution. In Chapter III.1 we carry out a brief survey of the existing theories of polymer in solution, with particular emphasis on the collapse process in poor solvents. We also introduce the concept of “hydrophobicity” and “hydrophobic collapse”, which is now a subject enormous interest, partly because it my help in understanding the initial processes involved in protein folding. We briefly discuss the subject of formation of beautiful self-organized structures by block copolymers, and also simple homopolymers which is essentially the focus of the work embodied in the next two chapters. In Chapter III.2 we demonstrated a chain length dependent crossover in the structural properties of linear hydrocarbon (n-alkane) chains using detailed atomistic simulations in explicit water. We identify a number of exotic structures o the polymer chain through energy minimization of representative snapshots collected from molecular dynamics trajectory. While the collapsed state is ring-like(circular) for small chains(CnH2n+2; n ≤ 20) and spherical for very long ones( n = 100), we find the emergence of ordered helical structures at intermediate lengths (n ~ 40). We find different types of disordered helices and toroid-like structures at n = 60. We also report a sharp transition in the stability of the collapsed state as a function of the chain length through relevant free energy calculations. While the collapsed state is only marginally metastable for C20H42, a clear bistable free energy surface emerges only when the chain is about 30 monomers long. For n = 30, the polymer exhibits an intermittent oscillation(characterized by well-developed 1/f noise, where f is the frequency ) between the collapsed and the coil structures, characteristic of two stable states separated by a small barrier. This appears to support a weakly first order phase transition between the extended and the collapsed states. Chapter III.3 extends the study of previous chapter to much longer chains (n ≥ 100), which irreversibly collapse in water into globular forms. Even though the collapsed form has a nearly spherical shape, close inspection shows a propensity towards local ordering in the alignment of the polymer segments. This tendency to maintain alignment in order to maximize the number of contacts leads to a core-shell like structure, where the shell is often characterized by a bent rod-like shape consisting of two adjacent segments running in parallel. A key event associated with the initial stage of collapse seems to be the formation of a skewed ring (or loop) that serves as a “nucleation center” for rest of the chain to collapse into. Time evolution of the radial distribution function of water surrounding the polymer, shows that the density of neighboring water decreases by only about 15-20% from that of bulk water. Even though interior of the ting-like structures is fully devoid of water, solvent accessible surface representation shows that these regions are geometrically/spatially inaccessible to water molecules. We suggest that the role of water is to stabilize such ring-like structures once formed by natural conformational fluctuations of the polymer chain. This view is confirmed by observation of spontaneous formation and melting away of such ring-like entities in a polar aprotic solvent(DMSO). We also comment on the role of the flexibility of polymer chains in determining the collapse kinetics. The last part(Part IV) of the thesis consists of two chapters that deal with the crystallization of linear polymer chains from dilute solution. The way long chain polymers crystallize is drastically different from their small molecule counterparts due to their topological connectivity. Linear polymers often crystallize from dilute solution in the form of thin lamellae with well-defined crystallographic features. In Chapter IV.1 we briefly survey the current theoretical understanding and confusions associated with the highly debated field of polymer crystallization. While the last few decades have seen the development of many successful phenomenological theories, the molecular mechanism of formation of such self-organized lamellae is extremely complex and very poorly understood. There are clearly two distinct steps in polymer crystallization. Firstly, the individual linear polymers must self-organize into bundles of somewhat regular structures. These structures then further aggregate to lamellar form and crystallize into a lattice. In this respect , it has marked similarity to the problem of protein crystallization. In chapter IV.2 we present Brownian dynamics simulation studies of a single polythelene chain of length 500. Such systems can reasonably mimic the process of crystallization from dilute solutions. Our simulations could successfully reproduce some of the interesting phenomena observed in experiments and very recent computer simulation studies, including multi-center nucleation of rod-like structures within a single polymer chain, an inverse relation between lamellar thickness and temperature etc. But our primary focus has been to understand the nature of the phase transition as one traverses along the melting temperature and the underlying free energy surface. Near the melting temperature we observe a very intriguing fluctuation between the disordered molten globule state and the ordered rod-like crystalline, where these two forms have highly different shape and structure. These fluctuations have strong signature of 1/f noise or intermittency. This clearly indicates the existence of a weakly first order transition, where two widely different states with large difference in values of order parameter are separated by a rather small free energy barrier. This can be related to the experimentally observed density fluctuations that resemble spinodal decomposition. It is important to note that very similar fluctuations have been observed in our previous studies on liquid crystals (Chapter 1.2) and intermediate sized alkalines in water(Chapter III.2) that signifies a universal underlying energy landscape for these systems. We have discussed the scope of future work at the end of each chapter whenever appropriate.

This thesis presents a theoretical study of Bose-Einstein condensates in a doublering trap. In particular, we determine the ground states of the condensate in the double-ring trap that arise from the interplay of quantum tunnelling and the trap’s rotation. The trap geometry is a concentric ring system, where the inner ring is of smaller radius than the outer ring and both lie in the same two-dimensional plane. Due to the difference in radii between the inner and outer rings, the angular momentum that minimises the kinetic energy of a condensate when confined in the individual rings is different at most frequencies. This preference is in direct competition with the tunnel coupling of the rings which favours the same angular momentum states being occupied in both rings. Our calculations show that at low tunnel coupling ground state solutions exist where the expectation value of angular momentum per atom in each ring differs by approximately an integer multiple. The energy of these solutions is minimised by maintaining a uniform phase difference around most of the ring, and introducing a Josephson vortex between the inner and outer rings. A Josephson vortex is identified by a 2p step in the relative phase between the two rings, and accounts for one quantum of circulation. We discuss similarities and differences between Josephson vortices in cold-atom systems and in superconducting Josephson junctions. Josephson vortices are actuated by a sudden change in the trapping potential. After this change Josephson vortices rotate around the double-ring system at a different frequency to the rotation of the double-ring potential. Numerical studies of the dependence of the velocity on the ground state tunnel coupling and interaction strength are presented. An analytical theory of the Josephson vortex dynamics is also presented which is consistent with our numerical results.

This thesis presents a theoretical study of Bose-Einstein condensates in a doublering trap. In particular, we determine the ground states of the condensate in the double-ring trap that arise from the interplay of quantum tunnelling and the trap’s rotation. The trap geometry is a concentric ring system, where the inner ring is of smaller radius than the outer ring and both lie in the same two-dimensional plane. Due to the difference in radii between the inner and outer rings, the angular momentum that minimises the kinetic energy of a condensate when confined in the individual rings is different at most frequencies. This preference is in direct competition with the tunnel coupling of the rings which favours the same angular momentum states being occupied in both rings. Our calculations show that at low tunnel coupling ground state solutions exist where the expectation value of angular momentum per atom in each ring differs by approximately an integer multiple. The energy of these solutions is minimised by maintaining a uniform phase difference around most of the ring, and introducing a Josephson vortex between the inner and outer rings. A Josephson vortex is identified by a 2p step in the relative phase between the two rings, and accounts for one quantum of circulation. We discuss similarities and differences between Josephson vortices in cold-atom systems and in superconducting Josephson junctions. Josephson vortices are actuated by a sudden change in the trapping potential. After this change Josephson vortices rotate around the double-ring system at a different frequency to the rotation of the double-ring potential. Numerical studies of the dependence of the velocity on the ground state tunnel coupling and interaction strength are presented. An analytical theory of the Josephson vortex dynamics is also presented which is consistent with our numerical results.

This thesis presents a theoretical study of Bose-Einstein condensates in a doublering trap. In particular, we determine the ground states of the condensate in the double-ring trap that arise from the interplay of quantum tunnelling and the trap’s rotation. The trap geometry is a concentric ring system, where the inner ring is of smaller radius than the outer ring and both lie in the same two-dimensional plane. Due to the difference in radii between the inner and outer rings, the angular momentum that minimises the kinetic energy of a condensate when confined in the individual rings is different at most frequencies. This preference is in direct competition with the tunnel coupling of the rings which favours the same angular momentum states being occupied in both rings. Our calculations show that at low tunnel coupling ground state solutions exist where the expectation value of angular momentum per atom in each ring differs by approximately an integer multiple. The energy of these solutions is minimised by maintaining a uniform phase difference around most of the ring, and introducing a Josephson vortex between the inner and outer rings. A Josephson vortex is identified by a 2p step in the relative phase between the two rings, and accounts for one quantum of circulation. We discuss similarities and differences between Josephson vortices in cold-atom systems and in superconducting Josephson junctions. Josephson vortices are actuated by a sudden change in the trapping potential. After this change Josephson vortices rotate around the double-ring system at a different frequency to the rotation of the double-ring potential. Numerical studies of the dependence of the velocity on the ground state tunnel coupling and interaction strength are presented. An analytical theory of the Josephson vortex dynamics is also presented which is consistent with our numerical results.

The effects of strain on the magnetic phases in perovskites are of interest in the highly active research field of multiferroics. A Monte Carlo program is written to investigate the influence of strain on the low– temperature magnetic phase diagram of the manganese perovskites, RMnO3, where R is a cation in the lanthanide series. A Metropolis simulation scheme is implemented together with parallel tempering to perform computations in a two–dimensional geometry using a conventional nearest–neighbor and next–nearest–neighbor Heisenberg Hamiltonian, extended to include spin–lattice couplings and single–ion anisotropies. The latter two are important to account for structural distortions such as octahedral tilting and the Jahn–Teller effect. It is shown that even weak single–ion anisotropies render incommensurability in the otherwise structurally commensurate E–type ordering, and that the Dzyaloshinskii–Moriya interaction, in combination with single–ion anisotropies, is crucial for the stabilization of previously experimentally observed incommensurate spin spirals. Simulations performed to account for strain in the crystallographic ab–plane show that tensile strain may improve stability of E–type ordering for R elements with small atomic radii and that compressive strain drives the magnetic ordering toward the incommensurate spiral states. / Spänningsinverkan på de magnetiska faserna i perovskiter är av intresse inom den just nu högaktiva forskningen om multiferroiska material. Ett Monte Carlo-program har skrivits för att undersöka effekterna av spän- ning på de magnetiska lågtemperaturfaserna i multiferroiska manganitpe- rovskiter, RMnO3, där R är en katjon i lantanoidserien. En kombination av Metropolisalgoritmen och parallelltemperering har använts för att utföra beräkningar i tvådimensionell geometri med en konventionell Heisenberghamiltonian, utökad till att även inkludera spinn–gitterkopplingar och enkeljonsanisotropier. De senare har visats vara viktiga för att ta i beaktande den strukturella distortion i materialet som följer av t.ex. syreoktahederförskjutning och Jahn–Tellereffekten. Det visas att även svaga anisotropier orsakar inkommensurabilitet i den i övrigt kommensurabla E–typsfasen, och att Dzyaloshinskii-Moriyainteraktionen, i kombination med anisotropitermerna, är avgörande för att kunna stabilisera de sedan tidigare experimentellt bekräftade inkommensurabla spinnspiralsfaserna. Simuleringar som modellerar spänning i materialets kristallografiska ab–plan visar att dragspänning kan förbättra stabiliteten hos E–typsfasen för R–atomer med liten radie och att tryckspänning leder den magnetiska ordningen mot inkommensurabla spiraltillstånd.

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