This thesis describes the synthesis of ruthenium based molecular clusters and their characterisation. Chapter 2 introduces the concept that the very large zero-field splitting (D = 2.9 cm–1) in the S = 5/2 ground state of [Ru2Mn(μ3-O)(tBuCO2)6(py)3] can be modelled by antisymmetric exchange effects. This is supported by measurement of the single ion D values from the Fe2Mn analogue. The same model is applied to the Ru2Ni analogue to describe the zero-field splitting in the S = 1 ground state, (DGS = +8.0 cm–1 from DNi = -4.0 cm–1) in Chapter 3.Chapters 3 and 4 give the full characterisation of each of the two families, [MIII2MII(μ3-O)(tBuCO2)6(py)3] (MIII = Ru or Fe, MII = Mn, Co, Ni or Zn), through IR, electronic absorption and NMR spectroscopy and are structurally characterised by X-ray diffraction. The total spin ground states and zero-field splitting of those ground states have been ascertained by SQUID magnetometry and EPR spectroscopy. Due to the redox activity of the Ru2M complexes chemical oxidations led to the isolation of [RuIII2CoIIIO(tBuCO2)6(py)3]+ (5) and [RuIIIRuIVNiIIO(tBuCO2)6(py)3]+ (6); the locus of their oxidation was determined with the aid of X-ray absorption spectroscopy (XAS).Chapter 5 shows that due to the ease of the substitution of the terminal ligand in Ru2M they can be linked to other molecular clusters with N-donor ligands, in this case [Cr7NiF8(tBuCO2)15(O2CC5H4N)][NH2Pr2] in order to synthesise [Ru2NiO(tBuCO2)6(py)(Cr7NiF8(tBuCO2)15(O2CC5H4N))2][NH2Pr2]2. In situ oxidation experiments have also been carried out to assess the switchabilty of the redox active linker. Chapter 6 demonstrates a new structural archetype for tetranuclear ruthenium mixed-metal complexes, with the formula, [Ru2M2(µ3-OH)2(tBuCO2)7(py)4], where M is either Co (1) or Ni (2). SQUID magnetometry and EPR spectroscopy have determined the spin ground states as, Seff = 1/2 in 1 and S = 3/2 in 2. The magnetic anisotropy in 2 has been determined as +2.02 cm–1 for the S = 3/2 ground state.

Inspired by the success of the ring-polymer molecular dynamics (RPMD) method, we derive a transition-state-theory version (RPTST) with a dividing surface which is, in general, conical in ring-polymer space. It is explained why this conical form is a good approximation to the optimal dividing surface and therefore why centroid-based quantum transition-state theories are inaccurate for asymmetric barriers at low temperatures. The geometry of the ring-polymer transition state is found to describe a finite-difference approximation to the semi-classical instanton trajectory (a classical periodic orbit of length βħ on the inverted potential). Based on this, a new practical method for locating multidimensional instantons is proposed, by computing saddle points on the ring-polymer surface, and a derivation for the reaction rate constant based on the "ImF" premise using the ring-polymer formalism is shown to be far simpler than in previous instanton approaches based on functional determinants. The resulting expression is based only on the ring-polymer potential at the transition-state and its Hessian, and is applied to evaluate the rate in a number of polyatomic systems. We show that a free-energy version of the ImF instanton theory is related to RPTST and thereby provide an explanation for why RPMD produces accurate results for thermal reaction rates in the deep-tunnelling regime and demonstrate how it can be made more efficient and systematically improved. From this, we also explain why RPMD is seen to underestimate the rates of symmetric reactions and overestimate the rates of asymmetric reactions. We also present a ring-polymer instanton derivation of a theory for calculating tunnelling splittings leading to another new practical method, which owing to its simple form, is easily extended to determine the entire tunnelling-splitting pattern of molecular clusters with two or more degenerate wells. This method is applied to the water dimer, trimer, and octamer, and shown to be in good overall agreement with experiment and to provide a deeper understanding of the tunnelling pathways.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第21590号 / 理博第4497号 / 新制||理||1646(附属図書館) / 京都大学大学院理学研究科化学専攻 / (主査)教授 寺西 利治, 教授 島川 祐一, 教授 吉村 一良 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

Efficient implementation of resource sharing strategies in a multi-user wireless environment can improve the performance of a network significantly. In this thesis we study various scheduling strategies for wireless networks and handle the problem of opportunistically scheduling transmissions using channel aware schemes. First we propose a scheme that can handle users with asymmetric channel conditions and is opportunistic in the sense that it exploits the multi-user diversity of the network. The scheme requires the users to have a priori knowledge of their channel distributions. The associated overhead is limited meaning it offers reduced feedback load, that does not scale with the increasing number of users. The main technique used to shrink the feedback load is the contention based distributed implementation of a splitting algorithm that does not require explicit feedback to the scheduler from every user. The users find the best among themselves, in a distributed manner, while requiring just a ternary broadcast feedback from the scheduler at the end of each mini-slot. In addition, it can also handle fairness constraints in time and throughput to various degrees. Next we propose another opportunistic scheduler that offers most of the benefits of the previously proposed scheme but is more practical because it can also handle heterogenous users whose channel distributions are unknown. This new scheme actually reduces the complexity and is also more robust for changing traffic patterns. Finally we extend both these schemes to the scenario where there are fixed thresholds, this enables us to handle opportunistic scheduling in practical systems that can only transmit over finite number of discrete rates with the additional benefit that full feedback session, even from the selected user, is never required.

L’étude de la cinétique de la photodissociation de l’eau assistée par lumière visible a été l’objectif principal de ce travail. En tant que matériau photo-excitable, le semi-conducteur SrTiO₃ dopé au Rh a été utilisé. Le dopage permet l’absorption de lumière visible et donc la transformation d’énergie solaire en combustibles chimiques. Le 1er Chapitre de cette thèse est consacré à une étude bibliographique couvrant les méthodes de caractérisation et les modèles de la cinétique photo-électrochimique. Le 2ème Chapitre traite la description des matériaux et méthodes expérimentaux. Le 3ème Chapitre concerne la caractérisation de la cinétique de la photodissociation de l’eau sur photo-électrodes à base de Rh:SrTiO₃, modifiées en surface par ajout d’un clathrochélate modèle, ou avec du Cu ou du Pt métalliques. Le 4ème Chapitre décrit une étude théorique du mécanisme de la réaction de dégagement d’hydrogène, catalysée par un clathrochélate modèle. Le spectre EXAFS du complexe a été analysé et modélisé, et les intermédiaires importants du mécanisme ont été mis en évidence. Le 5ème Chapitre est consacré à l’étude dynamique de photo-électrodes à base de Rh:SrTiO₃ en utilisant la technique de la photo-tension à lumière modulée. Ce Chapitre présente des résultats inattendus, qui sont rapportés pour la première fois. Ce comportement bizarre a été modélisé par un système d’équations différentielles usuellement utilisées pour décrire ce type de système photo-électrochimique. / The kinetics of water photo-dissociation assisted by visible light was the main topic of this work. The Rh doped SrTiO₃ semiconductor was employed as photo-excitable material. It can absorb visible light and therefore transform solar energy into useful chemical fuels. In this manuscript, a wide bibliographic overview is provided in the 1st Chapter, covering a description of the characterization methods and current models for photoelectrochemical kinetics. The 2nd Chapter is devoted to the description of the materials and methods. The 3rd Chapter deals with the full photoelectrochemical kinetic characterization of water splitting with Rh:SrTiO₃ photoelectrodes, surface-modified by addition of a model clathrochelate or with metallic Cu or Pt. In the 4th Chapter, a theoretical study of the mechanism of hydrogen evolution catalyzed by a model clathrochelate is provided. During the discussion, the EXAFS spectrum of the organometallic complex was thoroughly analyzed and modelled, and the relevant protonated intermediates involved in the mechanism were identified. The 5th Chapter deals with the photoelectrochemical dynamics of illuminated Rh:SrTiO₃ -based photo-electrodes, characterized by the light-modulated photovoltage technique. Unusual results were obtained and are reported in this thesis for the first time. This unexpected dynamic behavior has been modelled by a set of classical differential equations usually used to describe such photo-processes.

III-nitride nanostructures have generated tremendous scientific and technological interests in studying and engineering their low dimensional physics phenomena. Among these, 2D planar, free standing III-nitride nanomembranes are unrivalled in their scalability for high yield manufacture and can be mechanically manipulated. Due to the increase in their surface to volume ratio and the manifestation of quantum phenomena, these nanomembranes acquire unique physical properties. Furthermore, III-nitride membranes are chemically stable and biocompatible. Finally, nanomembranes are highly flexible and can follow curvilinear surfaces present in biological systems. However, being free-standing, requires especially new techniques for handling nanometers or micrometers thick membrane devices. Furthermore, effectively transferring these membrane devices to other substrates is not a direct process which requires the use of photoresists, solvents and/or elastomers. Finally, as the membranes are transferred, they need to be properly attached for subsequent device fabrications, which often includes spin coating and rinsing steps. These engineering complications have impeded the development of novel devices based on III-nitride membranes. In this thesis, we demonstrate the versatility of III-nitride membranes where we develop a thermal bio-sensor nanomembrane and solar energy photo-anode membrane. First, we present a novel preparation technique of nanomembranes with new characteristics; having no threading dislocation cores. We then perform optical characterization to reveal changes in their defect densities compared to the bulk crystal. We also study their mechanical properties where we successfully modulate their bandgap emission by 55 meV through various external compressive and tensile strain fields. Furthermore, we characterize the effect of phonon-boundary scattering on their thermal properties where we report a reduction of thermal conductivity from 130 to 9 W/mK. We employ these modifications to develop a thermal biosensor, which conformally gets attached to cells to measure their thermal properties. We also assess the statistical significance of our measurements to differentiate between different cell lines based on their measured thermal properties. Finally, we demonstrate the application of nanomembranes in solar-based water-splitting by merging them with nanowires to form nanowire membranes which are used to fabricate membrane photo-anodes. Finally, through optical, chemical and electrochemical measurements, we demonstrate their superior operations compared to typical fabrication techniques.

Converting solar energy to clean fuel has gained remarkable attention as an emerged renewable energy resource but optimum efficiency in photocatalytic applications has not yet been reached. One of the dominant factors is designing efficient photocatalytic semiconductors. The research reveals a theoretical investigation of optoelectronic properties of bismuth-based metal oxide and oxysulfide semiconductors using highly accurate first-principles quantum method based on density functional theory along with the range-separated hybrid HSE06 exchange-correlation functional. First, bismuth titanate compounds including Bi12TiO20, Bi4Ti3O12, and Bi2Ti2O7 were studied in a combined experimental and theoretical approach to prove its photocatalytic activity under UV light. They have unique bismuth layered structure, tunable electronic properties, high dielectric constant and low electron and effective masses in one crystallographic direction allowing for good charge separation and carrier diffusion properties. The accuracy of the investigation was determined by the good agreement between experimental and theoretical values. Next, BiVO4 with the highest efficiency for oxygen evolution was investigated. A discrepancy between the experimental and theoretical bandgap was reported and inspired a systematic study of all intrinsic defects of the material and the corresponding effect on the optical and transport properties. A candidate defective structure was proposed for an efficient photocatalytic performance. To overcome the carrier transport limitation, a mild hydrogen treatment was also introduced. Carrier lifetime was enhanced due to a significant reduction of trap-assisted recombination, either via passivation of deep trap states or reduction of trap state density. Finally, an accurate theoretical approach to design a new family of semiconductors with enhanced optoelectronic properties for water splitting was proposed. We simulated the solid solutions Bi1−xRExCuOS (RE = Y, La, Gd and Lu) from pure BiCuOS to pure RECuOS compositions. Starting from the thermodynamic stability of the solid solution, several properties were computed for each system including bandgaps, dielectric constants, effective masses and exciton binding energies. Several compositions with specific organization and density of Bi and RE atoms, were found to be appropriate for water splitting applications. In General, the presented results give further insights to the experimentalists and recommendations for appropriate future application and defect-design of each material.

This licentiate thesis comprises two complementary studiesdealing with the sheet-fed offset printing of paper. The firststudy addresses the further development of a practical methodto acoustically monitor and analyse the film splitting ofoffset inks. This method was tested on laboratory printingequipment, specifically monitoring the continuous ink splittingin the nip of an IGT ink distribution unit and the short-timeink splitting in the inked print disc-paper nip of the printingunit of an ISIT instrument. The study verified that the inksplitting component of the acoustic signal contributes to thehigher frequency range (10-20 kHz) of the audible spectrum, andcan thus be separated from the lower frequency machine noise.Furthermore, the film splitting component is sensitive tochanges in the ink and printing conditions, thus enabling itsuse in probing the fundamental mechanisms occurring during inktransfer and also suggesting its applicability fornon-intrusive monitoring of industrial printing presses. Anincrease in film thickness during ink distribution correspondsto an increased acoustic power, with the exception of very lowink amounts, which give reduced acoustic emission due to alubricating effect. The effect of the presence of fountainsolution was simulated by adding emulsion-forming, butnon-evaporative, ethylene glycol. This produces an increase inacoustic power at low amounts, due to resistance to glycol dropdeformation, followed by a decrease at higher amounts owing toexcess glycol lining the rolls. During test printing on paper,increasing ink amounts also display an increased acousticresponse. The second study further developed a theoretical model toexplain and predict the evolution of ink tack in terms of inksetting directly after offset printing on coated paper. Asmeasured by the ISIT, the tack of the printed ink rises duringshorter time periods, attains a maximum, and then falls atlonger times. The proposed model described how the ink tack,characterised by the impulse during disc pull-off, dependsdynamically on the viscoelastic properties of the ink, thecontact with paper and disc, and the flow geometry. The inksetting was modelled as a diffusion-limited transport of theoil vehicle through the ink film and into the pores of thecoated paper. The coupling of the tack and setting models,compared to the ISIT experimental measurements, then provided adiffusion coeffcient for ink setting during the tack riseperiod. This coeffcient decreases with time, and increasinglyrapidly with decreasing ink amounts due to theconcentration-dependent diffusion. For an accurate descriptionthe elasticity and adhesion effects also have to be considered,at least for explaining the tack fall period.

Let uxv be an induced path with center x in a graph G. The edge lifting of uv off x is defined as the action of removing edges ux and vx from the edge set of G, while adding the edge uv to the edge set of G. We study trees for which every possible edge lift changes the domination number. We show that there are no trees for which every possible edge lift decreases the domination number. Trees for which every possible edge lift increases the domination number are characterized.

Hydrogen is a carrier energy gas that can be utilized as a clean energy source instead of oil and natural gas. Splitting the water into hydrogen and oxygen is one of the most favorable methods to generate hydrogen. The catalytic properties of molybdenum disulfide (MoS2) could be valuable in this role, particularly due to its unique structure and ability to be chemically modified, enabling its catalytic activity to be further enhanced or made comparable to that of Pt-based materials. In general, these modification strategies may involve either structural engineering of MoS2 or enhancing the kinetics of charge transfer, including by confining to single metal atoms and clusters or integrating with a conductive substrate. We present the results of synergetic integration of MoS2 films with a Si-heterojunction solar cell for generating H2 via the photochemical water splitting approach. The results of the photochemical measurements demonstrated an efficient photocurrent of 36. 3 mA cm-2 at 0 V vs. RHE and an onset potential of 0.56 V vs. RHE. In addition to 25 hours of continuous photon conversion to H2 generation, this study points out that the integration of the Si-HJ with MoS2 is an effective strategy for enhancing the internal conductivity of MoS2 towards efficient and stable hydrogen production. Moreover, we studied the effect of doping an atomic scale of Pt on the catalytic activity of MoS2. The electrochemical results indicated that the optimum single Pt atoms loading amount demonstrated a distinct enhancement in the hydrogen generating, in which the overpotential was minimized to -0.0505 V to reach a current density of 10 mA cm−2 using only 10 ALD cycles of Pt. The Tafel slopes of the ALD Pt/ML-MoS2 electrodes were in the range of 55–120 mV/decade, which indicates a fast improvement in the HER velocity as a result of the increased potential. Stability is another important parameter for evaluating a catalyst. The same (10 ALD cycles) Pt/ML-MoS2 electrode was able to continuously generate hydrogen molecules at for 150 hours. These superior results demonstrate that the low conductivity of semiconductive MoS2 can be enhanced by anchoring the film with Pt SAs and clusters, leading to sufficient charge transport and a decrease in the overpotential.