Structural and Dynamical Properties of Solvated Electrons PDF Download
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Author: Cornelis van Huis
Publisher:
ISBN:
Category :
Languages : en
Pages : 120
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Book Description
Author: Cornelis van Huis
Publisher:
ISBN:
Category :
Languages : en
Pages : 120
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Book Description
Author: Cornelis van Huis
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Author: H. Ohtaki
Publisher: Elsevier
ISBN: 1483291421
Category : Science
Languages : en
Pages : 361
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Book Description
Recent advances in the study of structural and dynamic properties of solutions have provided a molecular picture of solute-solvent interactions. Although the study of thermodynamic as well as electronic properties of solutions have played a role in the development of research on the rate and mechanism of chemical reactions, such macroscopic and microscopic properties are insufficient for a deeper understanding of fast chemical and biological reactions. In order to fill the gap between the two extremes, it is necessary to know how molecules are arranged in solution and how they change their positions in both the short and long range. This book has been designed to meet these criteria. It is possible to develop a sound microscopic picture for reaction dynamics in solution without molecular-level knowledge of how reacting ionic or neutral species are solvated and how rapidly the molecular environment is changing with time. A variety of actual examples is given as to how and when modern molecular approaches can be used to solve specific solution problems. The following tools are discussed: x-ray and neutron diffraction, EXAFS, and XANES, molecular dynamics and Monte Carlo computer simulations, Raman, infrared, NMR, fluorescence, and photoelectron emission spectroscopic methods, conductance and viscosity measurements, high pressure techniques, and statistical mechanics methods. Static and dynamic properties of ionic solvation, molecular solvation, ion-pair formation, ligand exchange reactions, and typical organic solvents are useful for bridging the gap between classical thermodynamic studies and modern single-molecule studies in the gas phase. The book will be of interest to solution, physical, inorganic, analytical and structural chemists as well as to chemical kineticists.
Author: Michael J. Tauber
Publisher:
ISBN:
Category :
Languages : en
Pages : 404
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Author: Erik Peter Farr
Publisher:
ISBN:
Category :
Languages : en
Pages : 240
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Book Description
This thesis is broadly concerned with understanding the structural and energetic details of condensed phase chemistry, primarily on ultrafast timescales. The first chapter focuses on novel contributions regarding the nature of the hydrated electron. It has been thought that this quasi-free solvent-supported electron resided in a cavity by its repulsive Coulombic interactions with nearby water molecules. Instead, a relatively modern but controversial simulation of the hydrated electron has shown that many observables are in fact better described by a non-cavity structure in which the hydrated electron's wave function resides in the interstitial spaces between water that is at, or slightly above, bulk density near and within the electron. The novel contributions have been understanding the effects of temperature on the structure and dynamics of the hydrated electron. This newly observed experimental temperature dependence of dynamics is highly consistent with the new non-cavity model of the hydrated electron. Secondarily, we show that previous methods of determining the hydrated electron's first excited-state lifetime from transient absorption were fraught with parameter correlation, making clean identification of the lifetime impossible. To resolve this we employ a more sophisticated model in combination with better signal to noise from broadband transient absorption measurements to show with certainty that the first excited-state lifetime of the hydrated electron at room temperature is on the order of 100 fs---in agreement with recent time-resolved photoelectron experiments. The second chapter brings these concepts of time-resolved spectroscopy to an advanced undergraduate level through a novel laboratory experiment. In order to provide access to undergraduates, I built a low-cost combined transient absorption and time-resolved fluorescence spectrometer. Simultaneously, I developed an experiment limited by the temporal and spectral resolution of the instrument in which undergraduates measure the fluorescent and phosphorescent lifetimes of the dye Eosin B. With these lifetimes in hand, the undergraduates then arrive at a complete photophysical picture for the molecule and quantitatively interpret their results with introductory quantum mechanics for electronic spectroscopy. Finally, the third chapter highlights time-resolved and steady-state spectroscopic investigations of singly linked di-perylenediimide, a key acceptor material used in competitive organic photovoltaics. We show that this molecule exists in a range geometrical configurations at room temperature, and that these conformations are spectrally distinct. Furthermore, the typical approximations used to describe this dimer as a Kasha H-/J-aggregate do not appear reasonable evidenced by detailed deconvolution of underlying spectral components with a high density of states---further confirmed with time-dependent density functional theory. The overarching theme of these chapters is to understand molecular photophysics in condensed phases on ultrafast timescales by using or refining modern principles of physical chemistry.
Author: Saburo Nagakura
Publisher: Springer Science & Business Media
ISBN: 4431668683
Category : Science
Languages : en
Pages : 340
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Book Description
Molecular systems are assemblies of molecules designed to possess special qualities and desired functionality. Such systems are important because they provide materials with novel properties, and they will be particularly useful for minimizing electronic devices. Molecular systems often form organized molecular crystals, polymers, or thin films that are significantly more complex than current materials. To provide a sound basis for understanding these levels of complexity, this book provides an analysis of the fundamentals of electronic structures, dynamic processes in condensed phases, and the unique properties of organic molecular solids and the environmental effects on these properties. Also covered are the latest methods in physical chemistry that are particularly useful for deriving and controlling the functionality of molecular systems. A second volume subtitled From Molecular Systems to Molecular Devices is also being published.
Author: Jannis Samios
Publisher: Springer Science & Business Media
ISBN: 1402023847
Category : Science
Languages : en
Pages : 548
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Book Description
The unique behavior of the "liquid state", together with the richness of phenomena that are observed, render liquids particularly interesting for the scientific community. Note that the most important reactions in chemical and biological systems take place in solutions and liquid-like environments. Additionally, liquids are utilized for numerous industrial applications. It is for these reasons that the understanding of their properties at the molecular level is of foremost interest in many fields of science and engineering. What can be said with certainty is that both the experimental and theoretical studies of the liquid state have a long and rich history, so that one might suppose this to be essentially a solved problem. It should be emphasized, however, that although, for more than a century, the overall scientific effort has led to a considerable progress, our understanding of the properties of the liquid systems is still incomplete and there is still more to be explored. Basic reason for this is the "many body" character of the particle interactions in liquids and the lack of long-range order, which introduce in liquid state theory and existing simulation techniques a number of conceptual and technical problems that require specific approaches. Also, many of the elementary processes that take place in liquids, including molecular translational, rotational and vibrational motions (Trans. -Rot. -Vib. coupling), structural relaxation, energy dissipation and especially chemical changes in reactive systems occur at different and/or extremely short timescales.
Author: Chun C. Mak
Publisher:
ISBN:
Category :
Languages : en
Pages : 119
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Book Description
Photoexcitation of halides dissolved in polar liquids results in charge-transfer-to-solvent (CTTS) states in which a halide valence electron has been transferred to a delocalised, solvent-supported orbital. Subsequent relaxation of CTTS excited solvated halides results in the formation of solvated electrons, ubiquitous species implicated in numerous chemical and biochemical transformations. Analogues of the CTTS excited states of solvated halides have also been observed in small iodide-polar solvent clusters, and the relaxation of CTTS excited iodide-polar solvent clusters, [I–(Solv)n]*, has attracted significant interest as a paradigm for investigating the role of individual solvent molecules in trapping and solvating an excess electron. In this work, a combination of high-level quantum chemical calculations and first-principles molecular dynamics simulations is employed to elucidate the relaxation mechanism of [I–(Solv)n]* (Solv = H2O, CH3CN and CH3OH) and to develop an in-depth understanding of the nature of the molecular motions and interactions involved in the associated electron solvation processes. A ‘two-level’ approach is employed, in which [I–(Solv)n]* trajectories are propagated on a potential energy surface computed with a relatively modest treatment of electron correlation and a medium-sized basis set while electronic properties of cluster configurations sampled from the trajectories are computed with a much more rigorous quantum-chemical method and significantly larger basis sets. Results indicate that [I–(Solv)n]* relaxation involves rapid initial motion of the solvent molecules, leading to the separation of the excited electron from the iodine atom and a concomitant decrease in stability of the excited electron, followed by more gradual reorganisation of the cluster, which can have variable effects on the stability of the excited electron, depending on the type of solvent molecule in the cluster. In clusters with a strong network of solvent-solvent interactions, such as [I–(H2O)n]*, stabilisation of the excited electron occurs, while in clusters with a weaker network of solvent-solvent interactions, such as [I–(CH3OH)n]*, solvent cluster fragmentation ultimately results in destabilisation of the excited electron. Subtle differences in the structural properties of the molecules within the cluster can thus heavily influence the electron solvation process in [I–(Solv)n]*, a reflection of the important role of individual molecules in supporting a solvated electron.
Author: Jennifer Ryan Casey
Publisher:
ISBN:
Category :
Languages : en
Pages : 115
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Book Description
Since its discovery over fifty years ago, the hydrated electron has been the subject of much interest. Hydrated electrons, which are free electrons in water, are found in fields ranging from biochemistry to radiation chemistry, so it is important that we understand the structure and dynamics of this species. Because of its high reactivity, the hydrated electron's structure has proven difficult to pin down, especially its molecular details. One-electron mixed quantum/classical molecular dynamics simulations have proven useful in helping elucidate the structure of the hydrated electron. The picture most commonly presented from these studies is one of the electron residing in a cavity, disrupting the local water structure much like an anion the size of bromide. Our group has recently proposed a completely different structure for the hydrated electron, which arose from rigorous calculations of a new electron-water potential. The picture that emerged was of an electron that does not occupy a cavity but instead draws water within itself; this non-cavity electron resides in a region of enhanced water density. The one-electron cavity and non-cavity models all predict similar experimental observables that probe the electronic structure of the hydrated electron, such as the optical absorption spectrum, which makes it difficult to determine which model most accurately describes the true structure of the hydrated electron. In this thesis, we work to calculate experimental observables for various simulated cavity and non-cavity models that are particularly sensitive to the local water structure near the electron, in an effort to distinguish the various models from each other. Two particular observables we are interested in are the resonance Raman spectrum and the temperature dependent optical absorption spectrum of the hydrated electron. We find that for both of these experiments, only the non-cavity model has qualitative agreement with experiment; the cavity models miss the experimental temperature dependence in the optical absorption spectrum and show the wrong trends in the resonance Raman spectrum. We also explore the differences between non-cavity and cavity models by quantifying the electron-water overlap, referring to the non-cavity model as an `inverse plum pudding, ' where the water molecules are embedded within the electron density. Finally, we examine hydrated electrons in the presence of an air/water interface. Experiments indicate that most likely electrons do not reside at the surface, and if they do, they have structural and dynamical properties reminiscent of the bulk. Our calculated Potentials of Mean Force indicate that both cavity and non-cavity electrons prefer to be solvated by the bulk, but that the cavity electron has a local free energy minimum near the surface. These calculated interfacial cavity electrons behave very differently than cavity electrons in the bulk, in direct contrast to experimental evidence. From the work presented in this thesis, it is clear that the non-cavity electron is the most appropriate one-electron model we have for the structure of the hydrated electron.
Author: James F. Wishart
Publisher: World Scientific
ISBN: 9814282073
Category : Science
Languages : en
Pages : 634
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Book Description
This volume is a review of the trends in the field of radiation chemistry research. It covers a broad spectrum of topics, ranging from the historical perspective, instrumentation of accelerators in the nanosecond to femtosecond region, through the use ofradiation chemical methods in the study of antioxidants and nanomaterials, radiation-induced DNA damage by ionizing radiation involving both direct and indirect effects, to ultrafast events in free electron transfer, radiation-induced processes at solid-liquid interfaces and the recent work on infrared spectroscopy and radiation chemistry. The book is unique in that it covers a wide spectrum of topics that will be of great interest to beginners as well as experts. Recent data on ultrafast phenomena from the recently established world-class laser-driven accelerators facilities in the US, France and Japan are reviewed.
