Ultrafast Carrier and Structural Dynamics in Graphite Detected Via Attosecond Soft X-ray Absorption Spectroscopy

Ultrafast Carrier and Structural Dynamics in Graphite Detected Via Attosecond Soft X-ray Absorption Spectroscopy

Author: Nicola Di Palo

Publisher:

Published: 2020

Total Pages: 163

ISBN-13:

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Understanding most of the physical and chemical phenomena determining the world around us requires the possibility to interrogate their main characters on their natural scale in space and time. The insulating or conductive behavior of matter, its magnetic properties or the nature of chemical bonds are strongly dependent on the nuclear and electronic structure of the atoms, molecules or solids considered. Hence, tools are needed to probe electrons and nuclei directly at the atomic scale with a temporal resolution allowing the observation of electron dynamics (on the attosecond-to-femtosecond timescale) and structural dynamics (on the femtosecond-to-picosecond timescale) in real time.Attosecond science offers unique opportunities to investigate electronic and structural dynamics at the heart of important processes in atomic, molecular and solid-state physics. The generation of attosecond bursts of light, in the form of train of pulses or of isolated pulses, has been achieved on table-top sources by exploiting the high-order harmonic generation (HHG) process. The photons constituting the attosecond emission have energies that range from the extreme ultra-violet (XUV) up to the soft X-ray (SXR) region of the spectrum, allowing to interrogate the electronic structure of the probed material directly at the level of the inner electronic shells. Because of this property of accessing the characteristic electronic structure of the elements constituting the target, XUV and, especially, SXR spectroscopy are considered element-specific techniques. Attosecond pulses have already proven to be able to observe ultrafast phenomena in atoms, molecules or solids previously inaccessible.In this thesis, the application of time-resolved X-ray absorption fine-structure (XAFS) spectroscopy using attosecond SXR pulses to the study of carrier and structural dynamics in graphite is reported. In chapter 1, an introduction to the field of attoscience and the presentation of the state of the art of ultrafast dynamics in graphite are given. The established technique to generate attosecond pulses is described and a review of the most significant application of attosecond pulses to the study of electron dynamics is presented. The electronic and structural properties of graphite are then discussed, highlighting some of the most representative experiments detecting electron and lattice dynamics.The experimental setup developed at ICFO in the group of Prof. Dr. Jens Biegert and used for this Ph.D. thesis project is described in details in chapter 2. The system needed for the generation, propagation and detection of the attosecond SXR radiation is presented. The performances of the SXR source in terms of spectral tunability, photon flux and stability are discussed. The implementation of a IR pump - SXR probe scheme is reported, allowing beams' recombination in both collinear and non-collinear fashion. To conclude, the results of an attosecond streaking experiment are presented, through which a temporal characterization of the HHG emission has been achieved.A discussion on the spectroscopic capabilities of XAFS technique to interrogate the electronic and lattice structure of the observed material is presented in chapter 3. The potential of this technique has been demonstrated with an experimental investigation of a graphite thin film, with the results showing the possibility to probe the first unoccupied electronic bands and the characteristic distances defining the lattice structure.Finally, the XAFS capabilities have been exploited in a time-resolved experimental study of graphite to observe light-induced carrier and lattice dynamics, presented in chapter 4. The interpretation of the experimental data reveals insights on the ultrafast interaction of the pump laser field with charge carriers and on the effects of carrier-carrier and carrier-phonon scattering following photoexcitation.


Towards the Optical Control of Resonantly Bonded Materials

Towards the Optical Control of Resonantly Bonded Materials

Author: Yijing Huang

Publisher:

Published: 2022

Total Pages:

ISBN-13:

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There has been growing interest in using ultrafast light pulses to drive materials into nonequilibrium states with novel properties. In my study, I focus on a specific class of materials, the resonantly bonded materials with various functional properties including ferroelectricity, high thermoelectric figure of merit, and large change of optical constants upon crystallization and amorphization (or phase change materials). More importantly, this class of materials hosts a number of structural phases that are sensitive to external parameters including temperature, pressure, and chemical doping. It will be very interesting to structurally probe these materials under photoexcitation and explore possible new functionalities. The large polarizability in resonantly bonded materials means pronounced coupling between phonons and electronic states. Therefore, on top of probing the structural dynamics, we want to understand the photoexcited interatomic forces that drive the atomic motion and quantify the electron-phonon coupling. Using time-resolved X-ray scattering, I demonstrate that SnSe, one of the IV-VI resonantly bonded compounds, hosts a novel photo-induced lattice instability associated with an orthorhombic distortion of the rock-salt structure. This lattice instability is distinct from the one associated with the high-temperature phase, providing a counterexample of the conventional wisdom that laser pump pulse serves as a heat dump. I show that the driving mechanism for this new lattice instability is related to the removal of valence electrons from the lone pair orbital. Furthermore, using non-zone-center measurements of time-resolved X-ray scattering, I investigate the microscopic details of the photoinduced lattice instability from the perspective of interatomic interactions. I infer the photoexcited interatomic forces from the phonon dispersion and identify a certain bond that is largely overlapped with the lone pair orbital as responsible for the observed photoinduced lattice instability. The conclusion is contrary to the consensus that in thermal equilibrium, the resonant bonding network of chalcogen p orbitals is the main origin of lattice instability. And indeed, the photoexcited phonon modes have a significantly longer lifetime, which means less anharmonicity of the lattice, than those in thermal equilibrium. The results have implications for optical control of the thermoelectric, ferroelectric, and topological properties of the monochalcogenides and related materials. More generally, the results emphasize the need for structural probes to reveal distinct atomic-scale dynamics that are otherwise too subtle or invisible in conventional ultrafast spectroscopies. In the thesis, I also show that by combining time-resolved X-ray diffraction with time-resolved ARPES (angular-resolved photoemission spectroscopy) on Bi2Te3 and Bi2Se3 (V2-VI3 resonantly bonded materials) I can extract state-specific specific deformation potentials (DPs) in these topological insulators which are quantification of electron-phonon coupling. The measured DPs are comparable to those known in non-topological semiconductors. We observe an order of magnitude larger A1g1 phonon- surface state electron DP in Bi2Te3 than Bi2Se3 and reproduce such result with density functional theory. Our results generally help understanding fundamental processes in topological insulators such as surface state transport and potentially electron-phonon-coupling mediated unconventional Cooper-pairing. In investigations of ultrafast dynamics, the methodology holds implications for optical control of matter and even ultrafast switching between topological phases.


The Whys and How of Ultrafast X-ray Science

The Whys and How of Ultrafast X-ray Science

Author:

Publisher:

Published: 2007

Total Pages:

ISBN-13:

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The invention of ultrafast optical lasers with pulse durations comparable to vibrational periods in solids and motions of molecules undergoing structural changes has provided a look at the dynamics that govern important processes in nature. X-rays, on the other hand, with wave-lengths comparable to the distances between atoms, have been the key tool for the study of the average structure of liquids and solids at atomic resolution. With recent developments in ultrafast x-ray sources, the combination of appropriate temporal resolution and spatial resolution is opening new scientific opportunities for direct observation of atomic-scale dynamics. The Sub-Picosecond Pulse Source at SLAC is just such a source. The science and technology of ultrafast x-ray studies will be discussed in this context, as will the extension of these studies to opportunities afforded by the Linear Coherent Light Source x-ray free-electron laser.


Light Scattering in Solids IX

Light Scattering in Solids IX

Author: Manuel Cardona

Publisher: Springer Science & Business Media

Published: 2006-12-15

Total Pages: 435

ISBN-13: 3540344365

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This volume treats new materials (nanotubes and quantum dots) and new techniques (synchrotron radiation scattering and cavity confined scattering). In the past five years, Raman and Brillouin scattering have taken a place among the most important research and characterization methods for carbon nanotubes. Among the novel techniques discussed in this volume are those employing synchrotron radiation as a light source.


Encyclopedia of Interfacial Chemistry

Encyclopedia of Interfacial Chemistry

Author:

Publisher: Elsevier

Published: 2018-03-29

Total Pages: 5276

ISBN-13: 0128098945

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Encyclopedia of Interfacial Chemistry: Surface Science and Electrochemistry, Seven Volume Set summarizes current, fundamental knowledge of interfacial chemistry, bringing readers the latest developments in the field. As the chemical and physical properties and processes at solid and liquid interfaces are the scientific basis of so many technologies which enhance our lives and create new opportunities, its important to highlight how these technologies enable the design and optimization of functional materials for heterogeneous and electro-catalysts in food production, pollution control, energy conversion and storage, medical applications requiring biocompatibility, drug delivery, and more. This book provides an interdisciplinary view that lies at the intersection of these fields. Presents fundamental knowledge of interfacial chemistry, surface science and electrochemistry and provides cutting-edge research from academics and practitioners across various fields and global regions


Molecular Response to Ultra-intense X-rays Studied with Ion and Electron Momentum Imaging

Molecular Response to Ultra-intense X-rays Studied with Ion and Electron Momentum Imaging

Author: Xiang Li

Publisher:

Published: 2019

Total Pages: 0

ISBN-13:

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A new era in ultrafast science has started in the last decade with the advent of x-ray free-electron lasers (XFELs). These machines, which deliver ultra-intense (up to 1020 W/cm2) and ultrashort (down to hundreds of attoseconds) x-ray pulses, have enabled numerous exciting spectroscopic and imaging techniques for exploring structures and dynamics of atoms, molecules, nanomaterials and biological objects. This thesis aims at advancing our understanding of the fundamental interactions between XFEL pulses and molecules by employing experimental techniques based on coincident momentum spectroscopy of the resulting ions and electrons. The work presented here describes the dependence of molecular response on basic x-ray pulse parameters such as wavelength, pulse energy and pulse duration, which is essential for all XFEL applications, and explores the potential of the employed experimental approach for imaging of ultrafast molecular dynamics. More specifically, the dominant x-ray induced processes including sequential photoionization, ultrafast charge rearrangement and molecular fragmentation are studied. And it is observed that because of the charge rearrangement, molecules exposed to ultra-intense x-rays can be ionized more heavily than the isolated atoms with similar photoabsorption cross sections. While the pulse energy mainly determines what interaction products are created (i.e., what is the charge state distribution of the resulting ionic fragments), the pulse duration is found to be the key parameter which determines how fast a particular charge state is reached, and, thus, how large is the kinetic energy of the corresponding ion. With shorter pulses, a certain pair of ionic fragments is created faster and, thus, at a shorter internuclear distance, resulting in more efficient charge rearrangement. This, in turn, results in the enhancement of sequential ionization for shorter pulses. Moreover, signatures of resonance-enhanced x-ray multiple ionization, which were previously reported for atoms, are presented here for molecules. In addition to the fundamental investigations of x-ray - molecule interactions, two imaging schemes for studying molecular dynamics with free-electrons lasers are explored in proof-of-principle experiments. One is the so-called "Coulomb explosion imaging" method. The fragment momentum distribution from iodomethane molecules exploded by XFEL pulses is found to resemble the one expected from the instantaneous explosion of a molecule at equilibrium geometry, potentially providing a robust tool for ultrafast imaging of evolving molecular structures. A time-dependent explosion model is implemented to account for the charge buildup process. The other method is based on ion and electron coincidence measurement, which can fix the ejected electrons with respect to the molecular frame. Combining this method with a sequential two-photon absorption from a single XFEL pulse, a one-pulse pump-probe experiment is carried out on N2 molecules. The transition from the molecular ion N22 created by the first absorbed photon to two isolated atomic ions N+ and N+ is observed from the perspective of core-shell electrons, demonstrating the feasibility of time-resolved x-ray electron spectroscopy in the molecular frame


Ultrafast X-ray Science at the Advanced Light Source

Ultrafast X-ray Science at the Advanced Light Source

Author:

Publisher:

Published: 2000

Total Pages: 5

ISBN-13:

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Our scientific understanding of the static or time-averaged structure of condensed matter on the atomic scale has been dramatically advanced by direct structural measurements using x-ray techniques and modern synchrotron sources. Of course the structure of condensed matter is not static, and to understanding the behavior of condensed matter at the most fundamental level requires structural measurements on the time scale on which atoms move. The evolution of condensed-matter structure, via the making and breaking of chemical bonds and the rearrangement of atoms, occurs on the fundamental time scale of a vibrational period, (almost equal to)100 fs. Atomic motion and structural dynamics on this time scale ultimately determine the course of phase transitions in solids, the kinetic pathways of chemical reactions, and even the efficiency and function of biological processes. The integration of x-ray measurement techniques, a high-brightness femtosecond x-ray source, femtosecond lasers, and stroboscopic pump-probe techniques will provide the unique capability to address fundamental scientific questions in solid-state physics, chemistry, AMO physics, and biology involving structural dynamics. In this paper, we review recent work in ultrafast x-ray science at the ALS including time-resolved diffraction measurements and efforts to develop dedicated beamlines for femtosecond x-ray experiments.