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Full Description
It is the dream of every natural scientist to directly observe the motion of atoms and molecules in real time as they interact. The natural sciences by definition involve structural dynamics and the observation of molecules interconverting from one structure to another or other structures, which is, after all, the very essence of science. Each area of the natural sciences has unique intellectual goals; however, they are all united by the thought experiment in which we try to understand how molecules interconvert between different structures by passing through a reaction barrier, a transition state.
This concept of a "moment," an ultra-short time interval in the natural sciences, forces us to think about the relative positions of the atoms that define the barrier to the process of their interaction. It is the control of the barrier height that allows one of many possible atomic rearrangements to occur, since it occurs faster than competing processes. That is, the process of molecular transformation during interaction is inherently a "race against time." Manipulating the barrier height gives effective, exponential control over the yield of the reaction product. The problem of visualizing transition state structures is akin to finding a way from one valley to another in a very rugged mountainous area during an earthquake, where the mountains and the landscape change as you move across the terrain: suddenly a crack appears and the shaking takes you to a more stable valley. Without a detailed understanding of how fluctuations - in this analogy, shaking - affect the potential energy landscape, it would be difficult to guess where and when the crack will form or the path to the next valley.
At its most fundamental, chemistry is the study of structural dynamics, discussed both for synthetic purposes and for physical methods with the explicit goal of controlling the transformation of matter from one form/property to another. We now have tools to observe chemical reactions at the atomic level.
This monograph presents a picture of the development and evolution of methods for detecting ultrafast structural dynamics processes. It describes the theoretical foundations and principles of the relevant experimental techniques, as well as prospects for their improvement for application in the latest existing and developing technologies. The book presents the achievements of ultrafast methods of spectroscopy, electron diffraction, X-ray diffraction and electron microscopy for diagnostics of the structural dynamics of matter in states far from equilibrium and extreme states of matter. In general, the information obtained is of particular value for understanding the relationship between the elements of the structure-dynamics-function triad. In the future, this will ensure control over the functional capabilities of various materials far from equilibrium and the creation of new atomic and molecular technologies.
The monograph is recommended for a wide range of readers interested in the problems of the structure of matter, ultrafast structural dynamics, including the study of the structure and dynamics of nanomaterials: scientists, graduate students and students specializing in this interesting and rapidly developing area of modern natural science, which is now called "ultrafast science".
· Ultrafast transmission electron microscopy uncover structure-function relationships
· Ultra-short photoelectron pulses opened up the studying of structural dynamics
· One electron femtosecond pulses prevents damage of biological objects
· Ultrafast electron microscopy uncover simultaneous real space and diffraction imaging
· Ultrafast diffraction and tomography holds complete information of the quantum state
Contents
Acknowledgements
Foreword
Chapter One
Spectral methods for detecting dynamics of substances
1.1. Time-resolved optical spectroscopy
1.1.1. Time-resolved luminescence spectroscopy
1.1.2. Time-resolved difference absorption spectroscopy
1.1.3. Time-resolved Raman spectroscopy
1.1.4. Detection of laser-induced ultrafast processes in atomic-molecular structures
1.1.5. Intramolecular dynamics and the Born-Oppenheimer approximation
1.1.6. Ultrafast two-dimensional (2D) spectroscopy
1.1.7. Primary and stimulated photon echo
1.1.8. Progress in ultrafast laser spectroscopy
1.2. Attophysics
1.2.1. Angle-resolved attosecond photoelectron spectroscopy
1.2.2. Micro- and macroscopic aspects of the generation of high harmonics and ultrashort electromagnetic pulses of attosecond duration
1.3. Laser control of molecular degrees of freedom on a picosecond time scale
1.3.1. Optical molecular centrifuge: practical implementation and capabilities
1.3.2. Optical control of quantum rotors
Conclusion
References
Chapter Two
Dynamics of chemical reactions
2.1. Identification of photodissociation products by the TRXD signal at small X-ray scattering angles
2.2. Spectroscopic and structural study of molecular dynamics in an excited state by TRPES and UED methods
Conclusion
References
Chapter Three
Development of ultrafast electron microscopy
3.1. Examples in the field of UED
3.2. Detection of ultrafast coherent phenomena with UEM
3.2.1. UEM imaging of laser-induced phase transitions
3.2.2. UEM visualization of electromagnetic signals
3.2.3. Combining UEM with EELS (Electron Energy Loss Spectroscopy)
3.2.4. New trends in UEM: from 4D UEM to 5D UEM and attosecond electron microscopy
3.2.5. Holographic imaging of electromagnetic fields using electron-light quantum interference
3.2.6. UEM with laser nanoemitters
3.2.7. Ultrafast Lorentz Microscopy
3.3. Characterizing and controlling the out-of-equilibrium state of nanostructured Mott insulators
Conclusion
References
Chapter Four
Probing structural dynamics by ultra-short electron and X-ray pulses
4.1. Experimental setups for UEC
4.2. Diagnostics of the structural dynamics of condensed matter
4.2.1. Surfaces and crystals
4.2.2. Transition of graphite into diamond
4.2.3. Bilayers of the crystal structure of two-dimensional fatty acids: molecular assemblies
4.3. Photoswitching system changing properties from insulator to metal
4.4. Structural dynamics of nonequilibrium phase transitions
4.4.1. Vanadium dioxide
4.4.2. Superconducting cuprates
4.5. Quantum materials
4.5.1. Structural dynamics of quantum materials observed by UXRC, UXRnC and X-ray scattering methods
4.5.2. Structural dynamics of quantum materials observed by UXRC, UXRnC and X-ray scattering methods
4.5.3. "Anomalous" photoelectric effect in the UED method
Conclusion
References
Chapter Five
Methods for ultrafast electron and X-ray nanocrystallography
5.1. Time-resolved electron nano-crystallography
5.2. Basic Concepts
5.3. Sample preparation
5.4. Primary data processing
5.5. Some results of time resolved studies
5.5.1. Aluminum melting under tightly controlled conditions
5.5.2. Photoinduced heterogeneous changes in gold nanocrystals
5.5.3. Observation of coherent optical phonons excited by femtosecond laser radiation in Sb nanofilms
5.6. Time-resolved X-ray nanocrystallography
5.6.1. Spontaneous fluctuations and nanoscale heterogeneity
5.6.2. Structural dynamics of materials, energy transfer and phase transitions at the nanoscale
5.7. Nonequilibrium thermodynamics of colloidal gold nanocrystals
Conclusion
References
Chapter Six
Radiation sources and methods for ultrafast X-ray diffraction analysis
6.1. Processes studied by time resolved X-ray diffraction
6.2. Basics of X-ray Structure Analysis
6.3. Features of Time Resolved XRD (TRXRD)
6.3.1. Dynamics of slow processes—long-lived states
6.3.2. Short-lived states—dynamics of fast processes on a millisecond scale
6.4. The most important characteristics of instruments for X-ray diffraction studies of fast and ultrafast processes
6.4.1. The measures of radiation intensity
6.5. Synchrotron radiation
6.5.1. SR sources based on storage rings
6.5.2. Magnetic devices generating SR in storage rings
6.5.3. Classification of SR sources by generations
6.6. Free electron lasers - new sources of X-rays
6.6.1. Operating principles of free electron lasers
6.6.2. Examples of X-ray free electron lasers (XFELs)
6.7. Laser-plasma X-ray sources
6.7.1. Mechanisms of X-ray generation by laser plasma
6.7.2. Higher harmonics generation method
6.7.3. Hot laser plasma radiation
6.7.4. Laser-plasma accelerators and XFELs
6.8. Short-pulse X-ray generators based on inverse Compton scattering
6.8.1. Models of photon scattering by electrons
6.8.2. Inverse Compton effect - theoretical basis
6.8.3. On the duration of radiation pulses from laser-electron ICS sources and their polarization
6.8.4. Examples of operating ICS X-ray sources
6.8.5. Compton sources of X-rays based on FEL oscillators
6.8.6. ICS X-ray sources on linear electron accelerators
6.8.7. ICS X-ray sources based on small synchrotrons
6.8.8. Laser-plasma accelerators as X-ray generators
6.8.9. ICS X-ray sources with laser-plasma acceleration
6.8.10. Compact Compton X-ray sources
6.8.11. Examples of application of X-ray sources based on ICS
6.9. X-ray detectors for ultra-fast measurements
6.10. X-ray diffraction methods for studying structural dynamics using synchrotron, XFEL or ICS radiations
6.10.1. Experimental "pump-probe" methods
6.10.2. Stroboscopic measurements of diffraction patterns
6.10.3. Some problems in stroboscopic diffraction measurements by synchrotron radiation
6.10.4. Time-resolved diffraction studies using a laboratory diffractometer with an X-ray tube
6.10.5. Study of transition states in crystals using X-ray diffraction on synchrotron radiation
6.10.6. Problems of insufficient X-ray probe intensity in time-resolved XRSA
6.11. Time-resolved Laue X-ray diffraction for structure determination
6.12. SFXC - serial femtosecond X-ray crystallography
6.12.1. Sample delivery method for serial crystallography at XFEL
6.12.2. Data analysis using the SXC method
6.12.3. Improvements and modifications of X-ray diffraction analysis using the SXC method
6.12.4. Modifications of the SFXC method to SMXC
6.12.5. Practical application of SFXC
Chapter Seven
Visualization of structural dynamics in the femtosecond time domain: complementarity of spectroscopy and diffraction
7.1. Introduction
7.2. Transition State and Femtosecond Transition State Spectroscopy
7.3. Chemical dynamics via conical intersection between electronic states
7.4. Theory Elements of Time-Resolved Electron Diffraction
7.4.1. Basic assumptions and approximations
7.4.2. Aligned molecules
7.4.3. Solution of the inversion problem
7.4.4. The difference method for time-dependent diffraction data analysis
7.4.5. Time Dependent Diffraction from Single Crystals and Solution to the Inversion Problem
7.5. Dynamics of wave packets
7.5.1. Real time dynamics of transient states in photodissociation and photopredissociation
7.5.2. Quantum-dynamical simulations of photodissociation
7.6. The diffraction signatures of excited molecules
7.6.1. Molecular quantum state tomography
7.6.2. Non-adiabatic two-channel photo-dissociation of the CS₂ molecule
7.6.3. Diffraction signatures of aligned molecules
7.6.4. Photodissociation dynamics of aligned CS₂ and ICN molecules
7.7. Imaging the electrocyclic ring-opening reaction of 1,3-cyclohexadiene
7.7.1. The structure of the ground-state 1,3-cyclohexadiene molecule
7.7.2. Time-Resolved Electron Diffraction and Time-Resolved X-ray Diffraction of CHD
7.7.3. Convergence of Time-Resolved Electron and X-ray Diffraction, Femtosecond Spectroscopy and Quantum Chemistry
7.8. Dynamics of spectrally invisible structures
7.9. Photodissociation and ultrafast relaxation of iron pentacarbonyl
7.9.1. Ultrafast Electron Diffraction
7.9.2. Time-Resolved Femtosecond Spectroscopy and Mass-Spectrometry
7.9.3. Femtosecond-resolution Resonant Inelastic X-ray Scattering
7.10. Structure and nuclear dynamics in free radicals: the Jahn-Teller effect and pseudorotation in cyclopentadienyl radicals
7.11. Unimolecular photodissociation of 1,2-diiod-tetrafluoroethane
7.11.1. Structural dynamics of the elimination reaction of iodine atoms from the free C₂F₄I₂ molecules under collisionless conditions
7.11.2. Structural dynamics of iodine cleavage reaction in C₂H₄I₂ and C₂F₄I₂ molecules in solution
7.12. Laser-Induced Electron Diffraction
7.12.1. Ultrafast Electron Diffraction imaging of bond breaking in di-ionized acetylene
7.12.2. Molecular dynamics and electron density tomography
7.13. Atom Resolved Reaction Dynamics: Realization of the Chemists' Gedanken Experiment
7.14. Complementarity of spectroscopy and diffraction for studying structural dynamics
7.15. Theory: Closing the Loop
7.15.1. Short outline of computational techniques
7.15.2. Femtosecond quantum tomography: towards the quantum limit
7.16. Conclusions and future outlook
Supplement
References
List of abbreviations
index
