This work aims at development of new dynamical methods to control a resonant light-matter interaction as well as at their application for producing new sources of coherent intense sub-fs radiation in x-ray range. The dynamical control is based on modulation in time and in space of the parameters of the atomic transition (coupled to the resonant high-frequency field) by means of sufficiently strong off-resonant low-frequency control field. In particular, it may result in efficient transfer of quasi-monochromatic VUV or XUV radiation into ultrashort pulses via its resonant interaction with atomic hydrogen gas or plasma of hydrogen-like ions respectively by means of two different techniques: time and space dependent linear Stark effect or interruption of resonant interaction by the tunneling ionization, as shown in previous works of our group. \n\nIn this thesis, I further develop these ideas and demonstrate their important potential applications. First of all, both techniques are extended to arbitrary (non-hydrogen-like) atomic medium. Furthermore, advanced analytical and numerical solutions describing a process of pulses formation are found and shown to be in excellent agreement with each other. A deep physical analogy between the processes of coherent forward scattering of γ-ray radiation in the vibrated quasi-resonant nuclear absorber and the XUV field propagation in the quasi-resonant atomic medium in the presence of the moderately strong IR field is established. \n\nFinally, the application of the developed techniques for production of intense coherent attosecond sources of soft X-ray radiation, including so-called “water window” range (2.2-4.3nm) (especially promising for dynamical imaging of the proteins in a living cell) is proposed. Two different paths towards production of intense coherent attosecond pulses in a soft X-ray range are suggested: (i) via efficient transformation of the picosecond radiation of the high energy pulses of the existing x-ray plasma lasers into the trains of attosecond pulses in the resonant passive plasma, and (ii) via amplification of the low energy pulses of the existing high harmonic sources in the resonant active plasma of x-ray lasers.
This work aims at development of new dynamical methods to control a resonant light-matter interaction as well as at their application for producing new sources of coherent intense sub-fs radiation in x-ray range. The dynamical control is based on modulation in time and in space of the parameters of the atomic transition (coupled to the resonant high-frequency field) by means of sufficiently strong off-resonant low-frequency control field. In particular, it may result in efficient transfer of quasi-monochromatic VUV or XUV radiation into ultrashort pulses via its resonant interaction with atomic hydrogen gas or plasma of hydrogen-like ions respectively by means of two different techniques: time and space dependent linear Stark effect or interruption of resonant interaction by the tunneling ionization, as shown in previous works of our group. \n\nIn this thesis, I further develop these ideas and demonstrate their important potential applications. First of all, both techniques are extended to arbitrary (non-hydrogen-like) atomic medium. Furthermore, advanced analytical and numerical solutions describing a process of pulses formation are found and shown to be in excellent agreement with each other. A deep physical analogy between the processes of coherent forward scattering of γ-ray radiation in the vibrated quasi-resonant nuclear absorber and the XUV field propagation in the quasi-resonant atomic medium in the presence of the moderately strong IR field is established. \n\nFinally, the application of the developed techniques for production of intense coherent attosecond sources of soft X-ray radiation, including so-called “water window” range (2.2-4.3nm) (especially promising for dynamical imaging of the proteins in a living cell) is proposed. Two different paths towards production of intense coherent attosecond pulses in a soft X-ray range are suggested: (i) via efficient transformation of the picosecond radiation of the high energy pulses of the existing x-ray plasma lasers into the trains of attosecond pulses in the resonant passive plasma, and (ii) via amplification of the low energy pulses of the existing high harmonic sources in the resonant active plasma of x-ray lasers.
We suggest a highly efficient method of ultrashort pulse formation from resonant XUV radiation due to sub-laser-cycle modulation of the excited state of non-hydrogen-like atoms by a nonionizing IR laser field. This modulation results in formation of the Raman-Stokes and anti-Stokes sidebands in coherently forward-scattered radiation, which, in turn, leads to formation of short pulses, when the phases of the sidebands are matched. This method is a generalization of a recently suggested technique [V. A. Antonov et al., Phys. Rev. A 88, 053849 (2013)] for a non-hydrogen-like medium. The possibility to form 2-fs XUV pulses in the gas of helium atoms and 990-as XUV pulses in the plasma of Li+ ions with efficiencies over 80% is shown.
The past thirty years witnessed rapid developing of strong field physics that leads to the first generation of attosecond (10−18 s) pulses. The duration of available pulses has recently been reduced to less than 100 as, approaching the Kepler period of a classical electron revolving around the nucleus. For the first time, electron motions inside atoms, molecules and solids can be traced, probed and even steered in real time. It pushed the study on ultrafast dynamic processes into a new frontier, giving birth to attosecond physics. The development of attosecond pulses provides unprecedented coherent ultrashort XUV (extreme ultra-violet) of soft X-ray sources that enable imaging the atomic structure and resolving the related quantum dynamics for matter science. In particular, it allows the probing and monitoring of electron dynamics in the natural time scale of attoseconds with atomic spatial resolution. The generation and applications of attosecond pulses are directly related to the control and manipulation of the sub-cycle electron dynamics. Recent studies on the correlated multielectron dynamics have provided insight into the optical and dynamical properties of matter in the perspectives of time, phase and entanglement. It deepens our understanding on some of the fundamental questions, e.g., how the single or multiple photons are absorbed and how short are the quantum processes such as photoionization, tunneling ionization and charge migration. Although currently attosecond pulses are limited by the flux and pulse duration, the combination of attosecond pulses with intense infrared laser pulses paves new ways of controlling and probing electron dynamics in the domains of energy, time and space that lays the foundation for petahertz optoelectronics and attosecond pulse based transient spectroscopy. In this review, we will first briefly summarize the advancement of strong field and ultrafast physics including the relevant experimental findings, the theoretical explorations, the related technologies and the possible applications. Then we focus on the sub-cycle electron or multielectron dynamics and their manifestation on the ionization and coherent radiation properties. We start with the time behavior of Fano resonance and how it can be probed in time domain. In section 2, the correlated electron dynamics is discussed in term of anti-screening effect and Pauli effect that influence strong field ionization and high harmonic generation processes. In section 3, the coherent emission with frequency from terahertz to soft XUV and their joint measurement are discussed by emphasizing the generation mechanism of terahertz wave in two-color laser pulses. The developed high-harmonic and terahertz wave spectroscopy (HATS) is shown capable of imaging the molecular structure and dynamics. In section 4, the time-resolving of electron and hole dynamics and their coherence is proposed based on attosecond transient absorption technique. The coherence of ionization and the correlated electron dynamics is hinted crucial for electron-hole interaction. The topics are very limited and mainly selected from the perspectives of our group.
Extreme ultraviolet (XUV) light is a valuable frequency range for ultrafast optics experiments. The short wavelength is a requirement for ultrashort pulses, which are widely used to characterize fast dynamics. Additionally, the high photon energy enables quantum control of high frequency transitions in atoms. These transitions are of interest for ultrafast quantum control as the bandwidth of the control pulses needs to be less than the transition frequency. Presently, however, no good modulators exist for these frequencies, which significantly reduces the possible ultrafast optics experiments or applications in the XUV regime. This thesis addresses this problem and focuses on the control of XUV light in time and space. To enable control of XUV light a method is described which modulates the phase of XUV light emitted from a gas of noble atoms. The atoms are resonantly excited with a coherent XUV pulse generated through high order harmonic generation. After the excitation pulse has passed through the gas, the atoms will emit light in the absence of an external field, known as free induction. The phase of the emitted light is changed by shifting the resonance frequencies through the AC Stark shift with a non-resonant infrared control pulse. This phase-control of the emitting atoms also translates into a control of the phase of the emitted XUV field.With the method described in the previous paragraph, the direction of XUV light emitted from noble gases was controlled, and the temporal dynamics of the emission was studied. The redirection of the XUV emission, through the use of a spatially offset IR pulse, was found to change both with intensity of the control pulse and by changing the spatial offset between the pulses. By varying the delay between the excitation and the control pulse the time of redirection was controlled, which enabled high signal to noise study of the temporal dynamics of the emission. Furthermore, with two control pulses the emission was redirected twice, resulting in an XUV pulse shape with controlled duration emitted with a certain angle. Hopefully the presented work will result in more research into the development of this technique, to fully realize the possibility to shape the amplitude and phase of XUV pulses. Such a development would open the door for ultrafast XUV quantum control.
New generations of ultrashort and intense laser pulses as well ashigh power synchrotron radiation sources and x-ray free electronlasers have promoted fast developments in nonlinear optics andx-ray spectroscopy.The new experimental achievements and the appearance of varieties of novelnonlinear phenomena call for further development of theories. The objective of this thesis is to develop and apply thetheories to explain existing experimental data and to suggest new experiments. The first part of the thesis is devoted to nonlinear propagation of optical pulses. It is shown that the vibrational levels can be selectively populated by varying the duration, shape and intensity of the pump pulse. We obtained a strict analytical solution for the resonant two-photon interaction in a multilevel system beyond rotating wave approximation. Simulations show that the polarization anisotropy of the two-photon excitation affects strongly the anisotropy of photobleaching.The two-photon area theorem is reformulated with taking into account the dynamical Stark shift and the contribution from the permanent dipole moments. In general the dynamical Stark shift does not allow complete population of the excited state, but it can be compensated by detunings in atoms. A dynamical theory of the sequential two-photon absorption of microsecond pulses is developed to explore the role of transverse inhomogeneity of the light beam on optical limiting properties. The propagation of ultrashort laser pulses in nondipolar and dipolar media is investigated with special attention to the generation of superfluorescence and supercontinuum and the formation of attosecond pulses. The second part of the thesis addresses the interaction of molecules with x-ray radiation. We explore here the role of nuclear dynamics in resonant Auger scattering. Multimode simulations of the Auger spectra of ethylene molecule explain the main spectral features of the experimental spectra and show that the spectral profiles are formed mainly due to six vibrational modes. We predict the Doppler splitting of the atomic peak in resonant Auger scattering from SF6 molecule for circularly polarized x-rays. This effect is confirmed by the recent experiment. A new scheme of x-ray pump-probe spectroscopy, namely, resonant inelastic x-ray scattering accompanied by core-hole hopping induced by strong laser fields is suggested. The laser-induced promotion of core holes opens the symmetry forbidden scattering channels and gives rise to new spectral lines in the x-ray scattering spectrum. The strength of the symmetry forbidden lines becomes strong when the time of Rabi flopping is shorter than the lifetime of the core-excited state. We study the role of propagation of femtosecond x-ray free-electron pulses on the Auger process. Simulations show that there exists a strong competition between Auger decay and stimulated emission. The Auger yield and Auger branching ratio are strongly suppressed in the course of pulse propagation.
Abstract We establish a close physical analogy between coherent forward scattering of γ -ray radiation in the vibrating quasi-resonant nuclear absorber and the XUV field propagation in the quasi-resonant atomic medium in the presence of the moderately strong IR field. We prove that both processes, under certain conditions, are described by similar Maxwell–Bloch equations for a two-level medium with modulated parameters of the resonant transition. It results in similar transformation of both γ -ray and XUV fields at the exit from the medium, fully determined by the characteristics of applied modulation and spectral content of the incident fields. We find an appropriate analytical solution describing transformation of the electromagnetic field as a result of its propagation in the modulated medium. We show, in particular, that recently observed effects of (i) suppressed resonant absorption in coherent γ -ray scattering of vibrating absorber and (ii) ionization rate modulation in IR pump–XUV probe experiments, present themselves as different manifestations of the same general physical phenomenon of modulation induced transparency (MIT). That transparency is induced by modulating the parameters of the resonant transition. While only partial MIT was observed so far, we suggest certain conditions for conducting some realistic experiments, which should demonstrate nearly 100% transparency in both processes.
Abstract Ultrashort, coherent light pulses in the extreme ultraviolet (XUV) wavelength region are excellent tools for a wide range of experiments. These XUV pulses are in particular used to characterize electron dynamics. Additionally, the high photon energy enables quantum control of short-lived transitions in atoms. These transitions are of interest for ultrafast quantum control as the bandwidth of the control pulses needs to be less than the transition frequency. Coherent XUV pulses would be even more useful if the tools to control and manipulate them existed. Presently, however, no modulators exist for these frequencies, which significantly reduces the number of possible ultrafast optics experiments and applications in the XUV regime. This Ph.D. tutorial addresses this problem and focuses on the control of XUV light in time and space. To enable control of XUV light we have developed a method for opto-optical modulation (OOM), which modulates the phase of XUV light emitted from a gas of atoms. The atoms are resonantly excited with a coherent XUV pulse generated through high order harmonic generation and emit light after the excitation pulse passed. By shifting the resonance frequencies through the AC Stark shift with a non-resonant infrared control pulse, the phase of the emitted light, and therefore its wavefront, is controlled. With OOM the direction of XUV light emitted from noble gases has been controlled, and the temporal dynamics of the emission studied. By varying the delay between the excitation and the control pulse, the time of redirection was controlled, which enabled high signal to noise study of the temporal dynamics of the emission. Furthermore, a proof-of-principle experiment with two control pulses was performed, resulting in a shaped XUV pulse with controlled duration. The technique of OOM presented in this article is still at a very early stage and in order to obtain complete control of the amplitude and phase of the XUV pulses further development is necessary. Such development would present new opportunities for ultrafast XUV quantum control.