Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userCharacterizing Fano Resonances During Recollision
360
0
0.0
(
0
)
Added by
Graham Gardiner Brown
Publication date
2020
fields
Physics
and research's language is
English
Ask ChatGPT about the research
No Arabic abstract
When intense light irradiates a quantum system, an ionizing electron recollides with its parent ion within the same light cycle and, during that very brief (few femtosecond) encounter, its kinetic energy sweeps from low to high energy and back. Therefore, recollision offers unprecedented time resolution and it is the foundation on which attosecond science is built. For simple systems, recolliding trajectories are shaped by the strong field acting together with the Coulomb potential and they can be readily calculated and measured. However, for more complex systems, multielectron effects are also important because they dynamically alter the recolliding wave packet trajectories. Here, we theoretically study Fano resonances, one of the most accessible multielectron effects, and we show how multielectron dynamics can be unambiguously isolated when we use in situ measurement. The general class of in situ measurement can provide key information needed for time-dependent ab initio electronic structure theory and will allow us to measure the ultimate time response of matter.
rate research
Read More
Measuring the delay for an electron to emerge from different states is one of the major achievements of attosecond science. This delay can have two origins - the electron wave packet is reshaped during departure by the electrostatic field of the ionizing medium or it is modified by dynamic interaction with the remaining electrons. Most experiments have observed the former, but confirmation requires a complex calculation. A direct measurement of multielectron dynamics is needed. Photo-recombination - the inverse of photoionization - occurs naturally during electron recollision and can be measured by combining a perturbing beam to modify the recollision electron before recombination. These in situ methods allow us to unambiguously isolate multielectron dynamics - the reference being the spectral phase of an attosecond pulse simultaneously measured in spectral regions without multielectron interaction. Here, we measure the group delay of the recollision electron caused by plasmonic resonance dynamics in Xe, simulate the in situ measured spectral phase of a recollision electron generated in the presence of the plasmonic resonance in C$_{60}$ and present a corresponding semi-classical theory based on the strong-field approximation. Our results suggest that in situ techniques, together with 300 eV recollision electrons, will allow the ultimate time response of electronic matter to be measured.
Decay of bound states due to coupling with free particle states is a general phenomenon occurring at energy scales from MeV in nuclear physics to peV in ultracold atomic gases. Such a coupling gives rise to Fano-Feshbach resonances (FFR) that have become key to understanding and controlling interactions - in ultracold atomic gases, but also between quasiparticles such as microcavity polaritons. The energy positions of FFR were shown to follow quantum chaotic statistics. In contrast, lifetimes which are the fundamental property of a decaying state, have so far escaped a similarly comprehensive understanding. Here we show that a bound state, despite being resonantly coupled to a scattering state, becomes protected from decay whenever the relative phase is a multiple of $pi$. We observe this phenomenon by measuring lifetimes spanning four orders of magnitude for FFR of spin-orbit excited molecular ions with merged beam and electrostatic trap experiments. Our results provide a blueprint for identifying naturally long-lived states in a decaying quantum system.
Modern intense ultrafast pulsed lasers generate an electric field of sufficient strength to permit tunnel ionization of the valence electrons in atoms. This process is usually treated as a rapid succession of isolated events, in which the states of the remaining electrons are neglected. Such electronic interactions are predicted to be weak, the exception being recollision excitation and ionization caused by linearly-polarized radiation. In contrast, it has recently been suggested that intense field ionization may be accompanied by a two-stage `shake-up reaction. Here we report a unique combination of experimental techniques that enables us to accurately measure the tunnel ionization probability for argon exposed to 50 femtosecond laser pulses. Most significantly for the current study, this measurement is independent of the optical focal geometry, equivalent to a homogenous electric field. Furthermore, circularly-polarized radiation negates recollision. The present measurements indicate that tunnel ionization results in simultaneous excitation of one or more remaining electrons through shake-up. From an atomic physics standpoint, it may be possible to induce ionization from specific states, and will influence the development of coherent attosecond XUV radiation sources. Such pulses have vital scientific and economic potential in areas such as high-resolution imaging of in-vivo cells and nanoscale XUV lithography.
Characterizing quasibound states from coupled-channel scattering calculations can be a laborious task, involving extensive manual iteration and fitting. We present an automated procedure, based on the phase shift or S-matrix eigenphase sum, that reliably converges on a quasibound state (or scattering resonance) from some distance away. It may be used for both single-channel and multichannel scattering. It produces the energy and width of the state and the phase shift of the background scattering, and hence the lifetime of the state. It also allows extraction of partial widths for decay to individual open channels. We demonstrate the method on a very narrow state in the Van der Waals complex Ar--H$_2$, which decays only by vibrational predissociation, and on near-threshold states of $^{85}$Rb$_2$, whose lifetime varies over 4 orders of magnitude as a function of magnetic field.
The Fano resonance is a widespread wave scattering phenomenon associated with a peculiar asymmetric and ultra-sharp line shape, which has found applications in a large variety of prominent optical devices. While its substantial sensitivity to geometrical and environmental changes makes it the cornerstone of efficient sensors, it also renders the practical realization of Fano-based systems extremely challenging. Here, we introduce the concept of topological Fano resonance, whose ultra-sharp asymmetric line shape is guaranteed by design and protected against geometrical imperfections, yet remaining sensitive to external parameters. We report the experimental observation of such resonances in an acoustic system, and demonstrate their inherent robustness to geometrical disorder. Such topologically-protected Fano resonances, which can also be found in microwave, optical and plasmonic systems, open up exciting frontiers for the generation of various reliable wave-based devices including low-threshold lasers, perfect absorbers, ultrafast switches or modulators, and highly accurate interferometers, by circumventing the performance degradations caused by inadvertent fabrication flaws.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
