ترغب بنشر مسار تعليمي؟ اضغط هنا

Positive-energy spectra of atomic hydrogen in a magnetic field with an adiabatic-basis-expansion method

67   0   0.0 ( 0 )
 نشر من قبل Klaus Bartschat
 تاريخ النشر 2020
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The problem of photoionization of atomic hydrogen in a white-dwarf-strength magnetic field is revisited to understand the existing discrepancies in the positive-energy spectra obtained by a variety of theoretical approaches reported in the literature. Oscillator strengths for photoionization are calculated with the adiabatic-basis-expansion method developed by Mota-Furtado and OMahony [Phys. Rev. A {bf 76}, 053405 (2007)]. A comparative study is performed between the adiabatic-basis-expansion method and our previously developed coupled-channel theory [Phys. Rev. A {bf 94}, 033422 (2016)]. A detailed analysis of the positive-energy spectra obtained here and those from other theoretical approaches shows that the adiabatic-basis-expansion method can produce more accurate positive-energy spectra than other reported approaches for low field strengths.



قيم البحث

اقرأ أيضاً

223 - Daniel Trabert 2021
We present experimental data on the non-adiabatic strong field ionization of atomic hydrogen using elliptically polarized femtosecond laser pulses at a central wavelength of 390 nm. Our measured results are in very good agreement with a numerical sol ution of the time-dependent Schrodinger equation (TDSE). Experiment and TDSE show four above-threshold ionization (ATI) peaks in the electrons energy spectrum. The most probable emission angle (also known as attoclock-offset angle or streaking angle) is found to increase with energy, a trend that is opposite to standard predictions based on Coulomb interaction with the ion. We show that this increase of deflection-angle can be explained by a model that includes non-adiabatic corrections of the initial momentum distribution at the tunnel exit and non-adiabatic corrections of the tunnel exit position itself.
82 - J. Ahokas 2021
We describe the design and performance of a large magnetic trap for storing and cooling of atomic hydrogen (H). The trap operates in the vacuum space of a dilution refrigerator at a temperature of 1.5 K. Aiming at a large volume of the trap we implem ented the octupole configuration of linear currents (Ioffe bars) for the radial confinement, combined with two axial pinch coils and a 3 T solenoid for the cryogenic H dissociator. The octupole magnet consists of eight race-track segments which are compressed towards each other with magnetic forces. This provides a mechanically stable and robust construction with a possibility of replacement or repair of each segment. A maximum trap depth of 0.54 K (0.8 T) was reached, corresponding to an effective volume of 0.5 liters for hydrogen gas at 50 mK. This is an order of magnitude larger than ever used for trapping atoms.
We propose a method for measuring parity violation in neutral atoms. It is an adaptation of a seminal work by Fortson [Phys. Rev. Lett. {bf 70}, 2383 (1993)], proposing a scheme for a single trapped ion. In our version, a large sample of neutral atom s should be localised in an optical lattice overlapping a grid of detection sites, all tailored as the single site in Fortsons work. The methodology is of general applicability, but as an example we estimate the achievable signal in an experiment probing a nuclear spin independent parity violation on the line $6mathrm{s},^2mathrm{S}_{1/2}$--$5mathrm{d},^2mathrm{D}_{3/2}$ in $^{133}$Cs. The projected result is based on realistic parameters and textit{ab initio} calculations of transition amplitudes, using the relativistic coupled-cluster method. The final result is a predicted spectroscopic signature, evidencing parity violation, of the order of 1 Hz, for a sample of $10^8$ atoms. We show that a total interrogation time of 30000 s should suffice for achieving a precision of the order of 0.1% --- surpassing previous determinations of the weak charge in Cs by at least a factor of five.
89 - S. Eckart , D. Trabert , J. Rist 2021
Molecules are many body systems with a substantial amount of entanglement between their electrons. Is there a way to break the molecular bond of a diatomic molecule and obtain two atoms in their ground state which are still entangled and form a Bell- like state? We present a scheme that allows for the preparation of such entangled atomic states from single oxygen molecules on femtosecond time scales. The two neutral oxygen atoms are entangled in the magnetic quantum number of their valence electrons. In a time-delayed probe step, we employ non-adiabatic tunnel ionization, which is a magnetic quantum number-sensitive mechanism. We then investigate correlations by comparing single and double ionization probabilities of the Bell-like state. The experimental results agree with the predictions for an entangled state.
While typical theories of atom-light interactions treat the atomic medium as being smooth, it is well-known that microscopic optical effects driven by atomic granularity, dipole-dipole interactions, and multiple scattering can lead to important effec ts. Recently, for example, it was experimentally observed that these ingredients can lead to a fundamental, density-dependent dephasing of optical spin waves in a disordered atomic medium. Here, we go beyond the short-time and dilute limits considered previously, to develop a comprehensive theory of dephasing dynamics for arbitrary times and atomic densities. In particular, we develop a novel, non-perturbative theory based on strong disorder renormalization group, in order to quantitatively predict the dominant role that near-field optical interactions between nearby neighbors has in driving the dephasing process. This theory also enables one to capture the key features of the many-atom dephasing dynamics in terms of an effective single-atom model. These results should shed light on the limits imposed by near-field interactions on quantum optical phenomena in dense atomic media, and illustrate the promise of strong disorder renormalization group as a method of dealing with complex microscopic optical phenomena in such systems.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا