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Kjellsson Lindblom, TorORCID iD iconorcid.org/0000-0002-7544-5659
Publications (2 of 2) Show all publications
Kjellsson Lindblom, T. & Selsto, S. (2021). Relativistic photoionization with elliptically polarized laser fields in the ultraviolet region. Physical Review A: covering atomic, molecular, and optical physics and quantum information, 104(4), Article ID 043102.
Open this publication in new window or tab >>Relativistic photoionization with elliptically polarized laser fields in the ultraviolet region
2021 (English)In: Physical Review A: covering atomic, molecular, and optical physics and quantum information, ISSN 2469-9926, E-ISSN 2469-9934, Vol. 104, no 4, article id 043102Article in journal (Refereed) Published
Abstract [en]

We study relativistic effects in photoionization of a hydrogen atom exposed to an intense laser pulse of general ellipticity. The frequency of the laser pulse resides in the ultraviolet region. To this end, the semirelativistic approach introduced in Kjellsson Lindblom et al. [T. Kjellsson Lindblom, M. Forre, E. Lindroth, and S. Selsto, Phys. Rev. Lett. 121, 253202 (2018)] is applied. We present in some detail how this approximation is derived from the Dirac equation for elliptically polarized light within the so-called long-wavelength approximation. The validity of the semirelativistic approach is confirmed by direct comparison with the solution of the Dirac equation. It is found that the total ionization yield depends very weakly on ellipticity in the case of ionization from the isotropic ground state. With the excited initial state n = 2, l = m(l) = 1; however, pronounced ellipticity dependence is seen-in particular at the stabilization peak. Albeit small, relativistic corrections to the ionization probabilities are found. The correction is found to be largest for linear polarization. While relativistic effects tend to reduce the total ionization probability for most intensities considered, we also report a slight relativistic enhancement at comparatively modest field strengths.

Place, publisher, year, edition, pages
American Physical Society (APS), 2021
National Category
Atom and Molecular Physics and Optics
Identifiers
urn:nbn:se:kth:diva-303889 (URN)10.1103/PhysRevA.104.043102 (DOI)000704066400005 ()2-s2.0-85116736884 (Scopus ID)
Note

QC 20211021

Available from: 2021-10-21 Created: 2021-10-21 Last updated: 2023-12-07Bibliographically approved
Kjellsson Lindblom, T., Forre, M., Lindroth, E. & Selsto, S. (2020). Relativistic effects in photoionizing a circular Rydberg state in the optical regime. Physical Review A: covering atomic, molecular, and optical physics and quantum information, 102(6), Article ID 063108.
Open this publication in new window or tab >>Relativistic effects in photoionizing a circular Rydberg state in the optical regime
2020 (English)In: Physical Review A: covering atomic, molecular, and optical physics and quantum information, ISSN 2469-9926, E-ISSN 2469-9934, Vol. 102, no 6, article id 063108Article in journal (Refereed) Published
Abstract [en]

We study the photoionization process of a hydrogen atom initially prepared in a circular Rydberg state. The atom is exposed to a two-cycle laser pulse with a central wavelength of 800 nm. Before the atom approaches saturation, at field intensities of the order of 10(17) W/cm(2), relativistic corrections to the ionization probability are clearly seen. The ionization is predominantly driven by the radiation pressure in the propagation direction of the laser field, not by the electric field. Direct comparisons with the full numerical solution of the time-dependent Dirac equation demonstrate quantitative agreement with a semirelativistic approximation, which is considerably easier to implement.

Place, publisher, year, edition, pages
American Physical Society (APS), 2020
National Category
Atom and Molecular Physics and Optics
Identifiers
urn:nbn:se:kth:diva-289039 (URN)10.1103/PhysRevA.102.063108 (DOI)000597808100005 ()2-s2.0-85098129127 (Scopus ID)
Note

QC 20210125

Available from: 2021-01-25 Created: 2021-01-25 Last updated: 2023-12-07Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0002-7544-5659

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