Temporal coherent control of resonant two-photon double ionization of the hydrogen molecule via doubly excited states
Journal Article
·
· Physical Review A
- Univ. of Nebraska, Lincoln, NE (United States); OSTI
- Univ. of Nebraska, Lincoln, NE (United States)
Here, we use time-delayed, counter-rotating, circularly polarized few-cycle attosecond nonoverlapping pulses to study the temporal coherent control of the resonant process of two-photon double ionization (TPDI) of hydrogen molecule via doubly excited states for pulse propagation direction along $$\hat k$$ either parallel or perpendicular to the molecular axis $$\hat R$$. For $$\hat k$$∥ $$\hat R$$ and a pulse carrier frequency of 36 eV resonantly populating the Q21Π$$^+_u$$ (1) doubly excited state as well as other 1Π$$^+_u$$ doubly excited states, we find that the indirect ionization pathway through these doubly excited states changes the character of the kinematical vortex-shaped momentum distribution produced by the two direct ionization pathways from fourfold to twofold rotational symmetry. This result is similar to what found in TPDI of the He atom involving 1P$$^ o_ {±1}$$ doubly excited states; however, angular distributions exhibiting a quantum beat effect between the ground state and a doubly excited state seen for the He atom are observed here for its molecular counterpart with an anomaly in shape and magnitude, not in frequency. The sixfold differential probability integrated over the azimuthal angle of the photoelectron pair shows that this anomaly is due to autoionization decays and quantum beats between doubly excited states. For $$\hat k$$⟂$$\hat R$$ and a broadband pulse carrier frequency of 30 eV populating the Q11Π$$^+_u$$(1), Q11Σ$$^+_u$$(1), Q21Π$$^+_u$$(1) , and Q11Σ$$^+_u$$ (2) doubly excited states, the momentum distribution is shown to exhibit dynamical electron vortices with four spiral arms, which originates from the interplay between the 1Δ$$^+_ g$$ ,1Π$$^+_ g$$, and 1Σ$$^+_ g$$ dynamical ionization amplitudes. Our treatment within either the adiabatic-nuclei approximation or fixed-nuclei approximation shows that the latter provides a very good account for this correlated process.
- Research Organization:
- Univ. of Nebraska, Lincoln, NE (United States)
- Sponsoring Organization:
- Nebraska Research Initiative; USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- FG03-96ER14646; SC0021054
- OSTI ID:
- 1850232
- Journal Information:
- Physical Review A, Journal Name: Physical Review A Journal Issue: 5 Vol. 103; ISSN 2469-9926
- Publisher:
- American Physical Society (APS)Copyright Statement
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
74 ATOMIC AND MOLECULAR PHYSICS
atomic and molecular processes in external fields
auger processes
autoionization
coherent control
electron correlation calculation for atoms and ions
multiphoton or tunneling ionization and excitation
single-and few-photon ionization and excitation
ultrafast phenomena
atomic and molecular processes in external fields
auger processes
autoionization
coherent control
electron correlation calculation for atoms and ions
multiphoton or tunneling ionization and excitation
single-and few-photon ionization and excitation
ultrafast phenomena