We present combined experimental and theoretical results on strong-field ionization of oriented carbonyl sulfide molecules by circularly polarized laser pulses. The obtained molecular frame photoelectron angular distributions show pronounced asymmetries perpendicular to the direction of the molecular electric dipole moment. These findings are explained by a tunneling model invoking the laser-induced Stark shifts associated with the dipoles and polarizabilities of the molecule and its unrelaxed cation. The focus of the present article is to understand the strong-field ionization of one-dimensionally-oriented polar molecules, in particular asymmetries in the emission direction of the photoelectrons. In the following article [Phys. Rev. A 83, ...
The propensity of molecules to spatially align along the polarization vector of intense, pulsed ligh...
Kaya, Necati/0000-0001-9461-7623WOS: 000387090800006By measuring femtosecond laser driven strong-fie...
The transition between two distinct mechanisms for the laser-induced field-free orientation of CO mo...
We present combined experimental and theoretical results on strong-field ionization of oriented carb...
The combination of photoelectron spectroscopy and ultrafast light sources is on track to set new sta...
We present a combined experimental and theoretical study on strong-field ionization of a three-dimen...
We have studied, experimentally and theoretically, the ionization probability of carbonyl sulfide (O...
Laser-aligned carbonyl-sulfide molecules were strong-field ionized using mid-infrared light. Investi...
One of the big technical and scientific challenges today is to accomplish the ultimate dreamof filmi...
Strong-field ionization of aligned diatomic and polyatomic molecules such as O2, N2, C2H4, and other...
We demonstrate strong laser-field-free orientation of absolute-ground-state carbonyl sulfide molecul...
The propensity of molecules to spatially align along the polarization vector of intense, pulsed ligh...
Citation: Zigo, S., Le, A. T., Timilsina, P., & Trallero-Herrero, C. A. (2017). Ionization Study of ...
Through the use of the technique of time-of-flight mass spectroscopy, we obtain strong-field ionizat...
Jaron-Becker A, Becker A, Faisal F. Ionization of N-2, O-2, and linear carbon clusters in a strong l...
The propensity of molecules to spatially align along the polarization vector of intense, pulsed ligh...
Kaya, Necati/0000-0001-9461-7623WOS: 000387090800006By measuring femtosecond laser driven strong-fie...
The transition between two distinct mechanisms for the laser-induced field-free orientation of CO mo...
We present combined experimental and theoretical results on strong-field ionization of oriented carb...
The combination of photoelectron spectroscopy and ultrafast light sources is on track to set new sta...
We present a combined experimental and theoretical study on strong-field ionization of a three-dimen...
We have studied, experimentally and theoretically, the ionization probability of carbonyl sulfide (O...
Laser-aligned carbonyl-sulfide molecules were strong-field ionized using mid-infrared light. Investi...
One of the big technical and scientific challenges today is to accomplish the ultimate dreamof filmi...
Strong-field ionization of aligned diatomic and polyatomic molecules such as O2, N2, C2H4, and other...
We demonstrate strong laser-field-free orientation of absolute-ground-state carbonyl sulfide molecul...
The propensity of molecules to spatially align along the polarization vector of intense, pulsed ligh...
Citation: Zigo, S., Le, A. T., Timilsina, P., & Trallero-Herrero, C. A. (2017). Ionization Study of ...
Through the use of the technique of time-of-flight mass spectroscopy, we obtain strong-field ionizat...
Jaron-Becker A, Becker A, Faisal F. Ionization of N-2, O-2, and linear carbon clusters in a strong l...
The propensity of molecules to spatially align along the polarization vector of intense, pulsed ligh...
Kaya, Necati/0000-0001-9461-7623WOS: 000387090800006By measuring femtosecond laser driven strong-fie...
The transition between two distinct mechanisms for the laser-induced field-free orientation of CO mo...