scholarly journals Molecular frame photoemission by a comb of elliptical high-order harmonics: a sensitive probe of both photodynamics and harmonic complete polarization state

2016 ◽  
Vol 194 ◽  
pp. 161-183 ◽  
Author(s):  
K. Veyrinas ◽  
V. Gruson ◽  
S. J. Weber ◽  
L. Barreau ◽  
T. Ruchon ◽  
...  

Due to the intimate anisotropic interaction between an XUV light field and a molecule resulting in photoionization (PI), molecular frame photoelectron angular distributions (MFPADs) are most sensitive probes of both electronic/nuclear dynamics and the polarization state of the ionizing light field. Consequently, they encode the complex dipole matrix elements describing the dynamics of the PI transition, as well as the three normalized Stokes parameters s1, s2, s3 characterizing the complete polarization state of the light, operating as molecular polarimetry. The remarkable development of advanced light sources delivering attosecond XUV pulses opens the perspective to visualize the primary steps of photochemical dynamics in time-resolved studies, at the natural attosecond to few femtosecond time-scales of electron dynamics and fast nuclear motion. It is thus timely to investigate the feasibility of measurement of MFPADs when PI is induced e.g., by an attosecond pulse train (APT) corresponding to a comb of discrete high-order harmonics. In the work presented here, we report MFPAD studies based on coincident electron-ion 3D momentum imaging in the context of ultrafast molecular dynamics investigated at the PLFA facility (CEA-SLIC), with two perspectives: (i) using APTs generated in atoms/molecules as a source for MFPAD-resolved PI studies, and (ii) taking advantage of molecular polarimetry to perform a complete polarization analysis of the harmonic emission of molecules, a major challenge of high harmonic spectroscopy. Recent results illustrating both aspects are reported for APTs generated in unaligned SF6 molecules by an elliptically polarized infrared driving field. The observed fingerprints of the elliptically polarized harmonics include the first direct determination of the complete s1, s2, s3 Stokes vector, equivalent to (ψ, ε, P), the orientation and the signed ellipticity of the polarization ellipse, and the degree of polarization P. They are compared to so far incomplete results of XUV optical polarimetry. We finally discuss the comparison between the outcomes of photoionization and high harmonic spectroscopy for the description of molecular photodynamics.

2021 ◽  
Author(s):  
I. R. KHAIRULIN ◽  
V. А. АNTONOV ◽  
М. YU. RYABIKIN ◽  
M. A. BERRILL ◽  
V. N. SHLYAPTSEV ◽  
...  

Abstract Amplification of attosecond pulses produced via high harmonic generation is a formidable problem since none of the amplifiers can support the corresponding PHz bandwidth. Producing the well defined polarization state common for a set of harmonics required for formation of the circularly/elliptically polarized attosecond pulses (which are on demand for dynamical imaging and coherent control of the spin flip processes) is another big challenge. In this work we show how both problems can be tackled simultaneously on the basis of the same platform, namely, the plasma-based X-ray amplifier whose resonant transition frequency is modulated by an infrared field.


Author(s):  
Rambabu Rajpoot ◽  
Amol Holkundkar ◽  
Jayendra N. Bandyopadhyay

Abstract We study the high harmonic generation (HHG) using elliptically polarized two-color driving fields. The HHG via bi-chromatic counter-rotating laser fields is a promising source of circularly polarized ultrashort XUV radiation at the attosecond time scale. The ellipticity or the polarization of the attosecond pulses can be tweaked by modifying the emitted harmonics' ellipticity, which can be controlled by varying the driver fields. A simple setup is used to control the polarization of the driving fields, which eventually changes the ellipticity of the attosecond pulses. A well-defined scaling for the ellipticity of the attosecond pulse as a function of the rotation angle of the quarter-wave plate is also deduced by solving the time-dependent Schr\"odinger equation (TDSE) in two dimensions. The scaling can further be explored to obtain the attosecond pulses of the desired degree of polarization, ranging from linear to elliptical to circular polarization.


2017 ◽  
Vol 31 (29) ◽  
pp. 1750215 ◽  
Author(s):  
Feras Afaneh ◽  
Horst Schmidt-Böcking

In this paper, we study single and double ionizations of N2O in a short elliptically polarized 800 nm laser pulse using the COLTRIMS technique. The molecular-frame photoelectron angular distribution and the ion sum-momentum distribution of single and double ionizations of N2O molecules are reported for the single ionization dissociative channel NO[Formula: see text] + N and the double ionization dissociative channel NO[Formula: see text] + N[Formula: see text]. The ionizations of multiple orbitals for the two studied dissociative channels were identified via studying the orientation dependent ionization rates for their KERs. The results show that the shape of the ionizing orbitals governs the single and double ionization processes of N2O.


1998 ◽  
Vol 44 (1) ◽  
pp. 20-24 ◽  
Author(s):  
G Nienhuis ◽  
A. V Taichenachev ◽  
A. M Tumaikin ◽  
V. I Yudin

2007 ◽  
Vol 99 (24) ◽  
Author(s):  
Jérôme Levesque ◽  
Yann Mairesse ◽  
Nirit Dudovich ◽  
Henri Pépin ◽  
Jean-Claude Kieffer ◽  
...  

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Kotaro Nakagawa ◽  
Hideki Hirori ◽  
Yasuyuki Sanari ◽  
Fumiya Sekiguchi ◽  
Ryota Sato ◽  
...  

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