Photoelectron momentum distributions of Ne and Xe dimers in counter-rotating circularly polarized laser fields

The strong-field ionization of dimers is investigated theoretically in counter-rotating circularly polarized laser fields. By numerically solving the two-dimensional (2D) time-dependent Schrödinger equation (TDSE) with the single-electron approximation (SEA) frame, we present the photoelectron momen...

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Veröffentlicht in:Chinese physics B 2022-06, Vol.31 (6), p.63202-336
Hauptverfasser: Lei, Zhi-Xian, Xu, Qing-Yun, Yang, Zhi-Jie, He, Yong-Lin, Guo, Jing
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container_start_page 63202
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creator Lei, Zhi-Xian
Xu, Qing-Yun
Yang, Zhi-Jie
He, Yong-Lin
Guo, Jing
description The strong-field ionization of dimers is investigated theoretically in counter-rotating circularly polarized laser fields. By numerically solving the two-dimensional (2D) time-dependent Schrödinger equation (TDSE) with the single-electron approximation (SEA) frame, we present the photoelectron momentum distributions (PMDs) and photoelectron angular distribution (PADs) of aligned Ne and Xe dimers. It is found that the PMDs and PADs strongly depend on the time delays by counter-rotating circularly polarized laser pulses. The results can be explained by the ultrafast photoionization model and the evolution of electron wave packets for Ne and Xe dimers. Besides, We make a comparison of PMDs between Ne atom and Ne dimer.
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Phys. B</addtitle><date>2022-06-01</date><risdate>2022</risdate><volume>31</volume><issue>6</issue><spage>63202</spage><epage>336</epage><pages>63202-336</pages><issn>1674-1056</issn><abstract>The strong-field ionization of dimers is investigated theoretically in counter-rotating circularly polarized laser fields. By numerically solving the two-dimensional (2D) time-dependent Schrödinger equation (TDSE) with the single-electron approximation (SEA) frame, we present the photoelectron momentum distributions (PMDs) and photoelectron angular distribution (PADs) of aligned Ne and Xe dimers. It is found that the PMDs and PADs strongly depend on the time delays by counter-rotating circularly polarized laser pulses. The results can be explained by the ultrafast photoionization model and the evolution of electron wave packets for Ne and Xe dimers. 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subjects dimer
photoelectron momentum distributions
time-dependent Schrödinger equation
ultrafast photoionization model
title Photoelectron momentum distributions of Ne and Xe dimers in counter-rotating circularly polarized laser fields
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