Optical Interference Effect in Strong-field Electronic Coherence Spectroscopy

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: Weckwerth, Eleanor, Howard, Andrew J., Cheng, Chuan, Gabalski, Ian, Ghrist, Aaron M., Mohideen, Salma A., Lin, Chii-Dong, Yuen, Chi-Hong, Bucksbaum, Philip H.
Format: Preprint
Published: 2025
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866911158103965696
author Weckwerth, Eleanor
Howard, Andrew J.
Cheng, Chuan
Gabalski, Ian
Ghrist, Aaron M.
Mohideen, Salma A.
Lin, Chii-Dong
Yuen, Chi-Hong
Bucksbaum, Philip H.
author_facet Weckwerth, Eleanor
Howard, Andrew J.
Cheng, Chuan
Gabalski, Ian
Ghrist, Aaron M.
Mohideen, Salma A.
Lin, Chii-Dong
Yuen, Chi-Hong
Bucksbaum, Philip H.
contents We have investigated strong-field-induced electronic coherences in argon and molecular nitrogen ions created by high-intensity, few-cycle infrared laser pulses. This is a step toward the long-sought goal of strong-field coherent control in molecular chemistry. We employed high-intensity, few-cycle infrared laser pulses in a pump-probe setup to investigate a recent prediction that electronic coherences in nitrogen molecules change the ion yields vs. pump-probe delay. [Yuen and Lin, Phys. Rev. A 109, L011101 (2024)]. The predicted coherence signals in molecular nitrogen could not be resolved above the optical interference of the pump and probe pulses; a simultaneous measurement clearly resolved the induced cation fine-structure coherence in strong-field-ionized argon. The results of our comparison with simulations suggest that optical interference effects manifest differently in each ionic species and must be carefully accounted for when interpreting experimental data. We found that nonsequential double ionization in the low-intensity region of the focal volume can reduce the visibility of coherence generated by two-pulse sequential ionization, and we quantify the importance of pulse shape and spectral characteristics for isolating the desired coherence signals.
format Preprint
id arxiv_https___arxiv_org_abs_2505_21788
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Optical Interference Effect in Strong-field Electronic Coherence Spectroscopy
Weckwerth, Eleanor
Howard, Andrew J.
Cheng, Chuan
Gabalski, Ian
Ghrist, Aaron M.
Mohideen, Salma A.
Lin, Chii-Dong
Yuen, Chi-Hong
Bucksbaum, Philip H.
Atomic Physics
Chemical Physics
Optics
Quantum Physics
We have investigated strong-field-induced electronic coherences in argon and molecular nitrogen ions created by high-intensity, few-cycle infrared laser pulses. This is a step toward the long-sought goal of strong-field coherent control in molecular chemistry. We employed high-intensity, few-cycle infrared laser pulses in a pump-probe setup to investigate a recent prediction that electronic coherences in nitrogen molecules change the ion yields vs. pump-probe delay. [Yuen and Lin, Phys. Rev. A 109, L011101 (2024)]. The predicted coherence signals in molecular nitrogen could not be resolved above the optical interference of the pump and probe pulses; a simultaneous measurement clearly resolved the induced cation fine-structure coherence in strong-field-ionized argon. The results of our comparison with simulations suggest that optical interference effects manifest differently in each ionic species and must be carefully accounted for when interpreting experimental data. We found that nonsequential double ionization in the low-intensity region of the focal volume can reduce the visibility of coherence generated by two-pulse sequential ionization, and we quantify the importance of pulse shape and spectral characteristics for isolating the desired coherence signals.
title Optical Interference Effect in Strong-field Electronic Coherence Spectroscopy
topic Atomic Physics
Chemical Physics
Optics
Quantum Physics
url https://arxiv.org/abs/2505.21788