Probing the structure of stretched molecular ions with high-harmonic spectroscopy. (29th March 2017)

• Record Type: Journal Article
• Authors: Li, W Y; Wang, S; Shi, Y Z; Yang, S P; Chen, Y J
• Is Part Of: Journal of physics. Volume 50:Number 8(2017:Apr. 15)
• Publication Date: 2017-03-29
• Subjects: quantum-orbit theory -- strong-field approximations -- high-harmonic spectroscopy; Atoms -- Periodicals; Molecules -- Periodicals; Optics -- Periodicals; Nuclear physics -- Periodicals; 539.6
• DOI: 10.1088/1361-6455/aa63a3
• Languages: English
• ISSNs: 0953-4075

Abstract

Abstract: High-harmonic spectroscopy (HHS) is an emerging tool for probing the structure of molecules in ultrafast timescale. Here, through numerical solution of the time-dependent Schrödinger equation, we show that the present procedures in HHS cannot be directly applied to molecular ions such as H 2 + with large internuclear distances R . For the latter, besides the ground state, the excited state of the system also contributes importantly to the harmonic emission. A simple model based on developed strong-field approximations and quantum-orbit theory is proposed, which allows us to extract the structural and dynamical information of molecular ions with large R from the harmonic spectra obtained with considering only the contributions of the short trajectory. Our work gives suggestions on tracing the bond length of a molecular orbital in a chemical reaction as the molecule is stretched to large R .