The vibrational wavepacket of a diatomic molecular ion at the time of ionization is usually considered to be generated on the basis of the Franck-Condon principle. According to this principle, the amplitude of each vibrational wavefunction in the wavepacket is given by the overlap integral between each vibrational wavefunction and the ground vibrational wavefunction in the neutral molecule, and hence, the amplitude should be a real number, or equivalently, a complex number the phase of which is equal to zero. Here we report the observation of a non-trivial phase modulation of the amplitudes of vibrational wavefunctions in a wavepacket generated in the ground electronic state of a H₂⁺ molecular ion at the time of ionization. The phase modulation results in a group delay of the specific vibrational states of order 1 fs, which can be regarded as the settling time required to compose the initial vibrational wavepacket.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569855PMC
http://dx.doi.org/10.1038/ncomms9197DOI Listing

Publication Analysis

Top Keywords

vibrational wavepacket
12
vibrational wavefunction
12
settling time
8
vibrational
8
molecular ion
8
ion time
8
time ionization
8
phase modulation
8
wavepacket
5
time vibrational
4

Similar Publications

Differential Cross-Sections for the Vibrationally Excited H + HOD( = 1-4) → H + OD Reactions.

J Phys Chem A

December 2024

State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China.

Using the time-dependent wave-packet approach, we calculate the first fully converged state-to-state differential cross-sections for the H + HOD( = 1-4) → H + OD reactions on a highly accurate neural network PES. It is found that, unlike the loss of memory effect observed in the product distributions for low vibrational excitation reactions, high initial OH vibrational excitation significantly influences not only the product vibrational distribution but also the angular distribution. Furthermore, for the H + HOD( = 3,4) reactions, the total integral cross-sections maintain the pronounced oscillatory structures in the = 0 probabilities at low collision energies, which originate from the prereactive van der Waals resonances.

View Article and Find Full Text PDF

Quantum nuclear dynamics with wavepacket time evolution is classically intractable and viewed as a promising avenue for quantum information processing. Here, we use IonQ, Inc.'s 11-qubit trapped-ion quantum computer, Harmony, to study the quantum wavepacket dynamics of a shared-proton within a short-strong hydrogen-bonded system.

View Article and Find Full Text PDF

Rydberg-State Double-Well Potentials of Van der Waals Molecules.

Molecules

September 2024

Smoluchowski Institute of Physics, Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, Łojasiewicza 11, 30-348 Kraków, Poland.

Recent progress in studies of Rydberg double-well electronic energy states of MeNg (Me = 12-group atom, Ng = noble gas atom) van der Waals (vdW) molecules is presented and analysed. The presentation covers approaches in experimental studies as well as ab initio-calculations of potential energy curves (PECs). The analysis is shown in a broader context of Rydberg states of hetero- and homo-diatomic molecules with PECs possessing complex 'exotic' structure.

View Article and Find Full Text PDF

Attosecond Probing of Coherent Vibrational Dynamics in CBr.

J Phys Chem A

October 2024

Department of Chemistry, University of California, Berkeley, California 94720, United States.

A coherent vibrational wavepacket is launched and manipulated in the symmetric stretch (a) mode of CBr, by impulsive stimulated Raman scattering (ISRS) from nonresonant 400 nm laser pump pulses with various peak intensities on the order of tens of 10 W/cm. Extreme ultraviolet (XUV) attosecond transient absorption spectroscopy (ATAS) records the wavepacket dynamics as temporal oscillations in XUV absorption energy at the bromine M 3d edges around 70 eV. The results are augmented by nuclear time-dependent Schrödinger equation simulations.

View Article and Find Full Text PDF

Insights into Ultrafast Relaxation Dynamics of Electronically Excited Furfural and 5-Methylfurfural.

J Phys Chem A

October 2024

State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning 116023, China.

The ultrafast relaxation dynamics of furfural and 5-methylfurfural following excitation in the ultraviolet range is investigated using the femtosecond time-resolved photoelectron spectroscopy method. Specifically, the pump wavelength-dependent decay dynamics of electronically excited furfural and 5-methylfurfural is discussed on the basis of a detailed analysis of our measured time-resolved photoelectron spectroscopy spectra. Irradiation at all pump wavelengths prepares both furfural and 5-methylfurfural molecules with different vibrational levels in the first optically bright S (ππ*) state, the lifetime of which is measured to be at least hundreds of femtoseconds.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!