| 1. |
- Blinov, Svyatoslav N., et al.
(författare)
-
Mapping molecular potentials using pump-probe spectroscopy of vibrational wave packets' revival
- 2023
-
Ingår i: Physical Review A: covering atomic, molecular, and optical physics and quantum information. - : American Physical Society (APS). - 2469-9926 .- 2469-9934. ; 108:1
-
Tidskriftsartikel (refereegranskat)abstract
- In this study, we investigate the nuclear dynamics in nitrogen monoxide after valence ionization by a pump pulse and subsequent probing with a time-delayed x-ray pulse. We calculate the development of the resulting vibrational wave packet, taking into account three different ionization mechanisms: one-photon, multiphoton, and tunneling ionization. Using a two-time propagation method, we solve the nonstationary nuclear Schrödinger equation to obtain time-resolved x-ray absorption spectra (TRXAS), considering the finite duration of the probe pulse. Our simulations show that the TRXAS profile accurately reflects the vibrational wave packets' trajectory in the cationic ground state. Additionally, we find that the TRXAS evolution is highly sensitive to small changes in the probed potential energy curve, making it a useful tool for reconstructing molecular potentials and determining anharmonicity and equilibrium bond length. This method can be applied to other polyatomic molecules and pump mechanisms.
|
|
| 2. |
|
|
| 3. |
|
|
| 4. |
- Ignatova, Nina, 1989-, et al.
(författare)
-
Gradual collapse of nuclear wave functions regulated by frequency tuned X-ray scattering
- 2017
-
Ingår i: Scientific Reports. - London : Nature Publishing Group. - 2045-2322. ; 7:43891
-
Tidskriftsartikel (refereegranskat)abstract
- As is well established, the symmetry breaking by isotope substitution in the water molecule results in localisation of the vibrations along one of the two bonds in the ground state. In this study we find that this localisation may be broken in excited electronic states. Contrary to the ground state, the stretching vibrations of HDO are delocalised in the bound core-excited state in spite of the mass difference between hydrogen and deuterium. The reason for this effect can be traced to the narrow “canyon-like” shape of the potential of the state along the symmetric stretching mode, which dominates over the localisation mass-difference effect. In contrast, the localisation of nuclear motion to one of the HDO bonds is preserved in the dissociative core-excited state . The dynamics of the delocalisation of nuclear motion in these core-excited states is studied using resonant inelastic X-ray scattering of the vibrationally excited HDO molecule. The results shed light on the process of a wave function collapse. After core-excitation into the state of HDO the initial wave packet collapses gradually, rather than instantaneously, to a single vibrational eigenstate.
|
|
| 5. |
- Ignatova, Nina, 1989-, et al.
(författare)
-
Infrared-pump–x-ray-probe spectroscopy of vibrationally excited molecules
- 2017
-
Ingår i: Physical Review A. - 2469-9926 .- 2469-9934. ; 95:4
-
Tidskriftsartikel (refereegranskat)abstract
- We develop a theory of infrared (IR)-pump–x-ray-probe spectroscopy for molecular studies. We illustrate advantages of the proposed scheme by means of numerical simulations employing a vibrational wave packet technique applied to x-ray absorption and resonant inelastic x-ray scattering (RIXS) spectra of the water molecule vibrationally excited by a preceding IR field. The promotion of the vibrationally excited molecule to the dissociative 1a−114a1 and bound 1a−112b2 core-excited states with qualitatively different shapes of the potential energy surfaces creates nuclear wave packets localized along and between the OH bonds, respectively. The projection of these wave packets on the final vibrational states, governed by selection and propensity rules, results in spatial selectivity of RIXS sensitive to the initial vibrationally excited state, which makes it possible to probe selectively the ground state properties along different modes. In addition, we propose to use RIXS as a tool to study x-ray absorption from a selected vibrational level of the ground state when the spectral resolution is sufficiently high to resolve vibrational overtones. The proposed technique has potential applications for advanced mapping of multidimensional potential energy surfaces of ground and core-excited molecular states, for symmetry-resolved spectroscopy, and for steering chemical reactions.
|
|
| 6. |
- Kimberg, Victor, et al.
(författare)
-
Angular properties of band structures in one-dimensional holographic photonic crystals
- 2004
-
Ingår i: Journal of Optics. A, Pure and applied optics. - : Institute of Physics Publishing (IOPP). - 1464-4258 .- 1741-3567. ; 6:10, s. 991-996
-
Tidskriftsartikel (refereegranskat)abstract
- One-dimensional photonic crystals with continuous distribution of the dielectric constant were fabricated by the use of photopolymer materials and laser holography. The angular dependence of light propagation through the system was studied experimentally and theoretically. It is shown that the Brewster angles for different bands are different, in contrast to the conventional two-layer Bragg reflector with a step-like distribution of the dielectric constant. Comparison of the theory with experimental data allowed us to define the parameters of the hologram-the dielectric contrast and the shrinkage of the structure.
|
|
| 7. |
- Kimberg, V., et al.
(författare)
-
Single-Molecule X-Ray Interferometry : Controlling Coupled Electron-Nuclear Quantum Dynamics and Imaging Molecular Potentials by Ultrahigh-Resolution Resonant Photoemission and Ab Initio Calculations
- 2013
-
Ingår i: Physical Review X. - : American Physical Society. - 2160-3308. ; 3:1
-
Tidskriftsartikel (refereegranskat)abstract
- This paper reports an advanced study of the excited ionic states of the gas-phase nitrogen molecule in the binding-energy region of 22-34 eV, combining ultrahigh-resolution resonant photoemission (RPE) and ab initio configuration-interaction calculations. The RPE spectra are recorded for nine photon energies within the N 1s -> pi* absorption resonance of N-2 by using a photon bandwidth that is considerably smaller than lifetime broadening, and the dependence on excitation energy of the decay spectra is analyzed and used for the first assignment of 12 highly overlapped molecular states. The effect on the RPE profile of avoided curve crossings between the final N-2(+) ionic states is discussed, based on theoretical simulations that account for vibronic coupling, and compared with the experimental data. By use of synchrotron radiation with high spectral brightness, it is possible to selectively promote the molecule to highly excited vibrational sublevels of a core-excited electronic state, thereby controlling the spatial distribution of the vibrational wave packets, and to accurately image the ionic molecular potentials. In addition, the mapping of the vibrational wave functions of the core-excited states using the bound final states with far-from-equilibrium bond lengths has been achieved experimentally for the first time. Theoretical analysis has revealed the rich femtosecond nuclear dynamics underlying the mapping phenomenon. DOI: 10.1103/PhysRevX.3.011017
|
|
| 8. |
- Lindblad, Andreas, et al.
(författare)
-
Vibrational scattering anisotropy in O-2-dynamics beyond the Born-Oppenheimer approximation
- 2012
-
Ingår i: New Journal of Physics. - : IOP Publishing. - 1367-2630. ; 14, s. 113018-
-
Tidskriftsartikel (refereegranskat)abstract
- Born-Oppenheimer and Franck-Condon approximations are two major concepts in the interpretation of electronic excitations and modeling of spectroscopic data in the gas and condensed phases. We report large variations of the anisotropy parameter (beta) for the fully resolved vibrational sub-states of the X-2 Pi(g) electronic ground state of O-2(+) populated by participator resonant Auger decay following excitations of K-shell electrons into the sigma(star) resonance by monochromatic x-rays. Decay spectra for light polarization directions parallel and perpendicular to the electron detection axis recorded at four different excitation energies in the vicinity of the O 1s -> sigma(star) transition are presented. Breakdown of the Born-Oppenheimer approximation is for the first time selectively observed for the lower vibrational sub-states, where two quantum paths-resonant and direct-leading to the same final cationic state exist. The higher vibrational sub-states can only be populated by resonant photoemission; hence no interference between these channels can occur.
|
|
| 9. |
|
|
| 10. |
- Liu, X. J., et al.
(författare)
-
Young's double-slit experiment using core-level photoemission from N-2 : revisiting Cohen-Fano's two-centre interference phenomenon
- 2006
-
Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 39:23, s. 4801-4817
-
Tidskriftsartikel (refereegranskat)abstract
- The core-level photoelectron spectra of N-2 molecules are observed at high energy resolution, resolving the 1 sigma(g) and 1 sigma(u) components as well as the vibrational components in the extended energy region from the threshold up to 1 keV. The sigma(g)/sigma(u) cross section ratios display modulation as a function of photoelectron momentum due to the two-centre interference, analogous to the classical Young's double-slit experiment, as predicted by Cohen and Fano a long time ago. The Cohen-Fano interference modulations display different phases depending on the vibrational excitations in the core-ionized state. Extensive ab initio calculations have been performed within the Hartree-Fock and random phase approximations in prolate spheroidal coordinates. The dependence of photoionization amplitudes on the vibrational states was taken into account using the Born-Oppenheimer approximation. The ab initio results are in reasonable agreement with the experimental data. The theoretical analysis allows the modulation to be connected with the onset of transitions to the states of increasing orbital angular momentum which occurs at increasing photon energies. Deviation from the Cohen-Fano formula is found for both the experimental and the ab initio results and is attributed to electron scattering by the neighbouring atom. A new formula for the interference modulation is derived within the framework of the multiple scattering technique. It differs from the classical Cohen-Fano formula by the addition of twice the scattering phase of the photoelectron by the neighbouring atom. We demonstrate that one can measure directly the scattering phase by fitting our formula to the experimental results.
|
|
