Imaging Molecules from Within: Ultra-fast, Ångström Scale Structure Determination of Molecules via Photoelectron Holography using Free Electron Lasers
arXiv:0910.3078 · doi:10.1103/PhysRevA.81.033411
Abstract
A new scheme based on (i) upcoming brilliant X-ray Free Electron Laser (FEL) sources, (ii) novel energy and angular dispersive, large-area electron imagers and (iii) the well-known photoelectron holography is elaborated that provides time-dependent three-dimensional structure determination of small to medium sized molecules with Ångström spatial and femtosecond time resolution. Inducing molecular dynamics, wave-packet motion, dissociation, passage through conical intersections or isomerization by a pump pulse this motion is visualized by the X-ray FEL probe pulse launching keV photoelectrons within few femtoseconds from specific and well-defined sites, deep core levels of individual atoms, inside the molecule. On their way out the photoelectrons are diffracted generating a hologram on the detector that encodes the molecular structure at the instant of photoionization, thus providing 'femtosecond snapshot images of the molecule from within'. Detailed calculations in various approximations of increasing sophistication are presented and three-dimensional retrieval of the spatial structure of the molecule with Ångström spatial resolution is demonstrated. Due to the large photo-absorption cross sections the method extends X-ray diffraction based, time-dependent structure investigations envisioned at FELs to new classes of samples that are not accessible by any other method. Among them are dilute samples in the gas phase such as aligned, oriented or conformer selected molecules, ultra-cold ensembles and/or molecular or cluster objects containing mainly light atoms that do not scatter X-rays efficiently.
18 pages, 11 figures
References in corpus (4)
- Laser-induced alignment and orientation of quantum-state-selected large molecules
- Quantum-state selection, alignment, and orientation of large molecules using static electric and laser fields
- A selector for structural isomers of neutral molecules
- Ionization and expansion dynamics of atomic clusters irradiated with short intense VUV pulses
Cited by in corpus (17)
- Photoelectron angular distributions from strong-field ionization of oriented molecules
- Imaging an aligned polyatomic molecule with laser-induced electron diffraction
- Diffractive imaging of a molecular rotational wavepacket with femtosecond Megaelectronvolt electron pulses
- Spatially-controlled complex molecules and their applications
- State- and conformer-selected beams of aligned and oriented molecules for ultrafast diffraction studies
- Imaging Molecular Structure through Femtosecond Photoelectron Diffraction on Aligned and Oriented Gas-Phase Molecules
- Atomic, molecular and optical physics applications of longitudinally coherent and narrow bandwidth Free-Electron Lasers
- Strongly aligned and oriented molecular samples at a kHz repetition rate
- Spatially separated polar samples of the cis and trans conformers of 3-fluorophenol
- High-Energy Molecular-Frame Photoelectron Angular Distributions: A Molecular Bond-Length Ruler
- Theory on polarization-averaged core-level molecular-frame photoelectron angular distributions: II. Extracting the X-ray induced fragmentation dynamics of carbon monoxide dication from forward and backward intensities
- Strong laser alignment of solvent-solute aggregates in the gas-phase
- Rate equations for nitrogen molecules in ultrashort and intense x-ray pulses
- Photophysics of indole upon x-ray absorption
- Impulsive laser-induced alignment of OCS molecules at FERMI
- Laser Dressed Scattering of an Attosecond Electron Wave Packet
- Theory on polarization-averaged core-level molecular-frame photoelectron angular distributions: I. A Full-potential method and its application to dissociating carbon monoxide dication