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Philip Bucksbaum

Publications and source records attributed to Philip Bucksbaum.

3 recordsLinked to original sources

Disentangling the Sub-Cycle Electron Momentum Spectrum in Strong-Field Ionization

Quantum calculations of tunneling in strong-field ionization (SFI) predict intricate momentum distributions due to sub-laser-cycle attosecond electron dynamics. These are obscured in most experiments by the dominance of inter-cycle interference patterns which are the hallmark of above-threshold ionization (ATI). Highly controlled 1- to 2-cycle laser pulses produce less inter-cycle interference but cannot accurately recreate the sub-cycle features produced by uniform cycle calculations due to the effect of the carrier envelope of the pulse. We present a simple and effective technique to recover these sub-cycle features in experimental multi-cycle spectra. We time-filter the momentum distribution to highlight features originating from the interference of electron trajectory pairs with ionization times less than one field cycle apart. This method removes the ATI patterns and reveals sub-cycle interference structures in unprecedented detail. We can resolve new modulations in holographic structures that have not been previously noted in earlier experiments and which provide a new reference for comparing to calculations.

physics.atom-ph

X-ray diffractive imaging of controlled gas-phase molecules: Toward imaging of dynamics in the molecular frame

We report experimental results on the diffractive imaging of three-dimensionally aligned 2,5-diiodothiophene molecules. The molecules were aligned by chirped near-infrared laser pulses, and their structure was probed at a photon energy of 9.5 keV ($λ\approx130 \text{pm}$) provided by the Linac Coherent Light Source. Diffracted photons were recorded on the CSPAD detector and a two-dimensional diffraction pattern of the equilibrium structure of 2,5-diiodothiophene was recorded. The retrieved distance between the two iodine atoms agrees with the quantum-chemically calculated molecular structure to within 5 %. The experimental approach allows for the imaging of intrinsic molecular dynamics in the molecular frame, albeit this requires more experimental data which should be readily available at upcoming high-repetition-rate facilities.

physics.atm-clus

Strongly aligned gas-phase molecules at Free-Electron Lasers

We demonstrate a novel experimental implementation to strongly align molecules at full repetition rates of free-electron lasers. We utilized the available in-house laser system at the coherent x-ray imaging beamline at the Linac Coherent Light Source. Chirped laser pulses, i. e., the direct output from the regenerative amplifier of the Ti:Sa chirped pulse amplification laser system, were used to strongly align 2,5-diiodothiophene molecules in a molecular beam. The alignment laser pulses had pulse energies of a few mJ and a pulse duration of 94 ps. A degree of alignment of $\left<\cos^2\!θ_{2D}\right>$ = 0.85 was measured, limited by the intrinsic temperature of the molecular beam rather than by the available laser system. With the general availability of synchronized chirped-pulse-amplified near-infrared laser systems at short-wavelength laser facilities, our approach allows for the universal preparation of molecules tightly fixed in space for experiments with x-ray pulses.

physics.atm-clus