The long held objective of directly observing atomic motions during the defining moments of chemistry has been achieved based on ultrabright electron sources that have given rise to a new field of atomically resolved structural dynamics. This class of experiments requires not only simultaneous sub-atomic spatial resolution with temporal resolution on the 100 femtosecond time scale but also has brightness requirements approaching single shot atomic resolution conditions. The brightness condition is in recognition that chemistry leads generally to irreversible changes in structure during the experimental conditions and that the nanoscale thin samples needed for electron structural probes pose upper limits to the available sample or "film" for atomic movies. Even in the case of reversible systems, the degree of excitation and thermal effects require the brightest sources possible for a given space-time resolution to observe the structural changes above background. Further progress in the field, particularly to the study of biological systems and solution reaction chemistry, requires increased brightness and spatial coherence, as well as an ability to tune the electron scattering cross-section to meet sample constraints. The electron bunch density or intensity depends directly on the magnitude of the extraction field for photoemitted electron sources and electron energy distribution in the transverse and longitudinal planes of electron propagation. This work examines the fundamental limits to optimizing these parameters based on relativistic electron sources using re-bunching cavity concepts that are now capable of achieving 10 femtosecond time scale resolution to capture the fastest nuclear motions. This analysis is given for both diffraction and real space imaging of structural dynamics in which there are several orders of magnitude higher space-time resolution with diffraction methods. The first experimental results from the Relativistic Electron Gun for Atomic Exploration (REGAE) are given that show the significantly reduced multiple electron scattering problem in this regime, which opens up micron scale systems, notably solution phase chemistry, to atomically resolved structural dynamics.
The phenomenon of metastability shapes dynamical processes ranging from radioactive decay to chemical reactions. Here, we present a mechanism for metastability in which a quantum gas selfstabilizes against relaxation towards thermal equilibrium by establishing a transient ordered state. In this state, the direct relaxation channel is suppressed by destructive interference, which derives from the chiral order of the transient state. In particular, we consider the dynamical evolution of an ultracold bosonic gas in an optical lattice, that is quenched into a higher band of the lattice, which triggers the dynamical evolution. Following this quench, the self-stabilization phenomenon manifests itself in three stages of relaxation, subsequent to the preparation of the incoherent excited state. In the first stage, the gas develops coherence resulting in the ordered state, during the second stage the gas forms a long-lived state with inhibited relaxation and slow loss of coherence, followed by the third stage of fast relaxation to the thermal ground state. We demonstrate this mechanism experimentally and theoretically, and discuss its broader implications.
The linear accelerator REGAE at DESY produces short and low charged electron bunches, on the one hand to resolve the excitation transitions of atoms temporally by pump-probe electron diffraction experiments and on the other hand to investigate principal mechanisms of laser plasma acceleration. For both cases a high quality electron beam is required which can be identified with a small beam emittance. A standard magnet scan is used for the emittance measurement which is in case of a low charged bunch most sensitive to the beam size determination (RMS or 2 nd central moment of a distribution). Therefore the diagnostic and a routine to calculate proper central moments of an arbitrary distribution will be introduced and discussed.
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