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@ARTICLE{Manz:302028,
author = {Manz, Stephanie and Casandruc, Albert and Zhang, Dongfang
and Zhong, Yinpeng and Loch, Rolf A. and Marx, Alexander and
Hasegawa, Taisuke and Liu, Lai Chung and Bayesteh, Shima and
Delsim-Hashemi, Hossein and Hoffmann, Matthias and Felber,
Matthias and Hachmann, Max and Mayet, Frank and Hirscht,
Julian and Keskin, Sercan and Hada, Masaki and Epp, Sascha
W. and Flöttmann, Klaus and Miller, R. J. Dwayne},
title = {{M}apping {A}tomic {M}otions {W}ith {U}ltrabright
{E}lectrons: {T}owards {F}undamental {L}imits in
{S}pace-{T}ime {R}esolution},
journal = {Faraday discussions},
volume = {177},
issn = {1364-5498},
address = {Cambridge [u.a.]},
publisher = {Soc.},
reportid = {PUBDB-2016-03071},
pages = {467 - 491},
year = {2015},
note = {(c) The Royal Society of Chemistry},
abstract = {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
scatteringproblem in this regime, which opens up micron
scale systems, notably solution phase chemistry, to
atomically resolved structural dynamics.},
cin = {MPSD},
ddc = {540},
cid = {I:(DE-H253)MPSD-20120731},
pnm = {899 - ohne Topic (POF3-899)},
pid = {G:(DE-HGF)POF3-899},
experiment = {EXP:(DE-MLZ)NOSPEC-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000353034300027},
pubmed = {pmid:25631530},
doi = {10.1039/C4FD00204K},
url = {https://bib-pubdb1.desy.de/record/302028},
}