APS March Meeting 2011
Volume 56, Number 1
Monday–Friday, March 21–25, 2011;
Dallas, Texas
Session J38: Focus Session: Ultrafast Dynamics and Imaging II
11:15 AM–1:39 PM,
Tuesday, March 22, 2011
Room: A130/131
Sponsoring
Unit:
DCP
Chair: Markus Guehr, Stanford University
Abstract ID: BAPS.2011.MAR.J38.5
Abstract: J38.00005 : ``Making the Molecular Movie'': First Frames
12:51 PM–1:27 PM
Preview Abstract
Abstract
Author:
R.J. Dwayne Miller
(Max Planck Research Group for Atomically Resolved Dynamics, University of Hamburg, CFEL/DESY and University of Toronto)
Femtosecond Electron Diffraction has enabled atomic resolution to
structural
changes as they occur, essentially watching atoms move in real
time--directly observe transition states. This experiment has
been referred to as
``making the molecular movie'' and has been previously discussed
in the
context of a gedanken experiment. With the recent development of
femtosecond
electron pulses with sufficient number density to execute single
shot
structure determinations, this experiment has been finally
realized. A new
concept in electron pulse generation was developed based on a
solution to
the N-body electron propagation problem involving up to 10,000
interacting
electrons that has led to a new generation of extremely bright
electron
pulsed sources that minimizes space charge broadening effects.
Previously
thought intractable problems of determining t=0 and fully
characterizing
electron pulses on the femtosecond time scale have now been
solved through
the use of the laser pondermotive potential to provide a time
dependent
scattering source. Synchronization of electron probe and laser
excitation
pulses is now possible with an accuracy of 10 femtoseconds to
follow even
the fastest nuclear motions. The camera for the ``molecular
movie'' is well
in hand based on high bunch charge electron sources. Several movies
depicting atomic motions during passage through structural
transitions will
be shown. Atomic level views of the simplest possible structural
transition,
melting, will be presented for a number of systems in which both
thermal and
purely electronically driven atomic displacements can be
correlated to the
degree of directional bonding. Optical manipulation of charge
distributions
and effects on interatomic forces/bonding can be directly
observed through
the ensuing atomic motions. New phenomena involving strongly
correlated
electron systems will be presented in which an exceptionally
cooperative
phase transitions has been observed. The primitive origin of
molecular
cooperativity has also been discovered in recent studies of
molecular
crystals. These new developments will be discussed in the context of
developing the necessary technology to directly observe the
structure-function correlation in biomolecules--the fundamental
molecular basis of biological systems.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2011.MAR.J38.5