Mapping Atomic Motions with Electrons: Toward the Quantum Limit to Imaging Chemistry
Author(s) -
Zheng Li,
Sandeep Gyawali,
A. A. Ischenko,
Stuart A. Hayes,
R. J. Dwayne Miller
Publication year - 2019
Publication title -
acs photonics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.735
H-Index - 89
ISSN - 2330-4022
DOI - 10.1021/acsphotonics.9b01008
Subject(s) - degrees of freedom (physics and chemistry) , quantum , physics , quantum chemistry , reaction dynamics , statistical physics , quantum state , chemistry , chemical physics , nanotechnology , quantum mechanics , materials science , supramolecular chemistry , molecule
Recent advances in ultrafast electron and x-ray diffraction have pushed imaging of structural dynamics into the femtosecond time domain, i.e. the fundamental time scale of atomic motion. New physics can be reached beyond the scope of traditional diffraction or reciprocal space imaging. By exploiting the high time resolution, it has been possible to directly observe the collapse of nearly innumerable possible nuclear motions to a few key reaction modes that direct chemistry. It is this reduction in dimensionality in the transition state region that makes chemistry a transferable concept, with the same class of reactions being applicable to synthetic strategies to nearly arbitrary levels of complexity. The ability to image the underlying key reaction modes has been achieved with resolution to relative changes in atomic positions to better than .01 A, i.e. comparable to thermal motions. We have effectively reached the fundamental space-time limit with respect to the reaction energetics and imaging the acting...
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