2013 Joint Meeting of the APS Division of Atomic, Molecular & Optical Physics and the CAP Division of Atomic, Molecular & Optical Physics, Canada
Volume 58, Number 6
Monday–Friday, June 3–7, 2013;
Quebec City, Canada
Session J7: Invited Session: XFEL Science
2:00 PM–4:00 PM,
Wednesday, June 5, 2013
Room: 303
Chair: Oliver Gessner, Lawrence Berkeley National Laboratory
Abstract ID: BAPS.2013.DAMOP.J7.4
Abstract: J7.00004 : X-ray and optical wave mixing
3:30 PM–4:00 PM
Preview Abstract
Abstract
Author:
Ernest Glover
(Lawrence Berkeley National Laboratory)
Light-matter interactions have advanced our understanding of atoms,
molecules, and materials while also being central to a number of applied
areas. Though optical interactions have been heavily studied, their
microscopic details are often poorly understood. To date it has not been
possible to directly probe the microscopic details of light-matter
interactions.
X-ray and optical wave mixing, specifically sum frequency generation, was
proposed nearly a half century ago as an atomic-scale probe of light-matter
interactions. The process is, in essence, optically modulated x-ray
diffraction : x-rays inelastically scatter from optically induced charge
oscillations and probe optically polarized charge in direct analogy to how
conventional x-ray diffraction probes ground-state charge.
Here we use an x-ray free electron laser to demonstrate x-ray/optical sum
frequency generation through nonlinear interaction of the two fields in
single crystal diamond. Optically modulated x-ray diffraction from the (111)
planes generates a sum (x-ray $+$ optical) frequency pulse. The measured
conversion efficiency ($\sim$ 10$^{-7})$ determines the
(111) Fourier components of the optically induced charge and associated
microscopic field that arise in the illuminated sample. To within
experimental error bars the measured charge density is consistent with first
principles calculations of microscopic optical polarizability in diamond.
The measurements and calculations indicate that light predominantly perturbs
chemical bonds in the diamond lattice. This finding should be generally
applicable to covalent semiconductors and closely related materials such as
graphene. A simple bond charge model reproduces the measured charge density
to within $\sim$ 50{\%}, suggesting that these models can provide
reasonably accurate estimates of microscopic optical polarizability in, for
instance, photonic and photovoltaic devices based on silicon. The ability to
measure atomic-scale charges and fields induced by light should contribute
to a better understanding of materials while also creating new ways to study
phototriggered dynamics.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2013.DAMOP.J7.4