APS March Meeting 2013
Volume 58, Number 1
Monday–Friday, March 18–22, 2013;
Baltimore, Maryland
Session Y10: Invited Session: Advances in Actinide Measurement Techniques
8:00 AM–11:00 AM,
Friday, March 22, 2013
Room: 309
Sponsoring
Unit:
GIMS
Chair: Jason Cooley, Los Alamos National Laboratory
Abstract ID: BAPS.2013.MAR.Y10.5
Abstract: Y10.00005 : Transuranic Photoemission Using a Unique Light Source*
10:24 AM–11:00 AM
Preview Abstract
Abstract
Author:
John Joyce
(Los Alamos National Laboratory)
There has been a remarkable advance in the understanding of electronic
structure for complex materials in recent years. Much of this advance in
understanding has been realized through advanced spectroscopy capabilities
available at public synchrotron facilities. While the vast majority of
materials can take advantage of facilities at public synchrotrons,
transuranic materials are excluded from these facilities when multiple
containment barriers are incompatible with the chosen spectroscopy.
We have developed an advanced spectroscopy capability at Los Alamos for
photoemission on transuranic materials including Pu. Using several different
variants of photoemission we have explored a wide range of Pu materials
which has lead to a significant improvement in our understanding of
transuranic electronic structure. Examples of these successes will be given
along with details of the unique facility. Using the unique capabilities of
our transuranic photoemission system we exploit opportunities in
angle-resolved photoemission (ARPES) providing insight into the details of
both the energy and crystal momentum for a material. Additional information
is obtained using tunable photons which may be used to isolate the 5f
electron contribution to the valence electronic structure. Between ARPES and
tunable photoemission, one may construct a fairly detailed picture of the
bonding and hybridization for transuranic materials. By adding
temperature-dependent (10 - 350K) photoemission to the suite of tools, we
may cross over phase transition boundaries as well as quantify
electron-phonon coupling. We also have the capability for 1.5 and 3 KeV
core-level spectroscopy using a monochromatized x-ray source.
By combining the above photoemission tools with a variety of surface
preparation capabilities including cleaving, laser ablation, and thermal
desorption, we have a flexible and capable spectroscopy facility that
provides unique insight into the electronic structure of transuranic
materials.
*Work supported by DOE, BES, DMSE; Science Campaign 2; and the LANL LDRD program.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2013.MAR.Y10.5