X-ray Atomic and Molecular Science - Department of Chemistry, University of Nevada, Las Vegas



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Hydrogen storage

 

An effort to help understand the fundamental interaction between hydrogen and nanomaterials made of carbon, silicon, nickel, titanium and other metals.   For this project our group utilizes microscopy at UNLV and the Molecular Foundry at Lawrence Berkeley National Laboratory, and various forms of spectroscopy at LBNL’s Advanced Light source. The results may help to identify suitable material candidates for hydrogen storage in a solid state matrix.

 

Polarized X-Ray-Emission Spectroscopy

 

Current experiments in polarized x-ray-emission spectroscopy take place at the ALS’s beamline 9.3.1 using our new x-ray emission endstation.

 

*    Initial experiments have taken advantage of the atomic-site selectivity inherent to core-level spectroscopy (i.e., core levels for different atoms are well separated in energy), to study particular atomic sites in molecules. Over the last few years we have revisited molecular systems similar to those investigated in the pioneering studies, such as Cl-containing methane-derivatives (CF3Cl, CF2Cl2, etc.).  We are now moving onto other less-well-characterized molecules such as materials for hydrogen storage.

*    Resonant Inelastic X-ray Scattering (RIXS):  The incident x-ray is sufficient to resonantly remove a core-level electron to a higher unoccupied excited state.  Relaxation of this core-hole state is a two step process, an inner shell electron filling the hole while simultaneously an x-ray photon is emitted.

*    Non-Dipole:  The dipole approximation refers to the assumption that the expansion of exp(ik·r) for the interaction with the radiation field can be set equal to unity if k·r is small.   Previous non-dipole measurements at the ALS using electron time-of-flight techniques indicate that the extent and significance of these effects is larger than might be expected. For these experiments we must carefully study how the x-ray emission spectra change depending upon the emission polarization angle relative to the incoming photon beam axis.

 

Molecular Photoionization and Photofragmentation Dynamics

 

*    Anion/Cation Spectroscopy:

*    Molecular Photofragmentation:

*    Atomic Photoionization:

 

 

 


Questions? please mail to wcstolte@lbl.gov