Numéro |
J. Phys. Colloques
Volume 48, Numéro C9, Décembre 1987
X-Ray and Inner-Shell ProcessesVol. 1 |
|
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Page(s) | C9-761 - C9-763 | |
DOI | https://doi.org/10.1051/jphyscol:19879132 |
Vol. 1
J. Phys. Colloques 48 (1987) C9-761-C9-763
DOI: 10.1051/jphyscol:19879132
POLARIZATION EFFECTS IN MOLECULAR X-RAY FLUORESCENCE
D.W. LINDLE1, P.L. COWAN1, R.E. LaVILLA1, T. JACH1, R.D. DESLATTES1, R.C.C. PERERA2 and B. KARLIN31 National Bureau of Standards, Gaithersburg, MD 20899, U.S.A.
2 Center for X-Ray Optics, Lawrence Berkeley Laboratory, Berkeley, CA 94720, U.S.A.
3 National Synchrotron Light Source. Brookhaven National Laboratory, Upton, NY 11973, U.S.A.
Abstract
Highly polarized x-ray fluorescence has been observed following K-shell excitation of several Cl-containing molecules. Monochromatic synchrotron radiation (SR) with a high degree of linear polarization was used to resonantly excite Cl 1s electrons in CH3Cl, and the three Freons, CF3Cl, CF,Cl2, and CF3Cl. The subsequent Cl Kβ fluorescence was found to be strongly linearly polarized. The direction of polarization of the Kβ fluorescence is determined in part by the symmetry of the valence-orbital electron involved in the fluorescence decay which fills the Cl 1s hole. Our results illustrate that the core-level resonance lifetimes are short enough to preclude substantial disorientation of the molecule prior to fluorescence decay. Measurements of this type may prove to be a sensitive probe of orbital symmetry in more complicated molecular systems, condensed matter, and adsorbates.