Threshold Alignment Reversal and Circularly Polarized Fluorescence in Rotationally ResolvedH 2
Author(s) -
J.W. Maseberg,
Klaus Bartschat,
T. J. Gay
Publication year - 2013
Publication title -
physical review letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.688
H-Index - 673
eISSN - 1079-7114
pISSN - 0031-9007
DOI - 10.1103/physrevlett.111.253201
Subject(s) - physics , excitation , polarization (electrochemistry) , atomic physics , electron , linear polarization , optics , quantum mechanics , chemistry , laser
Using H2 and D2 targets, we have measured the polarization of Fulcher-band fluorescence resulting from spin-polarized electron-impact excitation of vibrationally and rotationally resolved d 3Π(u) → a 3Σ(g)+ transitions for incident electron energies from 14.3 to 28.5 eV. Near threshold, the linear polarization P1 descends from positive values through zero to negative values, indicating a dynamic production of M(N)=0 states. The circular polarization P3 is measured to be nonzero, indicating the orientation of rotationally resolved molecular states. For Q-branch transitions, P3 is consistent with theory based on Hund's case (b) coupling. The R-branch P3 values do not agree with theory equally well, indicating the effect of Σ-symmetry perturbation of the parent d 3Π(u)+ state.
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