VUV Spectroscopy of Atoms, Molecules and Surfaces
VUV Spectroscopy of Atoms, Molecules and Surfaces
VUV Spectroscopy of Atoms, Molecules and Surfaces
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56 High-resolution <strong>VUV</strong> spectroscopy <strong>of</strong> H −<br />
et al. in a hyperspherical close-coupling calculation [10]. The inadequacy <strong>of</strong><br />
this approach might have been expected on the basis <strong>of</strong> a comparison <strong>of</strong> the<br />
calculated cross section with the experimental results <strong>of</strong> Bryant et al. where<br />
the measured strength appeared to be much larger than predicted [10]. The<br />
widths obtained by Sadeghpour et al. [14], <strong>and</strong> Cortés <strong>and</strong> Martin [29], applying<br />
R-matrix- <strong>and</strong> L 2 methods, respectively, are outside the uncertainty <strong>of</strong><br />
the present value. The calculation <strong>of</strong> Sadeghpour et al. in addition predicts a<br />
resonance energy that deviates from the experimental value which, within the<br />
quoted uncertainty, agrees with those <strong>of</strong> all the other approaches. It should<br />
be noted that the improved resolution <strong>of</strong> the present experiment does not<br />
allow a more accurate determination <strong>of</strong> the resonance energy than previously<br />
reported. The uncertainty <strong>of</strong> this parameter is limited by the uncertainty<br />
<strong>of</strong> the D − beam orbit length [20]. The complex-rotation method applied in<br />
different variants by Ho [27], Lindroth et al. [16, 17], Kuan et al. [32], Chen<br />
[33] <strong>and</strong> Bylicki <strong>and</strong> Nicolaides [15] seems to provide a good description <strong>of</strong> the<br />
structure <strong>of</strong> the negative hydrogen ion. The measured magnitude <strong>of</strong> q agrees<br />
very well with the few theoretical predictions for this parameter [16, 29, 30]<br />
but this is to be expected since the q value couples to the width.<br />
3.4 Conclusion<br />
The natural width Γ <strong>and</strong> the asymmetry parameter q <strong>of</strong> the 1P o 2{0} − 3 resonance<br />
<strong>of</strong> D− have been determined to a precision that, for the first time, has<br />
allowed a critical test <strong>of</strong> the various theoretical models applied to this system.<br />
The measurement was performed with the technique <strong>of</strong> Doppler-tuned <strong>VUV</strong><br />
spectroscopy, for which the resolution was improved by a factor <strong>of</strong> ∼4with<br />
respect to previous experiments by electron cooling the D− beam. The energy<br />
resolution obtained in the present experiment cannot be improved much<br />
further, given the machine properties <strong>of</strong> the storage ring <strong>and</strong> the electron<br />
cooler, <strong>and</strong> will make an observation <strong>of</strong> the last member <strong>of</strong> the 2{0} − m series,<br />
the 1 P o 2 {0}− 5<br />
resonance, difficult. Figure 3.6 (a) shows the cross section in<br />
the vicinity <strong>of</strong> this resonance as predicted by Lindroth, with the 2p1/2, 2s<strong>and</strong> 2p3/2 thresholds <strong>of</strong> D(n=2) indicated by vertical lines. In figure 3.6 (b) this<br />
cross section has been convolved with the present experimental resolution,<br />
<strong>and</strong> the ratio <strong>of</strong> the resonant to <strong>of</strong>f-resonant contribution is seen to be ∼1.4<br />
with the 2p1/2 threshold being completely buried in the high-energy shoulder<br />
<strong>of</strong> the 2{0} − 5 resonance. Given the decrease in strength by a factor <strong>of</strong> ∼700<br />
when going from the 2 {0} − 3 to the 2 {0}− 5<br />
state [16], this structure can only<br />
be verified beyond statistical uncertainty by increasing the data-collection<br />
time by at least a factor <strong>of</strong> 50, assuming a grating efficiency similar to that<br />
<strong>of</strong> the 1996–97 experiments. Since the collection time for each data point is