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Picosecond lifetime measurements in 109Cd and 110Cd

Picosecond lifetime measurements in 109Cd and 110Cd

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164 S. Harissopulos et al. / Nuclear Physics A 683 (2001) 157–181<br />

As po<strong>in</strong>ted out <strong>in</strong> [27], nuclear deorientation is expected to have a significant <strong>in</strong>fluence<br />

to the <strong>in</strong>tensities of γ -transitions deexcit<strong>in</strong>g states with sp<strong>in</strong> J 4. In addition, <strong>in</strong> the<br />

case of E2 γ -transitions (J = 2) this <strong>in</strong>fluence is rather strong at 0 ◦ <strong>and</strong> rather weak<br />

at 55 ◦ . Hence, the ratio of the decay curve of a given excited state derived at a certa<strong>in</strong><br />

angle θ to this determ<strong>in</strong>ed at 55 ◦ , provides a reliable check for possible <strong>in</strong>fluence of the<br />

nuclear deorientation effect. In case this “anisotropy ratio” is constant, the decay curve<br />

derived at the certa<strong>in</strong> angle θ needs no corrections. In the present work, this check has<br />

been partially h<strong>in</strong>dered by the fact that dur<strong>in</strong>g the experiment the detector placed at 55 ◦ has<br />

provided spectra with long left tails <strong>in</strong> the γ -peaks, probably due to neutron damage, <strong>and</strong><br />

also irregular ga<strong>in</strong> shifts, which <strong>in</strong> many cases occurred <strong>in</strong> the same s<strong>in</strong>gle spectrum. Due<br />

to these problems anisotropy ratios have been derived via follow<strong>in</strong>g procedure: the “less<br />

damaged” 55 ◦ -spectra, i.e. the γ -s<strong>in</strong>gles spectra <strong>in</strong>clud<strong>in</strong>g relatively short left tails <strong>and</strong> no<br />

ga<strong>in</strong> shifts, have been normalized to the 260 keV γ -transition of 109 Cd. From the latter<br />

(normalized) spectra, the <strong>in</strong>tensities of the unshifted peak of the 2 + 1 → 0+ 1<br />

γ -transition<br />

of the 110 Cd nucleus have been derived via a very careful <strong>in</strong>tegration procedure. This<br />

procedure has also been carried out for the γ -s<strong>in</strong>gles spectra taken at 160 ◦ . Unfortunately,<br />

the quality of the 55 ◦ spectra did not allow to obta<strong>in</strong> anisotropy ratios for the 4 + 1 → 2+ 1<br />

γ -transition as well. In the follow<strong>in</strong>g, the <strong>in</strong>tensities of the unshifted peak of a γ -transition<br />

i → j obta<strong>in</strong>ed from spectra normalized to the 260 keV γ -transition of 109 Cd, which have<br />

beentakenatanangleθ, will be declared as R ij (x, θ). Hereby, it has to be po<strong>in</strong>ted out that<br />

R ij (x, θ) have not been determ<strong>in</strong>ed from difference spectra like quantities U ij (x).<br />

The <strong>in</strong>tensities R ij (x, θ = 55 ◦ ) of the 2 + 1 → 0+ 1<br />

γ -transition of 110 Cd have been<br />

compared with the respective R ij (x, 0 ◦ ) <strong>and</strong> R ij (x, 160 ◦ ). The correspond<strong>in</strong>g anisotropy<br />

ratios are shown <strong>in</strong> Fig. 4. Accord<strong>in</strong>g to this figure, the decay curves determ<strong>in</strong>ed at 0 ◦<br />

<strong>and</strong> 160 ◦ are <strong>in</strong>fluenced from the nuclear deorientation effect at distances x 100 µm<br />

<strong>and</strong> x 1000 µm, respectively. In addition, by fitt<strong>in</strong>g a s<strong>in</strong>gle exponential function of the<br />

form f(x)= a · exp(−x/τ R ) + c to the 0 ◦ /55 ◦ anisotropy ratio we obta<strong>in</strong>ed a relaxation<br />

time-constant τ R = 410(120) ps. It has to be emphasized that the fit function used serves<br />

only to correct the data measured at 0 ◦ , i.e. the data po<strong>in</strong>ts of the decay curve determ<strong>in</strong>ed<br />

Fig. 4. Anisotropy ratios measured <strong>in</strong> the present work for the 2 + 1 → 0+ 1 γ -transition of the 110 Cd.<br />

The solid curve shown <strong>in</strong> (a) has been obta<strong>in</strong>ed by the fitt<strong>in</strong>g of the s<strong>in</strong>gle exponential function<br />

f(x)= a · exp(−x/τ R ) + c to the data, which yielded a relaxation time-constant τ R = 410(120) ps.

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