Average-Resonance Method of Neutron-Captureγ-Ray Spectroscopy: States ofPd106,Gd156,Gd158,Ho166, andEr168

Abstract
The average-resonance method of neutron-capture γ-ray spectroscopy is critically examined by means of measurements on stable isotopes of palladium, gadolinium, holmium, and erbium. A mathematical model of the capture process is developed. This model shows that the intensities of the lines in average-resonance-capture spectra can yield the parities and set narrow limits on the spins of states in almost all nuclides with A>100 if the γ-ray strength function is a smooth function of γ-ray energy and if the random fluctuations in intensity result only from the Porter-Thomas distribution of partial radiation widths. The measurements give extensive data for Pd106, Gd156, Gd158, Ho166, and Er168, and some for Pd103, Pd105, Gd155, Gd157, Er165, Er167, and Er169. These data are examined for information relating to the mechanisms of radiative capture. All of the data are consistent with the hypothesis that the radiation widths are a smooth function of γ-ray energy and that the random fluctuations in intensity are well described by the Porter-Thomas distribution. The intensities of E1 transitions vary with γ-ray energy more rapidly than Eγ3, as expected from a giant-resonance description of the radiative process. The intensity of M1 radiation was measured over a 2-MeV range for Pd106 and Er168, and the reduced M1 widths for Pd106 form a giant-resonance-like curve that peaks at ∼7.8 MeV. Ratios of widths for E1 and M1 radiation and for E1 and E2 radiation are obtained for several nuclides. These properties of radiative capture are used to obtain spectroscopic information about final states. The most complete results are for Ho166, for which 16 rotational bands are identified and interpreted in terms of the collective model. Similar but less extensive data are obtained for Gd156, Gd158, and Er168. The measurements on Pd106 show that the shapes of the observed γ-ray lines may be used to determine the parities of final states.

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