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N. Mărginean

Publications and source records attributed to N. Mărginean.

4 recordsLinked to original sources

Isolated one-phonon mixed-symmetry 2+ state of the radioactive neutron-rich nuclide 132Te

The $M1$ transition strengths between excited $2^+$ states of the neutron-rich, radioactive nuclide $^{132}$Te have been studied through direct lifetime measurements using the Doppler-shift attenuation method in a two-neutron transfer reaction on a $^{130}$Te target. An unambiguous identification of the lowest-lying mixed-symmetry $2^+$ state has been achieved on the basis of the large $B(M1;2^+_2\rightarrow2^+_1$)=0.18(2) $μ_\mathrm{N}^2$ transition strength, in agreement with shell-model calculations. Results are compared to the shell model, and the analysis of both, data and calculations, unambiguously identifies the second-excited $2^+$ state of $^{132}$Te as the one-quadrupole phonon mixed-symmetry state of this isotope. A lowering of the energy and $B(M1;2^+_\mathrm{ms}\rightarrow 2^+_1)$ strength within the $N$=80 isotones toward the $Z$=50 shell closure is observed, which goes alongside with the lowering of the $E2$ collectivity approaching the magic proton shell.

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On the multipole mixing ratio of the $1066$ keV transition from the 0.52 $μs$ isomer of $^{180}$Hf

The nucleus $^{180}$Hf is one of the most primary of examples of an axially symmetric prolate rotor. Combined with the presence of high-$K$ isomers, spectroscopic studies can provide important information on the nature of its single-particle levels. Precise measurements are essential for constraining nuclear models and interpreting the nature of such isomeric states. In this work, the nucleus $^{180}$Hf was populated using the proton pick-up reaction $^{181}$Ta($^{11}$B,$^{12}$C)$^{180}$Hf at beam energy of 47 MeV at Horia Hulubei National Institute of Nuclear Physics and Engineering (IFIN-HH). The spin of the 1374 keV state and the mixing ratio of the $1066$ keV transition have been measured, the latter with an increased precision compared to the previous value from literature. The presently measured spin of the 1374 keV state, currently assigned a tentative value of $(4^-_1)$, favors one of the two different values reported in the literature. The particular state constitutes the band-head of a rotational band in $^{180}$Hf. The measured multipolarity mixing ratio of the inter-band transition $1374 \rightarrow 309$ keV can provide important information for the testing and constraining of theoretical nuclear models used for the study of the intrinsic properties of $^{180}$Hf as well as its neighboring isotopes.

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Shape Coexistence at Zero Spin in 64Ni Driven by the Monopole Tensor Interaction

The low-spin structure of the semimagic 64Ni nucleus has been considerably expanded: combining four experiments, several 0+ and 2+ excited states were identified below 4.5 MeV, and their properties established. The Monte Carlo shell model accounts for the results and unveils an unexpectedly complex landscape of coexisting shapes: a prolate 0+ excitation is located at a surprisingly high energy (3463 keV), with a collective 2+ state 286 keV above it, the first such observation in Ni isotopes. The evolution in excitation energy of the prolate minimum across the neutron N = 40 subshell gap highlights the impact of the monopole interaction and its variation in strength with N.

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Spectroscopy of Neutron-Rich 168,170Dy: Yrast Band Evolution Close to the NpNn Valence Maximum

The yrast sequence of the neutron-rich dysprosium isotope 168Dy has been studied using multi-nucleon transfer reactions following collisions between a 460-MeV 82Se beam and a 170Er target. The reaction products were identified using the PRISMA magnetic spectrometer and the gamma rays detected using the CLARA HPGe-detector array. The 2+ and 4+ members of the previously measured ground state rotational band of 168Dy have been confirmed and the yrast band extended up to 10+. A tentative candidate for the 4+ to 2+ transition in 170Dy was also identified. The data on these nuclei and on the lighter even-even dysprosium isotopes are interpreted in terms of Total Routhian Surface calculations and the evolution of collectivity in the vicinity of the proton-neutron valence product maximum is discussed.

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