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N. Karoussos

Publications and source records attributed to N. Karoussos.

6 recordsLinked to original sources
arXiv2001

Staggering effects in nuclear and molecular spectra

It is shown that the recently observed Delta J = 2 staggering effect (i.e. the relative displacement of the levels with angular momenta J, J+4, J+8, ..., relatively to the levels with angular momenta J+2, J+6, J+10, ...) seen in superdeformed nuclear bands is also occurring in certain electronically excited rotational bands of diatomic molecules (YD, CrD, CrH, CoH), in which it is attributed to interband interactions (bandcrossings). In addition, the Delta J = 1 staggering effect (i.e. the relative displacement of the levels with even angular momentum J with respect to the levels of the same band with odd J) is studied in molecular bands free from Delta J = 2 staggering (i.e. free from interband interactions/bandcrossings). Bands of YD offer evidence for the absence of any Delta J = 1 staggering effect due to the disparity of nuclear masses, while bands of sextet electronic states of CrD demonstrate that Delta J = 1 staggering is a sensitive probe of deviations from rotational behaviour, due in this particular case to the spin-rotation and spin-spin interactions.

physics.chem-ph↗
arXiv2001

Delta I = 1 staggering in octupole bands of light actinides: "Beat" patterns

The Delta I = 1 staggering (odd--even staggering) in octupole bands of light actinides is found to exhibit a ``beat'' behaviour as a function of the angular momentum I, forcing us to revise the traditional belief that this staggering decreases gradually to zero and then remains at this zero value. Various algebraic models (spf-Interacting Boson Model, spdf-IBM, Vector Boson Model, Nuclear Vibron Model) are shown to predict in their su(3) limits constant staggering for this case, being thus unable to describe the ``beat'' behaviour. An explanation of the ``beat'' behaviour is given in terms of two Dunham expansions (expansions in terms of powers of I(I+1)) with slightly different sets of coefficients for the ground state band and the negative parity band, the difference in the values of the coefficients being attributed to Coriolis couplings to other negative parity bands. Similar ``beat'' patterns have already been seen in rotational bands of some diatomic molecules, like AgH.

nucl-th↗
arXiv2001

Quantum algebraic symmetries in atomic clusters, molecules and nuclei

Quantum algebras (also called quantum groups) are deformed versions of the usual Lie algebras, to which they reduce when the deformation parameter q is set equal to unity. From the mathematical point of view they are Hopf algebras. Their use in physics became popular with the introduction of the q-deformed harmonic oscillator as a tool for providing a boson realization of the quantum algebra SUq(2), although similar mathematical structures had already been known. Initially used for solving the quantum Yang-Baxter equation, quantum algebras have subsequently found applications in several branches of physics, as, for example, in the description of spin chains, squeezed states, hydrogen atom and hydrogen-like spectra, rotational and vibrational nuclear and molecular spectra, and in conformal field theories. By now much work has been done on the q-deformed oscillator and its relativistic extensions, and several kinds of generalized deformed oscillators and SU(2) algebras have been introduced. Here we shall confine ourselves to a list of applications of quantum algebras in nuclear structure physics and in molecular physics and, in addition, a recent application of quantum algebraic techniques to the structure of atomic clusters will be discussed in more detail.

quant-ph↗
arXiv2001

Unified description of magic numbers of metal clusters in terms of the 3-dimensional q-deformed harmonic oscillator

Magic numbers predicted by a 3-dimensional q-deformed harmonic oscillator with Uq(3)>SOq(3) symmetry are compared to experimental data for atomic clusters of alkali metals (Li, Na, K, Rb, Cs), noble metals (Cu, Ag, Au), divalent metals (Zn, Cd), and trivalent metals (Al, In), as well as to theoretical predictions of jellium models, Woods-Saxon and wine bottle potentials, and to the classification scheme using the 3n+l pseudo quantum number. In alkali metal clusters and noble metal clusters the 3-dimensional q-deformed harmonic oscillator correctly predicts all experimentally observed magic numbers up to 1500 (which is the expected limit of validity for theories based on the filling of electronic shells), while in addition it gives satisfactory results for the magic numbers of clusters of divalent metals and trivalent metals, thus indicating that Uq(3), which is a nonlinear extension of the U(3) symmetry of the spherical (3-dimensional isotropic) harmonic oscillator, is a good candidate for being the symmetry of systems of several metal clusters. The Taylor expansions of angular momentum dependent potentials approximately producing the same spectrum as the 3-dimensional q-deformed harmonic oscillator are found to be similar to the Taylor expansions of the symmetrized Woods-Saxon and wine-bottle symmetrized Woods-Saxon potentials, which are known to provide successful fits of the Ekardt potentials.

physics.atm-clus↗
arXiv1999

The 3-Dimensional q-Deformed Harmonic Oscillator and Magic Numbers of Alkali Metal Clusters

Magic numbers predicted by a 3-dimensional q-deformed harmonic oscillator with Uq(3) > SOq(3) symmetry are compared to experimental data for alkali metal clusters, as well as to theoretical predictions of jellium models, Woods--Saxon and wine bottle potentials, and to the classification scheme using the 3n+l pseudo quantum number. The 3-dimensional q-deformed harmonic oscillator correctly predicts all experimentally observed magic numbers up to 1500 (which is the expected limit of validity for theories based on the filling of electronic shells), thus indicating that Uq(3), which is a nonlinear extension of the U(3) symmetry of the spherical (3-dimensional isotropic) harmonic oscillator, is a good candidate for being the symmetry of systems of alkali metal clusters.

quant-ph↗