On the asymptotic distribution of the spectrum of an operator over irreducible representations of its symmetry group

2006 ◽  
Vol 40 (3) ◽  
pp. 225-227
Author(s):  
V. N. Karpushkin
Symmetry ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1624
Author(s):  
Janos Polonyi ◽  
Ines Rachid

It is shown that the mixed states of a closed dynamics supports a reduplicated symmetry, which is reduced back to the subgroup of the original symmetry group when the dynamics is open. The elementary components of the open dynamics are defined as operators of the Liouville space in the irreducible representations of the symmetry of the open system. These are tensor operators in the case of rotational symmetry. The case of translation symmetry is discussed in more detail for harmonic systems.


2004 ◽  
Vol 7 ◽  
pp. 101-119 ◽  
Author(s):  
P. C. Matthews

AbstractThe process of classifying possible symmetry-breaking bifurcations requires a computation involving the subgroups and irreducible representations of the original symmetry group. It is shown how this calculation can be automated using a group theory package such as GAP. This enables a number of new results to be obtained for larger symmetry groups, where manual computation is impractical. Examples of symmetric and alternating groups are given, and the method is also applied to the spatial symmetry-breaking of periodic patterns observed in experiments.


1963 ◽  
Vol 18 (10) ◽  
pp. 1058-1064 ◽  
Author(s):  
Werner Kutzelnigg

The density operator (density matrix) of a quantum mechanical system can be decomposed into operators which transform as irreducible representations of the symmetry group in coordinate and spin space. Each of these components has a physical meaning connected with the expectation values of certain operators. The reduced density matrices can be decomposed in a completely analogous way.The symmetry properties of the total wave function give rise to degeneracies of the eigenvalues of the reduced density matrices. These degeneracies can be removed by requiring that the natural spin orbitals (NSO, defined as the eigenfunctions of the first order density matrix), as well as the natural spin geminais (NSG, the eigenfunctions of the second order density matrix) and their spinless counterparts transform as irreducible representations of the symmetry group and are eigenfunctions of S2 and Sz.In many important cases this requirement is compatible with the original definition of the NSO, the NSG etc. e. g., when there is no spatial degeneracy of the total wave function and when the Z-component of the total spin vanishes. When these conditions are not fulfilled an alternative definition of the NSO and the NSG is proposed.


2019 ◽  
Vol 19 (07) ◽  
pp. 2050124 ◽  
Author(s):  
Isabelle Baraquin

In this paper, we study (asymptotic) properties of the ∗-distribution of irreducible characters of finite quantum groups. We proceed in two steps, first examining the representation theory to determine irreducible representations and their powers, then we study the ∗-distribution of their trace with respect to the Haar measure. For the Sekine family, we look at the asymptotic distribution (as the dimension of the algebra goes to infinity).


2009 ◽  
Vol 7 (2) ◽  
pp. 211-214 ◽  
Author(s):  
Wojciech Florek ◽  
Katarzyna Jaśniewicz-Pacer ◽  
Leonard Kaliszan ◽  
Grzegorz Kamieniarz

AbstractA four-spin system with s=1 and the single-ion anisotropy, D∑ j [s jz ] 2 , is considered. When D≠0 the Hamiltonian of the system does not commute with S 2 and, therefore, S cannot be used as an additional label of energy levels. In this work we concentrate on the problem of mixing states with different total spins S. The Hamiltonian matrix is transformed to the symmetry-adapted basis (with subspaces labeled by the irreducible representations of the symmetry group) and next, after solving the eigenproblem for S 2, to the basis with vectors labeled by S. Each eigenproblem is solved exactly (at least numerically) and the eigenstates are expressed as ∑S a S ¦S〉. The coefficients aS are analyzed, especially for their D-dependence. Even in such a small system different schemes of level mixing can be observed.


A systematic study is made of the irreducible representations of the unitary unimodular group in three dimensions, an algebraic technique being used that is based on the well-known theory of the rotation group in three dimensions. Explicit representation matrices are found. The representations are characterized by the ranges of the ‘hypercharge’ and ‘isobaric spin’ that occur in them. The dimension formula is derived and the invariants are determined. Two identities are found relating the generators of the group.


Symmetry ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 548
Author(s):  
Thomas M. Mellor ◽  
Sergei N. Yurchenko ◽  
Per Jensen

Linear molecules usually represent a special case in rotational-vibrational calculations due to a singularity of the kinetic energy operator that arises from the rotation about the a (the principal axis of least moment of inertia, becoming the molecular axis at the linear equilibrium geometry) being undefined. Assuming the standard ro-vibrational basis functions, in the 3N−6 approach, of the form ∣ν1,ν2,ν3ℓ3;J,k,m⟩, tackling the unique difficulties of linear molecules involves constraining the vibrational and rotational functions with k=ℓ3, which are the projections, in units of ℏ, of the corresponding angular momenta onto the molecular axis. These basis functions are assigned to irreducible representations (irreps) of the C2v(M) molecular symmetry group. This, in turn, necessitates purpose-built codes that specifically deal with linear molecules. In the present work, we describe an alternative scheme and introduce an (artificial) group that ensures that the condition ℓ3=k is automatically applied solely through symmetry group algebra. The advantage of such an approach is that the application of symmetry group algebra in ro-vibrational calculations is ubiquitous, and so this method can be used to enable ro-vibrational calculations of linear molecules in polyatomic codes with fairly minimal modifications. To this end, we construct a—formally infinite—artificial molecular symmetry group D∞h(AEM), which consists of one-dimensional (non-degenerate) irreducible representations and use it to classify vibrational and rotational basis functions according to ℓ and k. This extension to non-rigorous, artificial symmetry groups is based on cyclic groups of prime-order. Opposite to the usual scenario, where the form of symmetry adapted basis sets is dictated by the symmetry group the molecule belongs to, here the symmetry group D∞h(AEM) is built to satisfy properties for the convenience of the basis set construction and matrix elements calculations. We believe that the idea of purpose-built artificial symmetry groups can be useful in other applications.


1993 ◽  
Vol 329 ◽  
Author(s):  
Frederick G. Anderson ◽  
H. Weidner ◽  
P. L. Summers ◽  
R. E. Peale ◽  
B. H. T. Chai

AbstractExpanding the crystal field in terms of operators that transform as the irreducible representations of the Td group leads to an intuitive interpretation of the crystal-field parameters. We apply this method to the crystal field experienced by Nd3+ dopants in the laser crystals YLiF4, YVO4, and KLiYF5.


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