On the modular isomorphism problem for groups of class 3 and obelisks

We study the Modular Isomorphism Problem applying a combination of existing and new techniques. We make use of the small group algebra to give a positive answer for two classes of groups of nilpotency class 3. We also introduce a new approach to derive properties of the lower central series of a finite 𝑝-group from the structure of the associated modular group algebra. Finally, we study the class of so-called 𝑝-obelisks which are highlighted by recent computer-aided investigations of the problem.

Universal Framework for Quantum Error-Correcting Codes

We present a universal framework for quantum error-correcting codes, i.e., a framework that applies to the most general quantum error-correcting codes. This framework is based on the group algebra, an algebraic notation associated with nice error bases of quantum systems. The nicest thing about this framework is that we can characterize the properties of quantum codes by the properties of the group algebra. We show how it characterizes the properties of quantum codes as well as generates some new results about quantum codes.

$$L^2$$-Betti numbers arising from the lamplighter group

We apply a construction developed in a previous paper by the authors in order to obtain a formula which enables us to compute $$\ell ^2$$ ℓ 2 -Betti numbers coming from a family of group algebras representable as crossed product algebras. As an application, we obtain a whole family of irrational $$\ell ^2$$ ℓ 2 -Betti numbers arising from the lamplighter group algebra $${\mathbb Q}[{\mathbb Z}_2 \wr {\mathbb Z}]$$ Q [ Z 2 ≀ Z ] . This procedure is constructive, in the sense that one has an explicit description of the elements realizing such irrational numbers. This extends the work made by Grabowski, who first computed irrational $$\ell ^2$$ ℓ 2 -Betti numbers from the algebras $${\mathbb Q}[{\mathbb Z}_n \wr {\mathbb Z}]$$ Q [ Z n ≀ Z ] , where $$n \ge 2$$ n ≥ 2 is a natural number. We also apply the techniques developed to the generalized odometer algebra $${\mathcal {O}}({\overline{n}})$$ O ( n ¯ ) , where $${\overline{n}}$$ n ¯ is a supernatural number. We compute its $$*$$ ∗ -regular closure, and this allows us to fully characterize the set of $${\mathcal {O}}({\overline{n}})$$ O ( n ¯ ) -Betti numbers.

CELLULAR AUTOMATA OVER ALGEBRAIC STRUCTURES

Let G be a group and A a set equipped with a collection of finitary operations. We study cellular automata $$\tau :{A^G} \to {A^G}$$ that preserve the operations AG of induced componentwise from the operations of A. We show τ that is an endomorphism of AG if and only if its local function is a homomorphism. When A is entropic (i.e. all finitary operations are homomorphisms), we establish that the set EndCA(G;A), consisting of all such endomorphic cellular automata, is isomorphic to the direct limit of Hom(AS, A), where S runs among all finite subsets of G. In particular, when A is an R-module, we show that EndCA(G;A) is isomorphic to the group algebra $${\rm{End}}(A)[G]$$ . Moreover, when A is a finite Boolean algebra, we establish that the number of endomorphic cellular automata over AG admitting a memory set S is precisely $${(k|S|)^k}$$ , where k is the number of atoms of A.

Artificial Symmetries for Calculating Vibrational Energies of Linear Molecules

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.