While the modern theory of the insulating state shows that the conducting or insulating properties of a system can be extracted solely from the ground state properties via the so-called localization tensor (LT), no chemical reading of this important quantity has ever been offered. Here, a remarkable link between the LT and the bond orders as described by the delocalization indices (DIs) of chemical bonding theory is reported. This is achieved through a real space partition of the LT into intra- and interatomic contributions. We show that the convergence or divergence of the LT in the thermodynamic limit, which signals the insulating or conducting nature of an extended system, respectively, can be nailed down to DIs. This allows for the exploitation of traditional chemical intuition to identify essential and spectator atomic groups in determining electrical conductivity. The thermodynamic limit of the LT is controlled by the spatial decay rate of the interatomic DIs, exponential in insulators and power-law in conductors. Computational data of a few selected toy systems corroborate our results.
While the modern theory of the insulating state shows that the conducting or insulating properties of a system can be extracted solely from the ground state properties via the so-called localization tensor (LT), no chemical reading of this important quantity has ever been offered. Here, a remarkable link between the LT and the bond orders as described by the delocalization indices (DIs) of chemical bonding theory is reported. This is achieved through a real space partition of the LT into intra- and interatomic contributions. We show that the convergence or divergence of the LT in the thermodynamic limit, which signals the insulating or conducting nature of an extended system, respectively, can be nailed down to DIs. This allows for the exploitation of traditional chemical intuition to identify essential and spectator atomic groups in determining electrical conductivity. The thermodynamic limit of the LT is controlled by the spatial decay rate of the interatomic DIs, exponential in insulators and power-law in conductors. Computational data of a few selected toy systems corroborate our results.
An ab initio analysis is made of the localized (in Mott’s sense) and delocalized (band) states of an electron in a crystal. The criterion of a difference between these states is the behavior of the off-diagonal elements in the one-particle electronic density matrix ⟨ψ^+(r)ψ^(r′)⟩ for T=0. Localization can be related to its exponential falloff for |r−r′|→∞, and delocalization, to its power-law decay. This corresponds to the analyticity of the density matrix in k space of the Brillouin zone in the first case, and to a singularity (Fermi step) in the second. This analyticity gives rise also to a power-law decay of the correlation functions. In a normal system, localization can be identified with the insulating state, and delocalization, with the conducting state. It is shown that the above localization criterion is applicable to disordered systems as well. Electron localization in superconductors is also discussed. It is pointed out that the above criterion of localization is met also in the BCS superconducting state and in the localized-pair model. The reason for the considerable difference between the properties of the insulating and superconducting states lies in that there are no static fluctuations in the number of electrons, 〈(ΔN)2〉0, in the ground state of an insulator whereas in a superconductor ODLRO results in nonzero fluctuations of N of a quantum nature.
We study in this contribution the spatial decay rate of real-space localization and delocalization indices in correlated systems. To that end, we examine Hubbard and quantum chemical models of simple cyclic hydrogen chains, showing that all descriptors of delocalization converge quickly toward the infinite chain limits. It is then shown that the localization index may be understood as a generalization of the standard order parameter in Mott insulator transitions and that the origin of the enigmatic sigmoidal profile of delocalization indices in chemical bond-breaking processes lies in the nonlinear mapping between intersite distances and correlation parameters. Although the long-range asymptotic decay of delocalization indices is exponential, we show that as the correlation parameter decreases quantum mechanical interference sets in and a switch to an oscillating pattern, related to core chemical concepts such as resonance or mesomerism, appears.
An insulator differs from a metal because of a different organization of the electrons in their ground state. In recent years this feature has been probed by means of a geometrical property, the quantum metric tensor, which addresses the system as a whole, and is therefore limited to macroscopically homogenous samples. Here we show that an analogous approach leads to a localization marker, which can detect the metallic versus insulating character of a given sample region using as the sole ingredient the ground state electron distribution, even in the Anderson case (where the spectrum is gapless). When applied to an insulator with a nonzero Chern invariant, our marker is capable of discriminating the insulating nature of the bulk from the conducting nature of the boundary. Simulations (both model Hamiltonian and first principles) on several test cases validate our theory.
The clear distinction between metals and insulators is a well established and appartently simple concept which can be clarified by studying the behavior of the electrical conductivity. However, a theoretical description of the processes leading to one of the two extremes is no trivial task. The widely accepted band structure theory relies on an one-electron picture to characterize the metallic/insulating behavior of a material. However, in spite of the fact that it can be used to make successful predictions, this description does not capture one of the essential elements characterizing the nature of an electronic quantum system, i.e. the electron correlation. The key to the different behaviors is clearly contained in the correlated many- electron wave function, but the analysis of such a high-dimensional object in configuration space can be quite cumbersome. Therefore the development of powerful tools to simplify this task is necessary. The total position-spread (TPS) tensor, which was derived by Walter Kohn’s theory of the insulating state, plays a key role in the field of metal-insulator transitions (MITs). This tool provides information about the electron localization, which is strongly connected to the electrical conductivity. Therefore, in this work particular attention was paid to the calculation of the TPS tensor of small and extended systems. Moreover, part of this thesis focuses on a new formalism, which allows the study of spin mobility and spin entanglement and provides therefore deeper insight into the effects of electron correlation. In the framework of quantum information theory (QIT), the quantum entanglement can be quantified by means of measures such as the von Neumann entropy. Also, the analysis of the elements of the two-orbital reduced density matrix provides an overview of the complexity of the many-electron wave function. These insights were used in this work for the analysis of the metallic/insulating character of a system. However, in order to perform such investigastions, the problem of achieving an accurate description of the many- electron wave function has to be dealt with. Despite the tremedous progress in the efficiency of quantum-chemical methods, the treatement of extended systems using standard approaches is still a difficult (if not unfeasible) task. Therefore the development and testing of sophisticated, low-scaling methods is currently the subject of many investigations. In this work, two approaches were employed: 1) the ab-initio density matrix renormalization group (DMRG) approach which, based on a tensor product ansatz, provides very precise results and exploits QIT to improve its performance; 2) the method of increments (MoI) which, using a many-body expansion in terms of localized orbitals, yields accurate correlation energies. By using both methods on strongly correlated one-dimesional model systems, we worked on a new formalism of the method of increments which can be used to describe the whole dissociation curve without inconvenient discontinuities. Finally, aiming to calculate the total position-spread tensor of extended systems, we worked on the application of the MoI for quantities other than the correlation energy.
The use of the mutual information (MI) as a measure of the entanglement in quantum systems has gained a consensus in recent years, even if there is an ongoing effort to distinguish the classical and quantum contributions contained therein. This quantity has been first introduced in condensed matter physics, in particular, in studies based on the density matrix renormalization group method. This method has been successfully adapted to quantum chemistry problems, opening the way to compute MI also in molecular systems. A key aspect of this quantity is its dependence on the one-electron (orbital) basis set, even for wave functions that are invariant under unitary transformation of the orbitals. In this work, we investigate the role of the orbital basis set (delocalized or localized, following different strategies) for wave functions expressed as linear combinations of Slater determinants and we give the analytic expression for the MI for a few special cases. This study aims to improve the knowledge of the relationship between the characteristics of the chemical bond (considering a few paradigmatic molecules, H 2, F 2, N 2, and short linear polyenes) and the properties of interest in the field of quantum information theory.
The localization tensor is a measure of distinguishability between insulators and metals. This tensor is related to the quantum metric tensor associated with the occupied bands in momentum space. In two dimensions and in the thermodynamic limit, it defines a flat Riemannian metric over the twist-angle space, topologically a torus, which endows this space with a complex structure, described by a complex parameter $\ensuremath{\tau}$. It is shown that the latter is a physical observable related to the anisotropy of the system. The quantity $\ensuremath{\tau}$ and the Riemannian volume of the twist-angle space provide an invariant way to parametrize the flat quantum metric obtained in the thermodynamic limit. Moreover, if, by changing the couplings of the theory, the system undergoes quantum phase transitions in which the gap closes, the complex structure $\ensuremath{\tau}$ is still well defined, although the metric diverges (metallic state), and it is fixed by the form of the Hamiltonian near the gap closing points. The Riemannian volume is responsible for the divergence of the metric at the phase transition.