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Czechoslovak Journal of Physics

Effective Hamiltonians from first principles

Jan Peřina

Published Jun 1, 1993• 2 citations
Publisher
DOI
10.1007/bf01591537

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Abstract First-principles approaches have been successful in solving many-body Hamiltonians for real materials to an extent when correlations are weak or moderate. As the electronic correlations become stronger often embedding methods based on first-principles approaches are used to better treat the correlations by solving a suitably chosen many-body Hamiltonian with a higher level theory. The success of such embedding theories, often referred to as second-principles, is commonly measured by the quality of self-energy Σ which is either a function of energy or momentum or both. However, Σ should, in principle, also modify the electronic eigenfunctions and thus change the real space charge distribution. While such practices are not prevalent, some works that use embedding techniques do take into account these effects. In such cases, choice of partitioning, of the parameters defining the correlated Hamiltonian, of double-counting corrections, and the adequacy of low-level Hamiltonian hosting the correlated subspace hinder a systematic and unambiguous understanding of such effects. Further, for a large variety of correlated systems, strong correlations are largely confined to the charge sector. Then an adequate nonlocal low-order theory is important, and the high-order local correlations embedding contributes become redundant. Here we study the impact of charge self-consistency within two example cases, TiSe2 and CrBr3, and show how real space charge re-distribution due to correlation effects taken into account within a first-principles Green’s function-based many-body perturbative approach is key in driving qualitative changes to the final electronic structure of these materials.
We investigate the effects of rotation on the excited bands of a tight-binding lattice, focusing particularly on the first excited (p)(p)(p) band. Both the on-site energies and the hopping between lattice sites are modified by the effective magnetic field created by rotation, causing a nontrivial splitting and magnetic fine structure of the ppp band. We show that Peierls substitution can be modified to describe ppp band under rotation, and use this method to derive an effective Hamiltonian. We compare the spectrum of the effective Hamiltonian with a first-principles calculation of the magnetic band structure and find excellent agreement, confirming the validity of our approach. We also discuss the on-site interaction terms for bosons and argue that many-particle phenomena in a rotating ppp band can be investigated starting from this effective Hamiltonian.