اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدSuccesses and failures of Bethe Ansatz Density Functional Theory
486
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
The response of a one-dimensional fermion system is investigated using Density Functional Theory (DFT) within the Local Density Approximation (LDA), and compared with exact results. It is shown that DFT-LDA reproduces surprisingly well some of the characteristic features of the Luttinger liquid, namely the vanishing spectral weight of low energy particle-hole excitations, as well as the dispersion of the collective charge excitations. On the other hand, the approximation fails, even qualitatively, for quantities for which backscattering is important, i.e., those quantities which are crucial for an accurate description of transport. In particular, the Drude weight in the presence of a single impurity is discussed.
قيم البحث
اقرأ أيضاً
We have evaluated the successes and failures of the Hubbard-corrected density functional theory (DFT+U) approach to study Mg doping of LiCoO$_2$. We computed the effect of the U parameter on the energetic, geometric and electronic properties of two p
ossible doping mechanisms: (1) substitution of Mg onto a Co (or Li) site with an associated impurity state and, (2) formation of impurity-state-free complexes of substitutional Mg and point defects in LiCoO$_2$. We find that formation of impurity states results in changes on the valency of Co in LiCoO$_2$. Variation of the Co U shifts the energy of the impurity state, resulting in energetic, geometric and electronic properties that depend significantly on the specific value of U. In contrast, the properties of the impurity-state-free complexes are insensitive to U. These results identify reasons for the strong dependence on the doping properties on the chosen value of U and for the overall difficulty of achieving agreement with the experimentally known energetic and electronic properties of doped transition metal oxides such as LiCoO$_2$.
Site-occupation embedding theory (SOET) is an alternative formulation of density-functional theory (DFT) for model Hamiltonians where the fully-interacting Hubbard problem is mapped, in principle exactly, onto an impurity-interacting (rather than a n
on-interacting) one. It provides a rigorous framework for combining wavefunction (or Green function) based methods with DFT. In this work, exact expressions for the per-site energy and double occupation of the uniform Hubbard model are derived in the context of SOET. As readily seen from these derivations, the so-called bath contribution to the per-site correlation energy is, in addition to the latter, the key density functional quantity to model in SOET. Various approximations based on Bethe ansatz and perturbative solutions to the Hubbard and single impurity Anderson models are constructed and tested on a one-dimensional ring. The self-consistent calculation of the embedded impurity wavefunction has been performed with the density matrix renormalization group method. It has been shown that promising results are obtained in specific regimes of correlation and density. Possible further developments have been proposed in order to provide reliable embedding functionals and potentials.
Conduction electrons coupled to a mesoscopic superconducting island hosting Majorana bound states have been shown to display a topological Kondo effect with robust non-Fermi liquid correlations. With $M$ bound states coupled to $M$ leads, this is an
SO($M$) Kondo problem, with the asymptotic high and low energy theories known from bosonization and conformal field theory studies. Here we complement these approaches by analyzing the Bethe ansatz equations describing the exact solution of these models at all energy scales. We apply our findings to obtain nonperturbative results on the thermodynamics of $Mrightarrow M-2$ crossovers induced by tunnel couplings between adjacent Majorana bound states.
We outline a Kohn-Sham-Dirac density-functional-theory (DFT) scheme for graphene sheets that treats slowly-varying inhomogeneous external potentials and electron-electron interactions on an equal footing. The theory is able to account for the the unu
sual property that the exchange-correlation contribution to chemical potential increases with carrier density in graphene. Consequences of this property, and advantages and disadvantages of using the DFT approach to describe it, are discussed. The approach is illustrated by solving the Kohn-Sham-Dirac equations self-consistently for a model random potential describing charged point-like impurities located close to the graphene plane. The influence of electron-electron interactions on these non-linear screening calculations is discussed at length, in the light of recent experiments reporting evidence for the presence of electron-hole puddles in nearly-neutral graphene sheets.
Deriving accurate energy density functional is one of the central problems in condensed matter physics, nuclear physics, and quantum chemistry. We propose a novel method to deduce the energy density functional by combining the idea of the functional
renormalization group and the Kohn-Sham scheme in density functional theory. The key idea is to solve the renormalization group flow for the effective action decomposed into the mean-field part and the correlation part. Also, we propose a simple practical method to quantify the uncertainty associated with the truncation of the correlation part. By taking the $varphi^4$ theory in zero dimension as a benchmark, we demonstrate that our method shows extremely fast convergence to the exact result even for the highly strong coupling regime.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
