arXiv subjects

Peter Fulde

Publications and source records attributed to Peter Fulde.

50 records · Page 3Linked to original sources

arXiv1998

Ground-state properties of rutile: electron-correlation effects

Electron-correlation effects on cohesive energy, lattice constant and bulk compressibility of rutile are calculated using an ab-initio scheme. A competition between the two groups of partially covalent Ti-O bonds is the reason that the correlation energy does not change linearly with deviations from the equilibrium geometry, but is dominated by quadratic terms instead. As a consequence, the Hartree-Fock lattice constants are close to the experimental ones, while the compressibility is strongly renormalized by electronic correlations.

cond-mat.mtrl-sci↗

arXiv1998

A Hartree-Fock ab initio band-structure calculation employing Wannier-type orbitals

An ab initio Wannier-function-based approach to electronic ground-state calculations for crystalline solids is outlined. In the framework of the linear combination of atomic orbitals method the infinite character of the solid is rigorously taken into account. The Hartree-Fock ground-state energy, cohesive energy, lattice constant and bulk modulus are calculated in a fully ab initio manner as it is demonstrated for sodium chloride, NaCl, using basis sets close to the Hartree-Fock limit. It is demonstrated that the Hartree-Fock band-structure can easily be recovered with the current approach and agrees with the one obtained from a more conventional Bloch-orbital-based calculation. It is argued that the advantage of the present approach lies in its capability to include electron correlation effects for crystalline insulators by means of well-established quantum chemical procedures.

cond-mat↗

arXiv1998

Towards a quantum-chemical description of crystalline insulators: A Wannier-function-based Hartree-Fock study of Li2O and Na2O

A recently proposed approach for performing electronic-structure calculations on crystalline insulators in terms of localized orthogonal orbitals is applied to the oxides of lithium and sodium, Li2O and Na2O. Cohesive energies, lattice constants and bulk moduli of the aforementioned systems are determined at the Hartree-Fock level, and the corresponding values are shown to be in excellent agreement with the values obtained by a traditional Bloch-orbital-based Hartree-Fock approach. The present Wannier-function-based approach is expected to be advantageous in the treatment of electron-correlation effects in an infinite solid by conventional quantum-chemical methods.

cond-mat↗

arXiv1997

Orbital Localization and Delocalization Effects in the U 5f^2 Configuration: Impurity Problem

Anderson models, based on quantum chemical studies of the molecule of U(C_8H_8)_2, are applied to investigate the problem of an U impurity in a metal. The special point here is that the U 5f-orbitals are divided into two subsets: an almost completely localized set and a considerably delocalized one. Due to the crystal field, both localized and delocalized U 5f-orbitals affect the low-energy physics. A numerical renormalization group study shows that every fixed point is characterized by a residual local spin and a phase shift. The latter changes between 0 and π/2, which indicates the competition between two different fixed points. Such a competition between the different local spins at the fixed points reflects itself in the impurity magnetic susceptibility at high temperatures. These different features cannot be obtained if the special characters of U 5f-orbitals are neglected.

cond-mat.str-el↗

arXiv1997

Obtaining Wannier Functions of a Crystalline Insulator within a Hartree-Fock approach: Applications to LiF and LiCl

An ab initio Hartree-Fock approach aimed at directly obtaining the localized orthogonal orbitals (Wannier functions) of a crystalline insulator is described in detail. The method is used to perform all-electron calculations on the ground states of crystalline lithium fluoride and lithium chloride, without the use of any pseudo or model potentials. Quantities such as total energy, x-ray structure factors and Compton profiles obtained using the localized Hartree-Fock orbitals are shown to be in excellent agreement with the corresponding quantities calculated using the conventional Bloch-orbital based Hartree-Fock approach. Localization characteristics of these orbitals are also discussed in detail.

cond-mat↗

arXiv1997

A Quantum Chemical Approach to Cohesive Properties of NiO

We apply ab-initio quantum chemical methods to calculate correlation effects on cohesive properties of NiO, thereby extending a recently proposed scheme to transition metal oxides with partially filled $d$-bands. We obtain good agreement with experiment for the cohesive energy and show that the deviation of the lattice constant at the Hartree-Fock level is mainly due to van der Waals-like interactions. Correlations enhance the stability of the magnetic ground state found at the Hartree-Fock level.

cond-mat.mtrl-sci↗

arXiv1996

Influence of electron correlations on ground-state properties of III-V semiconductors

Lattice constants and bulk moduli of eleven cubic III-V semiconductors are calculated using an ab initio scheme. Correlation contributions of the valence electrons, in particular, are determined using increments for localized bonds and for pairs and triples of such bonds; individual increments, in turn, are evaluated using the coupled cluster approach with single and double excitations. Core-valence correlation is taken into account by means of a core polarization potential. Combining the results at the correlated level with corresponding Hartree-Fock data, we obtain lattice constants which agree with experiment within an average error of -0.2%; bulk moduli are accurate to +4%. We discuss in detail the influence of the various correlation contributions on lattice constants and bulk moduli.

cond-mat.mtrl-sci↗

arXiv1996

On Metal-Insulator Transitions due to Self-Doping

We investigate the influence of an unoccupied band on the transport properties of a strongly correlated electron system. For that purpose, additional orbitals are coupled to a Hubbard model via hybridization. The filling is one electron per site. Depending on the position of the additional band, both, a metal--to--insulator and an insulator--to--metal transition occur with increasing hybridization. The latter transition from a Mott insulator into a metal via ``self--doping'' was recently proposed to explain the low carrier concentration in $\rm Yb_4As_3$. We suggest a restrictive parameter regime for this transition making use of exact results in various limits. The predicted absence of the self--doping transition for nested Fermi surfaces is confirmed by means of an unrestricted Hartree--Fock approximation and an exact diagonalization study in one dimension. In the general case metal--insulator phase diagrams are obtained within the slave--boson mean--field and the alloy--analog approximation.

cond-mat↗

arXiv1996

Cohesive energies of cubic III-V semiconductors

Cohesive energies for twelve cubic III-V semiconductors with zincblende structure have been determined using an ab-initio scheme. Correlation contributions, in particular, have been evaluated using the coupled-cluster approach with single and double excitations (CCSD). This was done by means of increments obtained for localized bond orbitals and for pairs and triples of such bonds. Combining these results with corresponding Hartree-Fock data, we recover about 92 \% of the experimental cohesive energies.

cond-mat↗

arXiv1996

Excitations in Spin Chains and Specific-Heat Anomalies in Yb(4)As(3)

An explanation is given for the observed magnetic-field dependence of the low-temperature specific heat coefficient of Yb(4)As(3). It is based on a recently developed model for that material which can explain the observed heavy-fermion behaviour. According to it the Yb(3+)-ions are positioned in a net of parallel chains with an effective spin coupling of the order of J = 25 K. The magnetic-field dependence can be understood by including a weak magnetic coupling J' between adjacent chains. The data require a ratio J'/J of about 10^{-4}. In that case the experimental results can be reproduced very well by the theory.

cond-mat↗

arXiv1995

Correlation effects in ionic crystals: I. The cohesive energy of MgO

High-level quantum-chemical calculations, using the coupled-cluster approach and extended one-particle basis sets, have been performed for (Mg2+)n (O2-)m clusters embedded in a Madelung potential. The results of these calculations are used for setting up an incremental expansion for the correlation energy of bulk MgO. This way, 96% of the experimental cohesive energy of the MgO crystal is recovered. It is shown that only 60% of the correlation contribution to the cohesive energy is of intra-ionic origin, the remaining part being caused by van der Waals-like inter-ionic excitations.

cond-mat↗

arXiv1995

Theoretical Model for the Semimetal Yb_4As_3

We present a model which can explain semiquantitatively a number of the unusual properties of \mbox{Yb$_4$As$_3$}. The structural phase transition at $T_{\text{c}}\simeq300\,\mbox{K}$ is described by a band Jahn-Teller effect of correlated electrons and is interpreted as a charge ordering of the Yb ions. The low carrier concentration in the low-temperature phase follows from the strong electron correlations of the 4f-holes on the Yb sites and can be viewed as self-doping of charge-ordered chains. The observed heavy-fermion behaviour is on a scale of $T^\ast\simeq50\,\mbox{K}$ and is due to spinon-like excitations in the Yb$^{3+}$-chains. The appearance of a second low-energy scale around 0.2\,K is due to the Fermi energy of the low-density carriers.

cond-mat↗

arXiv1995

Electron correlations for ground state properties of group IV semiconductors

Valence energies for crystalline C, Si, Ge, and Sn with diamond structure have been determined using an ab-initio approach based on information from cluster calculations. Correlation contributions, in particular, have been evaluated in the coupled electron pair approximation (CEPA), by means of increments obtained for localized bond orbitals and for pairs and triples of such bonds. Combining these results with corresponding Hartree-Fock (HF) data, we recover about 95 % of the experimental cohesive energies. Lattice constants are overestimated at the HF level by about 1.5 %; correlation effects reduce these deviations to values which are within the error bounds of this method. A similar behavior is found for the bulk modulus: the HF values which are significantly too high are reduced by correlation effects to about 97 % of the experimental values.

cond-mat↗

arXiv1994

Interaction of a Magnetic Impurity with Strongly Correlated Conduction Electrons

We consider a magnetic impurity which interacts by hybridization with a system of strongly correlated conduction electrons. The latter are described by a Hubbard Hamiltonian. By means of a canconical transformation the charge degrees of freedom of the magnetic impurity are eliminated. The resulting effective Hamiltonian $H_{\rm eff}$ is investigated and various limiting cases are considered. If the Hubbard interaction $U$ between the conduction electrons is neglected $H_{\rm eff}$ reduces to a form obtained by the Schrieffer-Wolff transformation, which is essentially the Kondo Hamiltonian. If $U$ is large and the correlations are strong $H_{\rm eff}$ is changed. One modification concerns the coefficient of the dominant exchange coupling of the magnetic impurity with the nearest lattice site. When the system is hole doped, there is also an antiferromagnetic coupling to the nearest neighbors of that site involving additionally a hole. Furthermore, it is found that the magnetic impurity attracts a hole. In the case of electron doping, double occupancies are repelled by the impurity. In contrast to the hole-doped case, we find no magnetic coupling which additionally involves a doubly occupied site.

cond-mat↗