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相关论文: Self-interaction Corrected Calculations of Correla…

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The electronic structures of the actinide elements U, Np, Pu, Am, Cm and Bk are investigated within the self-interaction corrected local spin density approximation. This method allows to describe a dual character of the 5f electrons, some…

强关联电子 · 物理学 2009-11-11 A. Svane , L. Petit , Z. Szotek , W. M. Temmerman

We report on the importance of GW self-energy corrections for the electronic structure of light actinides in the weak-to-intermediate coupling regime. Our study is based on calculations of the band structure and total density of states of…

强关联电子 · 物理学 2014-05-15 Towfiq Ahmed , R. C. Albers , A. V. Balatsky , C. Friedrich , Jian-Xin Zhu

The self-interaction corrected (SIC) local spin-density approximation (LSD) is used to investigate the groundstate valency configuration of the actinide ions in the actinide mono-carbides, AC (A = U, Np, Pu, Am, Cm), and the actinide…

强关联电子 · 物理学 2009-04-29 L. Petit , A. Svane , Z. Szotek , W. M. Temmerman , G. M. Stocks

The ground state electronic structures of the actinide oxides AO, A2O3 and AO2 (A=U, Np, Pu, Am, Cm, Bk, Cf) are determined from first-principles calculations, using the self-interaction corrected local spin-density (SIC-LSD) approximation.…

强关联电子 · 物理学 2015-05-13 L. Petit , A. Svane , Z. Szotek , W. M. Temmerman , G. M. Stocks

The electronic structure of UPd_2Al_3 is described using the self-interaction corrected local-spin-density approximation to density functional theory. The groundstate is found to be characterized by the coexistence of localized (f^2) and…

强关联电子 · 物理学 2009-11-10 L. Petit , A. Svane , W. M. Temmerman , Z. Szotek , R. Tyer

The electronic structure of lanthanide and actinide compounds is often characterized by orbital ordering of localized $f$-electrons. Density-functional theory (DFT) studies of such systems using the currently available LDA+$U$ method are…

强关联电子 · 物理学 2015-11-17 Fei Zhou , Vidvuds Ozolins

Local-spin-density functional calculations may be affected by severe errors when applied to the study of magnetic and strongly-correlated materials. Some of these faults can be traced back to the presence of the spurious self-interaction in…

材料科学 · 物理学 2009-11-10 Alessio Filippetti , Nicola Spaldin

In previous papers we showed that a division of the f-shell into two subsystems gives a better understanding of cohesive properties as well the general behavior of lanthanide systems. In this paper we present numerical computations using…

强关联电子 · 物理学 2007-05-23 U. Lundin , I. Sandalov , O. Eriksson

We present an overview of various theoretical methods with detailed emphasis on an intermediate Coulomb-U coupling model. This model is based on material-specific ab-initio band structure from which correlation effects are computed via…

强关联电子 · 物理学 2013-03-14 Tanmoy Das , Jian-Xin Zhu , Matthias J. Graf

We propose a self-consistent method for electronic structure calculations of correlated systems, which combines the local spin-density approximation (LSDA) and the dynamical mean field theory (DMFT). The LSDA part is based on the exact…

强关联电子 · 物理学 2007-05-23 L. Chioncel , L. Vitos , I. A. Abrikosov , J. Kollar , M. I. Katsnelson , A. I. Lichtenstein

The intricate interplay between itinerant-localized 5f states and strongly correlated electronic states have been systematically investigated in isostructural actinide compounds AnSn3 (An=U, Np, Pu) by using a combination of the density…

强关联电子 · 物理学 2024-01-10 Haiyan Lu , Li Huang

A general reformulation of the exchange energy of $5f$-shell is applied in the analysis of the magnetic structure of various actinides compounds in the framework of LDA+U method. The calculations are performed in an efficient scheme with…

强关联电子 · 物理学 2016-08-14 Fredrik Bultmark , Francesco Cricchio , Oscar Grånäs , Lars Nordström

We extend a tight-binding method to include the effects of spin-orbit coupling, and apply it to the study of the electronic properties of the actinide elements Th, U, and Pu. These tight-binding parameters are determined for the fcc crystal…

材料科学 · 物理学 2013-05-29 M. D. Jones , R. C. Albers

Using a recently developed method combining a nonspherical self-interaction corrected LDA+$U$ scheme and an on-site multi-body Hamiltonian [Phys.\ Rev.\ B 83, 085106 (2011)], we calculate the crystal field parameters and crystal field (CF)…

强关联电子 · 物理学 2015-11-17 Fei Zhou , Vidvuds Ozolins

In order to promote our understanding on electronic structure of actinide dioxides, we construct a tight-binding model composed of actinide $5f$ and oxygen $2p$ electrons, which is called $f$-$p$ model. After the diagonalization of the…

强关联电子 · 物理学 2014-05-30 Yu Hasegawa , Takahiro Maehira , Takashi Hotta

GICs doped with elements containing d and f orbitals have been studied rarely. We control the distribution and density of intercalated actinide metals (Th, U and Pu), and consider the effect of changing the distance of two adjacent carbon…

材料科学 · 物理学 2022-04-08 Kun Yan

We study the interaction of electrons with phonons in strongly correlated solids, having high-T_c cuprates in mind. Using sum-rules, we show that the apparent strength of this interaction strongly depends on the property studied. If the…

强关联电子 · 物理学 2007-05-23 O. Rösch , O. Gunnarsson

Uranium and plutonium's 5f electrons are tenuously poised between strongly bonding with ligand spd-states and residing close to the nucleus. The unusual properties of these elements and their compounds (eg. the six different allotropes of…

Accurately modeling compounds with partially filled $d$ and $f$ shells remains a hard challenge for density-functional theory, due to large self-interaction errors stemming from local or semi-local exchange-correlation functionals. Hubbard…

材料科学 · 物理学 2026-01-19 Kinga Warda , Eric Macke , Iurii Timrov , Lucio Colombi Ciacchi , Piotr M. Kowalski

In actinide systems, the 5f electrons experience a uniquely delicate balance of effects and interactions having similar energy scales, which are often difficult to properly disentangle. This interplay of factors such as the dual nature of…

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