Searcharxiv⌕ Search

arXiv subjects

Prasanjit Samal

Publications and source records attributed to Prasanjit Samal.

51 records · Page 3Linked to original sources
arXiv2017

Inhomogeneity Induced and Appropriately Parameterized Semilocal Exchange and Correlation Energy Functionals in Two-Dimensions

The construction of meta generalized gradient approximations based on the density matrix expansion (DME) is considered as one of the most accurate technique to design semilocal exchange energy functionals in two-dimensional density functional formalism. The exchange holes modeled using DME possess unique features that make it a superior entity. Parameterized semilocal exchange energy functionals based on the DME are proposed. The use of different forms of the momentum and flexible parameters is to subsume the non-uniform effects of the density in the newly constructed semilocal functionals. In addition to the exchange functionals, a suitable correlation functional is also constructed by working upon the local correlation functional developed for 2D homogeneous electron gas (2D-HEG). The non-local effects are induced into the correlation functional by a parametric form of one of the newly constructed exchange energy functionals. The proposed functionals are applied to the parabolic quantum dots with a varying number of confined electrons and the confinement strength. The results obtained with the aforementioned functionals are quite satisfactory which indicates why these are suitable for two-dimensional quantum systems.

cond-mat.mtrl-sci↗
arXiv2017

Employing semilocal exchange hole with an application to meta-GGA level screened range separated hybrid functional: A conventional wisdom method

Range separated hybrid density functionals are very successful in describing a wide range of molecular and solid state properties accurately. Range separated hybrid functionals are designed from spherically averaged or system averaged reversed engineered exchange hole. In the present attempt, we employ screened range separated hybrid functional scheme to the meta-GGA rung by using Tao-Mo semilocal exchange hole (or functional). The hybrid functional proposed here utilizes the spherically averaged density matrix expansion based exchange hole in range separation scheme. For slowly varying density correction, we employ range separation scheme only through the local density approximation (LDA) based exchange hole coupled with the slowly varying Tao-Mo enhancement factor through the conventional wisdom technique. Comprehensive performance and testing of the present functional shows, it accurately describes several molecular properties. The most appealing feature of this present screened hybrid functional is that it will be practically very useful in describing solid state properties in meta-GGA level.

cond-mat.mtrl-sci↗
arXiv2017

Density matrix expansion based semi-local exchange hole applied to range separated density functional theory

Exchange hole is the principle constituent in density functional theory, which can be used to accurately design exchange energy functional and range separated hybrid functionals coupled with some appropriate correlation. Recently, density matrix expansion (DME) based semi-local exchange hole proposed by Tao-Mo gained attention due to its fulfillment of some exact constraints. We propose a new long-range corrected (LC) scheme that combines meta-generalized gradient approximation (meta-GGA) exchange functionals designed from DME exchange hole coupled with the ab-initio Hartree-Fock (HF) exchange integral by separating the Coulomb interaction operator using standard error function. Associate with Lee-Yang-Parr (LYP) correlation functional, assessment and benchmarking of our functional using well-known test set shows that it performs remarkably well for a broad range of molecular properties, such as thermochemistry, noncovalent interaction and barrier height of chemical reactions.

cond-mat.mtrl-sci↗
arXiv2017

Performance of Range Separated Hybrids: Study within BECKE88 family and Semilocal Exchange Hole based Range Separated Hybrid

A long range corrected range separated hybrid functional is developed based on the density matrix expansion (DME) based semilocal exchange hole with Lee-Yang-Parr (LYP) correlation. An extensive study involving the proposed range separated hybrid for thermodynamic as well as properties related to the fractional occupation number is compared with different BECKE88 family semilocal, hybrid and range separated hybrids. It has been observed that using Kohn-Sham kinetic energy dependent exchange hole several properties related to the fractional occupation number can be improved without hindering the thermochemical accuracy. The newly constructed range separated hybrid accurately describe the hydrogen and non-hydrogen reaction barrier heights. The present range separated functional has been constructed using full semilocal meta-GGA type exchange hole having exact properties related to exchange hole therefore, it has a strong physical basis.

cond-mat.mtrl-sci↗
arXiv2017

Assessing The Band Gap Problem By Improving Upon The Semilocal Exchange Hole Potential

An asymptotic corrected exchange hole potential analogous to Becke-Roussel [A. D. Becke and M. R. Roussel, Phys. Rev. A 39, 3761 (1989)] is constructed by modeling the exchange hole using the generalized coordinate transformation based on density matrix expansion. The model potential is Laplacian free and the inhomogeneity present in the system is included in the momentum vector without affecting the uniform density limit. The parameters associated with the model exchange hole are fitted with the spherical atoms. The newly constructed potential along with Tran-Blaha modified Becke-Johnson (TBMBJ) [F. Tran and P. Blaha, Phys. Rev. Lett. 102, 226401 (2009)] potential quite accurately produces the band gap of various materials ranging from semiconductor through insulators. The results for band gap are improved compared to the TBMBJ and other standard semilocal exchange functionals.

cond-mat.mtrl-sci↗
arXiv2017

Role of Kohn-Sham Kinetic Energy Density in Designing Asymptotically Correct Semilocal Exchange-Correlation Functionals in Two Dimensions

The positive definite Kohn-Sham kinetic energy(KS-KE) density plays crucial role in designing semilocal meta generalized gradient approximations(meta-GGAs) for low dimensional quantum systems. It has been rigorously shown that near nucleus and at the asymptotic region, the KE-KS differ from its von Weizsäcker(VW) counterpart as contributions from different orbitals (i.e., s and p orbitals) play important role. This has been explored using two dimensional isotropic quantum harmonic oscillator as a test case. Several meta-GGA ingredients with different physical behaviors are also constructed and further used to design an accurate semilocal functionals at meta-GGA level. In the asymptotic region, a new exchange energy functional is constructed using the meta-GGA ingredients with formally exact properties of the enhancement factor. Also, it has been shown that exact asymptotic behavior of the exchange energy density and potential can be attained by choosing accurately the enhancement factor as a functional of meta-GGA ingredients.

cond-mat.mtrl-sci↗
arXiv2017

Semi-local Exchange Energy Functional For Two-Dimensional Quantum Systems: A Step Beyond Generalized Gradient Approximations

Semi-local density functionals for the exchange-correlation energy of electrons are extensively used as it produce realistic and accurate results for finite and extended systems. The choice of techniques play crucial role in constructing such functionals of improved accuracy and efficiency. An accurate and efficient semi-local exchange energy functional in two dimensions is constructed by making use of the corresponding hole based on the density matrix expansion. The exchange hole involved is localized under the generalized coordinate transformation and satisfies all the relevant constraints. Comprehensive testing and excellent performance of the functional is demonstrated versus exact exchange results. The functional also achieves remarkable accuracy by substantially reducing the errors present in the local and non-empirical density functionals proposed so far for two dimensional systems. The underlying principles involved in the functional construction are physically appealing and practically useful for developing range separated and non-local functionals in two dimensions.

cond-mat.mtrl-sci↗
arXiv2015

Excited-State Density-Functional Theory Revisited: on the Uniqueness, Existence, and Construction of the Density-to-Potential Mapping

The generalized constrained search formalism is used to address the issues concerning density-to-potential mapping for excited states in time-independent density-functional theory. The multiplicity of potentials for any given density and the uniqueness in density-to-potential mapping are explained within the framework of unified constrained search formalism for excited-states due to Görling, Levy-Nagy, Samal-Harbola and Ayers-Levy. The extensions of Samal-Harbola criteria and it's link to the generalized constrained search formalism are revealed in the context of existence and unique construction of the density-to-potential mapping. The close connections between the proposed criteria and the generalized adiabatic connection are further elaborated so as to keep the desired mapping intact at the strictly correlated regime. Exemplification of the unified constrained search formalism is done through model systems in order to demonstrate that the seemingly contradictory results reported so far are neither the true confirmation of lack of Hohenberg-Kohn theorem nor valid representation of violation of Gunnarsson-Lundqvist theorem for excited states. Hence the misleading interpretation of subtle differences between the ground and excited state density functional formalism are exemplified.

cond-mat.mtrl-sci↗
arXiv2008

A local-density approximation for the exchange energy functional for excited states : the band gap problem

We present excited states density functional theory (DFT) to calculate band gap for semiconductors and insulators. For the excited states exchange-correlation functional, we use a simple local density approximation (LDA) like functional and it gives the result which is very closed to experimental results. The linear muffin-tin potential is used to solve the self consistent Kohn-Sham equation

cond-mat.mtrl-sci↗
arXiv2006

Analysis of Floquet formulation of time-dependent density-functional theory

Floquet formulation of time-dependent density-functional theory is revisited in light of its recent criticism [Maitra and Burke, Chem. Phys. Lett. 359 (2002), 237]. It is shown that Floquet theory is well founded and its criticism has overlooked important points of both the Runge-Gross formalism and Floquet formulation itself. We substantiate our analysis by examples similar to that considered by Maitra and Burke.

cond-mat.mtrl-sci↗
arXiv2006

Density-to-potential map in time-independent excited-state density-functional theory

In light of the recent work by Sahni et al., Harbola, and Gaudoin and Burke, the question of mapping from an excited-state density of a many-electron interacting system to the potential of the related non-interacting system is analyzed. To do so, we investigate the Levy-Nagy criterion quantitatively for several excited-states. Our work indicates that Levy-Nagy criterion may fix the density to potential map uniquely.

cond-mat.mtrl-sci↗
arXiv2006

Exploring Foundations of Time-Independent Density Functional Theory for Excited-States

Based on the work of Gorling and that of Levy and Nagy, density-functional formalism for many Fermionic excited-states is explored through a careful and rigorous analysis of the excited-state density to external potential mapping. It is shown that the knowledge of the ground-state density is a must to fix the mapping from an excited-state density to the external potential. This is the excited-state counterpart of the Hohenberg-Kohn theorem, where instead of the ground-state density the density of the excited-state gives the true many-body wavefunctions of the system. Further, the excited-state Kohn-Sham system is defined by comparing it's non-interacting kinetic energy with the true kinetic energy. The theory is demonstrated by studying a large number of atomic systems.

cond-mat.mtrl-sci↗
arXiv2004

An accurate exchange energy functional in excited-state density functional theory

An exchange energy functional is proposed and tested for obtaining a class of excited-state energies using density-functional formalism. The functional is the excited-state counterpart of the local-density approximation functional for the ground-state. It takes care of the state-dependence of the energy functional and leads to highly accurate excitation energies.

cond-mat.other↗