THE VAN DER WAALS INTERACTION BETWEEN ALKALI MICROCLUSTERS

1993 ◽  
Vol 07 (09) ◽  
pp. 573-590 ◽  
Author(s):  
J. M. PACHECO ◽  
W. EKARDT
Keyword(s):  
Density Functional ◽  
Local Density ◽  
Van Der Waals ◽  
Van Der Waals Interaction ◽  
Functional Theory ◽  
Quantum Size ◽  
Valence Electrons ◽  
Sodium And Potassium ◽  
Neutral Sodium

The nonretarded van der Waals coefficients C6 and C8 are determined for all pairs of neutral sodium and potassium microclusters with 1, 2, 8 and 20 atoms. The spherical jellium approximation is used to replace their ionic cores, and the valence electrons are treated in the local density approximation of density functional theory. The dynamical polarizabilities of these systems are computed making use of three different methods, two microscopic and quantum mechanical linear response formulations and one classical. It is found that quantum size effects, in particular Landau fragmentation, play a crucial role in the determination of these coefficients. Furthermore, we find that self-interaction errors present in standard microscopic approximations lead to sizeable effects in the strength of the van der Waals coefficients. On the other hand, we find that the vibrational temperature of these clusters has a very small effect in the van der Waals interaction which can be disregarded within the range of temperatures presently reachable experimentally.

scholarly journals First-Principles Determination of the Polarizabilities of Carbon Tubules as a Function of Length

1994 ◽  
Vol 349 ◽  
Author(s):  
Andrew A. Quong ◽  
Mark R. Pederson
Keyword(s):  
First Principles ◽  
Density Functional ◽  
Valence Electron ◽  
Local Density ◽  
Density Approximation ◽  
Functional Theory ◽  
Size Dependent ◽  
The Density Functional Theory ◽  
Linear And Nonlinear

ABSTRACTWe use the local-density-approximation to the density-functional theory to determine the axial polarizabilities of fullerene tubules as a function of length and winding topologies. Specifically, we present linear polarizabilities for tubules of composition C12H24, C36H24, C40H20 and C60H24. The size-dependent variation in the dipole-coupled gaps between pairs of occupied and unoccupied levels leads to enhancements in the polarizability per valence electron as the length of the tubule increases. The results are compared to recent densityfunctional based calculations of the linear and nonlinear polarizabilities for fullerene and benzene molecules.

Nonempirical density-functional theory for van der Waals interactions

2010 ◽  
Vol 88 (11) ◽  
pp. 1057-1062 ◽  
Author(s):  
Axel D. Becke ◽  
Alya A. Arabi ◽  
Felix O. Kannemann
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Local Density ◽  
Van Der Waals ◽  
Van Der Waals Complexes ◽  
Basis Sets ◽  
Generalized Gradient ◽  
Dispersion Energy ◽  
Functional Theory ◽  
Grid Based

In previous work, Kannemann and Becke [ J. Chem. Theory Comput. 5, 719 (2009) and J. Chem. Theory Comput. 6, 1081 (2010) ] have demonstrated that the generalized gradient approximations (GGAs) of Perdew and Wang for exchange [Phys. Rev. B 33, 8800 (1986)] and Perdew, Burke, and Ernzerhof for correlation [Phys. Rev. Lett. 77, 3865 (1996)] , plus the dispersion density functional of Becke and Johnson [J. Chem. Phys. 127, 154108 (2007)] , comprise a nonempirical density-functional theory of high accuracy for thermochemistry and van der Waals complexes. The theory is nonempirical except for two universal cutoff parameters in the dispersion energy. Our calculations so far have been grid-based and have employed the local density approximation (LDA) for the orbitals. In this work, we employ orbitals from self-consistent GGA calculations using Gaussian basis sets. The results, on a benchmark set of 65 van der Waals complexes, are similar to our grid-based post-LDA results. This work sets the stage for van der Waals force computations and geometry optimizations.

ALL-ELECTRON LOCAL-DENSITY DETERMINATION OF THE ELECTRONIC STRUCTURE AND SURFACE ENERGY OF ZR(0001)

1993 ◽  
Vol 07 (01n03) ◽  
pp. 520-523
Author(s):  
J. I. LEE ◽  
S. K. HWANG ◽  
S. C. HONG ◽  
A. J. FREEMAN
Keyword(s):  
Electronic Structure ◽  
Surface Energy ◽  
Density Functional ◽  
Local Density ◽  
Full Potential ◽  
Functional Theory ◽  
Plane Wave Method ◽  
Local Density Functional Theory ◽  
Linearized Augmented Plane Wave

The electronic structure and surface energy of Zr(0001) is determined theoretically using the all-electron full-potential linearized augmented plane wave method based on local-density functional theory. We found the value of surface energy to be 1.6 J/m 2 which is comparable to the value estimated from experiments on liquid zirconium at the melting point. It is, however, much smaller than the surface energies of W(001), V(001) and bcc Co(001). The calculated valence charge density, workfunction, and layer projected density of states for Zr(0001) are also presented.

scholarly journals Density Functional Study on Benzene, Toluene, Ethylbenzene and Xylene Adsorptions on ZnO(100) Surface

Molekul ◽  
2019 ◽  
Vol 14 (1) ◽  
pp. 37 ◽  
Author(s):  
Nugraha Nugraha ◽  
Adhitya Gandaryus Saputro ◽  
Mohammad Kemal Agusta ◽  
Fiki Taufik Akbar ◽  
Aditya Dimas Pramudya
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Van Der Waals ◽  
Van Der Waals Interaction ◽  
Functional Study ◽  
Functional Theory ◽  
Covalent Interaction ◽  
Experimental Trend ◽  
Benzene Toluene ◽  
Adsorption Energies

We study the interaction between benzene, toluene, ethylbenzene and xylene (BTEX) molecules with ZnO(100) surface by means of density functional theory-based calculations. We find that these interactions result in the physical adsorptions of BTEX gases with adsorption distances larger than 2 Å. These adsorptions are governed by the van der Waals interaction instead of the covalent interaction. We also find that the trend of the strength of BTX adsorptions on ZnO(100) surface  is in line with the experimental trend of sensitivity of ZnO material towards BTX gases (benzene < tolune < xylene). We explain this relation by using one of the sensing mechanism within the ionosorption model. By using this relation, we also predict that the response of ZnO towards ethylbenzene will be similar to the response towards toluene since these two molecules have similar adsorption energies on ZnO(100) surface. 

Thermodynamic Stability of Hexagonal and Rhombohedral Bn at Cvd Conditions from Van der Waals Corrected First Principles Calculations

2019 ◽  
Author(s):  
Henrik Pedersen ◽  
Björn Alling ◽  
Hans Högberg ◽  
Annop Ektarawong
Keyword(s):  
Thin Films ◽  
Thermodynamic Stability ◽  
First Principles ◽  
Thermal Equilibrium ◽  
Density Functional ◽  
Van Der Waals ◽  
Chemical Vapor ◽  
First Principles Calculations ◽  
Functional Theory ◽  
The Stability

Thin films of boron nitride (BN), particularly the sp<sup>2</sup>-hybridized polytypes hexagonal BN (h-BN) and rhombohedral BN (r-BN) are interesting for several electronic applications given band gaps in the UV. They are typically deposited close to thermal equilibrium by chemical vapor deposition (CVD) at temperatures and pressures in the regions 1400-1800 K and 1000-10000 Pa, respectively. In this letter, we use van der Waals corrected density functional theory and thermodynamic stability calculations to determine the stability of r-BN and compare it to that of h-BN as well as to cubic BN and wurtzitic BN. We find that r-BN is the stable sp<sup>2</sup>-hybridized phase at CVD conditions, while h-BN is metastable. Thus, our calculations suggest that thin films of h-BN must be deposited far from thermal equilibrium.

scholarly journals Fully consistent density functional theory determination of the insulator-metal transition boundary in warm dense hydrogen

2020 ◽  
Vol 2 (3) ◽  
Author(s):  
Joshua Hinz ◽  
Valentin V. Karasiev ◽  
S. X. Hu ◽  
Mohamed Zaghoo ◽  
Daniel Mejía-Rodríguez ◽  
...  
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Functional Theory ◽  
Transition Boundary ◽  
Insulator Metal Transition

scholarly journals First-Principles Study of a MoS2-PbS van der Waals Heterostructure Inspired by Naturally Occurring Merelaniite

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1649
Author(s):  
Gemechis D. Degaga ◽  
Sumandeep Kaur ◽  
Ravindra Pandey ◽  
John A. Jaszczak
Keyword(s):  
Density Functional ◽  
Van Der Waals ◽  
Hole Mobility ◽  
Functional Theory ◽  
Mos2 Monolayer ◽  
Naturally Occurring ◽  
Weak Interlayer ◽  
Bulk Structure ◽  
P Type ◽  
Interlayer Bonding

Vertically stacked, layered van der Waals (vdW) heterostructures offer the possibility to design materials, within a range of chemistries and structures, to possess tailored properties. Inspired by the naturally occurring mineral merelaniite, this paper studies a vdW heterostructure composed of a MoS2 monolayer and a PbS bilayer, using density functional theory. A commensurate 2D heterostructure film and the corresponding 3D periodic bulk structure are compared. The results find such a heterostructure to be stable and possess p-type semiconducting characteristics. Due to the heterostructure’s weak interlayer bonding, its carrier mobility is essentially governed by the constituent layers; the hole mobility is governed by the PbS bilayer, whereas the electron mobility is governed by the MoS2 monolayer. Furthermore, we estimate the hole mobility to be relatively high (~106 cm2V−1s−1), which can be useful for ultra-fast devices at the nanoscale.

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