Tight-binding model for carbon from the third-generation LMTO method: A study of transferability

Bulletin of materials science

T Saha-Dasgupta²  D Nguyen-Manh³  O K Andersen¹ 

[1] Max-Planck-Institut für Festkorperforschung, 70569 Stuttgart, Germany$$Max-Planck-Institut für Festkorperforschung, 70569 Stuttgart, GermanyMax-Planck-Institut für Festkorperforschung, 70569 Stuttgart, Germany$$;Max-Planck-Institut für Festkorperforschung, 70569 Stuttgart, Germany$$S.N. Bose National Centre for Basic Science, Bidhan Nagar, Kolkata 700 098, India$$Max-Planck-Institut für Festkorperforschung, 70569 Stuttgart, GermanyMax-Planck-Institut für Festkorperforschung, 70569 Stuttgart, Germany$$S.N. Bose National Centre for Basic Science, Bidhan Nagar, Kolkata 700 098, India$$S.N. Bose National Centre for Basic Science, Bidhan Nagar, Kolkata 700 098, IndiaMax-Planck-Institut für Festkorperforschung, 70569 Stuttgart, Germany$$S.N. Bose National Centre for Basic Science, Bidhan Nagar, Kolkata 700 098, India$$;Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, UK$$Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, UKDepartment of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, UK$$

关键词: Carbon materials;    electronic structure;    ab initio calculations;    tight-binding;    transferability.;   

DOI  :  

学科分类：材料工程

来源: Indian Academy of Sciences

【 摘 要 】

The third-generation LMTO method provides a new wave function basis set in which the energy dependence of the interstitial region and inside muffinâ€�?�tin (MT) spheres is treated on an equal footing. Within the improved method, basis functions in the interstitial are the screened spherical waves (SSWs) with boundary condition defined in terms of a set of ‘hard’ sphere radii $a_{RL}$. Energy eigenvalues obtained from the singleparticle Schrödinger equation for MT potential is energetically accurate and very useful for predicting a reliable first-principles tight-binding (TB) model of widely different systems. In this study, we investigate a possibility of the new basis sets transferability to different environment which could be crucial for TB applications to very large and complicated systems in realistic materials modelling. For the case of C where the issue of $sp^2$ vs $sp^3$ bonding description is primarily important, we have found that by downfolding the unwanted channels in the basis, the TB electronic structure calculations in both hexagonal graphite and diamond structures are well compared with those obtained from the full LDA schemes if we use the same choice of hard sphere radii, aRL and a fixed, arbitrary energy, ðœ�?_𝜈. Moreover, the choice is robust and transferable to various situations, from different forms of graphite to a wide range of coordination. Using the obtained minimal basis set, we have been investigating the TB Hamiltonian and overlap matrices for different structure types for carbon, in particular we have predicted the on-site and hopping parameters (ð›�?₁, ð›�?₂, $cdots$, ð›�?₆) within an orthogonal representation for Slonczewskiâ€�?�Weissâ€�?�McClure (SWMcC) model of the Bernal structure. Our theoretical values are in excellent agreement with experimental ones from magnetoreflection measurements of Fermi surfaces for hexagonal graphite.

【 授权许可】

Unknown