Robust Periodic Hartree-Fock Exchange for Large-Scale Simulations Using Gaussian Basis Sets.
نویسندگان
چکیده
Hartree-Fock exchange with a truncated Coulomb operator has recently been discussed in the context of periodic plane-waves calculations [Spencer, J.; Alavi, A. Phys. Rev. B: Solid State, 2008, 77, 193110]. In this work, this approach is extended to Gaussian basis sets, leading to a stable and accurate procedure for evaluating Hartree-Fock exchange at the Γ-point. Furthermore, it has been found that standard hybrid functionals can be transformed into short-range functionals without loss of accuracy. The well-defined short-range nature of the truncated exchange operator can naturally be exploited in integral screening procedures and makes this approach interesting for both condensed phase and gas phase systems. The presented Hartree-Fock implementation is massively parallel and scales up to ten thousands of cores. This makes it feasible to perform highly accurate calculations on systems containing thousands of atoms or ten thousands of basis functions. The applicability of this scheme is demonstrated by calculating the cohesive energy of a LiH crystal close to the Hartree-Fock basis set limit and by performing an electronic structure calculation of a complete protein (rubredoxin) in solution with a large and flexible basis set.
منابع مشابه
An introductory guide to Gaussian basis sets in solid - state electronic structure calculations
The purpose of these notes is to provide some insight into Gaussian basis set technology as implemented in the CRYSTAL Hartree-Fock/density functional theory program for periodic systems. Essential differences between basis sets appropriate for use in solids and those used in purely molecular codes are explained. Examples of how to choose appropriate basis sets for particular problems, hints on...
متن کاملAb initio study & Density functional investigational of Adenine & Thymine; Comparison of primitive Gaussian and NBO calculation
We have performed quantum-chemical ab initio in various basis sets at the Hartree-Fock andB3LYP levels for Adenine and Thymine with the program GAUSSIAN98. The Dipole,Quadrupole, Octapole and Hexadecapole moments and primitive in nine basis sets for thesemolecules are presented. The most stabilized forms of these molecules are observed in 6-311++G** basis set. We have evaluated coefficient hybr...
متن کاملGaussian and Fourier Transform (GFT) Method and Screened Hartree-Fock Exchange Potential for First-principles Band Structure Calculations
The Gaussian and Fourier Transform (GFT) method is a first-principles quantum chemistry approach based on the Gaussian basis set, which can take into account the periodic boundary condition (PBC).(Shimazaki et al. 2009 a) The quantum chemistry method has mainly concentrated on isolated molecular systems even if target system becomes large such as DNA molecules and proteins, and the periodic nat...
متن کاملSpin eigenstate-dependent Hartree-Fock molecular dynamics
For the first time we present a fully ab initio molecular dynamics scheme for the treatment of many-electron ground and excited electronic states at the Hartree-Fock level using traditional Gaussian basis sets. The method is designed to simulate dynamics with first principles forces and to find global potential energy minima. Our first test examples concern the dynamics of singlet and triplet N...
متن کاملDensity functional Gaussian-type-orbital approach to molecular geometries, vibrations, and reaction energies
We present the theory, computational implementation, and applications of a density functional Gaussian-type-orbital approach called DGauss. For a range of typical organic and small inorganic molecules, it is found that this approach results in equilibrium geometries, vibrational frequencies, bond dissociation energies, and reaction energies that are in many cases significantly closer to experim...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of chemical theory and computation
دوره 5 11 شماره
صفحات -
تاریخ انتشار 2009