Extended Møller-Plesset perturbation theory for dynamical and static correlations.
نویسندگان
چکیده
We present a novel method that appropriately handles both dynamical and static electron correlations in a balanced manner, using a perturbation theory on a spin-extended Hartree-Fock (EHF) wave function reference. While EHF is a suitable candidate for degenerate systems where static correlation is ubiquitous, it is known that most of dynamical correlation is neglected in EHF. In this work, we derive a perturbative correction to a fully spin-projected self-consistent wave function based on second-order Møller-Plesset perturbation theory (MP2). The proposed method efficiently captures the ability of EHF to describe static correlation in degeneracy, combined with MP2's ability to treat dynamical correlation effects. We demonstrate drastic improvements on molecular ground state and excited state potential energy curves and singlet-triplet splitting energies over both EHF and MP2 with similar computational effort to the latter.
منابع مشابه
A Proposal for a Modified Møller-Plesset Perturbation Theory
A modified version of the Møller-Plesset approach for obtaining the correlation energy associated to a Hartree-Fock ground state is proposed. The method is tested in a model of interacting fermions that allows for an exact solution. Using up to third order terms improved results are obtained, even in the limit of loosely bound particles. The study of molecules and larger systems is seriously co...
متن کاملImplementation of dynamical nucleation theory with quantum potentials
A method is implemented within the context of dynamical nucleation theory in order to efficiently determine the ab initio water dimer evaporation rate constant. The drive for increased efficiency in a Monte Carlo methodology is established by the need to use relatively expensive quantum mechanical interaction potentials. A discussion is presented illustrating the theory, algorithm, and implemen...
متن کاملDevelopment of efficient computational techniques and codes for second-order Møller–Plesset perturbation calculation of extended systems
Electronic structure theory such as ab initio molecular orbital (MO) theory is the powerful tool in elucidating chemical phenomena such as electronic states, molecular structures, properties, and reaction mechanisms. The high-level quantum chemical calculations excellently reproduce the properties for small molecules in the same or better accuracy with the experiments. However, the computationa...
متن کاملImproved second-order Møller–Plesset perturbation theory by separate scaling of parallel- and antiparallel-spin pair correlation energies
Related Articles Basis set convergence of explicitly correlated double-hybrid density functional theory calculations J. Chem. Phys. 135, 144119 (2011) An explicitly correlated local coupled cluster method for calculations of large molecules close to the basis set limit J. Chem. Phys. 135, 144117 (2011) An efficient local coupled cluster method for accurate thermochemistry of large systems J. Ch...
متن کاملAuxiliary Basis Sets for Density Fitting Mp2 Calculations: Correlation Consistent Basis Sets for the 5d Elements Hf-pt
Auxiliary basis sets specifically matched to the correlation consistent cc-pVnZ-PP, ccpwCVnZ-PP, aug-cc-pVnZ-PP and aug-cc-pwCVnZ-PP orbital basis sets (used in conjunction with pseudopotentials) for the 5d transition metal elements Hf-Pt have been optimized for use in density fitting second-order Møller-Plesset perturbation theory and other correlated ab initio methods. Calculations of the sec...
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:
- The Journal of chemical physics
دوره 141 16 شماره
صفحات -
تاریخ انتشار 2014