Combinations of coupled cluster, density functionals, and the random phase approximation for describing static and dynamic correlation, and van der Waals interactions
arXiv:1509.03251 · doi:10.1080/00268976.2015.1123315
Abstract
Contrary to standard coupled cluster doubles (CCD) and Brueckner doubles (BD), singlet-paired analogues of CCD and BD (denoted here as CCD0 and BD0) do not break down when static correlation is present, but neglect substantial amounts of dynamic correlation. In fact, CCD0 and BD0 do not account for any contributions from multielectron excitations involving only same-spin electrons at all. We exploit this feature to add---without introducing double counting, self-interaction, or increase in cost---the missing correlation to these methods via meta-GGA density functionals (TPSS and SCAN). Furthermore, we improve upon these CCD0+DFT blends by invoking range separation: the short- and long-range correlations absent in CCD0/BD0 are evaluated with DFT and the direct random phase approximation (dRPA), respectively. This corrects the description of long-range van der Waals forces. Comprehensive benchmarking shows that the combinations presented here are very accurate for weakly correlated systems, while also providing a reasonable description of strongly correlated problems without resorting to symmetry breaking.
18 pages, 5 figures
References in corpus (12)
- A Higher-Accuracy van der Waals Density Functional
- Perspective: Advances and challenges in treating van der Waals dispersion forces in density functional theory
- The Ground State Correlation Energy of the Random Phase Approximation from a Ring Coupled Cluster Doubles Approach
- Adiabatic-connection fluctuation-dissipation density-functional theory based on range separation
- Long-range-corrected hybrids including RPA correlation
- Can single-reference coupled cluster theory describe static correlation?
- Density Matrix Renormalization Group with Efficient Dynamical Electron Correlation Through Range Separation
- A multiconfigurational hybrid density-functional theory
- Linearized Coupled Cluster Correction on the Antisymmetric Product of 1 reference orbital Geminals
- Pair extended coupled cluster doubles
- On the exact formulation of multi-configuration density-functional theory: electron density versus orbitals occupation
- Extended Møller-Plesset perturbation theory for dynamical and static correlations
Cited by in corpus (6)
- Benchmarking the accuracy of seniority-zero wavefunction methods for non-covalent interactions
- Actinide chemistry using singlet-paired coupled cluster and its combinations with density functionals
- Range-separated double-hybrid density-functional theory with coupled-cluster and random-phase approximations
- New Strategies in Modeling Electronic Structures and Properties with Applications to Actinides
- Restoring the Pauli principle in the random phase approximation ground state
- Expectation values of single-particle operators in the random phase approximation ground state