The coupled cluster method (CCM) is a method of quantum many-body theory that may provide accurate results for the ground-state properties of lattice quantum spin systems even in the presence of strong frustration and for lattices of arbitrary spatial dimensionality. Here we present a significant extension of the method by introducing an approach that allows an efficient parallelization of computer codes that carry out high-order CCM calculations. We find that we are able to extend such CCM calculations by an order of magnitude higher than ever before utilized in a high-order CCM calculation for an antiferromagnet. Furthermore we use only a relatively modest number of processors, namely, eight. Such very high-order CCM calculations are possible only by using such a parallelized approach. An illustration of the new approach is presented for the ground-state properties of a magnetic material, ${\mathrm{CaV}}_{4}{\mathrm{O}}_{9}$ .The coupled cluster method (CCM) is a method of quantum many-body theory that may provide accurate results for the ground-state properties of lattice quantum spin systems even in the presence of strong frustration and for lattices of arbitrary spatial dimensionality. Here we present a significant extension of the method by introducing an approach that allows an efficient parallelization of computer codes that carry out high-order CCM calculations. We find that we are able to extend such CCM calculations by an order of magnitude higher than ever before utilized in a high-order CCM calculation for an antiferromagnet. Furthermore we use only a relatively modest number of processors, namely, eight. Such very high-order CCM calculations are possible only by using such a parallelized approach. An illustration of the new approach is presented for the ground-state properties of a magnetic material, ${\mathrm{CaV}}_{4}{\mathrm{O}}_{9}$.

arXiv:cond-mat/0511544Physical Review BNov 15, 200522 citations

Coupled Cluster Treatment of the Alternating Bond Diamond Chain

Jian-Jun Jiang, Yong-Jun Liu, Fei Tang +1 more

By the analytical coupled cluster method (CCM), we study both the ground state and lowest-lying excited-state properties of the alternating bond diamond chain. The numerical exact diagonalization (ED) method is also applied to the chain to verify the accuracy of CCM results. The ED results show that the ground-state phase diagram contains two exact spin cluster solid ground states, namely, the tetramer-dimer (TD) state and dimer state, and the ferrimagnetic long-range-ordered state. We prove that the two exact spin cluster solid ground states can both be formed by CCM. Moreover, the exact spin gap in the TD state can be obtained by CCM. In the ferrimagnetic region, we find that the CCM results for some physical quantities, such as the ground-state energy, the sublattice magnetizations, and the antiferromagnetic gap, are comparable to the results obtained by numerical methods. The critical line dividing the TD state from the ferrimagnetic state is also given by CCM and is in perfect agreement with that determined by the ED method.By the analytical coupled cluster method (CCM), we study both the ground state and lowest-lying excited-state properties of the alternating bond diamond chain. The numerical exact diagonalization (ED) method is also applied to the chain to verify the accuracy of CCM results. The ED results show that the ground-state phase diagram contains two exact spin cluster solid ground states, namely, the tetramer-dimer (TD) state and dimer state, and the ferrimagnetic long-range-ordered state. We prove that the two exact spin cluster solid ground states can both be formed by CCM. Moreover, the exact spin gap in the TD state can be obtained by CCM. In the ferrimagnetic region, we find that the CCM results for some physical quantities, such as the ground-state energy, the sublattice magnetizations, and the antiferromagnetic gap, are comparable to the results obtained by numerical methods. The critical line dividing the TD state from the ferrimagnetic state is also given by CCM and is in perfect agreement with that determined by the ED method.

arXiv:1511.01985Journal of the Physical Society of JapanOct 29, 20154 citations

Coupled Superconductors

Brian D. Josephson

Reviews of Modern PhysicsJan 1, 1964495 citations

Approximation methods in a superconducting model

H. Mitter, K. Yamazaki

Nuclear PhysicsJun 1, 19631 citation

Coupled-cluster approach to electron correlations in the two-dimensional Hubbard model

Yoshihiro Asai, Hideki Katagiri

We have studied electron correlations in the doped two-dimensional (2D) Hubbard model by using the coupled-cluster method (CCM) to investigate whether or not the method can be applied to correct the independent particle approximations actually used in ab initio band calculations. The double excitation version of the CCM, implemented using the approximate coupled pair (ACP) method, accounts for most of the correlation energies of the 2D Hubbard model in the weak $(U/t\ensuremath{\simeq}1)$ and the intermediate $U/t$ regions $(U/t\ensuremath{\simeq}4).$ The error in this case is always less than $1%.$ The ACP approximation gets less accurate for large $U/t$ $(U/t\ensuremath{\simeq}8)$ and near half-filling. Further incorporation of electron correlation effects is necessary in this region. The accuracy depends neither on the system size, nor the gap between the lowest unoccupied level and the highest occupied level in the finite size effect. Hence, the CCM may be favorably applied to ab initio band calculations on metals as well as semiconductors and insulators.We have studied electron correlations in the doped two-dimensional (2D) Hubbard model by using the coupled-cluster method (CCM) to investigate whether or not the method can be applied to correct the independent particle approximations actually used in ab initio band calculations. The double excitation version of the CCM, implemented using the approximate coupled pair (ACP) method, accounts for most of the correlation energies of the 2D Hubbard model in the weak $(U/t\ensuremath{\simeq}1)$ and the intermediate $U/t$ regions $(U/t\ensuremath{\simeq}4).$ The error in this case is always less than $1%.$ The ACP approximation gets less accurate for large $U/t$ $(U/t\ensuremath{\simeq}8)$ and near half-filling. Further incorporation of electron correlation effects is necessary in this region. The accuracy depends neither on the system size, nor the gap between the lowest unoccupied level and the highest occupied level in the finite size effect. Hence, the CCM may be favorably applied to ab initio band calculations on metals as well as semiconductors and insulators.

arXiv:cond-mat/9904400Physical review. B, Condensed matterNov 15, 19996 citations

{\mathrm{CaV}}_{4}{\mathrm{O}}_{9}

U/t

regions $(U/t\ensuremath{\simeq}4).$ The error in this case is always less than

1%.

The ACP approximation gets less accurate for large

U/t

$(U/t\ensuremath{\simeq}8)$ and near half-filling. Further incorporation of electron correlation effects is necessary in this region. The accuracy depends neither on the system size, nor the gap between the lowest unoccupied level and the highest occupied level in the finite size effect. Hence, the CCM may be favorably applied to ab initio band calculations on metals as well as semiconductors and insulators.