State-specific frozen natural orbital for reduced-cost algebraic diagrammatic construction calculations: The application to ionization problem.

We have developed a reduced-cost algebraic diagrammatic construction (ADC) method based on state-specific frozen natural orbital and natural auxiliary functions. The newly developed method has been benchmarked on the GW100 test set for the ionization problem. The use of state-specific natural orbitals drastically reduces the size of the virtual space with a systematically controllable accuracy and offers a significant speedup over the standard ionization potential (IP)-ADC(3) method. The accuracy of the method can be controlled by two thresholds and nearly a black box to use. The inclusion of the perturbative correction significantly improves the accuracy of the calculated IP values, and the efficiency of the method has been demonstrated by calculating the IP of a molecule with 60 atoms and more than 2216 basis functions.

A similarity transformed second-order approximate coupled cluster method for the excited states: Theory, implementation, and benchmark.

We present a novel and cost-effective approach of using a second similarity transformation of the Hamiltonian to include the missing higher-order terms in the second-order approximate coupled cluster singles and doubles (CC2) model. The performance of the newly developed ST-EOM-CC2 model has been investigated for the calculation of excitation energies of valence, Rydberg, and charge-transfer excited states. The method shows significant improvement in the excitation energies of Rydberg and charge-transfer excited states as compared to the conventional CC2 method while retaining the good performance of the latter for the valence excited state. This method retains the charge-transfer separability of the charge-transfer excited states, which is a significant advantage over the traditional CC2 method. A second order many-body perturbation theory variant of the new method is also proposed.