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7.10 Coupled-Cluster Excited-State and Open-Shell Methods

7.10.15 Approximate EOM-CC Methods

(November 19, 2024)

7.10.15.1 EOM-MP2 and EOM-MP2T

Approximate EOM-CCSD models with T-amplitudes obtained at the MP2 level offer reduced computational cost compared to the full EOM-CCSD since the computationally demanding 𝒪(N6) CCSD step is eliminated from the calculation. Two methods of this type are implemented in Q-Chem. The first is invoked with the keyword METHOD = EOM-MP2. Its formulation and implementation follow the original EOM-CCSD(2) approach developed by Stanton and coworkers. 1205 Stanton J. F., Gauss J.
J. Chem. Phys.
(1995), 103, pp. 1064.
Link
The second method can be requested with the METHOD = EOM-MP2T keyword and is similar to EOM-MP2, but it accounts for the additional terms in ˉH that appear because the MP2 T-amplitudes do not satisfy the CCSD equations. EOM-MP2 ansatz is implemented for IP/EA/EE/SF energies, state properties, and interstate properties (EOM-EOM, but not REF-EOM). EOM-MP2t is available for the IP/EE/EA energy calculations only.

7.10.15.2 EOM-CCSD-S(D) and EOM-MP2-S(D)

These are very light-weight EOM methods in which the EOM problem is solved in the singles block and the effect of doubles is evaluated perturbatively. The ˉH is evaluated by using either CCSD or MP2 amplitudes, just as in the regular EOM calculations. The EOM-MP2-S(D) method, which is similar in level of correlation treatment to SOS-CIS(D), is particularly fast. These methods are implemented for IP and EE states. For valence states, the errors for absolute ionization or excitation energies against regular EOM-CCSD are about 0.4 eV and appear to be systematically blue-shifted; the EOM-EOM energy gaps look better. The calculations are set as in regular EOM-EE/IP, but using METHOD = EOM-CCSD-SD(D) or METHOD = EOM-MP2-SD(D). State properties and EOM-EOM transition properties can be computed using these methods (reference-EOM properties are not yet implemented). These methods are designed for treating core-level states. 1115 Sadybekov A., Krylov A. I.
J. Chem. Phys.
(2017), 147, pp. 014107.
Link

Note:  These methods are still in the experimental stage.