Chapter 10
Second-Order Approximate Coupled-Cluster (CC2) Calculations

ricc2 is a module for the calculation of excitation energies and response properties at a correlated ab initio level, in particular the second-order approximate coupled-cluster model CC2 [124]. All calculations employ the resolution-of-the-identity (RI) approximation for the electron repulsion integrals used in the correlation treatment and the description of excitation processes. At present the following functionalities are implemented:

ground state energies
for MP2 and CC2 and spin-component scaled variants thereof; the MP2 results are identical with those obtained with rimp2 (but usually the calculations are somewhat faster).
excitation energies
for the models CIS/CCS, CIS(D), CIS(D), ADC(2), and CC2 including spin-component scaled SCS and SOS version of of the latter four methods
transition moments
for ground state—excited and excited—excited state transitions for the models CCS and CC2; for ADC(2) only moments for ground state—excited state transitions are available
first-order properties
for the ground state with SCF (CCS), MP2, and CC2 and for excited states with CCS, CC2, ADC(2) and CIS(D)
geometric gradients
for the electronic ground state at the MP2 and the CC2 level; for electronically excited states at the CIS(D), ADC(2), and CC2 level
second-order properties
for the ground state with MP2 and CC2 and a closed-shell RHF reference wavefunction (currently restricted to the sequentical and SMP parallel versions)
gradients for auxiliary basis sets
for RI-MP2, -CC2, etc. calculations based on the RI-MP2 error functional
F12 corrections
to RI-MP2; MP2 ground-state energies can be computed (in C1 symmetry) using explicitly-correlated two-electron basis functions in the framework of the MP2-F12 model [121,125].
solvent effects
for the methods and states for which (orbital–relaxed) densities are available equilibrium solvent effects can be included in the framework of the cosmomode (for details see Chapter 19).

All functionalities at the MP2 and CC2 level are implemented for closed-shell RHF and open-shell UHF reference wavefunctions (with the exception of second-order propeties, which are only available for a closed-shell RHF reference). Ground state energies for MP2, MP2-F12 and CC2 and excited state energies for CC2 are also implemented for single determinant restricted open-shell Hartree-Fock (ROHF) reference wavefunctions (cmp. Sec. 9.3). (Note, that no gradients are available for MP2 and CC2 with ROHF reference wavefunctions.)

The second-order models MP2, CIS(D), CIS(D), ADC(2) and CC2 can be combined with a spin-component scaling (SCS or SOS). (Not yet available for second-order properties.) For the SOS variants one can switch to an implementation with O(N4)-scaling costs by setting the keyworkd for the numerical Laplace transformation (LT) ($laplace) .

For calculations with CCSD, CCSD(T) and other higher-order models beyond CC2 see Chapter 11.

 How To Perform a Calculation
 How to quote
 10.1 CC2 Ground-State Energy Calculations
 10.2 Calculation of Excitation Energies
 10.3 First-Order Properties and Gradients
  10.3.1 Ground State Properties, Gradients and Geometries
  10.3.2 Excited State Properties, Gradients and Geometries
  10.3.3 Visualization of densities and Density analysis
  10.3.4 Fast geometry optimizations with RI-SCF based gradients
 10.4 Transition Moments
  10.4.1 Ground to excited state transition moments
  10.4.2 Transition moments between excited states
 10.5 Ground State Second-order Properties with MP2 and CC2
 10.6 Parallel RI-MP2 and RI-CC2 Calculations
 10.7 Spin-component scaling approaches (SCS/SOS)