Weitao Yang. Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations[J]. 华南师范大学学报(自然科学版), 2014, 46(6): 137-138.
引用本文: Weitao Yang. Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations[J]. 华南师范大学学报(自然科学版), 2014, 46(6): 137-138.
Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations[J]. Journal of South China Normal University (Natural Science Edition), 2014, 46(6): 137-138.
Citation: Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations[J]. Journal of South China Normal University (Natural Science Edition), 2014, 46(6): 137-138.

Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations

Exchange-Correlation and Electronic Excitation Energies from Pairing Matrix Fluctuations

  • Abstract: We have developed an adiabatic connection to formulate the ground-state exchange-correlation energy in terms of pairing matrix linear fluctuations. This formulation of the exchange-correlation energy opens new a channel for density functional approximations based on the many-body perturbation theory. We illustrate the potential of such approaches with an approximation based on the particle-particle Random Phase Approximation (pp-RPA). This resulting method has many highly desirable properties. It has minimal delocalization error with a nearly linear energy behavior for systems with fractional charges, describes van der Waals interactions similarly and thermodynamic properties significantly better than the conventional RPA, and eliminates static correlation error for single bond systems. Most significantly, it is the first known functional with an explicit and closed-form dependence on the occupied and unoccupied orbitals, which captures the energy derivative discontinuity in strongly correlated systems. We also adopted pp-RPA and the particle-particle Tamm-Dancoff approximation (pp-TDA) to approximate the pairing matrix fluctuation and then determine excitation energies by the differences of two-electron addition/removal energies. This approach captures all types of interesting excitations: single and double excitations are described accurately, Rydberg excitations are in good agreement with experimental data and CT excitations display correct 1/R dependence. Furthermore, the pp-RPA and the pp-TDA have a computational cost similar to TDDFT and consequently are promising for practical calculations. To further explore the potential use of pairing matrix dependent functionals, we developed the linear-response time-dependent density-functional theory with pairing fields with both adiabatic and frequency-dependent kernels. The linear-response theory is established based on the representability assumption of the pairing matrix. The linear response theory justifies the use of approximated density functionals in the pp-RPA equation. This work sets the fundamentals for future density-functional development to enhance the description of ground state correlation energies and N 2 excitation energies.

     

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