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In a Physical Review B paper Chandross and Hicks claim that an analysis of the density-density correlation function in the dimerised Hubbard model of polyacetylene indicates that the optical exciton is bound, and that a previous study by Boman and Bursill that concluded otherwise was incorrect due to numerical innacuracy. We show that the method used in our original paper was numerically sound and well established in the literature. We also show that, when the scaling with lattice size is analysed, the interpretation of the density-density correlation function adopted by Chandross and Hicks in fact implies that the optical exciton is unbound.
Linear response theory for the density matrix renormalization group (DMRG-LRT) was first presented in terms of the DMRG renormalization projectors [Dorando et al., J. Chem. Phys. 130, 184111 (2009)]. Later, with an understanding of the manifold struc
Variational approaches for the calculation of vibrational wave functions and energies are a natural route to obtain highly accurate results with controllable errors. However, the unfavorable scaling and the resulting high computational cost of standa
We introduce the transcorrelated Density Matrix Renormalization Group (tcDMRG) theory for the efficient approximation of the energy for strongly correlated systems. tcDMRG encodes the wave function as a product of a fixed Jastrow or Gutzwiller correl
We introduce a versatile and practical framework for applying matrix product state techniques to continuous quantum systems. We divide space into multiple segments and generate continuous basis functions for the many-body state in each segment. By co
The similarities between Hartree-Fock (HF) theory and the density-matrix renormalization group (DMRG) are explored. Both methods can be formulated as the variational optimization of a wave-function ansatz. Linearization of the time-dependent variatio