Angular gausslets

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Abstract
Gausslets are one of the few basis constructions for electronic structure that combine locality, orthonormality, variable resolution, and an accurate diagonal approximation for the electron–electron interaction, but the original construction is tied to one dimension. Radial gausslets extended this idea to atoms while leaving the angular degrees of freedom in spherical harmonics, so the atomic interaction remained only partially diagonal in the combined basis. Here, we introduce generalized gausslets on the sphere and combine them shell by shell with radial gausslets to form an atom-centered basis in which the electron–electron interaction takes a two-index integral-diagonal form. The angular basis starts from localized spherical Gaussians and uses injection to make a low-ℓ spherical-harmonic subspace exact. Tests of the kinetic spectrum, low-ℓ Coulomb matrix elements, spherium, first-row Hartree–Fock calculations, and He exact diagonalization show systematic convergence with increasing angular resolution. We also develop density matrix renormalization group (DMRG) methods for this basis, including compact matrix-product operators, correlated small-space starting states, Givens-rotation transfers between nearby angular sizes, and embedded sampled variance extrapolation. We show that this combination of ingredients can be used to solve the Be atom, with extrapolations in the number of angular functions but with fixed radial resolution, to within about 0.1 mH of the complete-basis-set limit exact energy. This shows that DMRG calculations of first-row atoms that include both static and accurate dynamic correlation on the same footing are feasible.
Funding Information
  • National Science Foundation (DMR-2412638)

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