Ground and excited states of Li$^-$, Be$^-$ through a density-based approach

TL;DR

This study uses a density functional approach with a work-function-based exchange potential and Lee-Yang-Parr correlation to accurately compute energies and transition wavelengths of ground and excited states of Li$^-$ and Be$^-$ anions, showing good agreement with experimental data.

Contribution

It introduces a practical density functional method for calculating excited states of anions with high accuracy, using a generalized pseudospectral scheme.

Findings

Computed energies agree within 0.007-0.171% of theoretical and experimental data.

Transition wavelengths are within 0.438-0.891% of experimental values.

Method provides a reliable route for excited state calculations of anions.

Abstract

Density functional calculations are performed for ground [He]2s$^2$ $^1$S$^e$, and three metastable bound excited states, 1s2s2p$^2$ $^5$P$^e$, 1s2p$^3$ $^5$S$^o$, 1s2s2p3p $^5$P$^e$ of Li$^-$ and [He]2s2p$^2$ $^4$P$^e$, [He]2p$^3$ $^4$S$^o$, 1s2s2p$^3$ $^6$S$^o$ of Be$^-$ each. The work-function-based exchange potential is used, while the correlation effects are included by employing the Lee-Yang-Parr potential. The relevant nonrelativistic KS equation is solved by means of a generalized pseudospectral discretization scheme offering nonuniform and optimal spatial grid. Computed total energies, radial densities, selected density moments, as well as two transition wavelengths (1s2s2p$^2$ $^5$P$^e \to$1s2p$^3$ $^5$S$^o$ of Li$^-$, [He]2s2p$^2$ $^4$P$^e \to$ [He]2p$^3$ $^4$S$^o$ of Be$^-$) show reasonably good agreement with the available theoretical and experimental data. The term energies show an absolute deviation of 0.007--0.171% with the largest deviation being observed for the even-parity $^5$P state of Li$^-$. The transition wavelengths of Li$^-$, Be$^-$ are calculated within 0.891 and 0.438% of the experimental values. This offers a simple practical route towards accurate reliable calculation of excited states of anions within density functional theory.