Orbital-optimized density functional calculations of excited electronic states: Recent advances and perspectives

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Original abstract

Orbital-optimized (OO) density functional calculations provide a time-independent, variational route to electronic excitations that complements the presently widely used time-dependent density functional theory (TDDFT). As the orbitals are optimized in a state specific way, these methods can provide a balanced description of excited states with different character, thereby overcoming several limitations of practical implementations of TDDFT. Driven by recent developments in algorithms for obtained excited states as saddle points on the electronic energy surface, OO methods have seen an increased interest in recent years, maturing into an an active and rapidly developing area of research. Here, the theoretical foundations of the approach are clarified and an overview of the recent developments in methods for excited-state orbital optimization is provided. A unified overview of methods for treating open-shell singlet excited states and current approaches for computing transition properties and spectra is also provided. Finally, recent applications to molecular Rydberg, charge-transfer, and core excitations are reviewed, with the aim of assessing the present accuracy and range of applicability of OO density functional calculations.

Links and sources

• Official / arXiv page
• PDF from original source

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