An exciting approach to theoretical spectroscopy

Abstract: Theoretical spectroscopy, and more generally, electronic-structure theory, are powerful concepts for describing the complex many-body interactions in materials. They comprise a variety of methods that can capture all aspects, from ground-state properties to lattice excitations to different types of light-matter interaction, including time-resolved variants. Modern electronic-structure codes implement either a few or several of these methods. Among them, exciting is an all-electron full-potential package that has a very rich portfolio of all levels of theory, with a particular focus on excitations. It implements the linearized augmented planewave plus local orbital basis, which is known as the gold standard for solving the Kohn-Sham equations of density-functional theory. Based on this, it also offers benchmark-quality results for a wide range of excited-state methods. In this review, we provide a comprehensive overview of the features implemented in exciting in recent years, accompanied by short summaries on the state of the art of the underlying methodologies. They comprise density-functional theory and time-dependent density-functional theory, density-functional perturbation theory for phonons and electron-phonon coupling, many-body perturbation theory in terms of the $GW$ approach and the Bethe-Salpeter equation. Moreover, we capture resonant inelastic x-ray scattering, pump-probe spectroscopy as well as exciton-phonon coupling. Finally, we cover workflows and a view on data and machine learning. All aspects are demonstrated with examples for scientific relevant materials.