A perturbative derivation shows that X-ray-optical nonlinear signals in crystals carry a band-structure contribution, the joint density of states, separable from atomic-scale Wannier function contributions by polarization.
Observation of strong nonlinear interactions in parametric down-conversion of x-rays into ultraviolet radiation
1 Pith paper cite this work. Polarity classification is still indexing.
abstract
Nonlinear interactions between x-rays and long wavelengths can be used as a powerful atomic scale probe for light-matter interactions and for properties of valence electrons. This probe can provide novel microscopic information in solids that existing methods cannot reveal, hence to advance the understanding of many phenomena in condensed matter physics. However, thus far, reported x-ray nonlinear effects were very small and their observations required tremendous efforts. Here we report the observation of unexpected strong nonlinearities in parametric down-conversion (PDC) of x-rays to long wavelengths in gallium arsenide (GaAs) and in lithium niobate (LiNbO3) crystals, with efficiencies that are about 4 orders of magnitude stronger than the efficiencies measured in any material studied before. These strong nonlinearities cannot be explained by any known theory and indicate on possibilities for the development of a new spectroscopy method that is orbital and band selective. In this work we demonstrate the ability to use PDC of x-rays to investigate the spectral response of materials in a very broad range of wavelengths from the infrared regime to the soft x-ray regime.
citation-role summary
citation-polarity summary
fields
physics.optics 1years
2019 1verdicts
CONDITIONAL 1roles
background 1polarities
unclear 1representative citing papers
citing papers explorer
-
Theory of nonlinear interactions between x rays and optical radiation in crystals
A perturbative derivation shows that X-ray-optical nonlinear signals in crystals carry a band-structure contribution, the joint density of states, separable from atomic-scale Wannier function contributions by polarization.