Hard X-ray helical dichroism of disordered molecular media
Abstract
Chirality is a structural property of molecules lacking mirror symmetry that has strong implications in diverse fields, ranging from life to materials sciences. Established spectroscopic methods that are sensitive to chirality, such as circular dichroism (CD), exhibit weak signal contributions on an achiral background. Helical dichroism (HD), which is based on the orbital angular momentum (OAM) of light, offers a new approach to probe molecular chirality, but it has never been demonstrated on disordered samples. Furthermore, in the optical domain the challenge lies in the need to transfer the OAM of the photon to an electron that is localized on an {\AA}-size orbital. Here, we overcome this challenge using hard X-rays with spiral Fresnel zone, which can induce an OAM. We present the first HD spectra of a disordered powder sample of enantiopure molecular complexes of [Fe(4,4'-diMebpy)3]2+ at the iron K-edge (7.1 keV) with OAM-carrying beams. The HD spectra exhibit the expected inversions of signs switching from a left to a right helical wave front or from an enantiomer to the other. The asymmetry ratios for the HD spectra are within one to five percent for OAM beams with topological charges of one and three. These results open a new window into the studies of molecular chirality and its interaction with the orbital angular momentum of light.
Keywords
Cite
@article{arxiv.2204.06685,
title = {Hard X-ray helical dichroism of disordered molecular media},
author = {Jeremy R. Rouxel and Benedikt Rosner and Dmitry Karpov and Camila Bacellar and Giulia F. Mancini and Francesco Zinna and Dominik Kinschel and Oliviero Cannelli and Malte Oppermann and Cris Svetina and Ana Diaz and Jerome Lacour and Christian David and Majed Chergui},
journal= {arXiv preprint arXiv:2204.06685},
year = {2022}
}
Comments
15 pages, 5 figures