Vibrational wavepacket dynamics in Fe carbene photosensitizer determined with femtosecond X-ray emission and scattering.

ABSTRACT: The non-equilibrium dynamics of electrons and nuclei govern the function of photoactive materials. Disentangling these dynamics remains a critical goal for understanding photoactive materials. Here we investigate the photoinduced dynamics of the [Fe(bmip)₂]²⁺ photosensitizer, where bmip?=?2,6-bis(3-methyl-imidazole-1-ylidine)-pyridine, with simultaneous femtosecond-resolution Fe K? and K? X-ray emission spectroscopy (XES) and X-ray solution scattering (XSS). This measurement shows temporal oscillations in the XES and XSS difference signals with the same 278?fs period oscillation. These oscillations originate from an Fe-ligand stretching vibrational wavepacket on a triplet metal-centered (³MC) excited state surface. This ³MC state is populated with a 110?fs time constant by 40% of the excited molecules while the rest relax to a ³MLCT excited state. The sensitivity of the K? XES to molecular structure results from a 0.7% average Fe-ligand bond length shift between the 1?s and 2p core-ionized states surfaces.

SUBMITTER: Kunnus K 

PROVIDER: S-EPMC6994595 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature