• Media type: E-Article
  • Title: Vibrational wavepacket dynamics in Fe carbene photosensitizer determined with femtosecond X-ray emission and scattering
  • Contributor: Kunnus, Kristjan; Vacher, Morgane; Harlang, Tobias C. B.; Kjær, Kasper S.; Haldrup, Kristoffer; Biasin, Elisa; van Driel, Tim B.; Pápai, Mátyás; Chabera, Pavel; Liu, Yizhu; Tatsuno, Hideyuki; Timm, Cornelia; Källman, Erik; Delcey, Mickaël; Hartsock, Robert W.; Reinhard, Marco E.; Koroidov, Sergey; Laursen, Mads G.; Hansen, Frederik B.; Vester, Peter; Christensen, Morten; Sandberg, Lise; Németh, Zoltán; Szemes, Dorottya Sárosiné; [...]
  • imprint: Springer Science and Business Media LLC, 2020
  • Published in: Nature Communications
  • Language: English
  • DOI: 10.1038/s41467-020-14468-w
  • ISSN: 2041-1723
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>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)<jats:sub>2</jats:sub>]<jats:sup>2+</jats:sup> photosensitizer, where bmip = 2,6-bis(3-methyl-imidazole-1-ylidine)-pyridine, with simultaneous femtosecond-resolution Fe Kα and Kβ 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 (<jats:sup>3</jats:sup>MC) excited state surface. This <jats:sup>3</jats:sup>MC state is populated with a 110 fs time constant by 40% of the excited molecules while the rest relax to a <jats:sup>3</jats:sup>MLCT excited state. The sensitivity of the Kα 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.</jats:p>
  • Access State: Open Access