4.8 Article

Resonant Inelastic X-Ray Scattering Reveals Hidden Local Transitions of the Aqueous OH Radical

Journal

PHYSICAL REVIEW LETTERS
Volume 124, Issue 23, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.124.236001

Keywords

-

Funding

  1. U.S. Department of Energy, Office of Science, Basic Energy Science, Chemical Sciences, Geosciences and Biosciences Division [DE-AC02-06CH11357]
  2. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES) [DE-AC02-06CH11357, DE-AC02-76SF00515]
  3. Laboratory Directed Research and Development (LDRD) - Argonne National Laboratory
  4. Swedish Science Council [2018-04088]
  5. European X-ray Free Electron Laser
  6. Singapore Ministry of Education [MOE2014-T2-2-052, RG105/17, RG109/18]
  7. CNRS GotoXFEL program
  8. Cluster of Excellence Advanced Imaging of Matter of the Deutsche Forschungsgemeinschaft (DFG)-EXC 2056 [390715994]
  9. Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [DE-SC0019451]
  10. DTU Chemistry
  11. Independent Research Fund Denmark DFF-RP2 [7014-00258B]
  12. U.S. National Science Foundation [CHE-1856342]
  13. Hamburg Centre for Ultrafast Imaging
  14. Swedish Research Council [2018-04088] Funding Source: Swedish Research Council

Ask authors/readers for more resources

Resonant inelastic x-ray scattering (RIXS) provides remarkable opportunities to interrogate ultra-fast dynamics in liquids. Here we use RIXS to study the fundamentally and practically important hydroxyl radical in liquid water, OH(aq). Impulsive ionization of pure liquid water produced a short-lived population of OH(aq), which was probed using femtosecond x-rays from an x-ray free-electron laser. We find that RIXS reveals localized electronic transitions that are masked in the ultraviolet absorption spectrum by strong charge-transfer transitions-thus providing a means to investigate the evolving electronic structure and reactivity of the hydroxyl radical in aqueous and heterogeneous environments. First-principles calculations provide interpretation of the main spectral features.

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