4.8 Article

Stimulated X-Ray Emission Spectroscopy in Transition Metal Complexes

Journal

PHYSICAL REVIEW LETTERS
Volume 120, Issue 13, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.120.133203

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  2. DOE Office of Biological and Environmental Research
  3. National Institutes of Health, National Institute of General Medical Sciences [P41GM103393]
  4. Office of Science, Office of Basic Energy Sciences (OBES), Division of Chemical Sciences, Geosciences, and Biosciences (CSGB) of the Department of Energy (DOE) [DE-AC02-05CH11231]
  5. National Institutes of Health (NIH) [GM055302, GM110501]
  6. Ruth L. Kirschstein National Research Service Award [F32GM116423]
  7. Human Frontiers Science Project Award [RGP0063/2013 310]
  8. Department of Energy, Laboratory Directed Research and Development program at SLAC National Accelerator Laboratory [DE-AC02-76SF00515]

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We report the observation and analysis of the gain curve of amplified K alpha x-ray emission from solutions of Mn(II) and Mn(VII) complexes using an x-ray free electron laser to create the 1s core-hole population inversion. We find spectra at amplification levels extending over 4 orders of magnitude until saturation. We observe bandwidths below the Mn 1s core-hole lifetime broadening in the onset of the stimulated emission. In the exponential amplification regime the resolution corrected spectral width of similar to 1.7 eV FWHM is constant over 3 orders of magnitude, pointing to the buildup of transform limited pulses of similar to 1 fs duration. Driving the amplification into saturation leads to broadening and a shift of the line. Importantly, the chemical sensitivity of the stimulated x-ray emission to the Mn oxidation state is preserved at power densities of similar to 10(20) W/cm(2) for the incoming x-ray pulses. Differences in signal sensitivity and spectral information compared to conventional (spontaneous) x-ray emission spectroscopy are discussed. Our findings build a baseline for nonlinear x-ray spectroscopy for a wide range of transition metal complexes in inorganic chemistry, catalysis, and materials science.

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