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Stimulated X-Ray Emission Spectroscopy in Transition Metal Complexes

MPG-Autoren
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Weninger,  C.
LCLS, SLAC National Accelerator Laboratory, Menlo Park;
Quantum Optics with X-Rays, Independent Research Groups, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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Mercadier,  L.
Quantum Optics with X-Rays, Independent Research Groups, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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Majety,  V. P.
Quantum Optics with X-Rays, Independent Research Groups, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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Rohringer,  N.
Quantum Optics with X-Rays, Independent Research Groups, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Center for Free-Electron Laser Science, DESY;
Department of Physics, Universität Hamburg;

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PhysRevLett.120.133203.pdf
(Verlagsversion), 848KB

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supplementary.pdf
(Ergänzendes Material), 498KB

Zitation

Kroll, T., Weninger, C., Alonso-Mori, R., Sokaras, D., Zhu, D., Mercadier, L., et al. (2018). Stimulated X-Ray Emission Spectroscopy in Transition Metal Complexes. Physical Review Letters, 120(13): 133203. doi:10.1103/PhysRevLett.120.133203.


Zitierlink: https://hdl.handle.net/21.11116/0000-0001-AB94-7
Zusammenfassung
We report the observation and analysis of the gain curve of amplified Kα 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 ∼1.7  eV FWHM is constant over 3 orders of magnitude, pointing to the buildup of transform limited pulses of ∼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 ∼1020  W/cm2 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.