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Stimulated X-Ray Emission Spectroscopy in Transition Metal Complexes
- Kroll, Thomas;
- Weninger, Clemens;
- Alonso-Mori, Roberto;
- Sokaras, Dimosthenis;
- Zhu, Diling;
- Mercadier, Laurent;
- Majety, Vinay P;
- Marinelli, Agostino;
- Lutman, Alberto;
- Guetg, Marc W;
- Decker, Franz-Josef;
- Boutet, Sébastien;
- Aquila, Andy;
- Koglin, Jason;
- Koralek, Jake;
- DePonte, Daniel P;
- Kern, Jan;
- Fuller, Franklin D;
- Pastor, Ernest;
- Fransson, Thomas;
- Zhang, Yu;
- Yano, Junko;
- Yachandra, Vittal K;
- Rohringer, Nina;
- Bergmann, Uwe
- et al.
Published Web Location
https://doi.org/10.1103/physrevlett.120.133203Abstract
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 ∼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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