Spatially confined low-power optically pumped ultrafast synchrotron x-ray nanodiffraction

The combination of ultrafast optical excitation and time-resolved synchrotron x-ray nanodiffraction provides unique insight into the photoinduced dynamics of materials, with the spatial resolution required to probe individual nanostructures or small volumes within heterogeneous materials. Optically...

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Veröffentlicht in:Review of scientific instruments 2015-08, Vol.86 (8)
Hauptverfasser: Park, Joonkyu, Zhang, Qingteng, Chen, Pice, Cosgriff, Margaret P., Tilka, Jack A., Evans, Paul G., Adamo, Carolina, Schlom, Darrell G., Kavli Institute at Cornell for Nanoscale Science, Ithaca, New York 14853, Wen, Haidan, Zhu, Yi
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Sprache:eng
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Zusammenfassung:The combination of ultrafast optical excitation and time-resolved synchrotron x-ray nanodiffraction provides unique insight into the photoinduced dynamics of materials, with the spatial resolution required to probe individual nanostructures or small volumes within heterogeneous materials. Optically excited x-ray nanobeam experiments are challenging because the high total optical power required for experimentally relevant optical fluences leads to mechanical instability due to heating. For a given fluence, tightly focusing the optical excitation reduces the average optical power by more than three orders of magnitude and thus ensures sufficient thermal stability for x-ray nanobeam studies. Delivering optical pulses via a scannable fiber-coupled optical objective provides a well-defined excitation geometry during rotation and translation of the sample and allows the selective excitation of isolated areas within the sample. Experimental studies of the photoinduced lattice dynamics of a 35 nm BiFeO{sub 3} thin film on a SrTiO{sub 3} substrate demonstrate the potential to excite and probe nanoscale volumes.
ISSN:0034-6748
1089-7623