Generation and characterization of ultrathin free-flowing liquid sheets

The physics and chemistry of liquid solutions play a central role in science, and our understanding of life on Earth. Unfortunately, key tools for interrogating aqueous systems, such as infrared and soft X-ray spectroscopy, cannot readily be applied because of strong absorption in water. Here we use...

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Veröffentlicht in:Nature communications 2018-04, Vol.9 (1), p.1353-8, Article 1353
Hauptverfasser: Koralek, Jake D., Kim, Jongjin B., Brůža, Petr, Curry, Chandra B., Chen, Zhijiang, Bechtel, Hans A., Cordones, Amy A., Sperling, Philipp, Toleikis, Sven, Kern, Jan F., Moeller, Stefan P., Glenzer, Siegfried H., DePonte, Daniel P.
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Sprache:eng
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Zusammenfassung:The physics and chemistry of liquid solutions play a central role in science, and our understanding of life on Earth. Unfortunately, key tools for interrogating aqueous systems, such as infrared and soft X-ray spectroscopy, cannot readily be applied because of strong absorption in water. Here we use gas-dynamic forces to generate free-flowing, sub-micron, liquid sheets which are two orders of magnitude thinner than anything previously reported. Optical, infrared, and X-ray spectroscopies are used to characterize the sheets, which are found to be tunable in thickness from over 1 μm  down to less than 20 nm, which corresponds to fewer than 100 water molecules thick. At this thickness, aqueous sheets can readily transmit photons across the spectrum, leading to potentially transformative applications in infrared, X-ray, electron spectroscopies and beyond. The ultrathin sheets are stable for days in vacuum, and we demonstrate their use at free-electron laser and synchrotron light sources. X-ray spectroscopy is a tool used for the investigation of aqueous solutions but the strong absorption of water means that very thin liquid sheets are needed for accurate analysis. Here the authors produce free-flowing liquid sheets 2 orders of magnitude thinner than sheets obtained with existing techniques.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-03696-w