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Kado, Masataka; Ishino, Masahiko; Kishimoto, Maki; Tamotsu, Satoshi*; Yasuda, Keiko*; Shinohara, Kunio*
no journal, ,
Intense soft X-ray emissions are very useful for X-ray microscopy to observe living biological specimens. Increasing the photon flux in the range of wavelength 2.3 nm to 4.4 nm, so-called "water window", is a key issue for the soft X-ray microscopy. We have proposed to use ultra-thin foiled targets to limit the target mass to be heated by an intense pulsed laser. Thin foiled gold targets with various thicknesses from 10 nm to 50 m were irradiated with an intense laser pulse at the wavelength of 1.053 m generated from a Nd:glass laser system with 20 J output energy in 600 ps pulse duration. The soft X-ray emissions from the laser-produced plasmas were measured with a soft X-ray spectrometer and a soft X-ray plasma camera. The X-ray flux increased as the target thickness decreased and reached the maximum at the target thickness of 20 nm. We have observed living biological cells with the soft X-ray emissions generated from the thin-foiled gold targets.
Kado, Masataka; Kishimoto, Maki; Tamotsu, Satoshi*; Yasuda, Keiko*; Aoyama, Masato*; Shinohara, Kunio*
no journal, ,
Laser-plasma soft X-ray source produced by a high power pulsed laser is extremely bright and very suitable for biological X-ray microscopy to capture an image of living specimens for which require a single flash exposure to avoid imaging any damages on the specimens. We also have invented to use a fluorescent microscope to identify the cellular organelles in the images obtained with the soft X-ray microscope. The biological cells were cultivated directly onto the PMMA photo resists and observed with the soft X-ray microscope and the fluorescent microscope at the same time. The obtained soft X-ray images and fluorescence images of the cells were directly compared and each cellular organelle such as mitochondria, actin filaments, and chromosomes in the soft X-ray images were clearly identified. Since the soft X-ray microscope has higher spatial resolution than that of the fluorescent microscope, fine structures of the cellular organelles in the hydrated biological cells were observed.