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Daido, Hiroyuki; Suzuki, Yoji; Kawachi, Tetsuya; Fukuda, Takeshi*; Nakagiri, Toshio; Kaku, Masanori*; Kubodera, Masakazu*; Pirozhkov, A. S.
Proceedings of SPIE, Vol.8849, p.884908_1 - 884908_11, 2013/09
no abstracts in English
Ishino, Masahiko; Faenov, A.*; Tanaka, Momoko; Tamotsu, Satoshi*; Pikuz, T.; Hasegawa, Noboru; Nishikino, Masaharu; Inogamov, N.*; Skobelev, I.*; Fortov, V.*; et al.
Proceedings of SPIE, Vol.8849, p.88490F_1 - 88490F_8, 2013/09
Times Cited Count：2 Percentile：73.05(Optics)Nishikino, Masaharu; Hasegawa, Noboru; Tomita, Takuro*; Minami, Yasuo*; Takei, Ryota*; Baba, Motoyoshi*; Eyama, Tsuyoshi*; Takayoshi, Shodai*; Kawachi, Tetsuya; Hatomi, Daiki*; et al.
Proceedings of SPIE, Vol.8849, p.88490E_1 - 88490E_6, 2013/09
Times Cited Count：2 Percentile：73.05(Optics)We have developed the pump and probe interferometer and reflective imaging technique of the metal surfaces during the femtosecond laser ablation by using the laser-driven soft X-ray laser at the wavelength of 13.9 nm. The pumping laser used for ablation was a Ti: Sapphire laser pulse with the duration of 80 fs pulse at a central wavelength of 795 nm, and had a gaussian spatial profile. By using the X-ray imaging technique, the time resolved image of nano-scaled ablation dynamics of the platinum and the gold pumped by a femtosecond laser pulse was obtained.
Kado, Masataka; Kishimoto, Maki; Tamotsu, Satoshi*; Yasuda, Keiko*; Aoyama, Masato*; Shinohara, Kunio*
Proceedings of SPIE, Vol.8849, p.88490C_1 - 88490C_7, 2013/09
Times Cited Count：1 Percentile：55.65(Optics)We have proposed to use a fluorescence microscope to identify the cellular organelles in the images obtained with the soft X-ray microscope observing the same cells with both microscopes. The cells were stained with several fluorescent dyes such as Mito-tracker, Phalloidin, and DAPI and after taking many fluorescence images of cellular organelles the cells were exposed to the flash soft X-rays. The obtained soft X-ray images and fluorescence images of the cells were directly compared and each of the cellular organelles such as mitochondria, actin filaments, and chromosomes in the soft X-ray images was clearly identified. Since the soft X-ray microscope has higher spatial resolution than that of the fluorescence microscope, fine structures of the cellular organelles in the hydrated biological cells were observed for the first time.
