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-irradiated graphite surfaces using photon-stimulated desorption spectroscopySekiguchi, Tetsuhiro; Baba, Yuji; Shimoyama, Iwao; Nath, K. G.
Surface and Interface Analysis, 38(4), p.352 - 356, 2006/04
Times Cited Count：3 Percentile：7.13(Chemistry, Physical)We investigated the orientation nature at the top-most layers of F-irradiated graphite using polarization dependent near-edge X-ray absorption fine structure (NEXAFS) spectroscopy which incorporates partial electron yield (PEY) detection and photon-stimulated ion desorption (PSID) techniques. The fluorine K-edge NEXAFS spectra conducted in PEY mode show no significant dependence on polarization angles. In contrast, NEXAFS spectra recorded in F ion yield mode show enhanced yields at a feature of 
689.4 eV assigned as a 
*(C-F) state relevant to =C-F sites, which depend on polarization angles. The C-F bonds prefer relatively tilting down the surface at the top-most layer, while the C-F bonds are randomly directed at deeper regions. We conclude that the difference in the orientation structures between the top surface and bulk is reflected in the NEXAFS recorded in the two different detection modes. It was also found that H- and F
- PSID NEXAFS spectra are helpful in understanding desorption mechanism, thus in analysing NEXAFS data.
Sekiguchi, Tetsuhiro; Baba, Yuji; Shimoyama, Iwao; Wu, G.*; Kitajima, Yoshinori*
Surface Science, 593(1-3), p.310 - 317, 2005/11
Times Cited Count：2 Percentile：11.64(Chemistry, Physical)Using a newly developed rotatable time-of-flight mass spectrometer(R-TOF-MS) and polarized synchrotron radiation, orientation effect on fragmentation and desorption pathways occurring at the top-most layers of molecular solids have been investigated. Reported will be polarization-angle dependencies of TOF mass spectra, high-resolution electron- and ion-NEXAFS in condensed chlorobenzene.
Ikeura, Hiromi*; Sekiguchi, Tetsuhiro; Baba, Yuji; Imamura, Motoyasu*; Matsubayashi, Nobuyuki*; Shimada, Hiromichi*
Surface Science, 593(1-3), p.303 - 309, 2005/11
Times Cited Count：5 Percentile：26.1(Chemistry, Physical)no abstracts in English
Sekiguchi, Tetsuhiro; Baba, Yuji; Shimoyama, Iwao; Nath, K. G.
Journal of Electron Spectroscopy and Related Phenomena, 144-147, p.437 - 441, 2005/06
Times Cited Count：3 Percentile：17.55(Spectroscopy)no abstracts in English
Ikeura, Hiromi*; Sekiguchi, Tetsuhiro; Koike, Masaki*
Journal of Electron Spectroscopy and Related Phenomena, 144-147, p.453 - 455, 2005/06
Times Cited Count：16 Percentile：56.9(Spectroscopy)no abstracts in English
Kizaki, Hiroyuki*; Wada, Shinichi*; Sako, Erika*; Sumii, Ryohei*; Waki, Satoshi*; Isari, Koji*; Sekitani, Tetsuji*; Sekiguchi, Tetsuhiro; Tanaka, Kenichiro*
Journal of Electron Spectroscopy and Related Phenomena, 144-147, p.447 - 451, 2005/06
Times Cited Count：5 Percentile：27.33(Spectroscopy)no abstracts in English
Sekiguchi, Tetsuhiro; Baba, Yuji; Shimoyama, Iwao; Nath, K. G.
Free Electron lasers 2003, p.II_69 - II_70, 2004/00
no abstracts in English
Sekiguchi, Tetsuhiro; Ikeura-Sekiguchi, Hiromi*; Baba, Yuji; Shimoyama, Iwao; Nath, K. G.
Photon Factory Activity Report 2002, Part B, P. 80, 2003/11
no abstracts in English
Sekiguchi, Tetsuhiro; Ikeura, Hiromi*; Baba, Yuji
Surface Science, 532-535(1-3), p.1079 - 1084, 2003/06
Using a newly developed rotatable time-of-flight mass spectrometer(R-TOF-MS) and polarized synchrotron radiation, we have investigated orientation effect on fragmentation and desorption pathways occurring at the top-most layers of molecular solids. Reported will be polarization-angle dependencies of TOF mass spectra, high-resolution electron- and ion-NEXAFS in condensed formic acid, formamide and benzene. For condensed formamide(HCOND
), marked orientation effect was observed for the enhanced H-yields following C1s 
*
resonance. Direct photodissociation and charge-neutralization play an important role in the effect. For some fragment species, however, the bond scission showed no polarization dependence when dissociation sites were far from core-excited atoms. This is the case for N-D scission and D-desorption following C1s excitation, suggesting that indirect process governs, where secondary electrons would induce the fragmentation.
Wada, Shinichi*; Sumii, Ryohei*; Isari, Koji*; Waki, Satoshi*; Sako, Erika*; Sekiguchi, Tetsuhiro; Sekitani, Tetsuji*; Tanaka, Kenichiro*
Surface Science, 528(1-3), p.242 - 248, 2003/03
Times Cited Count：45 Percentile：84.36(Chemistry, Physical)no abstracts in English
Wada, Shinichi*; Sako, Erika*; Sumii, Ryohei*; Waki, Satoshi*; Isari, Koji*; Sekiguchi, Tetsuhiro; Sekitani, Tetsuji*; Tanaka, Kenichiro*
Nuclear Instruments and Methods in Physics Research B, 199, p.361 - 365, 2003/01
Times Cited Count：11 Percentile：59.28(Instruments & Instrumentation)no abstracts in English
Ikeura, Hiromi*; Sekiguchi, Tetsuhiro; Kitajima, Yoshinori*; Baba, Yuji
Applied Surface Science, 169-170, p.282 - 286, 2001/01
Times Cited Count：8 Percentile：44.9(Chemistry, Physical)Carbon and nitrogen K-shell excitation and dissociation of condensed formamide at 96 K were studied by near edge X-ray absorption fine structure (NEXAFS) recorded by total electron yield (TEY), total ion yield (TIY) and photon-stimulated desorption (PSD) yield of H+ measurements. It was found that electronic transitions from the C1s or the N1s to the *(C-H) and/or (N-H) enhanced ion yield of H+ from the C-H and/or N-H functional group. This selective dissociation indicates that the corresponding unoccupied molecular orbital has an antibonding character of the C-H and/or N-H. To investigate the molecular orientation of condensed formamide, incidence-angle-dependent TEY-NEXAFS spectra were measured. The CNO plane of the adsorbed formamide molecule is determined to be tilted away from the surface by an averaged angle of about 42 degrees.
