TRANSMISSION OF LOW-ENERGY (LESS-THAN-10 EV) O-16(+) IONS THROUGH CONDENSED AMMONIA AND WATER OVERLAYERS

被引:16
作者
AKBULUT, M
SACK, NJ
MADEY, TE
机构
[1] RUTGERS STATE UNIV,DEPT PHYS & ASTRON,PISCATAWAY,NJ 08855
[2] RUTGERS STATE UNIV,SURFACE MODIFICAT LAB,PISCATAWAY,NJ 08855
[3] STEVENS INST TECHNOL,DEPT PHYS,HOBOKEN,NJ 07030
关键词
D O I
10.1063/1.469695
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have studied the transmission of low energy (<10 eV) O-16(+) ions through ultrathin films of condensed molecular solids, NH3 and (H2O)-O-18, in order to address the fundamental scattering processes that occur in the desorption of ions from below the surface of solids. O-16(+) ions with a peak energy of similar to 7 eV and a narrow angular distribution [full-width at half-maximum (FWHM) similar to 15 degrees] are generated by means of electron stimulated desorption (ESD) from an O-16 oxidized W(100) surface and their yield, energy and angular distribution are measured with a digital ESDIAD (ESD ion angular distribution) detector. Ultrathin NH3 and (H2O)-O-18 films of known thickness are condensed on the oxidized surface at 25 K and changes in the ion yield, energy and angular distribution are observed as a function of coverage. We find that adsorption of only 0.5 monolayer of (H2O)-O-18 is enough to suppress the O-16(+) ion emission by a factor of 100, while three monolayers of NH3 are necessary for equivalent suppression of the O-16(+) ion emission. The angular distribution of the ions increases slightly with increasing overlayer coverage. We also fmd that a small percentage of (H2O)-O-18 dissociates upon adsorption. We suggest that one electron charge transfer between O-16(+) and (H2O)-O-18, and between O-16(+) and the dissociation product OH are the main reasons for the strong attenuation of O-16(+) ions by only a fraction of a monolayer of (H2O)-O-18. Charge transfer is also believed to be the main process that causes suppression of O-16(+) ions by ultrathin NH3 films. Other elastic and inelastic processes are not believed to contribute significantly to O-16(+) attenuation in NH3 or (H2O)-O-18 films. (C) 1995 American Institute of Physics.
引用
收藏
页码:2202 / 2215
页数:14
相关论文
共 56 条
  • [1] AKBULUT M, IN PRESS SURF SCI
  • [2] Albritton DL., 1978, ATOM DATA NUCL DATA, V22, P1, DOI [DOI 10.1016/0092-640X(78)90027-X, 10.1016/0092-640x(78)90027-x]
  • [3] A SURFACE CORE-LEVEL SHIFT PHOTOEMISSION-STUDY OF THE INTERACTION OF OXYGEN WITH W(100)
    ALNOT, P
    AUERBACH, DJ
    BEHM, J
    BRUNDLE, CR
    VIESCAS, A
    [J]. SURFACE SCIENCE, 1989, 213 (01) : 1 - 24
  • [4] AVOURIS P, 1989, ANNU REV PHYS CHEM, V40, P173
  • [5] ADSORPTION OF OXYGEN ON W(100) - ADSORPTION-KINETICS AND STRUCTURE
    BAUER, E
    POPPA, H
    VISWANATH, Y
    [J]. SURFACE SCIENCE, 1976, 58 (02) : 517 - 549
  • [6] Bransden B. H., 1992, CHARGE EXCHANGE THEO
  • [7] BROWN WL, 1988, PHYS REV B, V32, P1988
  • [8] DEPTH OF ORIGIN OF SPUTTERED ATOMS - EXPERIMENTAL AND THEORETICAL-STUDY OF CU/RU(0001)
    BURNETT, JW
    BIERSACK, JP
    GRUEN, DM
    JORGENSEN, B
    KRAUSS, AR
    PELLIN, MJ
    SCHWEITZER, EL
    YATES, JT
    YOUNG, CE
    [J]. JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1988, 6 (03): : 2064 - 2068
  • [9] ELASTIC-SCATTERING AND INTERFERENCE OF BACKSCATTERED PRIMARY, AUGER AND X-RAY PHOTOELECTRONS AT HIGH KINETIC-ENERGY - PRINCIPLES AND APPLICATIONS
    CHAMBERS, SA
    [J]. SURFACE SCIENCE REPORTS, 1992, 16 (06) : 261 - 331
  • [10] ADSORPTION AND ELECTRON-STIMULATED DESORPTION OF NH3/TIO2(110)
    DIEBOLD, U
    MADEY, TE
    [J]. JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1992, 10 (04): : 2327 - 2336