TY - JOUR
T1 - X-ray study of molecular oxygen adsorbed on graphite
AU - Heiney, P. A.
AU - Stephens, P. W.
AU - Mochrie, S. G.J.
AU - Akimitsu, J.
AU - Birgeneau, R. J.
AU - Horn, P. M.
N1 - Funding Information:
We would like to thank S. Fain, M. Toney, R. Diehl, J.P. McTague, and R.D. Etters for communicating their results prior to publication, R.F. Stewart for sending us unpublished calculations of the molecular form factor, and A. Thorny for furnishing the sample of vermicular graphite. We also acknowledge helpful discusions with A.N. Berker, J.P. McTague, M. Nielsen, O.E. Vilches, and E.K. Riedel. Work was supported by the Army Research Office under Contract No. DAAG-29-81-K-0029.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1983/2/2
Y1 - 1983/2/2
N2 - We have performed a detailed X-ray diffraction study of O2 adsorbed on UCAR-ZYX and Le Carbon Lorraine vermicular exfoliated graphite between 15 and 50 K. At least four phases of physisorbed oxygen are found. The monolayer δ phase consists of a centered parallelogram lattice, with the molecular axes parallel to the graphite surface. The data are consistent with a triple point at 26 K. The melting transition at a coverage of one monolayer appears to be first order. At higher coverages the molecules undergo a lying-down to standing-up transition; the higher coverage ζ phase froms an approximately triangular lattice with the molecular axes perpendicular to the graphite surface. Satellite peaks around the (1, 0) Bragg peak indicate, however, that this cannot be a simple triangular lattice; possible explanations include successively incommensurate layers or a sinusoidal density modulation. For coverages in the two-layer region the ζ phase modulation peaks disappear at 37 K, and at 40 K the adsorbed oxygen appears to undergo a first order melting transition into a fluid phase. With increasing coverage, the 2D X-ray diffraction profiles and phase boundaries do not connect smoothly onto those of the 3D α and β phases. At low temperatures (T < 30 K) the ζ phase always coexists with bulk crystallites; for temperatures near the 2D melting transition the 3D peaks are not observable. These data, taken together with the heat capacity results, suggest a wetting transition with only the bilayer lamellar phase or bulk O2 being stable at low temperatures.
AB - We have performed a detailed X-ray diffraction study of O2 adsorbed on UCAR-ZYX and Le Carbon Lorraine vermicular exfoliated graphite between 15 and 50 K. At least four phases of physisorbed oxygen are found. The monolayer δ phase consists of a centered parallelogram lattice, with the molecular axes parallel to the graphite surface. The data are consistent with a triple point at 26 K. The melting transition at a coverage of one monolayer appears to be first order. At higher coverages the molecules undergo a lying-down to standing-up transition; the higher coverage ζ phase froms an approximately triangular lattice with the molecular axes perpendicular to the graphite surface. Satellite peaks around the (1, 0) Bragg peak indicate, however, that this cannot be a simple triangular lattice; possible explanations include successively incommensurate layers or a sinusoidal density modulation. For coverages in the two-layer region the ζ phase modulation peaks disappear at 37 K, and at 40 K the adsorbed oxygen appears to undergo a first order melting transition into a fluid phase. With increasing coverage, the 2D X-ray diffraction profiles and phase boundaries do not connect smoothly onto those of the 3D α and β phases. At low temperatures (T < 30 K) the ζ phase always coexists with bulk crystallites; for temperatures near the 2D melting transition the 3D peaks are not observable. These data, taken together with the heat capacity results, suggest a wetting transition with only the bilayer lamellar phase or bulk O2 being stable at low temperatures.
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U2 - 10.1016/0039-6028(83)90584-8
DO - 10.1016/0039-6028(83)90584-8
M3 - Article
AN - SCOPUS:0000014548
SN - 0039-6028
VL - 125
SP - 539
EP - 564
JO - Surface Science
JF - Surface Science
IS - 2
ER -