Experiments on both single-crystal graphite and highly oriented pyrolytic graphite indicate that for 60Ͻ T Ͻ 300 K, C 60 forms single-layer islands of close-packed molecules at low coverages. Low-energy electrondiffraction measurements on the single crystal indicate that there is almost no preferred orientation of the C 60 lattice relative to the graphite lattice, producing continuous diffraction rings. A slight preference for the C 60 lattice oriented at 30°relative to the graphite lattice is explained as originating in the preference for the C 60 islands to nucleate and align at step edges, observed with scanning tunneling microscopy and low-energy electron microscopy. The energetics of this C 60 layer were investigated using the Novaco-McTague theory of epitaxial orientation, which found several minimum-energy angles near the experimental C 60 -C 60 spacing, inconsistent with the experiment and suggesting an extremely small C 60 -graphite corrugation. The thermal expansion of this "floating solid" C 60 lattice for 60Ͻ T Ͻ 120 K was compared to theoretical models using previously formulated C 60 -C 60 pair potentials. The calculated values, assuming perfect two-dimensional layers of spherical C 60 , are significantly smaller than the measured values, suggesting that additional thermal excitations, such as those involving molecular orientations, are present in this temperature range.
We report on the growth of Pb thin films deposited either on the Al-rich fivefold surface of the icosahedral AlCu-Fe quasicrystal or on the (111) surface of fcc Al. On the quasicrystalline substrate, the diffusion length of Pb adatoms is short due to heterogeneous nucleation that enforces a quasiperiodic structure in the monolayer. On the Al(111) substrate, the mobility of Pb adatoms is high and the interaction with the substrate is flatter, leading to the formation of a (√31×√31)R8.95° higher-order commensurate structure. This moiré structure propagates up to the highest coverages investigated.
Disciplines
Condensed Matter Physics | Metallurgy
CommentsThis article is from Physical Review B 79 (2009) We report on the growth of Pb thin films deposited either on the Al-rich fivefold surface of the icosahedral Al-Cu-Fe quasicrystal or on the ͑111͒ surface of fcc Al. On the quasicrystalline substrate, the diffusion length of Pb adatoms is short due to heterogeneous nucleation that enforces a quasiperiodic structure in the monolayer. On the Al͑111͒ substrate, the mobility of Pb adatoms is high and the interaction with the substrate is flatter, leading to the formation of a ͑ͱ31ϫ ͱ 31͒R8.95°higher-order commensurate structure. This moiré structure propagates up to the highest coverages investigated.
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