Dibromobianthryl ordering and polymerization on Ag(100)

We study the interaction between dibromobianthryl (DBBA) and the Ag(100) surface using scanning tunneling microscopy and density functional theory. DBBA is prochiral on adsorption and forms racemic domains with molecular rows aligned with the substrate nearest-neighbor [011] and [0 ̄11] directions. Deposition at elevated temperature leads to the formation of disordered meandering graphene nanowires of constant width

Quasiperiodic ordering in thick Sn layer on ii-Al-Pd-Mn: A possible quasicrystalline clathrate

Realization of an elemental solid-state quasicrystal has remained a distant dream so far in spite of extensive work in this direction for almost two decades. Here, we report the discovery of quasiperiodic ordering in a thick layer of elemental Sn grown on icosahedral ($i$)-Al-Pd-Mn. The STM images and the LEED patterns of the Sn layer show specific structural signatures that portray quasiperiodicity but are distinct from the substrate. Photoemission spectroscopy reveals the existence of the pseudogap around the Fermi energy up to the maximal Sn thickness. The structure of the Sn layer is modeled as a novel form of quasicrystalline clathrate on the basis of the following: Firstly, from ab-initio theory, the energy of bulk Sn clathrate quasicrystal is lower than the high temperature metallic $\beta$-Sn phase, but higher than the low temperature $\alpha$-Sn phase. A comparative study of the free slab energetics shows that surface energy favors clathrate over $\alpha$-Sn up to about 4 nm layer thickness, and matches $\beta$-Sn for narrow window of slab thickness of 2-3 nm. Secondly, the bulk clathrate exhibits gap opening near Fermi energy, while the free slab form exhibits a pronouced pseudogap, which explains the pseudogap observed in photoemission. Thirdly, the STM images exhibit good agreement with clathrate model. We establish the adlayer-substrate compatibility based on very similar (within 1%) the cage-cage separation in the Sn clathrate and the pseudo-Mackay cluster-cluster separation on the $i$-Al-Pd-Mn surface. Furthermore, the nucleation centers of the Sn adlayer on the substrate are identified and these are shown to be a valid part of the Sn clathrate structure. Thus, based on both experiment and theory, we propose that 4 nm thick Sn adlayer deposited on 5-fold surface of $i$-Al-Pd-Mn substrate is in fact a metastable realization of elemental, clathrate family quasicrystal.Comment: 10 figures in the Manuscript and the 8 figures in the Supplementary materia

Identification of Lone-Pair Surface States on Indium Oxide

Indium oxide is widely used as a transparent electrode in optoelectronic devices and as a photocatalyst with activity for reduction of CO₂. However, very little is known about the structural and electronic properties of its surfaces, particularly those prepared under reducing conditions. In this report, directional “lone-pair” surface states associated with filled 5s² orbitals have been identified on vacuum-annealed In₂O₃(111) through a combination of hard and soft X-ray photoemission spectroscopy and density functional theory calculations. The lone pairs reside on indium ad-atoms in a formal +1 oxidation state, each of which traps two electrons into a localized hybrid orbital protruding away from the surface and lying just above the valence band maximum in photoemission spectra. The third electron associated with the ad-atoms is delocalized into the conduction band, thus producing the surface electron accumulation layer identified previously on vacuum-annealed In₂O₃(111) (1 × 1) surfaces. The surface structure is further supported by low-energy electron diffraction, but there is no chemical shift in indium core level X-ray photoelectron spectra between surface In­(I) ad-atoms and bulk In­(III). The 5s² lone pairs confer Lewis basicity on the surface In sites and may have a pronounced impact on the catalytic or photocatalytic activity of reduced In₂O₃

Atomic oxygen adsorption on Pb(1 0 0)

We study atomic oxygen adsorption on a Pb(1 0 0) surface using density functional theory. The structures, binding energies, work function, and charge transfer of on-surface and subsurface adsorption are investigated at a range of coverages from 0.06 to 1.00 ML. The energetically favored adsorption site for on-surface adsorption is found to be a distorted hollow site for the whole coverage range studied. The distorted structures are stabilized by mixing of 6s and 6p states of lead mediated by the 2p states of oxygen. For subsurface adsorption, the sub-bridge site is found to be preferred to the sub-hollow site at low coverages, the two being nearly equal in energy at monolayer coverage. At 0.11 ML coverage, diffusion from an on-surface hollow site to a sub-bridge site is found to be barrierless, suggesting facile subsurface oxidation at low coverages. Combined on-surface and subsurface adsorption leads to the formation of a two-layer oxide structure resembling β-PbO

C60 Adsorbed on Ni(111) and Co(0001) Surfaces

Carbon-60 molecules were deposited on the fcc Ni(111) surface and, for the first time, the surface of bulk hcp Co(0001) and measured using low-energy electron diffraction and scanning tunneling microscopy. An adlayer with predominantly (4 × 4) domains is formed in each case. Other domains exemplify chiral epitaxial degeneracy. Annealing produces films with bright and dim molecules, with differing details per substrate. For C60 adsorption atop Ni(111), annealing results not only in vacancy formation beneath dim molecules but also in adatom nucleation below bright molecules

Reconstruction of the Al 13 Ru 4 (010) Approximant Surface Leading to Anisotropic Molecular Adsorption

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