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A Density Functional Study of Atomic Hydrogen and Oxygen Chemisorption on the Relaxed (0001) Surface of Double Hexagonal Close Packed Americium
Ab initio total energy calculations within the framework of density
functional theory have been performed for atomic hydrogen and oxygen
chemisorption on the (0001) surface of double hexagonal packed americium using
a full-potential all-electron linearized augmented plane wave plus local
orbitals method. Chemisorption energies were optimized with respect to the
distance of the adatom from the relaxed surface for three adsorption sites,
namely top, bridge, and hollow hcp sites, the adlayer structure corresponding
to coverage of a 0.25 monolayer in all cases. Chemisorption energies were
computed at the scalar-relativistic level (no spin-orbit coupling NSOC) and at
the fully relativistic level (with spin-orbit coupling SOC). The two-fold
bridge adsorption site was found to be the most stable site for O at both the
NSOC and SOC theoretical levels with chemisorption energies of 8.204 eV and
8.368 eV respectively, while the three-fold hollow hcp adsorption site was
found to be the most stable site for H with chemisorption energies of 3.136 eV
at the NSOC level and 3.217 eV at the SOC level. The respective distances of
the H and O adatoms from the surface were found to be 1.196 Ang. and 1.164 Ang.
Overall our calculations indicate that chemisorption energies in cases with SOC
are slightly more stable than the cases with NSOC in the 0.049-0.238 eV range.
The work functions and net magnetic moments respectively increased and
decreased in all cases compared with the corresponding quantities of bare dhcp
Am (0001) surface. The partial charges inside the muffin-tins, difference
charge density distributions, and the local density of states have been used to
analyze the Am-adatom bond interactions in detail. The implications of
chemisorption on Am 5f electron localization-delocalization are also discussed.Comment: 9 Tables, 5 figure
An investigation of the kinetics of hydrogen chemisorption on iron metal surfaces
The isothermal kinetics of H2, H2S, and O2 chemisorption onto epitaxially grown (III) oriented Fe films were studied. The measurements were made using the techniques of chemisorption induced resistance change and Auger electron spectroscopy (for adsorbed sulfur and oxygen). Also the origin of the chemisorption induced resistance change for these systems and its applicability to kinetic measurements were established. The chemisorption kinetics were interpreted as dissociative chemisorption via an adsorbed molecular species. The applicable rate constants were established. In none of the studies were the rate constants observed to be coverage dependent. By comparing the temperature dependence of the rate constants with absolute rate theory, the binding energies and activation energies of all the kinetic processes were obtained for the H2/Fe system. The initial sticking coefficient was pressure dependent for both the H2/Fe and H2S/Fe systems. This results from the step between the adsorbed molecular state and the dissociated chemisorbed state being the rate limiting step for absorption at certain pressures and temperatures. Estimates were obtained for the temperature dependence of the rate constants for the O2/Fe system
Adsorption of molecular oxygen on doped graphene: atomic, electronic and magnetic properties
Adsorption of molecular oxygen on B-, N-, Al-, Si-, P-, Cr- and Mn-doped
graphene is theoretically studied using density functional theory in order to
clarify if O2 can change the possibility of using doped graphene for gas
sensors, electronic and spintronic devices. O2 is physisorbed on B-, and Ndoped
graphene with small adsorption energy and long distance from the graphene
plane, indicating the oxidation will not happen; chemisorption is observed on
Al-, Si-, P-, Cr- and Mn-doped graphene. The local curvature caused by the
large bond length of X-C (X represents the dopants) relative to CC bond plays a
very important role in this chemisorption. The chemisorption of O2 induces
dramatic changes of electronic structures and localized spin polarization of
doped graphene, and in particular, chemisorption of O2 on Cr-doped graphene is
antiferromagnetic. The analysis of electronic density of states shows the
contribution of the hybridization between O and dopants is mainly from the p or
d orbitals. Furthermore, spin density shows that the magnetization locates
mainly around the doped atoms, which may be responsible for the Kondo effect.
These special properties supply a good choice to control the electronic
properties and spin polarization in the field of graphene engineering.Comment: 7 pages, 10 figure
Hydrogen on graphene: Electronic structure, total energy, structural distortions, and magnetism from first-principles calculations
Density functional calculations of electronic structure, total energy,
structural distortions, and magnetism for hydrogenated single-layer, bilayer,
and multi-layer graphene are performed. It is found that hydrogen-induced
magnetism can survives only at very low concentrations of hydrogen (single-atom
regime) whereas hydrogen pairs with optimized structure are usually
nonmagnetic. Chemisorption energy as a function of hydrogen concentration is
calculated, as well as energy barriers for hydrogen binding and release. The
results confirm that graphene can be perspective material for hydrogen storage.
Difference between hydrogenation of graphene, nanotubes, and bulk graphite is
discussed.Comment: 8 pages 8 figures (accepted to Phys. Rev. B
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