130 research outputs found
Theoretical study of metal borides stability
We have recently identified metal-sandwich (MS) crystal structures and shown
with ab initio calculations that the MS lithium monoboride phases are favored
over the known stoichiometric ones under hydrostatic pressure [Phys. Rev. B 73,
180501(R) (2006)]. According to previous studies synthesized lithium monoboride
tends to be boron-deficient, however the mechanism leading to this phenomenon
is not fully understood. We propose a simple model that explains the
experimentally observed off-stoichiometry and show that compared to such
boron-deficient phases the MS-LiB compounds still have lower formation enthalpy
under high pressures. We also investigate stability of MS phases for a large
class of metal borides. Our ab initio results suggest that MS noble metal
borides are less unstable than the corresponding AlB-type phases but not
stable enough to form under equilibrium conditions.Comment: 14 pages, 15 figure
Theoretical study of the thermal behavior of free and alumina-supported Fe-C nanoparticles
The thermal behavior of free and alumina-supported iron-carbon nanoparticles
is investigated via molecular dynamics simulations, in which the effect of the
substrate is treated with a simple Morse potential fitted to ab initio data. We
observe that the presence of the substrate raises the melting temperature of
medium and large nanoparticles ( = 0-0.16, = 80-1000, non-
magic numbers) by 40-60 K; it also plays an important role in defining the
ground state of smaller Fe nanoparticles ( = 50-80). The main focus of our
study is the investigation of Fe-C phase diagrams as a function of the
nanoparticle size. We find that as the cluster size decreases in the
1.1-1.6-nm-diameter range the eutectic point shifts significantly not only
toward lower temperatures, as expected from the Gibbs-Thomson law, but also
toward lower concentrations of C. The strong dependence of the maximum C
solubility on the Fe-C cluster size may have important implications for the
catalytic growth of carbon nanotubes by chemical vapor deposition.Comment: 13 pages, 11 figures, higher quality figures can be seen in article 9
at http://alpha.mems.duke.edu/wahyu
Generalized interaction coefficients.
Massachusetts Institute of Technology. Dept. of Metallurgy. Thesis. 1965. Sc.D.Sc.D
Discussion of thermodynamic consistency of the interaction parameter formalism
The apparent contradiction between the exact nature of the interaction parameter formalism as presented by Lupis and Elliott and the inconsistencies discussed recently by Pelton and Bale arise from the truncation of the Maclaurin series in the latter treatment. The truncation removes the exactness of the expression for the logarithm of the activity coefficient of a solute in a multi-component system. The integrals are therefore path dependent. Formulae for integration along paths of constant Xi,or X i/Xj are presented. The expression for In γsolvent given by Pelton and Bale is valid only in the limit that the mole fraction of solvent tends to one. The truncation also destroys the general relations between interaction parameters derived by Lupis and Elliott. For each specific choice of parameters special relationships are obtained between interaction parameters
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