43,267 research outputs found
Rules and mechanisms governing octahedral tilts in perovskites under pressure
The rotation of octahedra (octahedral tilting) is common in ABO3 perovskites
and relevant to many physical phenomena, ranging from electronic and magnetic
properties, metal-insulator transitions to improper ferroelectricity.
Hydrostatic pressure is an efficient way to tune and control octahedral
tiltings. However, the pressure behavior of such tiltings can dramatically
differ from one material to another, with the origins of such differences
remaining controversial. In this work, we discover several new mechanisms and
formulate a set of simple rules that allow to understand how pressure affects
oxygen octahedral tiltings, via the use and analysis of first-principles
results for a variety of compounds. Besides the known A-O interactions, we
reveal that the interactions between specific B-ions and oxygen ions contribute
to the tilting instability. We explain the previously reported trend that the
derivative of the oxygen octahedral tilting with respect to pressure (dR/dP)
usually decreases with both the tolerance factor and the ionization state of
the A-ion, by illustrating the key role of A-O interactions and their change
under pressure. Furthermore, three new mechanisms/rules are discovered. We
further predict that the polarization associated with the so-called hybrid
improper ferroelectricity could be manipulated by hydrostatic pressure, by
indirectly controlling the amplitude of octahedral rotations.Comment: Submitted to Phys. Re
Cation- and vacancy-ordering in Li_xCoO_2
Using a combination of first-principles total energies, a cluster expansion
technique, and Monte Carlo simulations, we have studied the Li/Co ordering in
LiCoO_2 and Li-vacancy/Co ordering in CoO_2. We find: (i) A ground state search
of the space of substitutional cation configurations yields the (layered) CuPt
structure as the lowest-energy state in the octahedral system LiCoO_2 (and
CoO_2), in agreement with the experimentally observed phase. (ii) Finite
temperature calculations predict that the solid-state order- disorder
transitions for LiCoO_2 and CoO_2 occur at temperatures (~5100 K and ~4400 K,
respectively) much higher than melting, thus making these transitions
experimentally inaccessible. (iii) The energy of the reaction E(LiCoO_2) -
E(CoO_2) - E(Li) gives the average battery voltage V of a Li_xCoO_2/Li cell.
Searching the space of configurations for large average voltages, we find that
CuPt (a monolayer superlattice) has a high voltage (V=3.78 V), but that
this could be increased by cation randomization (V=3.99 V), partial disordering
(V=3.86 V), or by forming a 2-layer Li_2Co_2O_4 superlattice along
(V=4.90 V).Comment: 12 Pages, RevTeX galley format, 5 figures embedded using epsf Phys.
Rev. B (in press, 1998
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