In the present work, based on the
density functional theory and
crystal structure prediction algorithms, we found novel structures
of alkali metal orthocarbonates Li4CO4-C2/c, Na4CO4-C2/c, and K4CO4-P21/c. The pressure of thermodynamic
stabilization of the obtained orthocarbonates with respect to decomposition
into the corresponding carbonate and oxide ranges from 21 GPa (for
K4CO4) to 25 GPa (for Li4CO4). All obtained structures contain isolated groups of [CO4]tetrahedra. The structures of lithium and sodium orthocarbonates
were found to be isotypic. As well as alkaline earth orthocarbonates,
orthocarbonates of alkali metals are structurally similar to orthosilicates
of the same metal. Na4CO4-C2/c was found to be dynamically stable at ambient
pressure, while all other structures are destabilized on decompression.
In addition, the P–T phase
diagrams of lithium, sodium, and potassium oxides have been calculated
for the first time. All oxides have a high-pressure phase transition
from the Fm3̅m (anti-fluorite)
structure to the Pnma (anti-cotunnite) structure
at 34 GPa for Li2O, at 10 GPa for Na2O, and
at 5 GPa for K2O at low temperatures. In the Na2O and K2O systems, high-temperature phase transition to
the P6̅2m (barringerite) structure
was revealed at temperatures above 1300 and 650 K, respectively.