High-pressure transformations of CaCO - a full structural trend from double [CO] triangles through the isolated group of [CO] tetrahedra to framework and layered structures
Over the past few years, the concept of carbonates, as the salts of MCO 3 or composition with [CO 3 ] triangles in the crystal structures, was sufficiently extended. In addition to carbonates, crystal structures with stoichiometry M 3 CO 5 , M 2 CO 4 and MC 2 O 5 were predicted and successfully synt...
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          | Published in | Physical chemistry chemical physics : PCCP Vol. 24; no. 38; pp. 23578 - 23586 | 
|---|---|
| Main Authors | , , , | 
| Format | Journal Article | 
| Published | 
          
        05.10.2022
     | 
| Online Access | Get full text | 
| ISSN | 1463-9076 1463-9084  | 
| DOI | 10.1039/d2cp01748b | 
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| Summary: | Over the past few years, the concept of carbonates, as the salts of MCO
3
or
composition with [CO
3
] triangles in the crystal structures, was sufficiently extended. In addition to carbonates, crystal structures with stoichiometry M
3
CO
5
, M
2
CO
4
and MC
2
O
5
were predicted and successfully synthesized. In the present study, based on density functional theory and crystal structure prediction algorithms, we found a novel structure of CaC
2
O
5
, namely Ca-pyrocarbonate with monoclinic symmetry
Cc
, which is one of the possible agents of the global carbon cycle. This structure is characterized by the isolated [C
2
O
5
] groups consisting of two [CO
3
] triangles connected through a common oxygen atom. The thermodynamic stability field of Ca-pyrocarbonate with respect to the decomposition reaction into calcium carbonate and carbon dioxide begins at a pressure of 10 GPa. As the pressure increases to 21 GPa, the structure of Ca-pyrocarbonate transforms into the recently synthesized tetragonal modification
I
4&cmb.macr;2
d
, in the structure of which carbon is in the sp
3
-hybridized state and [CO
4
] tetrahedra form isolated pyramidal [C
4
O
10
] anionic groups. At 59 GPa in the temperature range of 0-2500 K, CaC
2
O
5
-
I
4&cmb.macr;2
d
undergoes a phase transition to CaC
2
O
5
-
Fdd
2, with the framework structure of [CO
4
] tetrahedra. On further compression to about 80 GPa, the framework structure transforms into layered ones,
C
2 and
Pc
. In addition, we estimated the thermodynamic stability of CaC
2
O
5
with respect to the minerals of the Earth's mantle. We found that CaC
2
O
5
can coexist with bridgmanite up to pressures of 54 GPa at 300 K, where it reacts with the formation of a Ca-perovskite, magnesite, and solid CO
2
-V.
Using
ab initio
crystal structure prediction technique, we reveal novel structure of CaC
2
O
5
, Ca-pyrocarbonate with symmetry
Cc
, which stabilizes at 10 GPa. This structure is characterized by the isolated [C
2
O
5
] groups formed by polymerization of two [CO
3
] triangles. | 
|---|---|
| Bibliography: | https://doi.org/10.1039/d2cp01748b Electronic supplementary information (ESI) available. See DOI  | 
| ISSN: | 1463-9076 1463-9084  | 
| DOI: | 10.1039/d2cp01748b |