Orthocarbonates of Ca, Sr, and Ba The Appearance of sp3-Hybridized Carbon at a Low Pressure of 5 GPa and Dynamic Stability at Ambient Pressure

被引:24
作者
Gavryushkin, Pavel N. [1 ,2 ]
Sagatova, Dinara N. [1 ,2 ]
Sagatov, Nursultan [1 ,2 ]
Litasov, Konstantin D. [3 ]
机构
[1] Russian Acad Sci, Sobolev Inst Geol & Mineral, Siberian Branch, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
[3] RAS, Vereshchagin Inst High Pressure Phys, Moscow 108840, Russia
来源
ACS EARTH AND SPACE CHEMISTRY | 2021年 / 5卷 / 08期
关键词
crystallchemistry; mantle; transition zone; global carbon cycle; ab initio calculations; antiperovskite; anion-centered polyhedra; phase diagram; CRYSTAL-STRUCTURE PREDICTION; RAY-STRUCTURE DETERMINATION; TOTAL-ENERGY CALCULATIONS; EQUATION-OF-STATE; PHASE-TRANSITIONS; BEHAVIOR; CACO3; SRCO3; REFINEMENT; MINERALS;
D O I
10.1021/acsearthspacechem.1c00084
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Orthocarbonates are a newly discovered class of compounds that are stable at high pressures. The presence of sp3-hybridized carbon, having structural similarity to orthosilicates, and their potential participation in the global planetary carbon cycle have triggered intensive theoretical and experimental investigations into these compounds. Here, based on the density functional theory and crystal structure prediction calculations, we predict new stable crystal structures of the orthocarbonates Sr3C05-Cmcm, Sr3C05-I4/mcm, Ba,C04-Pnma, and Ba3C05-I4/mcm. Summarizing the obtained data, we show that orthocarbonates of alkaline -earth metals are isotypic to ambient-pressure orthosilicates with only rare exceptions. The lower -pressure stability limit for Ba-orthocarbonates is around 5 GPa. However, the stability limit increases with decreasing cation radius and reaches 13 GPa for Ca-orthocarbonates. Based on the calculations of Gibbs free energies with the quasi -harmonic approximation, the reaction 2M2C04 = M3CO5 + MCO3 (M = Sr and Ba) is established. At 20 GPa, this reaction is realized at temperatures above 1080 K for Sr,C04 and above 740 K for Ba,C04, and the Clapeyron slope is positive in both cases. The obtained P T diagrams for SrCO3 and BaCO3 show that equilibrium between the structures of aragonite and postaragonite is observed at 15-17 GPa for SrCO3 and 5-7 GPa for BaCO3. The transition pressure is almost independent of temperature. No other more favorable structures than postaragonite have been found for these compounds in the considered pressure range, up to 200 GPa. Thus, in contrast to CaCO3 and MgCO3, the transition from sp2 to sp3 hybridization is not realized for these compounds. Two of the found structures, Sr,C04-Pnma and Sr3C05-Cmcm, are dynamically stable at ambient pressure. This indicates the possibility of recovering the crystals from a high-pressure environment and conducting further laboratory investigation.
引用
收藏
页码:1948 / 1957
页数:10
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