Abstract
Magnesium Oxide (MgO) and water (H2O) are abundant in the interior of planets. Their properties, and in particular their interaction, significantly affect the planet interior structure and thermal evolution. Here, using crystal structure predictions and ab initio molecular dynamics simulations, we find that MgO and H2O can react again at ultrahigh pressure, although Mg(OH)2 decomposes at low pressure. The reemergent MgO-H2O compounds are: Mg2O3H2 above 400 GPa, MgO3H4 above 600 GPa, and MgO4H6 in the pressure range of 270–600 GPa. Importantly, MgO4H6 contains 57.3 wt % of water, which is a much higher water content than any reported hydrous mineral. Our results suggest that a substantial amount of water can be stored in MgO rock in the deep interiors of Earth to Neptune mass planets. Based on molecular dynamics simulations we show that these three compounds exhibit superionic behavior at the pressure-temperature conditions as in the interiors of Uranus and Neptune. Moreover, the water-rich compound MgO4H6 could be stable inside the early Earth and therefore may serve as a possible early Earth water reservoir. Our findings, in the poorly explored megabar pressure regime, provide constraints for interior and evolution models of wet planets in our solar system and beyond.
Original language | English |
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Article number | 1165 |
Pages (from-to) | 1165 |
Journal | Nature Communications |
Volume | 14 |
Issue number | 1 |
DOIs | |
State | Published - 1 Mar 2023 |
Bibliographical note
Funding Information:J.S. gratefully acknowledges the financial support from the National Key R&D Program of China (grant nos. 2022YFA1403201), the National Natural Science Foundation of China (grant nos. 12125404, 11974162, and 11834006), and the Fundamental Research Funds for the Central Universities. C.J.P is supported by the EPSRC through grants EP/P022596/1, and EP/S021981/1; A.V. acknowledges support by the ISF through grants 770/21 and 773/21. The calculations were carried out using supercomputers at the High Performance Computing Center of Collaborative Innovation Center of Advanced Microstructures, the high-performance supercomputing center of Nanjing University.
Funding Information:
J.S. gratefully acknowledges the financial support from the National Key R&D Program of China (grant nos. 2022YFA1403201), the National Natural Science Foundation of China (grant nos. 12125404, 11974162, and 11834006), and the Fundamental Research Funds for the Central Universities. C.J.P is supported by the EPSRC through grants EP/P022596/1, and EP/S021981/1; A.V. acknowledges support by the ISF through grants 770/21 and 773/21. The calculations were carried out using supercomputers at the High Performance Computing Center of Collaborative Innovation Center of Advanced Microstructures, the high-performance supercomputing center of Nanjing University.
Publisher Copyright:
© 2023, The Author(s).
© 2023. The Author(s).