Magnesium oxide-water compounds at megabar pressure and implications on planetary interiors.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36859401.
- Also identified by DOI 10.1038/s41467-023-36802-8 and PMC identifier 9977943.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Magnesium Oxide (MgO) and water (H<sub>2</sub>O) 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 H<sub>2</sub>O can react again at ultrahigh pressure, although Mg(OH)<sub>2</sub> decomposes at low pressure. The reemergent MgO-H<sub>2</sub>O compounds are: Mg<sub>2</sub>O<sub>3</sub>H<sub>2</sub> above 400 GPa, MgO<sub>3</sub>H<sub>4</sub> above 600 GPa, and MgO<sub>4</sub>H<sub>6</sub> in the pressure range of 270-600 GPa. Importantly, MgO<sub>4</sub>H<sub>6</sub> 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 MgO<sub>4</sub>H<sub>6</sub> 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.