Abstract
Dense hydrous magnesium silicate (DHMS) phases play a crucial role in transporting water in to the Earth’s interior. A newly discovered DHMS, phase H (MgSiO4H2), is stable at Earth’s lower mantle, i.e., at pressures greater than 30 GPa. Here we report the crystal structure and elasticity of phase H and its evolution upon compression. Using first principles simulations, we have explored the relative energetics of the candidate crystal structures with ordered and disordered configurations of magnesium and silicon atoms in the octahedral sites. At conditions relevant to Earth’s lower mantle, it is likely that phase H is able to incorporate a significant amount of aluminum, which may enhance the thermodynamic stability of phase H. The sound wave velocities of phase H are ~2–4% smaller than those of isostructural δ-AlOOH. The shear wave impedance contrast due to the transformation of phase D to a mixture of phase H and stishovite at pressures relevant to the upper part of the lower mantle could partly explain the geophysical observations. The calculated elastic wave velocities and anisotropies indicate that phase H can be a source of significant seismic anisotropy in the lower mantle.
Highlights
First principles simulations predicted a new Dense hydrous magnesium silicate (DHMS) phase, phase H (MgSiO4H2)[17], to be stable at pressures greater than the stability field of phase D
Structure consisting of magnesium (Mg) and silicon (Si) atoms in an octahedral coordination and is similar to the crystal structure of δ -AlOOH17,18 where aluminum (Al) atoms occur in octahedral sites
In this study, using first principles simulations, we report the crystal structure of phase H including the effect of ordering and disordering of Mg and Si atoms in the octahedral sites
Summary
First principles simulations predicted a new DHMS phase, phase H (MgSiO4H2)[17], to be stable at pressures greater than the stability field of phase D. In this study, using first principles simulations, we report the crystal structure of phase H including the effect of ordering and disordering of Mg and Si atoms in the octahedral sites.
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