Superionicity in Ammonium Polyhydrides at Extreme Pressures
Kyla de Villa, Xiaoyu Wang, Eva Zurek, Burkkhard Militzer

TL;DR
This study uses molecular dynamics simulations to explore superionic behavior in ammonium polyhydrides at high pressures, revealing phase transitions and melting trends relevant to planetary interiors.
Contribution
It provides the first detailed analysis of superionic phases in ammonium polyhydrides under extreme conditions, identifying transition metrics and the influence of proton fraction.
Findings
Hydrogen superionic diffusion occurs upon heating at high pressures.
Solid-to-superionic and superionic-to-liquid transitions decrease with increasing proton fraction.
Ammonium hydrides are likely to be liquid rather than superionic at ice giant interior conditions.
Abstract
Polyhydrides have been shown to form novel structures at high pressure, which may be found in the interiors of giant planets. With density functional molecular dynamics simulations we studied the behavior of ammonium polyhydride compounds with stoichiometries of NH, NH, NH, NH, NH, NH, and NH which were predicted with crystal structure search methods to be metastable at 100-300~GPa. For every compound, we performed simulations at a range of temperatures (and for several compounds, pressures) covering the solid, superionic and liquid phases. We show that when heated, high pressure ammonium polyhydride compounds exhibit hydrogen superionic diffusion. We demonstrate a number of metrics by which the solid-to-superionic and superionic-to-liquid transitions can be detected from simulation data, including changes in the internal energy and pressure,…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsHigh-pressure geophysics and materials · Material Dynamics and Properties · nanoparticles nucleation surface interactions
