High-pressure phase diagram of hydrogen and deuterium sulfides from first principles: structural and vibrational properties including quantum and anharmonic effects
Abstract
We study the structural and vibrational properties of the high-temperature superconducting sulfur trihydride and trideuteride in the high-pressure Im3m and R3m phases by first-principles density-functional-theory calculations. On lowering pressure, the rhombohedral transition Im3m → R3m is expected, with hydrogen bond desymmetrization and occurrence of trigonal lattice distortion. In hydrostatic conditions we find that, contrary to what suggested in some recent experiments, if the rhombohedral distortion exists it affects mainly the hydrogen-bonds, whereas the resulting cell distortion is minimal. We estimate that the occurrence of a stress anisotropy of approximately 10\% could explain this discrepancy. Assuming hydrostatic conditions, we calculate the critical pressure at which the rhombohedral transition occurs. Quantum and anharmonic effects, which are relevant in this system, are included at nonperturbative level with the stochastic self-consistent harmonic approximation (SSCHA). Within this approach, we determine the transition pressure by calculating the free energy Hessian. We find that quantum anharmonic effects are responsible for a strong reduction of the critical pressure with respect to the one obtained with the classical harmonic approach. Moreover, we observe a prominent isotope effect, as we estimate higher pressure transition for D3S than for H3S. Finally, within SSCHA we calculate the anharmonic phonon spectral functions in the Im3m phase. The strong anharmonicity of the system is confirmed by the occurrence of very large anharmonic broadenings leading to complex non-Lorentzian line shapes. However, for the vibrational spectra at zone center, accessible e.g. by infrared spectroscopy, the broadenings are very small (linewidth at most around 2~meV) and anharmonic phonon quasiparticles are well defined.
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