Origin of the large entropy change in the molecular caloric and ferroelectric ammonium sulfate

TL;DR

This study clarifies the origin of the large entropy change in ammonium sulfate's ferroelectric transition, revealing it stems from low-frequency librations of ammonium ions rather than molecular disorder.

Contribution

The paper demonstrates that vibrational entropy from librations, not molecular disorder, accounts for the large entropy change in ammonium sulfate's phase transition.

Findings

Entropy arises from low-frequency librations of ammonium ions.

Disorder-based models of entropy are invalid in this case.

Vibrational entropy from broad energy minima is crucial for functional molecular materials.

Abstract

The deceptively simple inorganic salt ammonium sulfate undergoes a ferroelectric phase transition associated with a very large entropy change and both electrocaloric and barocaloric functionality. While the structural origins of the electrical polarisation are now well established, those of the entropy change have been controversial for over fifty years. This question is resolved here using a combination of DFT phonon calculations with inelastic neutron scattering under variable temperature and pressure, supported by complementary total and quasielastic neutron scattering experiments. A simple model of the entropy in which each molecular ion is disordered across the mirror plane in the high symmetry phase, although widely used in the literature, proves to be untenable. Instead, the entropy arises from low-frequency librations of ammonium ions in this phase, with harmonic terms that are very small or even negative. These results suggest that, in the search for molecular materials with functionality derived from large entropy changes, vibrational entropy arising from broad energy minima is likely to be just as important as configurational entropy arising from crystallographic disorder.