Multiferroic domain relaxation in (NH4)2[FeCl5(H2O)]
Sebastian Biesenkamp, Karin Schmalzl, Petra Becker, Ladislav Bohaty,, and Markus Braden

TL;DR
This study investigates the domain relaxation dynamics in the multiferroic compound (NH4)2[FeCl5(H2O)] using neutron diffraction, revealing a slower relaxation process and complex magnetic ordering that does not affect domain wall pinning.
Contribution
It provides the first detailed analysis of multiferroic domain kinetics in (NH4)2[FeCl5(H2O)] and compares its relaxation behavior with other multiferroics, highlighting unique magnetic properties.
Findings
Multiferroic relaxation follows the Arrhenius-Merz law but with a larger time scale.
Higher-order magnetic contributions emerge upon cooling in the multiferroic phase.
Magnetic anharmonicity does not influence domain wall pinning or relaxation temperature dependence.
Abstract
The molecular compound (NH4)2[FeCl5(H2O)] is a type-II multiferroic material, in which incommensurate cycloidal order directly induces ferroelectric polarization. The multiferroic domain kinetics in (NH4)2[FeCl5(H2O)] were studied by time-resolved neutron diffraction experiments utilizing neutron polarization analysis. The temperature and electric-field dependent multiferroic relaxation obeys the simple combined Arrhenius-Merz law, which was reported to describe domain kinetics in the prototype multiferroics TbMnO3 and NaFeGe2O6. However, the characteristic time scale of the multiferroic relaxation is considerably larger than those in TbMnO3 or NaFeGe2O6. Temperature-dependent diffraction on (NH4)2[FeCl5(H2O)] reveals the emergence of higher-order and commensurate magnetic contributions upon cooling in the multiferroic phase in zero field. The good agreement with studies of…
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Taxonomy
TopicsSolid-state spectroscopy and crystallography · Inorganic Fluorides and Related Compounds · Crystal Structures and Properties
