Skip to main content

Research Repository

Advanced Search

A new avenue to relaxor-like ferroelectric behaviour found by probing the structure and dynamics of [NH3NH2]Mg(HCO2)3

Hitchings, Thomas J.; Wickins, Helen M.; Peat, George U. L.; Hodgkinson, Paul; Srivastava, Anant Kumar; Lu, Teng; Liu, Yun; Piltz, Ross O.; Demmel, Franz; Phillips, Anthony E.; Saines, Paul J.

A new avenue to relaxor-like ferroelectric behaviour found by probing the structure and dynamics of [NH3NH2]Mg(HCO2)3 Thumbnail


Authors

Thomas J. Hitchings

Helen Wickins helen.m.wickins@durham.ac.uk
PGR Student Doctor of Philosophy

George U. L. Peat

Anant Kumar Srivastava

Teng Lu

Yun Liu

Ross O. Piltz

Franz Demmel

Anthony E. Phillips

Paul J. Saines



Abstract

The field of relaxor ferroelectrics has long been dominated by ceramic oxide materials exhibiting large polarisations with temperature and frequency dependence. Intriguingly, the dense metal–organic framework (MOF) [NH3NH2]Mg(HCO2)3 was reported as one of the first coordination frameworks to exhibit relaxor-like properties. This work clarifies the origin of these relaxor-like properties through re-examining its unusual phase transition using neutron single crystal diffraction, along with solid-state NMR, quasielastic neutron scattering and dielectric spectroscopy studies. This reveals that the phase transition is caused by the partial reorientation of NH3NH2 within the pores of the framework, from lying in the planes of the channel at lower temperatures to along the channel direction above the transition temperature. The transition occurs via a dynamic process such that the NH3NH2 cations can slowly interconvert between parallel and perpendicular orientations, with an estimated activation energy of 50 kJ mol−1. Furthermore these studies are consistent with proton hopping between the hydrazinium cations oriented along the channel direction via a proton site intermediate. This study suggests the ferroelectric properties of [NH3NH2]Mg(HCO2)3 are likely driven by a hydrogen bonding mechanism. The relaxor behaviour is proposed to be the result of polar regions, which likely fluctuate due to increased cation dynamics at high temperature. The combination of cation reorientation and proton hopping fully describes this material's relaxor-like behaviour, suggesting a route to the future design of non-oxide-based relaxor ferroelectrics.

Citation

Hitchings, T. J., Wickins, H. M., Peat, G. U. L., Hodgkinson, P., Srivastava, A. K., Lu, T., …Saines, P. J. (2023). A new avenue to relaxor-like ferroelectric behaviour found by probing the structure and dynamics of [NH3NH2]Mg(HCO2)3. Journal of Materials Chemistry C Materials for optical and electronic devices, 11(28), 9695-9706. https://doi.org/10.1039/d3tc00480e

Journal Article Type Article
Acceptance Date Jun 12, 2023
Online Publication Date Jun 14, 2023
Publication Date 2023
Deposit Date Nov 7, 2023
Publicly Available Date Nov 7, 2023
Journal Journal of Materials Chemistry C
Print ISSN 2050-7526
Electronic ISSN 2050-7534
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 11
Issue 28
Pages 9695-9706
DOI https://doi.org/10.1039/d3tc00480e
Public URL https://durham-repository.worktribe.com/output/1900308

Files





You might also like



Downloadable Citations