Evolution of ferroelectricity in tetrathiafulvalene-p-chloranil as a function of pressure and temperature
arXiv:1312.6732 · doi:10.1063/1.4884964
Abstract
The neutral-to-ionic phase transition in the mixed-stack charge-transfer complex tetrathiafulvalene-p-chloranil (TTF-CA) has been studied by pressure-dependent infrared spectroscopy up to p=11 kbar and down to low temperatures, T = 10 K. By tracking the C=O antisymmetric stretching mode of CA molecules, we accurately determine the ionicity of TTF-CA in the pressure-temperature phase diagram. At any point the TTF-CA crystal bears only a single ionicity; there is no coexistence region or an exotic high-pressure phase. Our findings shed new light on the role of electron-phonon interaction in the neutral-ionic transition.
6 pages, 4 figures, accepted for publication in JCP
References in corpus (2)
Cited by in corpus (5)
- Separation of Charge Instability and Lattice Symmetry Breaking in an Organic Ferroelectric
- Phase Competition, Solitons, and Domain Walls in Neutral-Ionic Transition Systems
- Fate of a soliton matter upon symmetry-breaking ferroelectric order
- Molecular Dynamics at Electrical- and Optical-Driven Phase Transitions Time-Resolved Infrared Studies Using Fourier-Transform Spectrometers
- Experimental Verification of Charge Soliton Excitations in the Ionic Mott-Peierls Ferroelectric, TTF-CA