Metal-Insulator Transition in the Dimerized Organic Conductor -(BEDT-TTF)Hg(SCN)Br
arXiv:1706.08604 · doi:10.1103/PhysRevB.96.085116
Abstract
The organic charge-transfer salt -(BEDT-TTF)Hg(SCN)Br is a quasi two-dimensional metal with a half-filled conduction band at ambient conditions. When cooled below K it undergoes a pronounced transition to an insulating phase where the resistivity increases many orders of magnitude. In order to elucidate the nature of this metal-insulator transition we have performed comprehensive transport, dielectric and optical investigations. The findings are compared with other dimerized -(BEDT-TTF) salts, in particular the Cl-analogue, where a charge-order transition takes place at K.
arXiv commentsubmitted to Physical Review B, 9 pages, 7 figures
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Cited by in corpus (12)
- Evidence for a quantum dipole liquid state in an organic quasi-two-dimensional material
- Molecular Quantum Materials: Electronic Phases and Charge Dynamics in Two-Dimensional Organic Solids
- Evidence for electronically-driven ferroelectricity in the family of strongly correlated dimerized BEDT-TTF molecular conductors
- Impurity Moments Conceal Low-Energy Relaxation of Quantum Spin Liquids
- Melting of charge order in the low-temperature state of an electronic ferroelectric
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- Anomalously field-susceptible spin soft-matter emerging in an electric-dipole liquid candidate
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- Tuning Charge Order in -(BEDT-TTF)Hg(SCN)X (X=Br, Cl) via Uniaxial Strain
- C NMR observation of a nonmagnetic charge-ordered state in the organic conductor -(ET)Hg(SCN)Cl