CRYSTAL AND ELECTRONIC-STRUCTURES AND ELECTRICAL, MAGNETIC, AND OPTICAL-PROPERTIES OF 2 COPPER TETRAHALIDE SALTS OF BIS(ETHYLENEDITHIO)-TETRATHIAFULVALENE

Citation
Ir. Marsden et al., CRYSTAL AND ELECTRONIC-STRUCTURES AND ELECTRICAL, MAGNETIC, AND OPTICAL-PROPERTIES OF 2 COPPER TETRAHALIDE SALTS OF BIS(ETHYLENEDITHIO)-TETRATHIAFULVALENE, Physical review. B, Condensed matter, 50(4), 1994, pp. 2118-2127
Citations number
47
Categorie Soggetti
Physics, Condensed Matter
ISSN journal
01631829
Volume
50
Issue
4
Year of publication
1994
Pages
2118 - 2127
Database
ISI
SICI code
0163-1829(1994)50:4<2118:CAEAEM>2.0.ZU;2-2
Abstract
We report the crystal and electronic band structures at 295 K and meas urements of temperature-dependent magnetic susceptibility, electron pa ramagnetic resonance, optical reflectivity, conductivity, and thermopo wer for two copper tetrahalide salts of bis(ethylenedithio)-tetrathiaf ulvalene (BEDT-TTF), (BEDT-TTF)3CuBr4 and (BEDT-TTF)3CuCl2Br2. The two salts are isostructural with layers of BEDT-TTF having charges of 0 a nd + e separated by layers of pseudo-square-planar tetrahalides of cop per (II). At ambient pressure these salts show conductivities near 1 S cm-1, and the magnetic properties indicate coupled localized spins pr esent on both BEDT-TTF and the d9 copper layers. At 60 K, there is a d iscontinuous drop in susceptibility, a sharpening of the electron para magnetic resonance linewidth, and an increase in g value that we attri bute to the loss of the contribution from the BEDT-TTF sheets. This ma y be associated with a Jahn-Teller distortion of the planar copper com plexes. Below the transition temperature the susceptibility can be fit ted to a quadratic layer antiferromagnet with J = 15 K (CuBr4) and 8 K (CUCl2Br2) and one spin per formula unit. Under pressure there is a v ery rapid increase in conductivity, to 500 S/cm at 24 kbar, the larges t increase of conductivity under pressure in any molecular solid yet s tudied. There is a sharp transition from metal to insulator at tempera tures rising to 111 K near 5 kbar, and falling to 80 K at 20 kbar. We consider that these salts are nearly metallic at ambient pressure, wit h strongly enhanced susceptibilities, but are brought to a fully metal lic state under pressure as a result of increased intermolecular conta cts.