Two-dimensional radical-cationic Mott insulator based on an electron donor containing neither a tetrathiafulvalene nor tetrathiapentalene skeleton
We report the structure and physical properties of a new radical-cationic Mott insulator -(BEDT-BDT)PF 6 (BEDT-BDT: benzo[1,2- g :4,5- g ′]bis(thieno[2,3- b ][1,4]dithiin)). The crystal structure belongs to a monoclinic system with a 1 : 1 donor/anion ratio. Based on this composition, the salt is co...
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Veröffentlicht in: | CrystEngComm 2020-01, Vol.22 (36), p.5949-5953 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report the structure and physical properties of a new radical-cationic Mott insulator -(BEDT-BDT)PF
6
(BEDT-BDT: benzo[1,2-
g
:4,5-
g
′]bis(thieno[2,3-
b
][1,4]dithiin)). The crystal structure belongs to a monoclinic system with a 1 : 1 donor/anion ratio. Based on this composition, the salt is considered a half-filled Mott insulator, in which the BEDT-BDT molecules form a mode arrangement. Owing to the strong electron correlation, the temperature dependence of the resistivity exhibits semiconducting behaviour. The static magnetic susceptibility first follows the Curie-Weiss law down to 15 K, but then follows the two-dimensional (2D) triangular Heisenberg model with
J
= 7.5 K below 15 K. Even at 2 K, this salt is paramagnetic and no magnetic order is formed. The tight-binding band calculation reveals a 2D Fermi surface. It is remarkable that -(BEDT-BDT)PF
6
forms a 2D electronic structure without any 1,3-dithiol-2-ylidene units, unlike tetrathiafulvalene and tetrathiapentalene donors.
We have succeeded in developing a two-dimensional radical-cationic Mott insulator that does not contain a 1,3-dithiol-2-ylidene moiety. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d0ce00878h |