Abstract Single crystals of the semiconducting Ba 2 TeO are prepared from BaO and Te in a molten Ba flux in the molar ratio of 1:1:20 (steel crucible in evacuated quartz tube, 1000 °C, 20 h; cooling to 820 °C within 50 h).
Submillimeter and millimeter wave electron spin resonance (ESR) measurements of the pi-d correlated organic conductor lambda-(BETS)2Fe0.6Ga0.4Cl4 have been performed. Antiferromagnetic resonance (AFMR) has been observed in the insulating antiferromagnetic phase, and its frequency-field dependence can be reproduced by the biaxial anisotropic AFMR theory. We find that in this alloy system, the easy-axis is near the b-axis, unlike previous results for the pure lambda-(BETS)2FeCl4 salts where it is closer to the c*-axis. We have also observed electron paramagnetic resonance (EPR) in the metallic phase at higher fields where the g-value is shown to be temperature and frequency dependent for field applied along the c*-axis. This behavior indicates the existence of strong pi-d interaction. Our measurements further show the magnetic anisotropy associated with the anions (the D term in the spin Hamiltonian) is |D|~0.11 cm-1.
We report the first investigation of the photo-response of the conductivity of a new class of organic semiconductors based on functionalized pentacene. These materials form high quality single crystals that exhibit a thermally activated resistivity. Unlike pure pentacene, the functionalized derivatives are readily soluble in acetone, and can be evaporated or spin-cast as thin films for potential device applications. The electrical conductivity of the single crystal materials is noticeably sensitive to ambient light changes. The purpose, therefore, of the present study, is to determine the nature of the photo-response in terms of carrier activation vs. heating effects, and also to measure the dependence of the photo-response on photon energy. We describe a new method, involving the temperature dependent photo-response, which allows an unambiguous identification of the signature of heating effects in materials with a thermally activated conductivity. We find strong evidence that the photo-response in the materials investigated is predominantly a highly localized heating mechanism. Wavelength dependent studies of the photo-response reveal resonant features and cut-offs that indicate the photon energy absorption is related to the electronic structure of the material.
We investigated the optical properties of 4,4'-stilbenedinitrene at low temperature and in high magnetic fields and compared the results with complementary first principles calculations. Both physical tuning parameters allow us to manipulate the singlet-triplet equilibrium, and by doing so, control the optical contrast (which is on the order of -2.5 × 10(2) cm(-1) at 555 nm and 35 T). Moreover, analysis of the magneto-optical response using a combined population and Beer's law framework reveals the singlet-triplet spin gap and identifies particular features in the absorption difference spectrum as deriving from singlet or triplet state excitations. These findings deepen our understanding of coupling in open shell molecules and show how chemical structure modification can modulate charge-spin interactions in organic biradicals.
