Following the recent discovery of large magnetoresistance at room temperature in polyfluorence sandwich devices, we have performed a comprehensive magnetoresistance study on a set of organic semiconductor sandwich devices made from different pi-conjugated polymers and small molecules. The measurements were performed at different temperatures, ranging from 10K to 300K, and at magnetic fields, B < 100mT . We observed large negative or positive magnetoresistance (up to 10% at 300K and 10mT) depending on material and device operating conditions. We compare the results obtained in devices made from different materials with the goal of providing a comprehensive picture of the experimental data. We discuss our results in the framework of known magnetoresistance mechanisms and find that none of the existing models can explain our results.
We explore the possibility that hyperfine interaction causes the recently
discovered organic magnetoresistance (OMAR) effect. Our study employs both
experiment and theoretical modelling. An excitonic pair mechanism model based
on hyperfine interaction, previously suggested by others to explain magnetic
field effects in organics, is examined. Whereas this model can explain a few
key aspects of the experimental data, we, however, uncover several fundamental
contradictions as well. By varying the injection efficiency for minority
carriers in the devices, we show experimentally that OMAR is only weakly
dependent on the ratio between excitons formed and carriers injected, likely
excluding any excitonic effect as the origin of OMAR.Comment: 10 pages, 7 figures, 1 tabl
We perform charge-induced absorption and electroluminescence spectroscopy in a polyfluorene organic magnetoresistive device. Our experiments allow us to measure the singlet exciton, triplet exciton and polaron densities in a live device under an applied magnetic field, and to distinguish between three different models that were proposed to explain organic magnetoresistance. These models are based on different spin-dependent interactions, namely exciton formation, triplet excitonpolaron quenching and bipolaron formation. We show that the singlet exciton, triplet exciton and polaron densities and conductivity all increase with increasing magnetic field. Our data are inconsistent with the exciton formation and triplet-exciton polaron quenching models.
We study the recently discovered organic magnetoresistance ͑OMAR͒ effect in a pair of materials that have similar chemical structures except that one contains a heavy atom to enhance spin-orbit coupling. We use photoluminescence spectroscopy to estimate the spin-orbit coupling strength. In the material with weak spinorbit coupling the characteristic magnetic field scale is comparable to the hyperfine coupling strength. In the material with strong spin-orbit coupling we find that the OMAR is strongly reduced in size and the OMAR traces clearly exhibit a second, higher field scale which we identify with the spin-orbit coupling strength. We model our results using the standard spin-dynamics Hamiltonian.
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