Spintronics has shown a remarkable and rapid development, for example from the initial discovery of giant magnetoresistance in spin valves 1 to their ubiquity in hard-disk read heads in a relatively short time. However, the ability to fully harness electron spin as another degree of freedom in semiconductor devices has been slower to take off. One future avenue that may expand the spintronic technology base is to take advantage of the flexibility intrinsic to organic semiconductors (OSCs), where it is possible to engineer and control their electronic properties and tailor them to obtain new device concepts 2 . Here we show that we can control the spin polarization of extracted charge carriers from an OSC by the inclusion of a thin interfacial layer of polar material. The electric dipole moment brought about by this layer shifts the OSC highest occupied molecular orbital with respect to the Fermi energy of the ferromagnetic contact. This approach allows us full control of the spin band appropriate for charge-carrier extraction, opening up new spintronic device concepts for future exploitation.The development and understanding of new hybrid organic/inorganic interfaces will enable considerable progress in organic spintronics for technological purposes, including processing elements, sensors, memories and conceptually different future applications. In addition to the 'standard' spintronic applications, newly developed interfaces could bring spintronic effects to the field of organic light-emitting diodes (OLEDs), as well as in the fast progressing field of organic field-effect transistors. For example, the injection of carriers with a controlled spin state could enable the amplification of either singlet or triplet exciton states 2 leading to a significant increase in the efficiency of the electroluminescence in OLEDs. Although these considerations are conceptually straightforward, no efficiency amplification has yet been reported in the literature, despite several attempts 3 . The failure of those approaches was caused by the simple reason that light emission can be detected starting from an applied voltage of a few volts, whereas state-of-the-art spin injection in organic materials persists to a maximum of around 1 V (refs 4-6). As yet, this is unexplained. Further complications arise from the fact that various reports on working devices show a wide spread of performances for apparently similar structures, highlighting the issue of reproducibility [7][8][9] . The poor reproducibility is mainly due to the unknown interplay between processing and spin transfer performance and there is little deterministic control of the interface properties. However, it has recently been demonstrated that the insertion of a barrier

We report muon spin rotation (μSR) and infrared spectroscopy experiments on underdoped BaFe1.89Co0.11As2 which show that bulk magnetism and superconductivity (SC) coexist and compete on the nanometer length scale. Our combined data reveal a bulk magnetic order, likely due to an incommensurate spin density wave (SDW), which develops below T(mag)≈32  K and becomes reduced in magnitude (but not in volume) below Tc=21.7  K. A slowly fluctuating precursor of the SDW seems to develop already below the structural transition at T(s)≈50  K. The bulk nature of SC is established by the μSR data which show a bulk SC vortex lattice and the IR data which reveal that the majority of low-energy states is gapped and participates in the condensate at T≪T(c).

Publication date: 2012 Document VersionPublisher's PDF, also known as Version of record Link back to DTU Orbit Citation (APA): Bernhard, C., Wang, C. N., Nuccio, L., Schulz, L., Zaharko, O., Larsen, J., ... Niedermayer, C. (2012). Muon spin rotation study of magnetism and superconductivity in Using muon spin rotation (μSR) we investigated the magnetic and superconducting properties of a series of Ba(Fe 1−x Co x ) 2 As 2 single crystals with 0 x 0.15. Our study details how the antiferromagnetic order is suppressed upon Co substitution and how it coexists with superconductivity. In the nonsuperconducting samples at 0 < x < 0.04 the antiferromagnetic order parameter is only moderately suppressed. With the onset of superconductivity this suppression becomes faster and it is most rapid between x = 0.045 and 0.05. As was previously demonstrated by μSR at x = 0.055 [P. Marsik et al., Phys. Rev. Lett. 105, 57001 (2010)], the strongly weakened antiferromagnetic order is still a bulk phenomenon that competes with superconductivity. The comparison with neutron diffraction data suggests that the antiferromagnetic order remains commensurate whereas the amplitude exhibits a spatial variation that is likely caused by the randomly distributed Co atoms. A different kind of magnetic order that was also previously identified [C. Bernhard et al., New J. Phys. 11, 055050 (2009)] occurs at 0.055 < x < 0.075 where T c approaches the maximum value. The magnetic order develops here only in parts of the sample volume and it seems to cooperate with superconductivity since its onset temperature coincides with T c . Even in the strongly overdoped regime at x = 0.11, where the static magnetic order has disappeared, we find that the low-energy spin fluctuations are anomalously enhanced below T c . These findings point toward a drastic change in the relationship between the magnetic and superconducting orders from a competitive one in the strongly underdoped regime to a constructive one in near-optimally and overdoped samples.

We report on a particular type of CdSe nanocrystals (NCs) that exhibit a single optical absorption doublet. The two peaks in the doublet are relatively sharp with a full width half-maximum as narrow as 10 nm. The peak positions vary with passivation ligands (at ∼426 and ∼453 nm for amine ligand passivation and at ∼432 and ∼460 nm for carboxylate ligand passivation). To date, it has been generally concluded that these NCs have a two-dimension (2D) morphology with 1D quantum confinement. Here, we report that zero-dimension (0D) NCs with 3D quantum confinement can exhibit a very similar static optical feature consisting of a sharp absorption doublet. We show that our as-prepared CdSe NCs (without further purification) were mainly 0D NCs, as observed when they were deposited on transmission electron microscopy (TEM) grids directly from toluene or hexane dispersions. We further demonstrate that it was possible to alter this 0D morphology by using dispersion additives and/or purification solvents to result in the appearance of 2D NCs under TEM. Although the 0D and selfassembled 2D NCs displayed similar static optical features, the two morphologies behaved quite differently in polarized emission. The 2D NCs exhibited detection angle dependent polarized emission, whereas the 0D NCs do not. Our findings indicate that a well-like morphology can be induced by the presence of hexadecylamine (HDA) in the dispersion with sonication for aminepassivated 0D NCs or by the use of ethanol during purification with dispersion storage for carboxylate-passivated 0D NCs. In this way, it is possible to manipulate the NC morphology for a targeted application through the appropriate post-treatment. This study highlights that more sophisticated theoretical studies are required to account for the experimental observations in which both 0D NCs and their self-assembled 2D NC products display similar static optical features.