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    Confined crystals of the smallest phase-change material
    (Washington, DC : American Chemical Society, 2013) Giusca, C.E.; Stolojan, V.; Sloan, J.; Börrnert, F.; Shiozawa, H.; Sader, K.; Rümmeli, M.H.; Büchner, B.; Silva, S.R.P.
    The demand for high-density memory in tandem with limitations imposed by the minimum feature size of current storage devices has created a need for new materials that can store information in smaller volumes than currently possible. Successfully employed in commercial optical data storage products, phase-change materials, that can reversibly and rapidly change from an amorphous phase to a crystalline phase when subject to heating or cooling have been identified for the development of the next generation electronic memories. There are limitations to the miniaturization of these devices due to current synthesis and theoretical considerations that place a lower limit of 2 nm on the minimum bit size, below which the material does not transform in the structural phase. We show here that by using carbon nanotubes of less than 2 nm diameter as templates phase-change nanowires confined to their smallest conceivable scale are obtained. Contrary to previous experimental evidence and theoretical expectations, the nanowires are found to crystallize at this scale and display amorphous-to-crystalline phase changes, fulfilling an important prerequisite of a memory element. We show evidence for the smallest phase-change material, extending thus the size limit to explore phase-change memory devices at extreme scales.
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    The magneto-optical gradient effect in an exchange-biased thin film: Experimental evidence for classical diffraction theory
    (Milton Park : Taylor & Francis, 2010) Schäfer, R.; Hamann, C.; McCord, J.; Schultz, L.; Kamberský, V.
    The magneto-optical gradient effect decorates the boundaries of in-plane domains even at perpendicular incidence of light in an optical polarization microscope. For its explanation, the classical magneto-optical diffraction theory was previously used to derive the effect from the same gyrotropic interaction as the Kerr effect. In order to explain the symmetry of the experimentally observed contrast on bulk ferromagnetic crystals, planar as well as perpendicular subsurface gradients in the magnetization had to be assumed. This was particularly needed when the surface magnetizations in neighboring domains pointed head-on and a gradient contrast appeared also in conditions of vanishing gyrotropic interaction at the surface. The gradient contrast in such conditions should not appear in very thin films where perpendicular magnetization gradients are not enforced by reduction of magnetostatic energy. Here we present the first experimental confirmation of this expectation, thus closing an experimental gap in verifying the predictions of the diffraction theory.