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    Magnetic properties of individual Co2FeGa Heusler nanoparticles studied at room temperature by a highly sensitive co-resonant cantilever sensor
    (London : Nature Publishing Group, 2017) Körner, Julia; Reiche, Christopher F.; Ghunaim, Rasha; Fuge, Robert; Hampel, Silke; Büchner, Bernd; Mühl, Thomas
    The investigation of properties of nanoparticles is an important task to pave the way for progress and new applications in many fields of research like biotechnology, medicine and magnetic storage techniques. The study of nanoparticles with ever decreasing size is a challenge for commonly employed methods and techniques. It requires increasingly complex measurement setups, often low temperatures and a size reduction of the respective sensors to achieve the necessary sensitivity and resolution. Here, we present results on how magnetic properties of individual nanoparticles can be measured at room temperature and with a conventional scanning force microscopy setup combined with a co-resonant cantilever magnetometry approach. We investigate individual Co2FeGa Heusler nanoparticles with diameters of the order of 35 nm encapsulated in carbon nanotubes. We observed, for the first time, magnetic switching of these nanoparticles in an external magnetic field by simple laser deflection detection. Furthermore, we were able to deduce magnetic properties of these nanoparticles which are in good agreement with previous results obtained with large nanoparticle ensembles in other experiments. In order to do this, we expand the analytical description of the frequency shift signal in cantilever magnetometry to a more general formulation, taking unaligned sensor oscillation directions with respect to the magnetic field into account.
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    Universal electronic structure of polar oxide hetero-interfaces
    (London : Nature Publishing Group, 2015) Treske, Uwe; Heming, Nadine; Knupfer, Martin; Büchner, Bernd; Di Gennaro, Emiliano; Khare, Amit; Di Uccio, Umberto Scotti; Granozio, Fabio Miletto; Krause, Stefan; Koitzsch, Andreas
    The electronic properties of NdGaO3/SrTiO3, LaGaO3/SrTiO3, and LaAlO3/SrTiO3 interfaces, all showing an insulator-to-metal transition as a function of the overlayer-thickness, are addressed in a comparative study based on x-ray absorption, x-ray photoemission and resonant photoemission spectroscopy. The nature of the charge carriers, their concentration and spatial distribution as well as the interface band alignments and the overall interface band diagrams are studied and quantitatively evaluated. The behavior of the three analyzed heterostructures is found to be remarkably similar. The valence band edge of all the three overlayers aligns to that of bulk SrTiO3. The near-interface SrTiO3 layer is affected, at increasing overlayer thickness, by the building-up of a confining potential. This potential bends both the valence and the conduction band downwards. The latter one crossing the Fermi energy in the proximity of the interface and determines the formation of an interfacial band offset growing as a function of thickness. Quite remarkably, but in agreement with previous reports for LaAlO3/SrTiO3, no electric field is detected inside any of the polar overlayers. The essential phenomenology emerging from our findings is discussed on the base of different alternative scenarios regarding the origin of interface carriers and their interaction with an intense photon beam.
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    Spin-orbit coupling control of anisotropy, ground state and frustration in 5d2 Sr2MgOsO6
    (London : Nature Publishing Group, 2016) Morrow, Ryan; Taylor, Alice E.; Singh, D.J.; Xiong, Jie; Rodan, Steven; Wolter, A.U.B.; Wurmehl, Sabine; Büchner, Bernd; Stone, M.B.; Kolesnikov, A.I.; Aczel, Adam A.; Christianson, A.D.; Woodward, Patrick M.
    The influence of spin-orbit coupling (SOC) on the physical properties of the 5d2 system Sr2MgOsO6 is probed via a combination of magnetometry, specific heat measurements, elastic and inelastic neutron scattering, and density functional theory calculations. Although a significant degree of frustration is expected, we find that Sr2MgOsO6 orders in a type I antiferromagnetic structure at the remarkably high temperature of 108 K. The measurements presented allow for the first accurate quantification of the size of the magnetic moment in a 5d2 system of 0.60(2) μB –a significantly reduced moment from the expected value for such a system. Furthermore, significant anisotropy is identified via a spin excitation gap, and we confirm by first principles calculations that SOC not only provides the magnetocrystalline anisotropy, but also plays a crucial role in determining both the ground state magnetic order and the size of the local moment in this compound. Through comparison to Sr2ScOsO6, it is demonstrated that SOC-induced anisotropy has the ability to relieve frustration in 5d2 systems relative to their 5d3 counterparts, providing an explanation of the high TN found in Sr2MgOsO6.
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    One-sign order parameter in iron based superconductor
    (Basel : MDPI, 2012) Borisenko, Sergey V.; Zabolotnyy, Volodymyr B.; Kordyuk, Alexnader A.; Evtushinsky, Danil V.; Kim, Timur K.; Morozov, Igor V.; Follath, Rolf; Büchner, Bernd
    The onset of superconductivity at the transition temperature is marked by the onset of order, which is characterized by an energy gap. Most models of the iron-based superconductors find a sign-changing (s±) order parameter [1–6], with the physical implication that pairing is driven by spin fluctuations. Recent work, however, has indicated that LiFeAs has a simple isotropic order parameter [7–9] and spin fluctuations are not necessary [7,10], contrary to the models [1–6]. The strength of the spin fluctuations has been controversial [11,12], meaning that the mechanism of superconductivity cannot as yet be determined. We report the momentum dependence of the superconducting energy gap, where we find an anisotropy that rules out coupling through spin fluctuations and the sign change. The results instead suggest that orbital fluctuations assisted by phonons [13,14] are the best explanation for superconductivity.