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    Two types of magnetic shape-memory effects from twinned microstructure and magneto-structural coupling in Fe1 +yTe
    (Washington : National Academy of Sciences, 2019) Rößler, S.; Koz, C.; Wang, Z.; Skourski, Y.; Doerr, M.; Kasinathan, D.; Rosner, H.; Schmidt, M.; Schwarz, U.; Rößler, U.K.; Wirth, S.
    A detailed experimental investigation of Fe1+yTe (y = 0.11, 0.12) using pulsed magnetic fields up to 60 T confirms remarkable magnetic shape-memory (MSM) effects. These effects result from magnetoelastic transformation processes in the low-temperature antiferromagnetic state of these materials. The observation of modulated and finely twinned microstructure at the nanoscale through scanning tunneling microscopy establishes a behavior similar to that of thermoelastic martensite. We identified the observed, elegant hierarchical twinning pattern of monoclinic crystallographic domains as an ideal realization of crossing twin bands. The antiferromagnetism of the monoclinic ground state allows for a magnetic-field–induced reorientation of these twin variants by the motion of one type of twin boundaries. At sufficiently high magnetic fields, we observed a second isothermal transformation process with large hysteresis for different directions of applied field. This gives rise to a second MSM effect caused by a phase transition back to the field-polarized tetragonal lattice state.
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    Single molecule magnet with an unpaired electron trapped between two lanthanide ions inside a fullerene
    (London : Nature Publishing Group, 2017) Liu, F.; Krylov, D.S.; Spree, L.; Avdoshenko, S.M.; Samoylova, N.A.; Rosenkranz, M.; Kostanyan, A.; Greber, T.; Wolter, A.U.B.; Büchner, B.; Popov, A.A.
    Increasing the temperature at which molecules behave as single-molecule magnets is a serious challenge in molecular magnetism. One of the ways to address this problem is to create the molecules with strongly coupled lanthanide ions. In this work, endohedral metallofullerenes Y 2 @C 80 and Dy 2 @C 80 are obtained in the form of air-stable benzyl monoadducts. Both feature an unpaired electron trapped between metal ions, thus forming a single-electron metal-metal bond. Giant exchange interactions between lanthanide ions and the unpaired electron result in single-molecule magnetism of Dy 2 @C 80 (CH 2 Ph) with a record-high 100 s blocking temperature of 18 K. All magnetic moments in Dy 2 @C 80 (CH 2 Ph) are parallel and couple ferromagnetically to form a single spin unit of 21 μ B with a dysprosium-electron exchange constant of 32 cm -1. The barrier of the magnetization reversal of 613 K is assigned to the state in which the spin of one Dy centre is flipped.
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    Cartesian product of synchronization transitions and hysteresis
    (Bristol : Institute of Physics Publishing, 2017) Wang, C.; Zou, Y.; Guan, S.; Kurths, J.
    We present theoretical results when applying the Cartesian product of two Kuramoto models on different network topologies. By a detailed mathematical analysis, we prove that the dynamics on the Cartesian product graph can be described by the canonical equations as the Kuramoto model. We show that the order parameter of the Cartesian product is the product of the order parameters of the factors. On the product graph, we observe either continuous or discontinuous synchronization transitions. In addition, under certain conditions, the transition from an initially incoherent state to a coherent one is discontinuous, while the transition from a coherent state to an incoherent one is continuous, presenting a mixture state of first and second order synchronization transitions. Our numerical results are in a good agreement with the theoretical predictions. These results provide new insight for network design and synchronization control.
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    Fully solvable lower dimensional dynamics of Cartesian product of Kuramoto models
    ([London] : IOP, 2019) Chen, Zewen; Zou, Yong; Guan, Shuguang; Liu, Zonghua; Kurths, Jürgen
    Implementing a positive correlation between the natural frequencies of nodes and their connectivity on a single star graph leads to a pronounced explosive transition to synchronization, additionally presenting hysteresis behavior. From the viewpoint of network connectivity, a star has been considered as a building motif to generate a big graph by graph operations. On the other hand, we propose to construct complex synchronization dynamics by applying the Cartesian product of two Kuramoto models on two star networks. On the product model, the lower dimensional equations describing the ensemble dynamics in terms of collective order parameters are fully solved by the Watanabe-Strogatz method. Different graph parameter choices lead to three different interacting scenarios of the hysteresis areas of two individual factor graphs, which further change the basins of attraction of multiple fixed points. Furthermore, we obtain coupling regimes where cluster synchronization states are often present on the product graph and the number of clusters is fully controlled. More specifically, oscillators on one star graph are synchronized while those on the other star are not synchronized, which induces clustered state on the product model. The numerical results agree perfectly with the theoretic predictions. © 2019 The Author(s). Published by IOP Publishing Ltd on behalf of the Institute of Physics and Deutsche Physikalische Gesellschaft.