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Register a new userFrustrating frustration in snap-induced morphing
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The bistability of embedded elements provides a natural route through which to introduce reprogrammability to elastic meta-materials. However, attempts to leverage this programmability in objects that can change shape, or morph, have been limited by the tendency for the deformations induced by multiple elastic elements to be incompatible --- deformation is frustrated by geometry. We study the root cause of this frustration in a particular system, the soft morphable sheet, which is caused by an azimuthal buckling instability of bistable elements embedded within a sheet. With this understanding we show that, for this system at least, the root of frustration can itself be frustrated by an appropriate design of the lattice on which bistable elements are placed.
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We describe a combined experimental and theoretical investigation of shape-morphing structures assembled by actuating composite (Janus) fibers, taking into account multiple relevant factors affecting shape transformations, such as strain rate, composition, and geometry of the structures. Starting with simple bending experiments, we demonstrate the ways to attain multiple out-of-plane shapes of closed rings and square frames. Through combining theory and simulation, we examine how the mechanical properties of Janus fibers affect shape transitions. This allows us to control shape changes and to attain target 3D shapes by precise tuning of the material properties and geometry of the fibers. Our results open new perspectives of design of advanced mechanical metamaterials capable to create elaborate structures through sophisticated actuation modes.
Using the example of Zn-doped La2CuO4, we demonstrate that a spinless impurity doped into a non-frustrated antiferromagnet can induce substantial frustrating interactions among the spins surrounding it. This counterintuitive result is the key to resolving discrepancies between experimental data and earlier theories. Analytic and quantum Monte Carlo studies of the impurity-induced frustration are in a close accord with each other and experiments. The mechanism proposed here should be common to other correlated oxides as well.
The title compound Ba3RuTi2O9 crystallizes with a hexagonal unit cell. It contains layers of edge shared triangular network of Ru4+ (S=1) ions. Magnetic susceptibility chi(T) and heat capacity data show no long range magnetic ordering down to 1.8K. A Curie-Weiss (CW) fitting of chi(T) yields a large antiferromagnetic CW temperature theta_CW=-166K. However, in low field, a splitting of zero field cooled (ZFC) and field cooled (FC) chi(T) is observed below ~30K. Our measurements suggest that Ba3RuTi2O9 is a highly frustrated system but only a small fraction of the spins in this system undergo a transition to a frozen magnetic state below ~30K.
Using spin-polarized low-energy electron microscopy to study magnetization in epitaxial layered systems, we found that the area vs perimeter relationship of magnetic domains in the top Fe layers of Fe/NiO/Fe(100) structures follows a power-law distribution, with very small magnetic domain cutoff radius (about 40 nm) and domain wall thickness. This unusual magnetic microstructure can be understood as resulting from the competition between antiferromagnetic and ferromagnetic exchange interactions at the Fe/NiO interfaces, rather than from mechanisms involving the anisotropy and dipolar forces that govern length scales in conventional magnetic domain structures. Statistical analysis of our measurements validates a micromagnetic model that accounts for this interfacial exchange coupling.
Shape morphing magnetic soft materials, composed of magnetic particles in a soft polymer matrix, can transform shapes reversibly, remotely, and rapidly, finding diverse applications in actuators, soft robotics, and biomedical devices. To achieve on-demand and sophisticated shape morphing, the manufacturing of structures with complex geometry and magnetization distribution is highly desired. Here, we report a magnetic dynamic polymer composite composed of hard-magnetic microparticles in a dynamic polymer network with thermal-responsive reversible linkages, which permit functionalities including targeted welding, magnetization reprogramming, and structural reconfiguration. These functions not only provide highly desirable structural and material programmability and reprogrammability but also enable the manufacturing of structures with complex geometry and magnetization distribution. The targeted welding is exploited for modular assembling of fundamental building modules with specific logics for complex actuation. The magnetization reprogramming enables altering the morphing mode of the manufactured structures. The shape reconfiguration under magnetic actuation is coupled with network plasticity to remotely transform two-dimensional tessellations into complex three-dimensional architectures, providing a new strategy of manufacturing functional soft architected materials such as three-dimensional kirigami. We anticipate that the reported magnetic dynamic polymer provides a new paradigm for the design and manufacturing of future multifunctional assemblies and reconfigurable morphing architectures and devices.
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