Publications by authors named "Manfred Wuttig"

Feroxyhite (-FeOOH) nanomaterials were successfully synthesized through the atmospheric AC microplasma method at room temperature from ferrous sulfate aqueous solutions. Various syntheses conditions, including electric voltage, electric field strength, ferrous concentration, hydrogen peroxide concentration, and reaction duration, were systematically investigated. The synthesized products were characterized through x-ray diffraction, UV-vis absorption spectroscopy, photoluminescence spectroscopy, infra-red spectroscopy, and electron microscopy.

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High- molecular magnets have amassed much promise; however, the long-standing obstacle for its practical applications is the inaccessibility of high-temperature molecular magnets showing dynamic and nonvolatile magnetization control. In addition, its functional durability is prone to degradation in oxygen and heat. Here, we introduce a rapid prototyping and stabilizing strategy for high (360 K) molecular magnets with precise spatial control in geometry.

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Recent progress in molecular ferroelectrics (MOFEs) has been overshadowed by the lack of high-quality thin films for device integration. We report a water-based air-processable technique to prepare large-area MOFE thin films, controlled by supersaturation growth at the liquid-air interface under a temperature gradient and external water partial pressure. We used this technique to fabricate ImClO thin films and found a large, tunable room temperature electroresistance: a 20-fold resistance variation upon polarization switching.

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FePd exhibits an anomalously large magnetostriction of ~400 ppm at room temperature as well as linear, isotropic, and hysteresis free magnetization behavior. This near perfectly reversible magnetic response is attributable to the presence of a large number of premartensitic magnetoelastic twin clusters present in the system made possible through the elastic softening that occurs near a martensitic transformation temperature of 252 K. It is proposed that the twin clusters in the material reduce both internal elastic and magnetic energy, causing the elastic and magnetic behavior of the material to be intimately linked.

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Room temperature multiferroics has been a frontier research field by manipulating spin-driven ferroelectricity or charge-order-driven magnetism. Charge-transfer crystals based on electron donor and acceptor assembly, exhibiting simultaneous spin ordering, are drawing significant interests for the development of all-organic magnetoelectric multiferroics. Here, we report that a remarkable anisotropic magnetization and room temperature multiferroicity can be achieved through assembly of thiophene donor and fullerene acceptor.

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Functional shape memory alloys need to operate reversibly and repeatedly. Quantitative measures of reversibility include the relative volume change of the participating phases and compatibility matrices for twinning. But no similar argument is known for repeatability.

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All magnets elongate and contract anisotropically when placed in a magnetic field, an effect referred to as Joule magnetostriction. The hallmark of Joulian magnetostriction is volume conservation, which is a broader definition applicable to self-accommodation of ferromagnetic, ferroelectric or ferroelastic domains in all functional materials. Here we report the discovery of 'giant' non-volume-conserving or non-Joulian magnetostriction (NJM).

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A new type of carbon charge-transfer magnet, consisting of a fullerene acceptor and single-walled carbon nanotube donor, is demonstrated, which exhibits room temperature ferromagnetism and magnetoelectric (ME) coupling. In addition, external stimuli (electric/magnetic/elastic field) and the concentration of a nanocarbon complex enable the tunabilities of the magnetization and ME coupling due to the control of the charge transfer.

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Tetragonal FeCo nanostructures are becoming particularly attractive because of their high magnetocrystalline anisotropy and magnetization achievable without rare-earth elements, . Yet, controlling their metastable structure, size and stoichiometry is a challenging task. In this study, we demonstrate AuCu templated FeCo shell growth followed by thermally induced phase transformation of AuCu core from face-centered cubic to L10 structure, which triggers the FeCo shell to transform from the body-centered cubic structure to a body-centered tetragonal phase.

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The renaissance of multiferroics has yielded a deeper understanding of magneto-electric coupling of inorganic single-phase multiferroics and composites. Here, we report charge-transfer polymeric multiferroics, which exhibit external field-controlled magnetic, ferroelectric, and microwave response, as well as magneto-dielectric coupling. The charge-transfer-controlled ferroic properties result from the magnetic field-tunable triplet exciton which has been validated by the dynamic polaron-bipolaron transition model.

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The structure and properties of the ferromagnet Tb(1-x)Dy(x)Fe(2) are explored through the morphotropic phase boundary (MPB) separating ferroic phases of differing symmetry. Our synchrotron data support a first order structural transition, with a broadening MPB width at higher temperatures. The optimal point for magnetomechanical applications is not centered on the MPB but lies on the rhombohedral side, where the high striction of the rhombohedral majority phase combines with the softened anisotropy of the MPB.

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A substantial magnetoelectric coupling effect of an excitonic all-conjugated block copolymer multiferroics consisting of electronically distinct polythiophene derivatives is reported. The observations open new avenues for the multifunctional all-conjugated block copolymer synthesis and electric field tunable multiferroic devices.

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Chemical and structural heterogeneity and the resulting interaction of coexisting phases can lead to extraordinary behaviours in oxides, as observed in piezoelectric materials at morphotropic phase boundaries and relaxor ferroelectrics. However, such phenomena are rare in metallic alloys. Here we show that, by tuning the presence of structural heterogeneity in textured Co(1-x)Fe(x) thin films, effective magnetostriction λ(eff) as large as 260 p.

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A new class of functional materials with giant nonhysteretic strain responses to applied fields is considered. They are decomposed two-phase systems consisting of single-domain nanoprecipitates of a low-symmetry phase. Their strain response is caused by the field-induced change of structural orientation of the domain states of these precipitates.

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A near-field room temperature scanning magnetic probe microscope has been developed using a laminated magnetoelectric sensor. The simple trilayer longitudinal-transverse mode sensor, fabricated using Metglas as the magnetostrictive layer and polyvinylidene fluoride as the piezoelectric layer, shows an ac field sensitivity of 467+/-3 microV/Oe in the measured frequency range of 200 Hz-8 kHz. The microscope was used to image a 2 mm diameter ring carrying an ac current as low as 10(-5) A.

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Reversibility of structural phase transformations has profound technological implications in a wide range of applications from fatigue life in shape-memory alloys (SMAs) to magnetism in multiferroic oxides. The geometric nonlinear theory of martensite universally applicable to all structural transitions has been developed. It predicts the reversibility of the transitions as manifested in the hysteresis behaviour based solely on crystal symmetry and geometric compatibilities between phases.

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