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  • 1
    Publication Date: 2016-06-08
    Description: It has been challenging to achieve combined strong magnetoelectric coupling and narrow ferromagnetic resonance (FMR) linewidth in multiferroic heterostructures. Electric field induced large effective field of 175 Oe and narrow FMR linewidth of 40 Oe were observed in FeCoSiB/Si/SiO 2 /PMN-PT heterostructures with substrate clamping effect minimized through removing the Si substrate. As a comparison, FeCoSiB/PMN-PT heterostructures with FeCoSiB film directly deposited on PMN-PT showed a comparable voltage induced effective magnetic field but a significantly larger FMR linewidth of 283 Oe. These multiferroic heterostructures exhibiting combined giant magnetoelectric coupling and narrow ferromagnetic resonance linewidth offer great opportunities for integrated voltage tunable RF magnetic devices.
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 9289-9300 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper presents ion yields resulting from multiphoton ionization and fragmentation of gaseous toluene (C7H8) in the focus of an 80 fs Ti:sapphire laser beam (λ=800 nm) with a sufficiently small B-integral [Siegman, Lasers (University Science Books, Mill Valley, CA, 1986)]. The peak intensity was varied between 1.9×1013 and 2.8×1014 W cm−2, and both linear and circular polarization were used. Over the whole range of intensities studied, only the singly charged parent ion and its fragment, C7H7+, are found. Although the Keldysh adiabaticity parameter equals 0.86 for the saturation intensity of ∼1×1014 W cm−2, there is no indication of tunneling. The parent ion yield is found to be effectively proportional to the sixth power of the peak intensity. This is shown to be in good agreement with a multiple lowest-order perturbation multiphoton ionization model which takes into account successive channel closing for increasing peak intensities and orders up to 11 inclusive. On the assumption that the excess energy acquired by the toluene cation as a result of the interaction with the electromagnetic field is of the order of the ponderomotive energy for the intensity prevailing at the moment of the ionization, the internal energy distribution of the toluene cations created that is brought about by this multiple-order multiphoton ionization model is calculated. This internal energy distribution is in perfect agreement with the measured C7H7+ yield, if the rate-energy curve for the fragmentation of excited toluene cations as given by Golovin et al. [Sov. J. Chem. Phys. 2, 632 (1985)] is moderately reduced by a factor of 4.5. © 2000 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 8226-8230 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The influence of confinement on morphology formation in copolymer systems is an important area of interest in theoretical research. We apply dynamic density functional theory to investigate the effect of pores on the morphology formation in a symmetric diblock copolymer system. The pore is represented by a perfect cylindrical tube. Porous systems are important in biology and are gaining interest for applications in nanotechnology. We show that for the pore sizes under investigation two equilibrium morphologies are possible depending on the surface interaction: a perpendicular or slab morphology and a parallel or multiwall tube morphology. The latter is referred to in the article as dartboard morphology. In the dynamic pathway towards this morphology an intermediate metastable helical phase is found. An important observation is that, for a wide range of pore radii and variations of polymer chain length, no mixed parallel/perpendicular morphologies were found: All observed morphologies are insensitive to the pore diameter. © 2001 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 744-753 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Using the photo-electron-product-ion-coincidence method (PEPICO) we have measured state-selective cross sections for the following processes: (A) N+2(X,A;v)+H2→N2H++H, (B) H+2(X;v)+N2→N2H++H, (C) N+2(X,A;v)+H2→H+2+N2, and (D) H2+(X;v)+N2→N2++H2. The measurements were performed at thermal velocities (Ec.m.≈40 meV). We have found that the charge transfer processes (C) and (D) have cross sections that are at least an order of magnitude smaller than the cross sections for the rearrangement processes (A) and (B). The cross section for reaction (A) with N2+(A;v) as reactant is found to be (50.2±2.4)% of the cross section for the same reaction with N2+(X;v) as reactant. The cross section for reaction (B) is found to be independent of the internal energy of the reactant ion. The measured variation of the cross sections as a function of the internal energy of the reacting ion is compared with calculations based on a RRKM type statistical model and an electronic correlation diagram of the (N2–H2)+ system. Excellent agreement is found, indicating complete randomization of internal energy within the collision complex. Absolute cross sections are determined for the rearrangement reactions: for reaction (A) the cross section is 76.1 A(ring)2 starting with N2+(X;v=0,1) and 38.05 A(ring)2 starting with N2+(A;v=0–5). For reaction (B) the cross section is 114 A(ring) 2 for H2+(X;v=0–6). © 1995 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 5121-5136 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The H2+LiF(001) system was used to investigate the performance of the hybrid close-coupling wave packet (CCWP) method and of a symmetry adapted, fully close-coupled wave packet (SAWP) method for a molecule–surface problem characterized by fairly high corrugation. In the calculations, a realistic, φ-dependent model potential was used. The calculations were performed for a collision energy of 0.2 eV, with H2 initially in its j=0 rotational state at normal incidence to the surface. Large increases in the computational efficiencies of both wave packet methods were achieved by taking advantage of the potential coupling matrices associated with both methods becoming sparser with increasing molecule–surface distance. For the present model problem and employing this increased sparseness at longer range, the SAWP method is faster than the CCWP method by a factor of 2. The potential usefulness of the SAWP method for dissociative chemisorption problems is discussed. © 1995 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 7850-7855 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: For the two reactive systems, NH3+(Eint)+N H3→NH4++NH2 and H2+(Eint)+H2→H3++H, for which the relative cross sections were measured earlier in our group for Ec.m.≈40 meV we calculated the relative cross section as a function of internal energy using the statistical Rice–Ramsperger–Kassel–Marcus (RRKM) theory that implicitly conserves total energy and total angular momentum. We found satisfactory agreement between theory and experiment by imposing rather mild constraints upon the loose transition state configuration. These constraints involve inactive vibrations and steric hindrance. The steric hindrance imposed in case of the (NH3–NH3)+ system is interpreted as being due to the anisotropic interaction of the ionic charge with the permanent electric dipole of the respective neutral collision partner in the two dissociation channels. We cannot be absolutely sure that the specific combination of modifications we propose for each of the two systems is the only one that agrees well with experiment. However, we find it striking that an agreement can be obtained by such weak and physically meaningful modifications, and we take this as a strong indication that the two studied systems do behave statistical. © 1995 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 5512-5524 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have investigated the performance of a fully close-coupled wave packet method and its symmetry-adapted version for a model problem of H2 scattering from LiF(001). The computational cost of the fully close-coupled methods scales linearly with the number of rotation-diffraction states present in the basis set, provided that the sparseness of the potential coupling matrix is taken into account. For normal incidence, the symmetry adapted version is faster than the conventional close-coupling wave packet method by almost an order of magnitude. An extension of the method to more realistic molecule-surface problems is considered. © 1995 American Institute of Physics.
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  • 8
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The magnetic structure of nanoscale alloy films has been probed using the magnetic x-ray linear dichroism in photoelectron spectroscopy. FeNi and CoFe epitaxial films were grown on Cu(001), in situ and using molecular beam epitaxy techniques. The magnetic x-ray linear dichroism measurements were made at the Spectromicroscopy Facility of the Third Generation Advanced Light Source. Because soft x-rays were used to generate photoemission from the 3p core levels, both elemental selectivity and magnetic sensitivity were achieved simultaneously. © 1996 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 2250-2256 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dynamic mean-field density functional method is adapted to describe phase separation in the presence of geometrical constraints. We observe that inclusion of small filler particles (such as rods) already has a dramatic effect on the morphology of polymer melts. The effect is comparable to the effect of applied simple steady shear. Mesostructures in the presence of large filler particles such as plates are totally governed by the geometry of the particle. Effects of polymer–surface interactions on morphology formation are investigated in detail. © 1999 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 8751-8754 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The first three-dimensional (3D) simulation of meso-phase formation in a specific polymer system—55% aqueous solution of the triblock polymer surfactant (EO)13(PO)30(EO)13—under simple steady shear is performed. The method is based on dynamic mean-field density functional theory. The hexagonal phase is investigated. The simulations reproduce recent experimental observations on the same polymer system. © 1998 American Institute of Physics.
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