Coercive field behavior of permalloy antidot arrays based on self-assembled template fabrication

High-density magnetic antidot arrays have been fabricated by deposition of Fe₂₀Ni₈₀ thin films on self-assembled nanoporous alumina membranes (NAM) with high-order hexagonal symmetry. The magnetic properties induced by the size and the geometry configuration of the holes introduced in a Fe₂₀Ni₈₀ thin film are discussed based on hysteresis loops measured as a function of temperature. The precursor NAMs have pore diameters ranging between 35 and 95 nm (55 and 75 nm after the film deposition) and a lattice parameter of 105 nm. An enormous increase of coercitivity, as compared with the corresponding continuous films, was observed for temperatures between 2 and 300 K. This effect depends on the size and surface density of holes in the Fe₂₀Ni₈₀ antidot arrays. Rutherford backscattering spectrometry (RBS) measurements were performed in order to better clarify the magnetic material that was eventually deposited within the NAM pores.     

Ordered magnetic nanohole and antidot arrays prepared through replication from anodic alumina templates

Highly ordered arrays of Ni nanoholes and Fe₂₀Ni₈₀ antidots have been prepared, respectively, by replica/antireplica processing and sputtering techniques using nanoporous alumina membranes as templates. Geometrical characteristics as nanohole/antidot diameter, interpore distance and the overall hexagonal symmetry of arrays are controlled through the original templates. Experimental data on their hysteresis and magnetic domain structure have been taken by vibrating sample magnetometry and magnetic force microscopy, respectively. An analysis of the magnetization process, resulting magnetic anisotropy and magnetic domain structure is summarized considering the influence of those geometry aspects. In particular, the hexagonal symmetry and the density of nanohole/antidots determine the overall magnetic behavior, which is of interest in future high-density magnetic storage systems.     

Irreducible finite-size effects in the surface free energy of NaCl crystals from crystal-nucleation data

In this Letter we report a simulation study in which we compare the solid-liquid interfacial free energy of NaCl at coexistence, gamma_{LS}, with the value that follows from the height of the homogeneous nucleation barrier. The two estimates differ by more than 100%. Smaller discrepancies are found for gamma_{LS} of hard-sphere and of Lennard-Jones particles. We consider a variety of possible causes for this discrepancy and conclude that it is due to a finite-size effect that cannot be corrected for by any simple thermodynamic procedure. By taking into account the finite-size effects of gamma_{LS} obtained in real nucleation experiments, we obtain quantitative agreement between gamma_{LS} estimated in the simulations and derived from the experiments. Our finding suggests that most published solid-liquid surface free energies derived from nucleation experiments will have to be revised.     

String order and symmetries in quantum spin lattices

We show that the existence of string order in a given quantum state is intimately related to the presence of a local symmetry by proving that both concepts are equivalent within the framework of finitely correlated states. Once this connection is established, we provide a complete characterization of local symmetries in these states. The results allow us to understand in a straightforward way many of the properties of string order parameters, like their robustness or fragility under perturbations and their typical disappearance beyond strictly one-dimensional lattices. We propose and discuss an alternative definition, ideally suited for detecting phase transitions, and generalizations to two and more spatial dimensions.     

The Shapes of Sulfonamides: A Rotational Spectroscopy Study

Benzenesulfonamides are a class of molecules of extreme interest in the biochemical field because many of them are active against a variety of diseases. In this work, the pharmacophoric group benzensulfonamide, its derivatives para-toluensulfonamide and ortho-toluensulfonamide, and the bioactive molecule sulfanilamide, were investigated using rotational spectroscopy to determine their conformations and the influence of different substituents on their structures. For all species, the hyperfine structure due to the ¹⁴N atom was analyzed, and this provided crucial information for the unambiguous identification of the observed conformation of all molecules. In addition, for ortho-toluensulfonamide, the vibration–rotation hyperfine structure related to the methyl torsion was analyzed, and the methyl group rotation barrier was determined. For benzensulfonamide, partial r_S and r₀ structures were established from the experimental rotational constants of the parent and two deuterated isotopic species. In all compounds except ortho-toluensulfonamide, the amino group of the sulfonamide group lies perpendicular to the benzene plane with the aminic hydrogens eclipsing the oxygen atoms. In ortho-toluensulfonamide, where weak attractive interactions occur between the nitrogen lone pair and the methyl hydrogen atoms, the amino group lies in a gauche orientation, retaining the eclipsed configuration with respect to the SO₂ frame. A comparison of the geometrical arrangements found in the PDB database allowed us to understand that the bioactive conformations are different from those found in isolated conditions. The conformations within the receptor are reached with an energy cost, which is balanced by the interactions established in the receptor.     

A Comparative Study of Methyl Methacrylate/Butyl Acrylate Copolymerization Kinetics by Atom‐Transfer and Conventional Radical Polymerization

Methyl methacrylate and butyl acrylate monomers are copolymerized by atom‐transfer radical polymerization, affording polymers with well‐controlled molecular weight and low polydispersity. A kinetic analysis of this system is compared with the corresponding free‐radical polymerization system. The copolymerization rate follows an opposite trend to that observed in conventional copolymerization. This fact is attributed to a smaller population of radicals generated in the reaction, since the relative fraction of propagating radicals is the same as that in classical copolymerization.     

XRD Line Broadening Studies on Mullite

An X-ray diffraction microstructural study on 110, 220, 001 and 111 peaks has been performed on mullite in the temperature range of primary mullite formation in order to monitor nucleation and growth process. Considering the crystallinity of the starting kaolinites, a greater disorder of the kaolinite has been found to enhance the mullite formation. Isothermal growth is related to a decrease in the Al₂O₃ content of mullite.     

On the Formation of Dislocation Hollow Cores on Cleaved {100} Faces of L-Arginine Phosphate Monohydrate Single Crystals

Thermodynamic conditions and energy considerations for the formation of hollow cores at the emergence points of monolayer cleavage steps associated with screw dislocations on the cleaved {100} faces of LAP single crystals are discussed. Analysis of the formation of hollow cores and the change of the curvature of steps in the vicinity of their origins reveals that dislocations responsible for the origin of hollow cores have stress fields due to trapped mother liquor of different supersaturations. The results also show that (1) the radius of a hollow core is inversely proportional to the one-third power of the interface supersaturation while the volume of hollow corés increases exponentially with their radius, and that (2) the strain energy associated with a dislocation is responsible for the formation of an equilibrium hollow core of a particular depth at the origins of cleavage steps associated with dislocations.