Voltage-controlled spin electronics is crucial for continued progress in information technology. It aims at reduced power consumption, increased integration density and enhanced functionality where non-volatile memory is combined with highspeed logical processing. Promising spintronic device concepts use the electric control of interface and surface magnetization. From the combination of magnetometry, spin-polarized photoemission spectroscopy, symmetry arguments and first-principles calculations, we show that the (0001) surface of magnetoelectric Cr 2 O 3 has a roughness-insensitive, electrically switchable magnetization. Using a ferromagnetic Pd/Co multilayer deposited on the (0001) surface of a Cr 2 O 3 single crystal, we achieve reversible, room-temperature isothermal switching of the exchange-bias field between positive and negative values by reversing the electric field while maintaining a permanent magnetic field. This effect reflects the switching of the bulk antiferromagnetic domain state and the interface magnetization coupled to it. The switchable exchange bias sets in exactly at the bulk Néel temperature.S pintronics strives to exploit the spin degree of freedom of electrons for an advanced generation of electronic devices 1,2 . In particular, voltage-controlled spin electronics is of vital importance to continue progress in information technology. The main objective of such an advanced technology is to reduce power consumption while enhancing processing speed, integration density and functionality in comparison with presentday complementary metal-oxide-semiconductor electronics [3][4][5][6] . Almost all existing and prototypical solid-state spintronic devices rely on tailored interface magnetism, enabling spin-selective transmission or scattering of electrons. Controlling magnetism at thin-film interfaces, preferably by purely electrical means, is a key challenge to better spintronics [7][8][9][10] . The absence of direct coupling between magnetization and electric field makes the electric control of collective magnetism in general, and surface and interface magnetism in particular, a scientific challenge. The significance of controlled interface magnetism started with the exchange-bias effect. Exchange bias is a coupling phenomenon at magnetic interfaces that manifests itself most prominently in the shift of the ferromagnetic hysteresis loop along the magnetic-field axis and is quantified by the magnitude µ 0 H EB of the shift 11 . The exchange-bias pinning of ferromagnetic thin films is employed in giant magnetoresistance and tunnelling magnetoresistance structures of magnetic-field sensors and modern magnetic read heads 12 . Electric control of exchange bias has been proposed for various spintronic applications that go beyond giant magnetoresistance and tunnelling magnetoresistance technology 5 . One approach to such voltage control requires a reversible, laterally uniform, isothermal electric tuning of the exchange-bias field at room temperature, which remains a significant challenge.Early attemp...
Objective The purpose of this study was to reveal the effectiveness of non-thermal atmospheric plasma brush in surface wettability and modification of four dental substrates. Methods Specimens of dental substrates including dentin, enamel, and two composites Filtek Z250, Filtek LS Silorane were prepared (~2 mm thick, ~10 mm diameter). The prepared surfaces were treated for 5–45 s with a non-thermal atmospheric plasma brush working at temperatures from 36 to 38 °C. The plasma-treatment effects on these surfaces were studied with contact-angle measurement, X-ray photoemission spectroscopy (XPS) and scanning electron microscopy (SEM). Results The non-thermal atmospheric argon plasma brush was very efficient in improving the surface hydrophilicity of four substrates studied. The results indicated that water contact angle values decreased considerably after only 5 s plasma treatment of all these substrates. After 30 s treatment, the values were further reduced to <5°, which was close to a value for super hydrophilic surfaces. XPS analysis indicated that the percent of elements associated with mineral in dentin/enamel or fillers in the composites increased. In addition, the percent of carbon (%C) decreased while %O increased for all four substrates. As a result, the O/C ratio increased dramatically, suggesting that new oxygen-containing polar moieties were formed on the surfaces after plasma treatment. SEM surface images indicated that no significant morphology change was induced on these dental substrates after exposure to plasmas. Significance Without affecting the bulk properties, a super-hydrophilic surface could be easily achieved by the plasma brush treatment regardless of original hydrophilicity/hydrophobicity of dental substrates tested.
We have fabricated a new class of diode from two different polytypes of boron carbide. Diodes were fabricated by chemical vapour deposition from two different isomers of closo-dicarbadodecaborane: closo-1,2-dicarbadodecaborane (orthocarborane, C 2 B 10 H 12) and closo-1,7-dicarbadodecaborane (metacarborane, C 2 B 10 H 12), differing only by the carbon placement within the icosahedral cage. We find that the electronic structure (molecular orbitals) of these two isomer molecules and the resulting decomposition reflect the tendency of metacarborane to form an n-type semiconductor while orthocarborane is an effective source compound for a slightly p-type semiconducting boron carbide. The diodes of this novel class are effective solid state neutron detectors, and have a number of unique applications.
Detection of neutrons, at high total efficiency, with greater resolution in kinetic energy, time and/or real-space position, is fundamental to the advance of subfields within nuclear medicine, high-energy physics, non-proliferation of special nuclear materials, astrophysics, structural biology and chemistry, magnetism and nuclear energy. Clever indirect-conversion geometries, interaction/transport calculations and modern processing methods for silicon and gallium arsenide allow for the realization of moderate- to high-efficiency neutron detectors as a result of low defect concentrations, tuned reaction product ranges, enhanced effective omnidirectional cross sections and reduced electron-hole pair recombination from more physically abrupt and electronically engineered interfaces. Conversely, semiconductors with high neutron cross sections and unique transduction mechanisms capable of achieving very high total efficiency are gaining greater recognition despite the relative immaturity of their growth, lithographic processing and electronic structure understanding. This review focuses on advances and challenges in charged-particle-based device geometries, materials and associated mechanisms for direct and indirect transduction of thermal to fast neutrons within the context of application. Calorimetry- and radioluminescence-based intermediate processes in the solid state are not included.
Recent advances in thin-film deposition techniques, such as molecular beam epitaxy and pulsed laser deposition, have allowed for the manufacture of heterostructures with nearly atomically abrupt interfaces. Although the bulk properties of the individual heterostructure components may be well-known, often the heterostructures exhibit novel and sometimes unexpected properties due to interface effects. At heterostructure interfaces, lattice structure, stoichiometry, interface electronic structure (bonding, interface states, etc.), and symmetry all conspire to produce behavior different from the bulk constituents. This review discusses why knowledge of the electronic structure and composition at the interfaces is pivotal to the understanding of the properties of heterostructures, particularly the (spin polarized) electronic transport in (magnetic) tunnel junctions.
Proximity-induced superconductivity in a 3D topological insulator represents a new avenue for observing zero-energy Majorana fermions inside vortex cores. Relatively small gaps and low transition temperatures of conventional s-wave superconductors put the hard constraints on these experiments. Significantly larger gaps and higher transition temperatures in cuprate superconductors might be an attractive alternative to considerably relax these constraints, but it is not clear whether the proximity effect would be effective in heterostructures involving cuprates and topological insulators. Here, we present angle-resolved photoemission studies of thin Bi2Se3 films grown in-situ on optimally doped Bi2Sr2CaCu2O 8+δ substrates that show the absence of proximity-induced gaps on the surfaces of Bi2Se3 films as thin as a 1.5 quintuple layer. These results suggest that the superconducting proximity effect between a cuprate superconductor and a topological insulator is strongly suppressed, likely due to a very short coherence length along the c-axis, incompatible crystal and pairing symmetries at the interface, small size of the topological surface state's Fermi surface and adverse effects of a strong spin-orbit coupling in the topological material.
We compare the adsorption, bonding, and electronic structure of closo-1,2 dicarbadodecaborane (orthocarborane, C2B10H12) and closo-1,7 dicarbadodecaborane (metacarborane, C2B10H12) on metal surfaces. The electronic structure (molecular orbitals) of these two isomer molecules are calculated to be very similar, but there are significant differences in the experimental binding energies for each isomer as an adsorbed species. Metacarborane adsorbs on both Co and Au with the Fermi level (chemical potential) placed closer to the lowest unoccupied molecular orbital than is observed with orthocarborane adsorbed on Co and Cu.
Abstract:The molecular orbitals of 1, 1′-biphenyl-4,4′-dimethyldithiol (HS-CH 2 -C 6 H 4 -C 6 H 4 -CH 2 -SH) are identified from combined photoemission and inverse photoemission studies and compared with theory for several different surfaces, molecular conformations and molecular orientations. The preferential molecular orientations of biphenyldimethyldithiol, on both Au(111) and polycrystalline Co, are identified from polarization resolved photoemission studies. Two different molecular orientations are adopted by biphenyldimethyldithiol on gold depending on adsorption conditions. Biphenyldimethyldithiol is observed to bond more strongly to cobalt than gold surfaces.
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