Submicron (100–500 nm) room-temperature ferromagnets of MnAs have been successfully incorporated into GaAs semiconductor substrates by Mn+ ion implantation and subsequent heat treatment at 920 °C for 1 s in a nitrogen gas. Atomic force microscopy indicates an epitaxial relation of [0001] oriented hexagonal MnAs crystallites on (001) GaAs substrates: [11 2̄0]MnAs∥[110]GaAs. A stronger shape anisotropy along [110]GaAs is observed for the smaller crystallites. Magnetic characterizations by superconducting quantum interference device reveal uniaxial in-plane magnetic anisotropy of the sample. Magnetic force microscopy imaging shows that the uniaxial magnetic anisotropy comes from the alignment of magnetic dipoles along the magnetic easy [11 2̄0] axis of MnAs, which is parallel to [110]GaAs.
Quantum information processing requires quantum registers based on coherently interacting quantum bits. The dipolar couplings between nitrogen vacancy (NV) centres with nanometre separation makes them a potential platform for room-temperature quantum registers. The fabrication of quantum registers that consist of NV centre arrays has not advanced beyond NV pairs for several years. Further scaling up of coupled NV centres by using nitrogen implantation through nanoholes has been hampered because the shortening of the separation distance is limited by the nanohole size and ion straggling. Here, we demonstrate the implantation of C 5 N 4 H n from an adenine ion source to achieve further scaling. Because the C 5 N 4 H n ion may be regarded as an ideal point source, the separation distance is solely determined by straggling. We successfully demonstrate the fabrication of strongly coupled triple NV centres. Our method may be extended to fabricate small quantum registers that can perform quantum information processing at room temperature.
Neutron scattering measurements were carried out for liquid Se, liquid Te, and liquid Te50Se50. The results are discussed in the context of semiconductor-to-metal transition. As to liquid Te50Se50, the vibrational modes show a remarkable change when the semiconductor-to-metal transition occurs by temperature increase. A soft stretching mode was observed for the metallic phase and it shows the structural change; the appearance of long bonds in the metallic phase. The vibrational modes for liquid Se and liquid Te were obtained and agreed well with former works. The crossover from collective to single-particle-like regime was also observed for all liquid samples and the transition ranges (Q=4.5–8 Å−1) are presented. The diffusive features in the low-Q region and single-particle-like properties in the high-Q region are discussed and are shown to be consistent with the results for the vibrational modes.
Inelastic x-ray scattering measurements on liquid Bi were carried out. Prominent acoustic mode excitations were observed in the dynamic structure factor to beyond 12 nm −1 , which resolves previously conflicting results as to their presence beyond 6 nm −1 . We find the dispersion curve of the excitation energy with momentum transfer is nearly flat from 7 to 15 nm −1 consistent with ab initio calculations of liquid Bi [J. Souto et al., Phys. Rev. B 81, 134201 (2010)]. Our ab initio and classical molecular dynamics simulations suggest that a long-range force is needed to reproduce the flatness of the dispersion curve, and the long-range force is correlated with a local structure consisting of shorter and longer bonds in the liquid.
In small-angle X-ray scattering from highly oriented pyrolytic graphite, radial streak patterns are observed. The streaks change their direction with sample rotation and appear and disappear in pairs. This streak pattern can be explained by double Bragg scattering. The directions of the streaks calculated as functions of the rotation angle are in good agreement with experiment. In addition, asymmetry in the intensity of the streaks and a small deviation from the radial pattern are observed, and they can be explained by the finite sample-size effect. The necessity of taking double Bragg scattering into account in small-angle X-ray scattering studies of crystalline materials is emphasized. research papers J. Appl. Cryst. (2016). 49, 835-844 Yoshinori Ohmasa et al. Double Bragg scattering in HOPG 837
This study reports that high fluence fullerene ion (C60+) irradiation of 1–6 MeV, which was made possible by a new-type of high-flux ion source, elongates metal nanoparticles (NPs) in amorphous SiO2 as efficiently as swift heavy ions (SHIs) of 200 MeV Xe14+, i.e., two orders of the magnitude higher energy ions. Comparing the irradiation effects induced by both the beams, the stopping processes of C60 ions in SiO2 are discussed in this paper. Despite of having almost the same elongation efficiency, the C60+ irradiation induced ~10 times more efficient sputtering due to the clustering enhancement and/or the synergy effect. Ion tracks of ~10.4 nm in diameter and 60–80 nm in length were observed in crystalline SiO2 under 4 MeV C60 irradiation. While the track diameter was comparable to those by SHIs of the same electronic stopping, much shorter track lengths than those predicted by a rigid C60 molecule model indicates that the fragmentation occurred due to nuclear collisions. The elongation of the metal NPs was induced only down to the depth where the tracks were observed but not beyond.
Articles you may be interested inSecondary ion counting for surface-sensitive chemical analysis of organic compounds using time-of-flight secondary ion mass spectroscopy with cluster ion impact ionization Rev. Sci. Instrum. 82, 033101 (2011); 10.1063/1.3541799Time-of-flight secondary ion mass spectroscopy analysis of Na adatoms interacting with water-ice film Surface composition and morphology of polyimidesiloxane copolymers with short polydimethylsiloxane segments studied by electron spectroscopy for chemical analysis and time-of-flight secondary ion mass spectrometry Determination of trace metallic impurities on 200-mm silicon wafers by time-of-flight secondary-ion-mass spectroscopy J. Vac. Sci. Technol. B 15, 1908 (1997; 10.1116/1.589577 Thermal desorption spectroscopy and molecular beam time-of-flight studies of silicon wafer ultraviolet/ozone cleaning J.
Nanostructures composed of conjugated polymers or π-conjugated molecules provide sensing platforms with large specific surface areas. One of the feasible approaches to accessing such nanostructured miniaturized sensors with ultrahigh sensitivity is to develop a network of organic nanowires with optical/electronic properties that can measure signals upon interacting with the analytes at their surfaces. In this work, organic nanowires with controlled number density and uniform length were fabricated by one-dimensional solid-state polymerization of 9,9'-spirobi[9 H-fluorene] (SBF) derivatives triggered by high-energy single particles. SBF was chosen as a conjugated molecular motif with the interplay of high density of π-electrons, high solubility, and uniform solid-state structures, allowing us to fabricate sensing platforms via solution processing. The as-deposited energy density in linear polymerization nanospace was theoretically analyzed by a collision model, interpreting nanowire sizes at subnanometer levels. The substitution of bromine atoms was confirmed to be effective not only for the higher collision probability of the incident particles but also for the remarkable increase in radiolytic neutral radical yield via C-Br cleavages or electron-dissociative attachments onto the bromine atoms. The fluorescence spectra of SBF-based nanowires were different from those of SBF derivatives due to extended bond formation as a result of polymerization reactions. Fluorescence was quenched by the addition of nitrobenzene, indicating the potential use of our nanowires for fluorometric sensing applications. Microwave-based conductivity measurements revealed that the SBF-based nanowires exhibited charge carrier transport property upon photoexcitation, and that the conductivity was changed upon treatment with nitrobenzene vapors. The presented strategy of bromination of aromatic rings for efficient fabrication of controlled nanowire networks with favorable fluorescent and charge transport properties of nanowires advances the development of nanostructured sensing systems.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.