On the relationship of magnetocrystalline anisotropy and stoichiometry in epitaxial L1(0) CoPt (001) and FePt (001) thin films

Two series of epitaxial CoPt and FePt films, with nominal thicknesses of 42 or 50 nm, were prepared by sputtering onto single-crystal MgO(001) substrates in order to investigate the chemical ordering and the resultant magnetic properties as a function of alloy composition. In the first series, the film composition was kept constant, while the substrate temperature was increased from 144 to 704 degrees C. In the second series the substrate temperature was kept constant at 704 degrees C for CoPt and 620 degrees C for FePt, while the alloy stoichiometry was varied in the nominal range of 40-60-at. % Co(Fe). Film compositions and thicknesses were measured via Rutherford backscattering spectrometry. The lattice and long-range order parameter for the L1(0) phase were obtained for both sets of films using x-ray diffraction. The room-temperature magnetocrystalline anisotropy constants were determined for a subset of the films using torque magnetometry. The order parameter was found to increase with increasing temperature, with ordering occurring more readily in FePt when compared with CoPt. A perpendicular anisotropy developed in CoPt for substrate temperatures above 534 degrees C and in FePt above 321 degrees C. The structure and width of the magnetic domains in CoPt and FePt, as seen by magnetic force microscopy, also demonstrated an increase in magnetic anisotropy with increasing temperature. For the films deposited at the highest temperatures (704 degrees C for CoPt and 620 degrees C for FePt), the order parameter reached a maximum near the equiatomic composition, whereas the magnetocrystalline anisotropy increased as the concentration of Co or Fe was increased from below to slightly above the equiatomic composition. It is concluded that nonstoichiometric L1(0) CoPt and FePt, with a slight excess of Co or Fe, are preferable for applications requiring the highest anisotropies

Stoichiometry-anisotropy connections in epitaxial L1(0) FePt(001) films

The order parameters and anisotropy constants of a series of epitaxial L1(0) FePt films with compositions in the range of 45-55 at. % Fe and nominal thicknesses of 50 nm have been characterized. The films were made by cosputtering the elements onto single crystal MgO(001) substrates. The substrates were coated with 1 nm Pt/1 nm Fe bilayer seeds prior to alloy deposition. Both the bilayer seed and the alloy film were deposited at 620 degreesC. Lattice and order parameters were obtained by x-ray diffraction. Film compositions and thicknesses were determined by Rutherford backscattering spectrometry, and room-temperature magnetocrystalline anisotropies were determined with a torque magnetometer. It was found that the order parameter had a maximum for the film composition closest to the equiatomic composition, whereas the magnetocrystalline anisotropy increased as the Fe content increased from below to slightly above the equiatomic composition. These results imply that nonstoichiometric FePt compositions, with a slight excess of Fe, may in fact be preferred for applications that require high anisotropy

A multistate outbreak of Escherichia coli O157:H7 infections linked to alfalfa sprouts grown from contaminated seeds.

A multistate outbreak of Escherichia coli O157:H7 infections occurred in the United States in June and July 1997. Two concurrent outbreaks were investigated through independent case-control studies in Michigan and Virginia and by subtyping isolates with pulsed-field gel electrophoresis (PFGE). Isolates from 85 persons were indistinguishable by PFGE. Alfalfa sprouts were the only exposure associated with E. coli O157:H7 infection in both Michigan and Virginia. Seeds used for sprouting were traced back to one common lot harvested in Idaho. New subtyping tools such as PFGE used in this investigation are essential to link isolated infections to a single outbreak

General Post-annealing Method Enables High-Efficiency Two-Dimensional Perovskite Solar Cells

Two-dimensional (2D) perovskites, with a formula of (RNH3)2MAn-1PbnI3n+1, have shown impressive photovoltaic device efficiency with improved stability. The operating mechanism of such photovoltaic devices is under debate and the scope of incorporated organic cations (RNH3 +) is limited. We report a general post-annealing method to incorporate a variety of organic cations into 2D perovskites, which demonstrate significant device efficiencies (7-12%). A detailed investigation of the archetypical (C4H9NH3)2MA3Pb4I13 (n = 4) reveals that such perovskites thin films contain multiple 2D phases (i.e., 2D quantum wells, n = 2, 3, 4,...). These phases appear to be distributed with decreasing n values from the top to the bottom of the 2D perovskites thin film, enabling efficient energy transfer in the first 500 ps and possible charge transfer at longer time scale, thereby accounting for high device efficiencies. Our post-annealing method is compatible with ambient condition and only requires relatively low annealing temperature for a very short period of time, offering significant prospects for scalable manufacturing of 2D perovskites solar cells

Spectroscopic and Mechanistic Studies of Heterodimetallic Forms of Metallo-β-lactamase NDM-1

In an effort to characterize the roles of each metal ion in metallo-β-lactamase NDM-1, heterodimetallic analogues (CoCo-, ZnCo-, and CoCd-) of the enzyme were generated and characterized. UV–vis, 1H NMR, EPR, and EXAFS spectroscopies were used to confirm the fidelity of the metal substitutions, including the presence of a homogeneous, heterodimetallic cluster, with a single-atom bridge. This marks the first preparation of a metallo-β-lactamase selectively substituted with a paramagnetic metal ion, Co(II), either in the Zn1 (CoCd-NDM-1) or in the Zn2 site (ZnCo-NDM-1), as well as both (CoCo-NDM-1). We then used these metal-substituted forms of the enzyme to probe the reaction mechanism, using steady-state and stopped-flow kinetics, stopped-flow fluorescence, and rapid-freeze-quench EPR. Both metal sites show significant effects on the kinetic constants, and both paramagnetic variants (CoCd- and ZnCo-NDM-1) showed significant structural changes on reaction with substrate. These changes are discussed in terms of a minimal kinetic mechanism that incorporates all of the data

An instrument for in situ time-resolved X-ray imaging and diffraction of laser powder bed fusion additive manufacturing processes

In situ X-ray-based measurements of the laser powder bed fusion (LPBF) additive manufacturing process produce unique data for model validation and improved process understanding. Synchrotron X-ray imaging and diffraction provide high resolution, bulk sensitive information with sufficient sampling rates to probe melt pool dynamics as well as phase and microstructure evolution. Here, we describe a laboratory-scale LPBF test bed designed to accommodate diffraction and imaging experiments at a synchrotron X-ray source during LPBF operation. We also present experimental results using Ti-6Al-4V, a widely used aerospace alloy, as a model system. Both imaging and diffraction experiments were carried out at the Stanford Synchrotron Radiation Lightsource. Melt pool dynamics were imaged at frame rates up to 4 kHz with a ∼1.1 μm effective pixel size and revealed the formation of keyhole pores along the melt track due to vapor recoil forces. Diffraction experiments at sampling rates of 1 kHz captured phase evolution and lattice contraction during the rapid cooling present in LPBF within a ∼50 × 100 μm area. We also discuss the utility of these measurements for model validation and process improvement

Pressure-induced quenching of the charge-density-wave state observed by x-ray diffraction

We report an x-ray diffraction study on the charge-density-wave (CDW) LaTe$_3$ and CeTe$_3$ compounds as a function of pressure. We extract the lattice constants and the CDW modulation wave-vector, and provide direct evidence for a pressure-induced quenching of the CDW phase. We observe subtle differences between the chemical and mechanical compression of the lattice. We account for these with a scenario where the effective dimensionality in these CDW systems is dependent on the type of lattice compression and has a direct impact on the degree of Fermi surface nesting and on the strength of fluctuation effects

Subsurface Cooling Rates and Microstructural Response during Laser Based Metal Additive Manufacturing

Laser powder bed fusion (LPBF) is a method of additive manufacturing characterized by the rapid scanning of a high powered laser over a thin bed of metallic powder to create a single layer, which may then be built upon to form larger structures. Much of the melting, resolidification, and subsequent cooling take place at much higher rates and with much higher thermal gradients than in traditional metallurgical processes, with much of this occurring below the surface. We have used in situ high speed X-ray diffraction to extract subsurface cooling rates following resolidification from the melt and above the β-transus in titanium alloy Ti-6Al-4V. We observe an inverse relationship with laser power and bulk cooling rates. The measured cooling rates are seen to correlate to the level of residual strain borne by the minority β-Ti phase with increased strain at slower cooling rates. The α-Ti phase shows a lattice contraction which is invariant with cooling rate. We also observe a broadening of the diffraction peaks which is greater for the β-Ti phase at slower cooling rates and a change in the relative phase fraction following LPBF. These results provide a direct measure of the subsurface thermal history and demonstrate its importance to the ultimate quality of additively manufactured materials