Search

A set of GaAs1−xBix/GaAs multilayer quantum-well structures was deposited by metal-organic vapor phase epitaxy at 390 °C and 420 °C. The precursor fluxes were introduced with the intent of growing discrete and compositionally uniform GaAs1−xBix well and GaAs barrier layers in the epitaxial films. High-resolution high-angle annular-dark-field (or “Z-contrast”) scanning transmission electron microscopy imaging revealed concentration profiles that were periodic in the growth direction, but far more complicated in shape than the intended square wave. The observed composition profiles could explain various reports of physical properties measurements that suggest compositional inhomogeneity in GaAs1−xBix alloys as they currently are grown.

GaAs1−zBiz/GaAs1−yPy strained-compensated quantum well (QW) structures for laser applications were grown by metalorganic vapor phase epitaxy. The band offsets for the GaAs1−zBiz/GaAs1−yPy heterojunction were calculated by the density functional theory, and the design of strain-compensated structures was undertaken by the zero stress analysis. The post-growth thermal annealing of the structures dramatically increases the photoluminescence intensity compared to that from as-grown GaAs1−zBiz QW samples. Transmission electron microscopy studies verified layer thicknesses as well as the presence of abrupt interfaces in the annealed GaAs1−zBiz/GaAs1−yPy QW structure. Electroluminescence measurements from ridge-waveguide devices show broad spectral emission characteristics and lasing was not observed up to a current injection of 4 kA cm−2. [ABSTRACT FROM AUTHOR]

Controlled-release, and especially long-acting, drug delivery systems hold promise for improving treatments for numerous medical conditions. Previously, we reported an additive manufacturing or "three-dimensional (3D) printing" approach for fabricating liquid-core-shell-cap microcarriers comprising standard photoresists. Here we explore the potential to extend this strategy to achieve microcarriers comprising biodegradable materials as a new pathway to controlled-release drug delivery options. Specifically, we investigate the use of "Two-Photon Direct Laser Writing (DLW)" as a means to 3D print microcarriers composed of: ( i ) a bottle-shaped "shell" with an orifice, ( ii ) an aqueous liquid "core", and ( iii ) a biodegradable "cap". The cap, which is DLW-printed directly onto the shell's orifice, is designed to degrade over time in the body- e.g ., with degradation time proportional to cap thickness-to ultimately facilitate release of the liquid core at desired time points. Fabrication results based on the use of a biodegradable poly(ethylene glycol) diacrylate (PEGDA) photomaterial for the cap revealed that shell designs incorporating microfluidic obstruction structures appeared to limit undesired entry of the liquid-phase PEGDA into the shell ( i.e ., directly preceding cap printing), thereby resulting in improved retention of the liquid core after completion of the cap printing process. These results mark an important first step toward evaluating the utility of the presented DLW 3D printing strategy for possible drug delivery applications., Competing Interests: CONFLICT OF INTEREST Sharon Flank is Founding CEO of InfraTrac, Inc., which has a potential interest in commercializing the microcarriers presented in this work.

Precession electron diffraction (PED) was used to measure the long-range order parameter in lattice-mismatched AlInP epitaxial films under investigation for solid-state-lighting applications. Both double- and single-variant films grown at 620, 650 and 680 °C were analysed in TEM cross-section. PED patterns were acquired in selected-area-diffraction mode through external microscope control using serial acquisition, which allows inline image processing. The integrated peak intensities from experimental patterns were fit using dynamical simulations of diffraction from the ordered domain structures. Included in the structure-factor calculations were mean atomic displacements of the anions (P) due to ordering, which were found by valence-force-field calculations to have a nearly linear dependence on order parameter. A maximum order parameter of S = 0.36 was measured for a double-variant specimen grown at 650 °C., (© 2021 Royal Microscopical Society.)