RESUMEN
Semiconducting quantum dots (QDs) have potential applications in light-emitting diodes, single-photon sources and quantum computing due to shape-dependent (opto) electronic properties. Atomic resolution 3D-structure determination is important in understanding growth kinetics and improving device performance. 3D-reconstruction of large QDs was reported using characterization techniques like atomic force microscopy, atom probe tomography and tilt series electron tomography, but, still, atomic resolution tomography of QDs, especially those sized below 10 nm, is a challenge. Inline-3D-holography is an emerging and promising technique to perform atomic resolution tomography at low electron doses. In the present study, atomically resolved 3D structures of QDs were reconstructed using inline-3D-holography, implemented on InN QDs (<10 nm) grown on a Si substrate. The residual amorphous glue distorts the exit surface geometry; hence an error correction method was proposed. This is the first experimental evidence of pre-pyramid shaped 3D structure of QDs sized below 10 nm that supports theoretical predictions.
RESUMEN
Nanoparticles have a wide range of applications due to their unique geometry and arrangement of atoms. For a precise structure-property correlation, information regarding atomically resolved 3D structures of nanoparticles is utmost beneficial. Though modern aberration-corrected transmission electron microscopes can resolve atoms with the sub-angstrom resolution, an atomic-scale 3D reconstruction of a nanoparticle using Scanning Transmission Electron Microscopy (STEM) based tomographic method faces hurdles due to high electron irradiation damage and "missing-wedge". Instead, inline 3D holography based tomographic reconstructions from single projection registered at low electron doses is more suitable for defining atomic positions at nanostructures. Nanoparticles are generally supported on amorphous carbon film for Transmission Electron Microscopy (TEM) experiments. However, neglecting the influence of carbon film on the tomographic reconstruction of the nanoparticle may lead to ambiguity. To address this issue, the effect of amorphous carbon support was quantitatively studied using simulations and experiments and it was revealed that increasing thickness and/or density of carbon support increases distortion in tomograms.
RESUMEN
Biocompatible ß-type Ti alloys with high ultimate tensile strength (UTS) and yield strength are potential candidates for certain orthopedic and cardiovascular implants. Aiming for these applications, Ti alloy with 14 wt % Mn (Ti-14 Mn) as ß-stabilizer was processed through thermomechanical treatment along with solutionizing and quenching, followed by 95% cold rolling, which resulted in ultrahigh UTS and yield strength. 3-[4,5-Dimethylthiazol-2-yl]-2,5-diphenyltetrazolimbromide assay with different cell lines suggests efficient cell growth on alloy surface without compromising biocompatibility. Cell adhesion and spreading assay show that cells are not only able to attach to the alloy surface but also able to spread and grow with normal morphology, which projects this material as a potential candidate for biomedical application. Previous studies on binary ß-type Ti alloy systems treated with the above-mentioned processing route confirm the presence of nanoscale phase separation, which enhances its mechanical properties. To discover the same phenomena in the alloy of the present study, bright-field and high-resolution transmission electron microscopy (HRTEM) imaging experiments were performed and nanoscale contrast-modulated lamella regions were observed. Geometrical phase analysis on complex-valued exit wave, reconstructed using focal series HRTEM images, demonstrates that the lamella is a result of d-spacing modulation. Ab initio calculation indicates that d-spacing modulation with the same crystal structure occurs due to composition modulation and was proved by scanning transmission electron microscopy imaging coupled with quantitative energy-dispersive X-ray spectroscopy. Correlating contrast, strain, and composition modulation confirms nanoscale phase separation, which is the first report of this phenomenon in Ti-Mn alloy system.