We report atomic resolution Z-contrast scanning transmission electron microscopy images that reveal the incorporation of I atoms in the form of helical chains inside single-walled carbon nanotubes. Density functional calculations and topological considerations provide a consistent interpretation of the experimental data. Charge transfer between the nanotube walls and the I chains is associated with the intercalation.
Batteries based on magnesium are an interesting alternative to current state-of-the-art lithium-ion systems; however, high-energy-density cathodes are needed for further development. Here we utilize TEM, EDS, and EELS in addition to soft-XAS to determine electrochemical magnesiation mechanism of a high-energy density cathode, K-αMnO2. Rather than following the typical insertion mechanism similar to Li(+), we propose the gradual reduction of K-αMnO2 to form Mn2O3 then MnO at the interface of the cathode and electrolyte, finally resulting in the formation of K-αMnO2@(Mg,Mn)O core-shell product after discharge of the battery. Understanding the mechanism is a vital guide for future magnesium battery cathodes.
The nucleation pathway for single-wall carbon nanotubes on a metal surface is demonstrated by a series of total energy calculations using density functional theory. Incorporation of pentagons at an early stage of nucleation is energetically favorable as they reduce the number of dangling bonds and facilitate curvature of the structure and bonding to the metal. In the presence of the metal surface, nucleation of a closed cap or a capped single-wall carbon nanotube is overwhelmingly favored compared to any structure with dangling bonds or to a fullerene.
The growth times of single-wall carbon nanotubes ͑SWNT's͒ within a high-temperature laser-vaporization ͑LV͒ reactor were measured and adjusted through in situ imaging of the plume of laser-ablated material using Rayleigh-scattered light induced by time-delayed, 308-nm laser pulses. Short SWNT's were synthesized by restricting the growth time to less than 20 ms for ambient growth temperatures of 760-1100°C. Statistical analysis of transmission electron microscope photographs indicated most-probable lengths of 35-77 nm for these conditions. Raman spectra ͑E ex ϭ1.96 and 2.41 eV͒ of the short nanotubes indicate that they are wellformed SWNT's. The temperature of the particles in the vortex-ring-shaped plume during its thermalization to the oven temperature was estimated by collecting its blackbody emission spectra at different spatial positions inside the oven and fitting them to Planck's law. These data, along with detailed oven temperature profiles, were used to deduce a complete picture of the time spent by the plume at high growth temperatures ͑760-1100°C͒. The upper and lower limits of the growth rates of SWNT's were estimated as 0.6 and 5.1 m/s for the typical nanosecond Nd:YAG laser-vaporization conditions used in this study. These measurements permit the completion of a general picture of SWNT growth by LV based on imaging, spectroscopy, and pyrometry of ejected material at different times after ablation, which confirms our previous measurements that the majority of SWNT growth occurs at times greater than 20 ms after LV by the conversion of condensed phase carbon.
The atomic structures of two symmetric [001] tilt grain boundaries in yttria-stabilized cubic-zirconia, ⌺5 (310) and near-⌺13 (510), are studied by Z-contrast scanning transmission electron microscopy. Both boundaries are composed of periodic arrays of highly symmetric structural units, with a distinct unit for each boundary. Oxygen K-edge electron energy-loss spectra show that the oxygen coordination is similar between the bulk and grain boundary, indicating that oxygen ions within the grain boundary reside in distorted tetrahedral sites. Atomic models of the grain boundaries are proposed that are consistent with the experimental data. The core structures are different from previously studied metal or oxide grain boundaries and are unique to the fluorite structure. Yttrium segregation to the grain boundaries is also investigated by electron energy-loss spectroscopy. Yttrium is found to segregate preferentially to the ⌺5 grain boundary, and the spatial distribution of the segregation layer is confined to within 1 nm of the boundary plane.
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