Elemental Analysis and Fine Structure of Mitochondrial Granules in Growth Plate Chondrocytes Studied by Electron Energy Loss Spectroscopy and Energy Dispersive X-Ray Microanalysis

Electron energy loss spectrometry - EELS, and energy dispersive X-ray microanalysis - XRMA, were used to study the elemental composition of mitochondrial dense granules - mdg. The study was performed on dry cut thin sections (80-200 nm) of freeze-dried and low temperature embedded cartilage. Results obtained by means of XRMA clearly showed high phosphorus and calcium content in the mdg. Using EELS at 100 kV primary voltage we found that small concentrations of elements (i.e. below typically 1% atomic weight) are difficult to analyze and map, this especially in sections thicker than 50-60 nm. Surprisingly, analysis of calcium can be successfully performed on thicker sections though the edge lies above the carbon K edge while this is not possible for the phosphorus edge which is located at lower energies. This is likely due to the edge shapes (sharp for calcium and delayed for phosphorus), and to the more intense contribution of multiple low loss scattering in the background for phosphorus between 100 and 130 eV. By means of EELS elemental mapping a centrally located core was found in numerous mdg. In the calcium map the signal was strongest in the middle of mdg which corresponds to the area of reduced carbon signal. We found that carbon maps might be used for high resolution structural studies of chemically unfixed and anhydrously processed biological tissues. As carbon is the main constituent of Lowicryl resin its distribution is reversed to the distribution of biological tissue in which the proportion of carbon is lower, but is proportional to water content in the specimen in vivo. Use of EELS in combination with electron microscope with accelerating voltages in range of 140-200 kV together with anhydrous techniques of the tissue preparation will provide a new type of information which might lead to better understanding of the etiology and function of small structures in the cell

Electron energy loss spectroscopy determination of Ti oxidation state at the (001) LaAlO3/SrTiO3 interface as a function of LaAlO3 growth conditions

At the (001) interface between the two band-insulators LaAlO3 and SrTiO3, a high-mobility electron gas may appear, which has been the object of numerous works over the last four years. Its origin is a subject of debate between the interface polarity and unintended doping. Here we use electron energy loss 'spectrum images', recorded in cross-section in a scanning transmission electron microscope, to analyse the Ti3+ ratio, characteristic of extra electrons. We find an interface concentration of Ti3+ that depends on growth conditions.Comment: 6 page

Spectroscopic mapping of local structural distortions in ferroelectric PbTiO3/SrTiO3 superlattices at the unit-cell scale

The local structural distortions in polydomain ferroelectric PbTiO3/SrTiO3 superlattices are investigated by means of high spatial and energy resolution electron energy loss spectroscopy combined with high angle annular dark field imaging. Local structural variations across the interfaces have been identified with unit cell resolution through the analysis of the energy loss near edge structure of the Ti-L2,3 and O-K edges. Ab-initio and multiplet calculations of the Ti-L2,3 edges provide unambiguous evidence for an inhomogeneous polarization profile associated with the observed structural distortions across the superlattice.Comment: 5 pages, 4 figure

Ab initio study of bilateral doping within the MoS2-NbS2 system

We present a systematic study on the stability and the structural and electronic properties of mixed molybdenum-niobium disulphides. Using density functional theory we investigate bilateral doping with up to 25 % of MoS2 (NbS2) by Nb (Mo) atoms, focusing on the precise arrangement of dopants within the host lattices. We find that over the whole range of considered concentrations, Nb doping of MoS2 occurs through a substitutional mechanism. For Mo in NbS2 both interstitial and substitutional doping can co-exist, depending upon the particular synthesis conditions. The analysis of the structural and electronic modifications of the perfect bulk systems due to the doping is presented. We show that substitutional Nb atoms introduce electron holes to the MoS2, leading to a semiconductor-metal transition. On the other hand, the Mo doping of Nb2, does not alter the metallic behavior of the initial system. The results of the present study are compared with available experimental data on mixed MoS2-NbS2 (bulk and nanoparticles).Comment: 7 pages, 6 figure

From early to present and future achievements of EELS in the TEM

This paper reviews the implementation of Electron Energy Loss Spectroscopy (EELS) in a Transmission Electron Microscope (TEM), as an essential tool for advanced analytical studies, exhibiting a unique level of performance in terms of spatial resolution down to the interatomic distances for imaging and sensitivity down to the single atom for elemental identification. In terms of spectral resolution, it offers access with a resolution as good as a few meV, to a very broad spectral domain extending from tens of meV (in the IR) up to a few keV (in the X-ray). This new generation of instrument (EELS+(S)TEM) is now routinely used to investigate the structural, spectral, electronic and chemical properties of a wide range of materials and to broaden spectacularly the field of novel information which it provides. A first part of the paper describes the major progress in advanced instrumentation brought by the novel pieces of equipment (spectrometers, monochromators, aberration correctors and detectors) together with the newly elaborated tools for the acquisition and processing of huge data collections. The second part is devoted to the description of the information contained in a global EELS spectrum: (i) from the core-loss domain implying excitations from inner-shell atomic electrons and its application in elemental, chemical and electronic mapping; (ii) from the low-energy domain exhibiting individual or collective excitations of the valence and conduction electron gas, with its most recent developments in band gap mapping and nanoplasmonics; (iii) in the ultra-low energy domain, which is now in its infancy, the surface collective electron excitations, molecular bonds and the vibrations of phonons at surfaces and in the bulk of nanostructures. The third part is devoted to the exploration of unconventional domains of applications, which in many cases associate the EELS acquisition with the generation and the capture of other signals in various environments, in situ operation (temperature, pressure...), absorption or generation of photons (cathodoluminescence, X-ray emission), acquisition and handling of multidimension data (space, energy, momentum, time). In conclusion, EELS fifty years after its first recognition as a useful actor in the development and promotion of the analytical microscopy, has nowadays become an essential tool for the acquisition of many physical parameters with ultimate resolution, thus opening new routes in nanophysics to be explored

The impact of EELS in materials science

This summary paper emphasizes the highlights of the workshop which are particularly relevant for applications in materials science. It reviews progress in EELS instrumentation, data recording and processing, and in the use and interpretation of EELS fine structures. We point out the possibilities of EELS as a local analytical tool, discuss EELS detection limits, and indicate potential fields of applications for EELS fine structure studies