X-ray mapping without STEM

Author(s):  
Judith M. Brock ◽  
Max T. Otten

A knowledge of the distribution of chemical elements in a specimen is often highly useful. In materials science specimens features such as grain boundaries and precipitates generally force a certain order on mental distribution, so that a single profile away from the boundary or precipitate gives a full description of all relevant data. No such simplicity can be assumed in life science specimens, where elements can occur various combinations and in different concentrations in tissue. In the latter case a two-dimensional elemental-distribution image is required to describe the material adequately. X-ray mapping provides such of the distribution of elements.The big disadvantage of x-ray mapping hitherto has been one requirement: the transmission electron microscope must have the scanning function. In cases where the STEM functionality – to record scanning images using a variety of STEM detectors – is not used, but only x-ray mapping is intended, a significant investment must still be made in the scanning system: electronics that drive the beam, detectors for generating the scanning images, and monitors for displaying and recording the images.

Author(s):  
T. Yaguchi ◽  
M. Konno ◽  
T. Kamino ◽  
M. Ogasawara ◽  
K. Kaji ◽  
...  

Abstract A technique for preparation of a pillar shaped sample and its multi-directional observation of the sample using a focused ion beam (FIB) / scanning transmission electron microscopy (STEM) system has been developed. The system employs an FIB/STEM compatible sample rotation holder with a specially designed rotation mechanism, which allows the sample to be rotated 360 degrees [1-3]. This technique was used for the three dimensional (3D) elemental mapping of a contact plug of a Si device in 90 nm technology. A specimen containing a contact plug was shaped to a pillar sample with a cross section of 200 nm x 200 nm and a 5 um length. Elemental analysis was performed with a 200 kV HD-2300 STEM equipped with the EDAX genesis Energy dispersive X-ray spectroscopy (EDX) system. Spectrum imaging combined with multivariate statistical analysis (MSA) [4, 5] was used to enhance the weak X-ray signals of the doped area, which contain a low concentration of As-K. The distributions of elements, especially the dopant As, were successfully enhanced by MSA. The elemental maps were .. reconstructed from the maps.


2021 ◽  
Author(s):  
Kadriye Ozlem saygi ◽  
Birgul Kacmaz ◽  
Serdar Gul

Abstract Bacterial infections are one of the most serious health problems all over the world, which cause need for the discovery of new drug. Since antibiotic resistance is a major threat to both humans and the environment, there is a need for studies on the antimicrobial properties of different forms of traditionally used plants. Herein, the seeds of coriander were used to isolate essential oil (EO) and to synthesise silver nanoparticles (C-AgNPs). The major oil constituents were characterized by GC-MS as Linalool (79.12%), Camphor (6.16%), γ-Terpinene (2.82%) and α-Pinene (2.67%). The synthesized AgNPs were characterized by UV-Visible spectrophotometry, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX), X-ray difraction (XRD) and Fourier Tranmission Infrared (FTIR). The surface plasmon resonance (SPR) of C-AgNPs at 437 nm was recorded on the UV-Vis spectrometer. The spherical and homogenous of AgNPs was presented in SEM images. EDX showed elemental distribution and confirmed AgNPs. A characteristic intense peak was at 3.0 keV. The antibacterial activities of the essential oil and AgNPs form of coriander seed against Staphylococcus aureus ATCC 29213 and Escherichia coli ATCC 25922 bacteria were investigated by broth microdilution test. AgNPs and essential oil of coriander can be expected to provide future opportunities in nanomedicine and materials science. AgNPs can be displayed synergistic antimicrobial effect when used in combination with essential oil.


1998 ◽  
Vol 4 (S2) ◽  
pp. 856-857
Author(s):  
David M. Longo ◽  
James M. Howe ◽  
William C. Johnson

The focused ion beam (FIB) has become an indispensable tool for a variety of applications in materials science, including that of specimen preparation for the transmission electron microscope (TEM). Several FIB specimen preparation techniques have been developed, but some problems result when FIB specimens are analyzed in the TEM. One of these is X-ray fluorescence from bulk material surrounding the thin membrane in FIB-prepared samples. This paper reports on a new FIB specimen preparation method which was devised for the reduction of X-ray fluorescence during energy dispersive X-ray spectroscopy (EDS) in the TEM.Figure 1 shows three membrane geometries that were investigated in this study on a single-crystal Si substrate with a RF sputter-deposited 50 nm Ni film. Membrane 1 is the most commonly reported geometry in the literature, with an approximately 20 urn wide trench and a membrane having a single wedge with a 1.5° incline.


1993 ◽  
Vol 1 (4) ◽  
pp. 6-10
Author(s):  
Stephen E. Rice

Great strides have been made in the last decade in high resolution transmission electron microscopes (TEMs) which can also provide elemental information via energy dispersive X-ray analysis (EDX) or energy loss spectroscopy (EELS), and proponents of various TEM techniques make bold claims. Convergent beam elecjron diffraction and microdifff action shine as techniques for defect structure analysis and means for solving crystal structures. The spectroscopies can now be used to map chemical state information at a level which until recently might be encountered in science fiction. As a pure imaging device, electron holography holds great promise for providing Ehe ultimate (would you believe 0.1Å?) imaging resolution. Although conventional TEMs will never approach this, it appears that we are learning more and more about less and less, until we will soon know everything there is to know about nothing.


2016 ◽  
Vol 16 (4) ◽  
pp. 3821-3826 ◽  
Author(s):  
Wang Dexuan ◽  
Li Guian ◽  
Han Qingyan ◽  
Wang Ziqiang ◽  
Pan Liping ◽  
...  

We report a simple and environmentally friendly approach to the synthesis of Au-SiO2 composite nanospheres. Our method presents a route for the decoration of preformed amine functionalized SiO2 nanospheres by in situ formation of Au nanoparticles at three different concentrations of Au precursor (HAuCl4). Herein, the silane coupling agent (KH-550) is used as an intermediary to connect the Au nanoparticles to the surfaces of the SiO2 nanospheres, which helps avoid the aggregation of Au nanoparticles. The crystal structure, chemical elements, morphology and catalytic properties of the Au-SiO2 composite nanospheres were analyzed by transmission electron microscopy (TEM), X-Ray powder diffraction (XRD), UV-vis-spectrophotometer (UV-vis) and X-ray photoelectron spectroscopy (XPS). The analytical results demonstrate that the Au nanoparticles (4–9 nm) were homogeneously distributed on the surface of the SiO2 nanospheres, which had a good FCC crystal structure. Moreover, the Au-SiO2 composite nanospheres exhibited good catalytic properties, measured by their ability to reduce organic dyes. The Au-SiO2 composite nanospheres are promising candidates for applications in catalysis and wastewater treatment.


2015 ◽  
Vol 233-234 ◽  
pp. 513-516 ◽  
Author(s):  
A.P. Safronov ◽  
Galina V. Kurlyandskaya ◽  
S.M. Bhagat ◽  
I.V. Beketov ◽  
A.M. Murzakaev ◽  
...  

Spherical nickel nanoparticles were prepared by the electrical explosion of wire. The as-prepared nanoparticles were modified immediately after fabrication at room temperature in order to provide tunable surface properties with focus on the development of composites filled with nanoparticles. Following liquid modificators were used: hexane, toluene and the solution of polystyrene in toluene. In one case the surface modification by carbon was made in gas phase as a result of hydrocarbon injection. The average size of the nanoparticles was about 50 nm and unit cell parameters were close to 0.351 nm. Detailed characterization was done by X-ray diffraction, transmission electron microscopy, and magnetization measurements. Sphericity was also checked using microwave resonant absorption.


2018 ◽  
Vol 2 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Brent L. Nannenga ◽  
Tamir Gonen

Micro-electron diffraction, or MicroED, is a structure determination method that uses a cryo-transmission electron microscope to collect electron diffraction data from nanocrystals. This technique has been successfully used to determine the high-resolution structures of many targets from crystals orders of magnitude smaller than what is needed for X-ray diffraction experiments. In this review, we will describe the MicroED method and recent structures that have been determined. Additionally, applications of electron diffraction to the fields of small molecule crystallography and materials science will be discussed.


1973 ◽  
Vol 56 (4) ◽  
pp. 930-943
Author(s):  
John L Brown ◽  
James W Johnson

Abstract The optical microscope has long been an important tool in forensic analysis for the comparison of firearms markings and the examination and identification of other minute bits of evidence. The electron microscope permits the examination of even smaller details and offers analytical capabilities unique to the type of instrument used. The transmission electron microscope can be used to identify very small amounts of crystalline materials through the process of electron diffraction. The scanning electron microscope can frequently supersede the optical microscope because of its superior depth of focus and range of magnification. When it is equipped with an energy dispersive X-ray analyzer, most of the chemical elements in a sample can be determined. Applications of these instruments have provided some interesting and instructive results in forensic analysis.


1987 ◽  
Vol 111 ◽  
Author(s):  
Pankaj K. Sinha ◽  
Timothy S. Cale

AbstractThe distribution of nickel and copper between crystallites supported on high surface area silica (Cabosil HS5) has been studied using a Philips 400 series transmission electron microscope equipped with super twin lenses, a field emission gun and EDAX energy dispersive X-ray spectroscope. The same Ni-Cu catalysts have previously been characterized and used in cyclopropane hydrogenolysis kinetics. The good intercrystallite homogeneity found in a well reduced sample having 31% nominal copper validates a critical assumption made in these previous studies. Limited data on unreduced and partially reduced samples also highlight the need to carefully control the degree of reduction in kinetic and characterization studies.


1999 ◽  
Vol 590 ◽  
Author(s):  
N. Mölders ◽  
P.J. Schilling ◽  
J.M. Schoonmaker

ABSTRACTAn x-ray microprobe beamline was recently developed and commissioned at the Center for Advanced Microstructures and Devices (CAMD), Louisiana State University. It achieves a moderate horizontal and vertical focal spot size of 18.8 µm × 7.0 µm (σ), respectively. The beamline and end-station are designed and optimized to perform (i) spatially-resolved x-ray fluorescence spectroscopy (spectro-microscopy) using the broad intense spectrum of the white synchrotron radiation, and (ii) spatially-resolved x-ray absorption spectroscopy (micro-spectroscopy) in the energy region of 2100eV to 12000 eV. These dual capabilities enable K-edge measurements and mapping, in non-vacuum conditions, of low-Z elements down to Cl, S, and P that are of both environmental interest and technological importance. In this paper, an application of this novel synchrotron tool to elucidate the elemental distribution (microstructure) and chemical state (speciation) of Mn, Cl, S, and P-containing particulates emitted from automobile engines burning methylcyclopentadienyl manganese tricarbonyl- (MMT-) added fuel will be discussed in detail. Future opportunities of this microbeam technique in materials science and materials characterization will also be outlined.


Sign in / Sign up

Export Citation Format

Share Document