A New High Performance Electron Energy Loss Spectrometer for use with Monochromated Microscopes

2001 ◽  
Vol 7 (S2) ◽  
pp. 908-909
Author(s):  
H.A. Brink ◽  
M. Barfels ◽  
B. Edwards ◽  
P. Burgner

A new type of electron energy loss spectrometer for use with monochromated microscopes is presented. The energy resolution of the spectrometer is better than 0.100 eV. A completely new electron optical design with a number of extra optical elements and advanced tuning software makes it possible to correct spectrum aberrations to 4th order, which increases sensitivity and collection angles. New high-stability electronics make it possible to maintain energy resolution over a period of several minutes in a practical laboratory environment.The energy resolution of Transmission Electron Microscopes (TEMs) equipped with electron energy loss spectrometers is determined by a combination of the energy spread of the electron source, the stability of the microscope’s high voltage power supply, and the energy resolution of the spectrometer. Commercial microscopes usually employ electron sources with an energy distributions of around 0.5 eV or more (FWHM), limiting the energy ultimate energy resolution that can be achieved. Recently FEI constructed a special 200 kV TEM with a built-in monochromator which makes it possible to monochromize the electron source to better than 0.100 eV. A prototype of the presented spectrometer has been installed on this microscope.

Author(s):  
Ondrej L. Krivanek

The electron energy loss spectrometer developed at Berkeley differs from most other ones in four ways: 1) it uses the projector lens crossover as the spectrometer entrance object plane, 2) its magnet is asymmetric so that the entrance object is de-magnified about 5x, 3) it counts electrons admitted through the energy-selecting slit singly at rates up to 20MHz while adding zero dark count, and 4) it fits neatly at the back of the available leg space of the electron microscope, and requires no substantial alterations to the microscope. The energy resolution attainable routinely at any primary voltage is 3eV over an energy loss range 0 to 1keV, as illustrated by resolving the π* transition on the K-edge of amorphous carbon (Fig. 1). The 3 eV limit comes mainly from 120Hz stray magnetic fields (the 60Hz component has been compensated out). Fast scanning of the spectrum improves the resolution to 1eV (Fig. 2). This indicates that with proper magnetic shielding of the electron flight path, especially in the microscope viewing chamber which is made out of brass, the energy resolution attainable with the spectrometer will be limited only by the energy spread of the primary beam.


Author(s):  
C. Colliex ◽  
P. Trebbia

The physical foundations for the use of electron energy loss spectroscopy towards analytical purposes, seem now rather well established and have been extensively discussed through recent publications. In this brief review we intend only to mention most recent developments in this field, which became available to our knowledge. We derive also some lines of discussion to define more clearly the limits of this analytical technique in materials science problems.The spectral information carried in both low ( 0<ΔE<100eV ) and high ( >100eV ) energy regions of the loss spectrum, is capable to provide quantitative results. Spectrometers have therefore been designed to work with all kinds of electron microscopes and to cover large energy ranges for the detection of inelastically scattered electrons (for instance the L-edge of molybdenum at 2500eV has been measured by van Zuylen with primary electrons of 80 kV). It is rather easy to fix a post-specimen magnetic optics on a STEM, but Crewe has recently underlined that great care should be devoted to optimize the collecting power and the energy resolution of the whole system.


Author(s):  
Eckhard Quandt ◽  
Stephan laBarré ◽  
Andreas Hartmann ◽  
Heinz Niedrig

Due to the development of semiconductor detectors with high spatial resolution -- e.g. charge coupled devices (CCDs) or photodiode arrays (PDAs) -- the parallel detection of electron energy loss spectra (EELS) has become an important alternative to serial registration. Using parallel detection for recording of energy spectroscopic large angle convergent beam patterns (LACBPs) special selected scattering vectors and small detection apertures lead to very low intensities. Therefore the very sensitive direct irradiation of a cooled linear PDA instead of the common combination of scintillator, fibre optic, and semiconductor has been investigated. In order to obtain a sufficient energy resolution the spectra are optionally magnified by a quadrupole-lens system.The detector used is a Hamamatsu S2304-512Q linear PDA with 512 diodes and removed quartz-glas window. The sensor size is 13 μm ∗ 2.5 mm with an element spacing of 25 μm. Along with the dispersion of 3.5 μm/eV at 40 keV the maximum energy resolution is limited to about 7 eV, so that a magnification system should be attached for experiments requiring a better resolution.


2012 ◽  
Vol 18 (4) ◽  
pp. 667-675 ◽  
Author(s):  
Paul Cueva ◽  
Robert Hovden ◽  
Julia A. Mundy ◽  
Huolin L. Xin ◽  
David A. Muller

AbstractThe high beam current and subangstrom resolution of aberration-corrected scanning transmission electron microscopes has enabled electron energy loss spectroscopy (EELS) mapping with atomic resolution. These spectral maps are often dose limited and spatially oversampled, leading to low counts/channel and are thus highly sensitive to errors in background estimation. However, by taking advantage of redundancy in the dataset map, one can improve background estimation and increase chemical sensitivity. We consider two such approaches—linear combination of power laws and local background averaging—that reduce background error and improve signal extraction. Principal component analysis (PCA) can also be used to analyze spectrum images, but the poor peak-to-background ratio in EELS can lead to serious artifacts if raw EELS data are PCA filtered. We identify common artifacts and discuss alternative approaches. These algorithms are implemented within the Cornell Spectrum Imager, an open source software package for spectroscopic analysis.


2000 ◽  
Vol 6 (S2) ◽  
pp. 206-207
Author(s):  
Huifang Xu

Because of similar chemical properties of the rare earth elements (Ree), whole series of the Ree may occur in natural Ree-bearing crystals. Relative concentration of the Ree may vary as the crystallization environments change. Electron energy-dispersive spectroscopy (EDS) associated with TEM is unable to resolve Ree and other coexistence elements, such as Ba nd Ti, because of peak overlap and energy resolution (∼ 150 eV) of EDS. Figure A indicate multiple peaks from Ce only. The Cu peaks are from Cu grid holding the specimen. Electron energy-loss spectroscopy (EELS) with energy resolution of < 1 eV is able to resolve all Ree in natural Ree-bearing crystals.Natural carbonate crystals from a Ree ore deposit were investigated by using EELS associated with field emission-gun (FEG) TEM. The crystals are in a chemical series of BaCO3 - Ree(CO3)F [1]. In Figure B, EEL spectra A and B are from Ce-rich and La-rich bastnaesite (Ree(CO3)F), respectively; spectrum D is from cordylite (BaCO3 (Ree(CO3)F); spectrum E is from huanghoite (BaCO3 Ree(CO3)F), spectrum F is from BaCO3; spectrum C is from an unknown Ree-rich phase.


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