scholarly journals Introduction to ‘electron interference microscopy’

Microscopy ◽  
2020 ◽  
Author(s):  
Ken Harada ◽  
Tadahiro Kawasaki
Author(s):  
Akira Tonomura

An electron beam is often modulated, only in phase and not in intensity. When the beam passes through a magnetic field or a ferromagnetic thin film which can be regarded as pure phase objects. Therefore, great defocusing is indispensable for magnetic domain observation in Lorentz microscopy. Electron interference microscopy, however, can directly display the phase distribution of an electron beam in an in-focus electron micrograph, and consequently should provide direct information about magnetic fields.The development of a coherent field emission electron beam has opened a way to such a possibility using electron holography in which the phase-amplified phase distribution can be displayed as an interference micrograph. In addition, contour fringes have been interpreted as in-plane magnetic lines of force. Such an intuitive interpretation is possible for the following reason (Fig.1). An incident wavefront is displaced by the vector potential circulating around a magnetic field.


A simple electrostatic device has been constructed which, when inserted in the optical system of an electron microscope, functions as an absorbing phase plate. Its operation depends on the central portion of a thin poorly conducting thread generating a stable potential under the influence of the electron beam and creating a particular form of electric field. An electron interference technique is employed to study the stabilizing mechanism and to develop a method for achieving the required magnitude of potential. The performance of this device is gauged by optical diffraction of electron micrographs of a thin carbon film; its application is illustrated by examining some negatively stained biological specimens. The results indicate that such an ‘electrostatic phase plate’ can provide significant improvements in contrast and signal/noise ratio over normal bright field images without loss in resolution.


1994 ◽  
Vol 332 ◽  
Author(s):  
Akira Tonomura

ABSTRACTFlux lines in superconducting thin films are observed statically in a holographic electron interference micrograph, and dynamically in a Lorentz micrograph with a “coherent” and 300kV electron beam. In interference microscopy, projected magnetic lines of force in a tilted Nb thin film are observed quantitatively as contour fringes drawn on an in-focus electron micrograph. Whereas in Lorentz microscopy, flux lines are observed as spots with bright and dark contrast pairs due to defocusing of the image. Although the image is blurred due to a large amount of defocusing, this method is suitable for real-time observation. By making the best use of this feature, flux line movement can be observed when the applied magnetic field or the film temperature changes.


Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).


iScience ◽  
2021 ◽  
pp. 102940
Author(s):  
Neha Goswami ◽  
Yiyang Lu ◽  
Mikhail E. Kandel ◽  
Michael J. Fanous ◽  
Kathrin Bohn-Wippert ◽  
...  

2014 ◽  
Vol 8 (4) ◽  
pp. 231-241 ◽  
Author(s):  
Peter Lehmann ◽  
Jan Niehues ◽  
Stanislav Tereschenko

2008 ◽  
Vol 13 (3) ◽  
pp. 034004 ◽  
Author(s):  
Alexey R. Brazhe ◽  
Nadezda A. Brazhe ◽  
Georgy V. Maksimov ◽  
Pavel S. Ignatyev ◽  
Andrey B. Rubin ◽  
...  

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