High Resolution Tem of Semiconductor Defects

Author(s):  
J. C. H. Spence

Computational techniques are now well developed for the determination of the electronic structure of semiconductor surfaces and their line and planar defects. These calculations depend sensitively on the atomic structure assumed for the defect, and so provide an outstanding challenge for high resolution electron microscopy, while it is unlikely that the details of the charge redistribution which controls the electronic structure of defects will be directly imaged for many years, the use of a-priori chemical knowledge may frequently greatly limit the number of likely defect structures. New high resolution imaging methods for the study of surface roughness, an area of almost total ignorance, are described elsewhere in this volume (1). It seems likely that the electronic structure of the line and planar defects will only be solved when all the information available from such techniques as EPR, SDP Hall effect measurements, CTS and EBIC are considered (see (2) for a review of recent work). The unique contribution of high resolution electron microscopy (HREM) is its non-statistical capability of analysing isolated, well characterised defects. The outstanding problems which semiconductor defects offer for HREM are (i) the difficulty of obtaining three dimensional defect structure information (ii) the need to extract information beyond the point resolution limit of current machines (but within their information resolution limit (3)) (iii) the need for chemical (atomic number) information. These three problems are briefly discussed below in the light of recent work.

1980 ◽  
Vol 2 ◽  
Author(s):  
Fernando A. Ponce

ABSTRACTThe structure of the silicon-sapphire interface of CVD silicon on a (1102) sapphire substrate has been studied in crøss section by high resolution transmission electron microscopy. Multibeam images of the interface region have been obtained where both the silicon and sapphire lattices are directly resolved. The interface is observed to be planar and abrupt to the instrument resolution limit of 3 Å. No interfacial phase is evident. Defects are inhomogeneously distributed at the interface: relatively defect-free regions are observed in the silicon layer in addition to regions with high concentration of defects.


Author(s):  
J. C. Barry

The National Facility for High Resolution Electron Microscopy, within the Center for Solid State Science at Arizona State University, was established in 1979 by the National Science Foundation. The Facility was established for the purposes of advancing knowledge in the field of high resolution electron microscopy, and promoting the application of new research methods to problems of current scientific and technological importance. The current Director of the Facility is Dr. John M. Cowley.The major equipment at the Facility is as follows.JEM 4000EX 400keV ultra-high resolution electron microscope (installed 1984). Structure resolution limit of 1.7 Å, and information limit of 1.6 Å. The 4000EX can be placed under computer control (using a system developed at ASU) for the purposes of alignment; that is, the computer automatically corrects the focus, stigmation and beam tilt. At 1.7 Å resolution, direct structure images of virtually all crystalline materials can be obtained, and individual atomic columns may be resolved in many samples. The 4000EX has been applied to characterization of defects, interfaces and surfaces of ceramics, metals and semiconductors.


Author(s):  
David J. Smith

The recent advent of high-resolution electron microscopes (HREMs) capable of resolving sub-2-Ångstrom detail on a routine basis has led to an enormous increase in the range of materials which can be usefully studied. Not only is it possible to resolve individual atomic columns in low index zones of most common metals but observations of semiconductors, for example, are no longer restricted to the traditional [110] zone, thereby making it feasible at last to obtain two-dimensional information about surfaces, interfaces and other planar defects. There is a worldwide upsurge of interest in the capabilities of these machines and the so-called medium-voltage (300-400kV) HREMs are selling rapidly despite their considerable expense. Our objective here is to provide a brief and selective overview of the latest applications and likely trends in HREM studies of materials - further details can be found elsewhere in these proceedings. No attempt is made to review instrumentation developments since they are being considered separately.


1996 ◽  
Vol 466 ◽  
Author(s):  
L. D. Marks ◽  
E. Bengu ◽  
R. Plass ◽  
T. Ichimiya ◽  
P. M. Ajayan ◽  
...  

ABSTRACTRecent work has demonstrated that high resolution electron microscopy in plan-view imaging mode is capable of directly imaging surfaces at a resolution of better than 2 Å. For the particular case of the Si (111) 7×7 surface, we have been able to image not only the adatoms visible in STM images, but all the atoms in the top three atomic layers including the dimers. The potential applications of this approach and its limitations will be discussed.


Author(s):  
W. H. Wu ◽  
R. M. Glaeser

Spirillum serpens possesses a surface layer protein which exhibits a regular hexagonal packing of the morphological subunits. A morphological model of the structure of the protein has been proposed at a resolution of about 25 Å, in which the morphological unit might be described as having the appearance of a flared-out, hollow cylinder with six ÅspokesÅ at the flared end. In order to understand the detailed association of the macromolecules, it is necessary to do a high resolution structural analysis. Large, single layered arrays of the surface layer protein have been obtained for this purpose by means of extensive heating in high CaCl2, a procedure derived from that of Buckmire and Murray. Low dose, low temperature electron microscopy has been applied to the large arrays.As a first step, the samples were negatively stained with neutralized phosphotungstic acid, and the specimens were imaged at 40,000 magnification by use of a high resolution cold stage on a JE0L 100B. Low dose images were recorded with exposures of 7-9 electrons/Å2. The micrographs obtained (Fig. 1) were examined by use of optical diffraction (Fig. 2) to tell what areas were especially well ordered.


Author(s):  
Robert A. Grant ◽  
Laura L. Degn ◽  
Wah Chiu ◽  
John Robinson

Proteolytic digestion of the immunoglobulin IgG with papain cleaves the molecule into an antigen binding fragment, Fab, and a compliment binding fragment, Fc. Structures of intact immunoglobulin, Fab and Fc from various sources have been solved by X-ray crystallography. Rabbit Fc can be crystallized as thin platelets suitable for high resolution electron microscopy. The structure of rabbit Fc can be expected to be similar to the known structure of human Fc, making it an ideal specimen for comparing the X-ray and electron crystallographic techniques and for the application of the molecular replacement technique to electron crystallography. Thin protein crystals embedded in ice diffract to high resolution. A low resolution image of a frozen, hydrated crystal can be expected to have a better contrast than a glucose embedded crystal due to the larger density difference between protein and ice compared to protein and glucose. For these reasons we are using an ice embedding technique to prepare the rabbit Fc crystals for molecular structure analysis by electron microscopy.


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