Defect creation by 10‐keV electron irradiation in phosphorous‐dopeda‐Si:H

1990 ◽  
Vol 67 (6) ◽  
pp. 2800-2805 ◽  
Author(s):  
Suvarna Babras ◽  
V. G. Bhide ◽  
N. R. Rajopadhye ◽  
S. V. Bhoraskar
1994 ◽  
Vol 336 ◽  
Author(s):  
A. Scholz ◽  
B. Schröder ◽  
H. Oechsner

ABSTRACTThe interaction mechanisms of keV-electrons with the hydrogenated Amorphous semiconductor are briefly discussed and the differences to the metastable defect creation by photons are set out. Based on the knowlegde of the energy dissipation mechanisms of keV-electrons in the hydrogenated Amorphous semiconductor, a model for the creation of metastable defects by keV-electron irradiation is developed and its quantitative agreement with the experimental results is shown.


NANO ◽  
2016 ◽  
Vol 11 (06) ◽  
pp. 1630001 ◽  
Author(s):  
Noriaki Itoh ◽  
Chihiro Itoh ◽  
Jun'ichi Kanasaki

Modification by electronic excitation of semiconductor surfaces and carbon-related quasi-two-dimensional (2D) nanostructured materials, namely graphene, carbon nanotubes is reviewed. Defect creation in these materials takes place not by low-intensity photoirradiation, but by laser or electron irradiation. The defect creation processes are different from ordinary photochemical processes in molecules or in some solids like alkali halides, which can be modified by a localized exciton. It is pointed out that there are common features in defect creation by electronic excitation in semiconductor surfaces and carbon-related quasi-2D nanomaterials: the yield-intensity relation shows strong superlinearity for laser irradiation near the bandgap energies and linearity or weak superlinearity for higher energy electron or photon irradiation. These results are explained in terms of multi-hole localization, in which bonds are weakened more strongly and more energy is available upon recombination with trapped electrons in comparison with excitons. The multi-hole localized state is considered to be realized by the creation of dense excitons or by cascade excitation for laser irradiation and by multiple excitations or multiple exciton generation by single impacts for electron irradiation. The review includes also polymerization of C[Formula: see text] films by electronic excitation, which is induced by low-intensity photoirradiation as well as by laser or electron irradiation. The experimental observation that laser or electron irradiation polymerize C[Formula: see text] films differently from low-intensity photoirradiation is explained in terms of multi-hole localization similar to the defect formation mechanism. Although fragmentation of C[Formula: see text] is due to electronic excitation of the molecule, it is included in the review because its yield is strongly superlinear for laser irradiation near bandgap energies and weakly superlinear for high-energy electron or photon irradiation as for other cases.


Author(s):  
W. Kunath ◽  
E. Zeitler ◽  
M. Kessel

The features of digital recording of a continuous series (movie) of singleelectron TV frames are reported. The technique is used to investigate structural changes in negatively stained glutamine synthetase molecules (GS) during electron irradiation and, as an ultimate goal, to look for the molecules' “undamaged” structure, say, after a 1 e/Å2 dose.The TV frame of fig. la shows an image of 5 glutamine synthetase molecules exposed to 1/150 e/Å2. Every single electron is recorded as a unit signal in a 256 ×256 field. The extremely low exposure of a single TV frame as dictated by the single-electron recording device including the electron microscope requires accumulation of 150 TV frames into one frame (fig. lb) thus achieving a reasonable compromise between the conflicting aspects of exposure time per frame of 3 sec. vs. object drift of less than 1 Å, and exposure per frame of 1 e/Å2 vs. rate of structural damage.


Author(s):  
T. Mukai ◽  
T. E. Mitchell

Radiation-induced homogeneous precipitation in Ni-Be alloys was recently observed by high voltage electron microscopy. A coupling of interstitial flux with solute Be atoms is responsible for the precipitation. The present investigation further shows that precipitation is also induced at thin foil surfaces by electron irradiation under a high vacuum.


Author(s):  
L.E. Murr

The production of void lattices in metals as a result of displacement damage associated with high energy and heavy ion bombardment is now well documented. More recently, Murr has shown that a void lattice can be developed in natural (colored) fluorites observed in the transmission electron microscope. These were the first observations of a void lattice in an irradiated nonmetal, and the first, direct observations of color-center aggregates. Clinard, et al. have also recently observed a void lattice (described as a high density of aligned "pores") in neutron irradiated Al2O3 and Y2O3. In this latter work, itwas pointed out that in order that a cavity be formed,a near-stoichiometric ratio of cation and anion vacancies must aggregate. It was reasoned that two other alternatives to explain the pores were cation metal colloids and highpressure anion gas bubbles.Evans has proposed that void lattices result from the presence of a pre-existing impurity lattice, and predicted that the formation of a void lattice should restrict swelling in irradiated materials because it represents a state of saturation.


Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.


Author(s):  
E.A. Kenik ◽  
T.A. Zagula ◽  
M.K. Miller ◽  
J. Bentley

The state of long-range order (LRO) and short-range order (SRO) in Ni4Mo has been a topic of interest for a considerable time (see Brooks et al.). The SRO is often referred to as 1½0 order from the apparent position of the diffuse maxima in diffraction patterns, which differs from the positions of the LRO (D1a) structure. Various studies have shown that a fully disordered state cannot be retained by quenching, as the atomic arrangements responsible for the 1½0 maxima are present at temperatures above the critical ordering temperature for LRO. Over 20 studies have attempted to identify the atomic arrangements associated with this state of order. A variety of models have been proposed, but no consensus has been reached. It has also been shown that 1 MeV electron irradiation at low temperatures (∼100 K) can produce the disordered phase in Ni4Mo. Transmission electron microscopy (TEM), atom probe field ion microscopy (APFIM), and electron irradiation disordering have been applied in the current study to further the understanding of the ordering processes in Ni4Mo.


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