valency electron
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1992 ◽  
Vol 242 ◽  
Author(s):  
Y. Hamakawa ◽  
H. Okamoto

ABSTRACTA review is given on recent progress in amorphous and microcrystalline silicon-carbide (a-SiC, nc-SiC) semiconductors and their technological applications to optoelectronic functional devices. Firstly, some significant properties in this alloy as a new synthetic material are pointed out with recent advances of thin film technologies, such as plasma CVD, ECR-CVD and ion-beam CVD etc. There exists an energy gap controllability from 1.7eV to 3.6 eV with retaining the valency electron control from n-type through i- to p-type semiconductors. While its conductivity can also be controlled more than ten order of magnitudes, e.g., from 10-9to 102 Scm-1 by controlling the impurity doping and preparation conditions.Secondly, a series of technical data on the electronic and optoelectronic properties of a-Si, C1−x C1−x and μ-SiC are demonstrated from recent achievements. In the final part of the paper, current state of the art in the field of optoelectronic applications from live technologies on amorphous silicon solar cells. a-SiC visible light LED and EL devices are reviewed. A technological evolution from “microelectronics” to “macroelectronlcs” will be discussed.


1989 ◽  
Vol 164 ◽  
Author(s):  
Y. Hamakawa ◽  
Y. Matsumoto ◽  
G. Hirata ◽  
H. Okamoto

AbstractA review is given of the electrical and optical properties of hydrogenated microcrystalline silicon carbide (μc-SiC:H) films prepared by ECR (Electron Cyclotron Resonance) plasma chemical vapor deposition. The material produced with the ECR plasma technology has a very wide energy gap from 2 to 2.8 eV with good valency electron controllability, e.g., a dark conductivity as high as 10 Scmg− which is more than seven orders of magnitude larger than that of amorphous SiC:H.Employing this material as a wide gap heterojunction window, 15.4% and 12.0% conversion efficiencies have been achieved with the structures of ITO/p type μc-SiC:H/n type poly-Si and p type vc-SiC:H/i type a-Si:H/n type Pc-Si:H heterojunction solar cells, respectively. The successful development of a visible light thin film light emitting diode show the promise of microcrystalline materials for optoelectronic applications.


1988 ◽  
Vol 24 (3) ◽  
pp. 298-303 ◽  
Author(s):  
V. V. Shumilov ◽  
V. M. Cherkashenko ◽  
M. Ya. Khodos

1981 ◽  
Vol 42 (C4) ◽  
pp. C4-471-C4-474 ◽  
Author(s):  
Y. Tawada ◽  
M. Kondo ◽  
H. Okamoto ◽  
Y. Hamakawa

Measurements have been made of the lattice spacings of solid solutions of lithium, magnesium, silicon, copper, zinc, germanium and silver in aluminium. The lattice of aluminium is expanded by the solution of magnesium or germanium, and contracted by the solution of lithium, silicon, copper or zinc. No change in lattice spacing can be detected when silver is dissolved in aluminium, although microscopic examination shows that a solid solution is formed, and this is confirmed by the absence of any diffraction lines other than those of the solid solution in aluminium. If the lattice spacing/composition curve for dilute solutions is extrapolated to 100% of solute, the resulting lattice spacing refers to a hypothetical face-centred cubic modification of the solute, and the corresponding closest distance of approach of the atoms is called the apparent atomic diameter (A. A. D.) of the solute when in solution in aluminium. Previous work enables the corresponding A. A. D. values to be deduced for the above solute elements when dissolved in univalent copper, silver or gold, and in divalent magnesium. The differences between the A. A. D. values of a given element when dissolved in various solvents are discussed, and it is suggested that they are controlled by the interplay of four factors: (1) the relative volume per valency electron in crystals of the solvent and solute, (2) the relative radii of the ions of solvent and solute, (3) Brillouin zone effects, and (4) the difference between solvent and solute in the electrochemical series. If this line of approach adopted be correct, it follows that it is only in exceptional circumstances that the so-called Vegard’s law will apply to metallic solid solutions.


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