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Development for liguid phase epitaxy by solvent evaporation

Development for liguid phase epitaxy by solvent evaporation
溶剂蒸发液相外延技术的发展
批准号:
09650013
负责人:
TAKEI Humihiko
金额:
$2.11万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1998

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中文摘要
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英文摘要
Because of high convenience and productivity, the epitaxial growth techniques possess high utilities for fabricating many electronic devices. The liquid phase epitaxy is one of the most useful method among these epitaxial techniques due to high growth rate and reproducibility. The solvent evaporation epitaxy, which has been developed by us, is conducted in a following simple way : a solid mixture of solute and solvent is plastered on a surface of substrate crystals and then the solvent is evaporated by heating them. Despite of the simplicity, only a few trials of this epitaxy have been reported and many points for developping the technique have remained. In this study, we applied the technique for several oxide systems. The (100) surfaces of MgO single crystals were used as a substrate and experiments on simple oxides of MnO, CoO and NiO, oxide-superconductors of the BSCCO system and a transparent conductive spinel of ZnGa_2O_4 were reported. From the results of this study, the following superior points became clear : 1) The method is simple. 2) Epitaxial growth proceeds reproductively when the experimental conditions are settled. 3) No further treatment for separating the epitaxed layers from the solutions is needed. On the other hand, the next disadvantageous points existed : 1) Solvent materials is important but limited. 2) Because of the high heating temperatures, unexpected chemical reactions often occur between films and substrates. 3) Uniform epitaxial growth proceeds only when the appropriate growth conditions are settled sharply. As a conclusion, the solvent evaporation epitaxy is actually a prominent method for preparing oxide crystal films. However, it also became clear that there remain many problems to produce perfect films for many devices.
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H.Hasegawa et al.: "Origin of the metallic conductivity in PdCoO2 with delafossite structure" Physica B. 245. 157-163 (1998)
H.Hasekawa 等人:“具有铜铁矿结构的 PdCoO2 中金属电导率的起源”Physica B. 245. 157-163 (1998)
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T.Suzuki et al.: "Phase relation studies on the(Bi0.8Pb0.2)2Sr2CuO6-CaCuO2 system between 850 and 1020℃" Physica C. (in press).
T. Suzuki等:“850至1020℃之间(Bi0.8Pb0.2)2Sr2CuO6-CaCuO2体系的相关系研究”Physica C.(出版中)。
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H.Asaoka, Y.Kazumata, H.Takei and K.Noda: "Influence of growth condition on magnetic flux pinning in YBa_2Cu_3O_x single crystals" Physica C. 279. 246-252 (1997)
H.Asaoka、Y.Kazumata、H.Takei 和 K.Noda:“生长条件对 YBa_2Cu_3O_x 单晶中磁通量钉扎的影响”Physica C. 279. 246-252 (1997)
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T.R.Zhao and H.Takei: "Study of the oxidation and reduction kinetics of copper iron oxide [CuFeO_2] in the Cu-Fe-O system" Mater.Res.Bull.32. 1377-1393 (1997)
T.R.Zhao和H.Takei:“Cu-Fe-O体系中铜铁氧化物[CuFeO_2]的氧化和还原动力学研究”Mater.Res.Bull.32。
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