首页> 外文期刊>Applied Superconductivity, IEEE Transactions on >Comparison Study of src='/images/tex/21851.gif' alt='hbox {YBa}_{2}hbox {Cu}_{3}hbox {O}_{7-{rm x}}'> Films Deposited by Using Various Carboxylate Solutions
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Comparison Study of src='/images/tex/21851.gif' alt='hbox {YBa}_{2}hbox {Cu}_{3}hbox {O}_{7-{rm x}}'> Films Deposited by Using Various Carboxylate Solutions

机译:的比较研究 src =“ / images / tex / 21851.gif” alt =“ hbox {YBa} _ {2} hbox {Cu} _ {3} hbox {O} _ {7- { rm x}}“> 使用各种羧酸盐溶液沉积的薄膜

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In this work, four fluorine-free solutions based on various carboxylates (propionates, butyrates, valerates, and hexanoates, respectively) were prepared and used for deposition of YBCO films on single-crystal substrates, in order to further understand the role of precursors on properties of the final films. After the same pyrolysis and sintering processes, the films from propionates and butyrates show pure YBCO phase and were epitaxially grown, as determined by X-ray diffractometer analysis. There are clear differences in morphologies of these four films, i.e., the films from propionates and butyrates exhibit platelike grains without distinct grain boundaries, while almost randomly orientated grains were observed on the surface of the other two films. As a result, we noticed significant discrepancies on their superconducting performance. The films from propionates and butyrates give values (at 77 K, self-field) of 2.1 and 1.3 , respectively, while no superconducting transition above 70 K was observed in the other two films. A relatively larger amount of carbonaceous residue left as a by-product after decomposition of carboxylates with longer ligands, particularly under fast pyrolysis and sintering processes, could be one of the explanations of the poor superconductivity in the films from the valerate- and hexanoate-based precursors.
机译:在这项工作中,制备了四种基于各种羧酸盐(分别为丙酸酯,丁酸酯,戊酸酯和己酸酯)的无氟溶液,并将其用于在单晶基板上沉积YBCO膜,以进一步了解前驱物在硅上的作用。最终膜的性质。经过相同的热解和烧结过程,丙酸酯和丁酸酯的薄膜显示出纯的YBCO相,并通过X射线衍射仪分析确定其外延生长。这四种薄膜的形态存在明显差异,即,丙酸酯和丁酸酯的薄膜呈现出无明显晶界的板状晶粒,而在其他两种薄膜的表面上观察到几乎随机取向的晶粒。结果,我们注意到它们的超导性能存在显着差异。来自丙酸酯和丁酸酯的薄膜给出的值(在77 K,自电场下)分别为2.1和1.3,而在其他两幅薄膜中未观察到高于70 K的超导转变。具有较长配体的羧酸盐分解后,尤其是在快速热解和烧结过程中,相对大量的碳残留物可能作为副产物残留,这可能是由于戊酸酯和己酸酯基薄膜超导性差的原因之一。前体。

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