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A simple method for the normal pressure synthesis of Cu1-xTlxBa2Ca3Cu4O12-delta superconductor

机译:一种常压合成Cu1-xTlxBa2Ca3Cu4O12-δ超导体的简单方法

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摘要

A very simple method for the direct synthesis of Cu1-xTlxBa2Ca3Cu4O12-delta (Cu1-xTlx-1234) superconductor is reported. A predominant single phase Cu1-xTlx-1234 is achieved by the solid state reaction of Ba(NO3)(2), CaCO3 and Cu(CN) at first stage and with appropriate amount of Tl2O3 at the second stage. These materials were fired twice for 24 h at 880 degrees C followed by intermediate grinding. Thoroughly ground and fired material was mixed with Tl2O3 in appropriate amount and pellets were made by applying a pressure of 5 tons. Pellets were wrapped in an aluminum foil and sintered at 880 degrees C for 3-30 min. A predominantly single phase of Cu1-xTlxBa2Ca3Cu4O12-delta was achieved with an inclusion of unknown impurity. The resistivity measurements established the onset temperature of superconductivity [T-c (onset)] at 120 K and zero resistivity critical temperature [T-c(R = 0)] at 106 K. Bulk superconductivity was also confirmed by ac-magnetic susceptibility measurements. The surface of the samples was analyzed by electron microscopy and their composition by energy dispersive X-ray spectroscopy (EDX) measurements. For optimizing the carriers in the final compound, post-annealing experiments were carried out in the flowing nitrogen atmosphere. For the study of the doping mechanisms, in the post-annealed samples, the phonon modes of Cu1-xTlx-1234 were investigated by infrared absorption measurements. The absorption mode of O-delta [O3] atoms decreased in intensity after the post-annealing and the apical oxygen modes were softened to lower wave numbers. The softening of these phonon modes suggested the reduction of thallium from Tl3+ to Tl1+; which resulted in an increase of [T-c(R = 0)] of the material. (c) 2005 Elsevier B.V. All rights reserved.
机译:报道了一种非常简单的直接合成Cu1-xTlxBa2Ca3Cu4O12-δ(Cu1-xTlx-1234)超导体的方法。通过在第一阶段进行Ba(NO3)(2),CaCO3和Cu(CN)的固态反应,并在第二阶段进行适量的Tl2O3,可以实现主要的单相Cu1-xTlx-1234。将这些材料在880摄氏度下烧制两次,持续24小时,然后进行中间研磨。将经过充分研磨和煅烧的材料与适量的Tl2O3混合,并通过施加5吨的压力制成颗粒。将粒料包裹在铝箔中并在880℃下烧结3-30分钟。 Cu1-xTxxBa2Ca3Cu4O12-δ的主要单相包含未知杂质。电阻率测量确定了120 K时的超导率[T-c(起始)]的起始温度,106 K时确定了零电阻率的临界温度[T-c(R = 0)]。通过交流磁化率测量也证实了体超导率。通过电子显微镜分析样品的表面,并通过能量色散X射线光谱(EDX)测量分析其组成。为了优化最终化合物中的载体,在流动的氮气气氛中进行了后退火实验。为了研究掺杂机理,在退火后的样品中,通过红外吸收测量研究了Cu1-xTlx-1234的声子模式。后退火后,O-δ[O3]原子的吸收模式强度降低,并且顶部氧模式被软化以降低波数。这些声子模态的软化表明of从Tl3 +减少到Tl1 +。这导致材料的[T-c(R = 0)]增加。 (c)2005 Elsevier B.V.保留所有权利。

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