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Apical oxygen, 3D-2D cross over and superconductivity in Sm_(2-x)Ce_xCuO_(4-δ)

机译:SM_(2-x)CE_XCUO_(4-δ)中的顶端氧气,3D-2D交叉和超导性

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In spite of the vast amount of experimental and theoretical articles accumulated in HTSC, the mechanism of the interaction driving charge carriers to form Cooper pairs below T_c is still unknown. The comparison of the normal state transport properties of Yba_2Cu_3O_(7-δ) and the Sm_(2-x)Ce_xCuO_(4-δ)^s[1,2] might shed some light on the microscopic origin of HTSC. In comparison to the YBCO, the apical oxygen in Sm_(2-x)Ce_xCuO_(4-δ)^s[3] destroys the superconductivity via the vertical ionic bonding which localizes the charge in the Cu-O squares, however the hole transfer by moving O(4) towards the CuO+2 planes, leads to the optimization of YBCO properties. The behaviour of C axis parameter vs the oxygen content cannot be explained by a BSC mechanism. The high amount of anisotropy ratio [4] is explained by the sheer square planes in NCCO system, i.e. without apical oxygen (SC with Tc maximum). From the data of the resistivity in the normal state, we conclude the observation of a 3D-2D cross over only in Sm_(2-x)Ce_xCuO_(4-δ)^s[2] and Nd_(2-x)Ce_xCuO_(4-δ)^s[5] which is also related to its high anisotropy. The competition between anisotropy and superconductivity destroys the superconducting state in the 2D limit even in the ground state. In this material the superconductivity cannot be enhanced at high temperature because the compound is a quasi 2D system (sheer square planes of CuO_2) and the cuprate superconductors is a genuine three-dimensional (3D) phenomenon [6]. The Josephson coupling between the different layers is S-I-S for NCCO and S-N-S for YBCO, thus the Lawrence and Doniach model (LD) [7] with neighbouring layers coupled by the Josephson tunnelling is appropriate. In summary the behaviour of apical oxygen is intrinsically different in the two kinds of cuprates.
机译:尽管HTSC中积累了大量的实验和理论物品,但相互作用驱动电荷载体的机制仍然未知。 YBA_2CU_3O_(7-Δ)和SM_(2-X)CE_XCUO_(4-Δ)^ S [1,2]的正常状态传输性能的比较可能在HTSC的显微源上脱光。与YBCO相比,SM_(2-X)CE_XCUO_(4-Δ)^ S [3]中的顶端氧气通过垂直离子键来破坏超导性,所述垂直离子键合,所述垂直离子键能定位CU-O平方中的电荷,但是孔转印通过向CUO + 2平面移动O(4),导致YBCO属性的优化。 C轴参数VS的行为VS不能通过BSC机制来解释氧气含量。高量的各向异性比[4]由NCCO系统中的纯方平面解释,即没有顶端氧气(最大TC的SC)。从正常状态的电阻率数据中,我们得出仅在SM_(2-x)CE_xcuo_(4-Δ)^ s [2]和nd_(2-x)ce_xcuo_( 4-Δ)^ S [5],其与其高各向异性有关。各向异性和超导之间的竞争使得即使在地面状态也会破坏2D限制中的超导状态。在该材料中,在高温下不能增强超导性,因为该化合物是准2D系统(CuO_2的纯度平面),铜酸酯超导体是真正的三维(3D)现象[6]。不同层之间的Josephson耦合是用于NCCO和用于YBCO的S-N-S的S-I-S,因此劳伦斯和Doniach模型(LD)[7]与Josephseon隧道耦合的相邻层是合适的。总之,在两种铜酸盐中,顶端氧的行为在本质上不同。

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