arXivDaily arXiv每日学术速递 周一至周五更新
arXiv 1703.03350cond-mat.supr-con
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Cs-C $_{60}$库仑作用控制的Cs-PDMATHAAB-C $_{60}$化合物的高$T_\textrm {C}$超导电性

High-$T_\textrm {C}$ superconductivity in Cs$_3$C$_{60}$ compounds governed by local Cs-C$_{60}$ Coulomb interactions

Dale R. Harshman, Anthony T. Fiory

摘要:

在碱金属掺杂的$\textit {A}$ $_3$ C $_{60}$富勒烯化合物中,A15和fcc形式的Cs $_3$ C $_{60}$表现出在静水压力下变化的超导态,最高转变温度分别为$T_\textrm {C}$ $^\textrm {meas}$ = 38.3和35.2 K。本文认为,这两种化合物在压力下代表的最佳材料的$\textit {A}$ $_3$ C $_{60}$家庭,和C $_{60}$相关的超导性介导的库仑相互作用与电荷的碱。采用非平面几何推导了高$T_\textrm {C}$超导性的层间库仑配对模型,将两个相互作用层的图像推广到位于C $_{60}$上的电荷库与碱金属离子之间的相互作用。最佳转变温度遵循代数表达式,$T_\textrm {C0}$ =(12.474 nm $^2$ K)/ $\ell$ $ζ$,其中$\ell$涉及C $_{60}$上相互作用的表面电荷之间的平均间距,并且$ζ$是C $_{60}$表面与相邻Cs离子之间的平均径向距离。测量的阳离子化学计量的Cs $_{3-\textrm{x}}$ C $_{60}$与x $\approx$ 0的$T_\textrm {C0}$值被发现是38.19和36.88 K的A15和fcc形式,分别与二分法的转变温度反映较大的$ζ$和结构无序的fcc形式。在A15的形式,模拟相互作用的电荷和库仑势e $^2$ / $ζ$的核自旋弛豫和中红外光学电导率的结果定量同意。在fcc形式中,$T_\textrm {C}$ $^\textrm {meas}$的抑制低于$T_\textrm {C0}$归因于天然结构紊乱。声子效应与库仑配对进行了讨论。

英文摘要:

Unique among alkali-doped $\textit {A}$$_3$C$_{60}$ fullerene compounds, the A15 and fcc forms of Cs$_3$C$_{60}$ exhibit superconducting states varying under hydrostatic pressure with highest transition temperatures at $T_\textrm {C}$$^\textrm {meas}$ = 38.3 and 35.2 K, respectively. Herein it is argued that these two compounds under pressure represent the optimal materials of the $\textit {A}$$_3$C$_{60}$ family, and that the C$_{60}$-associated superconductivity is mediated through Coulombic interactions with charges on the alkalis. A derivation of the interlayer Coulombic pairing model of high-$T_\textrm {C}$ superconductivity employing non-planar geometry is introduced, generalizing the picture of two interacting layers to an interaction between charge reservoirs located on the C$_{60}$ and alkali ions. The optimal transition temperature follows the algebraic expression, $T_\textrm {C0}$ = (12.474 nm$^2$ K)/$\ell$$ζ$, where $\ell$ relates to the mean spacing between interacting surface charges on the C$_{60}$ and $ζ$ is the average radial distance between the C$_{60}$ surface and the neighboring Cs ions. Values of $T_\textrm {C0}$ for the measured cation stoichiometries of Cs$_{3-\textrm{x}}$C$_{60}$ with x $\approx$ 0 are found to be 38.19 and 36.88 K for the A15 and fcc forms, respectively, with the dichotomy in transition temperature reflecting the larger $ζ$ and structural disorder in the fcc form. In the A15 form, modeled interacting charges and Coulomb potential e$^2$/$ζ$ are shown to agree quantitatively with findings from nuclear-spin relaxation and mid-infrared optical conductivity. In the fcc form, suppression of $T_\textrm {C}$$^\textrm {meas}$ below $T_\textrm {C0}$ is ascribed to native structural disorder. Phononic effects in conjunction with Coulombic pairing are discussed.

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