Planar oxygen nuclear magnetic resonance (NMR) relaxation and shift data from all cuprate superconductors available in the literature are analyzed. They reveal a temperature-independent pseudogap at the Fermi surface, which increases with decreasing doping in family-specific ways, i.e., for some materials, the pseudogap is substantial at optimal doping while for others it is nearly closed at optimal doping. The states above the pseudogap, or in its absence are similar for all cuprates and doping levels, and Fermi liquid-like. If the pseudogap is assumed exponential it can be as large as about 1500 K for the most underdoped systems, relating it to the exchange coupling. The pseudogap can vary substantially throughout a material, being the cause of cuprate inhomogeneity in terms of charge and spin, so consequences for the NMR analyses are discussed. This pseudogap appears to be in agreement with the specific heat data measured for the YBaCuO family of materials, long ago. Nuclear relaxation and shift show deviations from this scenario near Tc, possibly due to other in-gap states.
Nuclear magnetic resonance (NMR) provides local, bulk information about the electronic properties of materials, and it has been influential for theory of high-temperature superconducting cuprates. Importantly, NMR found early that nuclear relaxation is much faster than what one expects from coupling to fermionic excitations above the critical temperature for superconductivity (Tc), i.e. what one estimates from the Knight shift with the Korringa law. As a consequence, special electronic spin fluctuations have been invoked. Here, based on literature relaxation data it is shown that the electronic excitations, to which the nuclei couple with a material and doping dependent anisotropy, are rather ubiquitous and Fermi liquid-like. A suppressed NMR spin shift rather than an enhanced relaxation leads to the failure of the Korringa law for most materials. Shift and relaxation below Tc support the view of suppressed shifts, as well. A simple model of two coupled electronic spin components, one with 3d(x 2 −y 2 ) orbital symmetry and the other with an isotropic s-like interaction can explain the data. The coupling between the two components is found to be negative, and it must be related to the pseudogap behavior of the cuprates. We can also explain the negative shift conundrum and the long-standing orbital shift discrepancy for NMR in the cuprates.
Nuclear relaxation is an important thermodynamic probe of electronic excitations, in particular in conducting and superconducting systems. Here, an empirical phenomenology based on all available literature data for planar Cu in hole-doped cuprates is developed. It is found that most of the seemingly different relaxation rates among the systems are due to a temperature independent anisotropy that affects the mostly measured 1/T 1 , the rate with an external magnetic field along the crystal c-axis, while 1/T 1⊥ is largely independent on doping and material above the critical temperature of superconductivity (Tc). This includes very strongly overdoped systems that show Fermi liquid behavior and obey the Korringa law. Below Tc the relaxation rates are similar, as well, if plotted against the reduced temperature T /Tc. Thus, planar Cu nuclear relaxation is governed by a simple, dominant mechanism that couples the nuclei with varying anisotropy to a rather ubiquitous bath of electronic excitations that appear Fermi liquid-like irrespective of doping and family. In particular, there is no significant enhancement of the relaxation due to electronic spin fluctuations, different from earlier conclusions. Only the La2−xSrxCuO4 family appears to be an outlier as additional relaxation is present, however, the anisotropy remains temperature independent. Also systems with very low doping levels, for which there is a lack of data, may behave differently.
Very recently, there has been significant progress with establishing a common phenomenology of the superconducting cuprates in terms of nuclear magnetic resonance (NMR) shift and relaxation. Different from the old interpretation, it was shown that the shifts demand two coupled spin components with different temperature dependencies. One spin component couples isotropically to the planar Cu nucleus and is likely to reside at planar O, while the other, anisotropic component has its origin in the planar copper 3d(x 2 − y 2 ) orbital. Nuclear relaxation, on the other hand, was found to be rather ubiquitous and Fermi liquid-like for planar Cu, i.e., it is independent of doping and material, apart from the sudden drop at the superconducting transition temperature, Tc. However, there is a doping and material dependent anisotropy that is independent on temperature, above and below Tc. Here we present a slightly different analysis of the shifts that fits all planar Cu shift data. In addition we are able to derive a simple model that explains nuclear relaxation based on these two spin components. In particular, the only outlier so far, La2−xSrxCuO4, can be understood, as well. While this concerns predominantly planar Cu, it is argued that the two component model should fit all cuprate shift and relaxation data.March 25, 2020 ⊥ arXiv:2002.09903v2 [cond-mat.supr-con]
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