Model of nuclear relaxation inYBa2Cu3O7−δ

Abstract
We examine nuclear spin-lattice relaxation rates (1/T1) at copper (Cu), oxygen (O), and yttrium (Y) sites in YBa2 Cu3 O7δ. We use a two-hole band model consisting of strongly Heisenberg superexchange coupled spins (S=1/2) on Cu sites that are exchange coupled with strength Jpd to itinerant oxygen holes introduced by doping. The Cu(1) (chain) spins are modeled by one-dimensional Heisenberg chains; the Cu(2) (planar) spins are modeled by two-dimensional Schwinger boson mean-field theory. We first consider the limit of Jpd=0 to explain the following: (i) qualitatively the superlinear behavior of 1/T1 versus temperature T on Cu(1) (chain sites) in terms of their quasi-one-dimensional character, (ii) the insufficiency of arguments producing a T1/2 temperature dependence on Cu(2) (planar) sites due to the vastly stronger temperature dependence of the antiferromagnetic fluctuations, (iii) the development of an anomaly in 1/T1T similar to experimental data due to anisotropy and/or quantum disorder induced ‘‘spin gaps,’’ (iv) the need to produce some recalibration of estimates of transferred Cu(2) to Cu nuclear coupling with proper account of intersite fluctuations, and (v) the dramatic reduction of the transferred Cu spin fluctuation contribution to 1/T1 on Y and O(2,3) (planar) sites arising from form-factor effects (and hence the observation of metallic Korringa behavior at these nuclei). Next, we demonstrate formally that for finite values of Jpd the low-temperature proportionality of O(2,3) and Cu(2) rates may be understood as arising from coupling of Cu- and O-hole spin susceptibilities in the presence of a Cu(2) anisotropy or spin gap.