NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
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- 23 -<br />
to the lattice directly via the time-dependent magnetic field of<br />
the unpaired electron of the impurity ion. However most of the<br />
nuclei are coupled only indirectly by spin diffusion through<br />
dipole-dipole interactions. The spin-lattice relaxation time<br />
resulting from such a process depends upon the nature of the impur-<br />
ities and the impurity concentration. Where the concentration<br />
of impurities is low, T1 depends upon the rate of spin diffusion.<br />
2.3.4 <strong>IN</strong>TERACTION WITH CONDUCTION ELECTRONS<br />
This mechanism is the dominant relaxation process in metals.<br />
The non-localized conduction electrons create relatively large<br />
time varying local magnetic fields at a nucleus, which can induce<br />
simultaneous but opposite flips of the electron and nuclear spins.<br />
The resulting energy difference is made up by an increase in the<br />
kinetic energy of the electrons. To a first approximation only<br />
those s character electrons near the top of the Fermi distribut-<br />
ion are able to take part in this process. From Slichter, p. 126,<br />
the relaxation rate induced by this mechanism is given by<br />
1 64 33222 222<br />
T19 YeYnSt Fp (EF)kBT<br />
where p(EF) is the density of states at the Fermi surface and kB<br />
is Boltzmann's constant.<br />
Xs<br />
Y2 t1z<br />
e<br />
2<br />
P(EF)<br />
For a non-interacting electron gas<br />
Hence equations (2.10) and (2.22) lead to the simple Korringa relat-<br />
ionship(l7) between the Knight shift<br />
and spin-lattice relaxation<br />
(2.22)