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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)

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