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NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...

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- 29 -<br />

where En are the Zeeman energy levels (-yM n). This leads to<br />

the expression<br />

with<br />

11a<br />

1<br />

f (I)<br />

40<br />

f (I) (eQ)2cT*2E(T*) JE1(co) + 4E2(o) I<br />

21 +3<br />

I2(2I - 1)<br />

Such an equation is not specific to zinc blende crystal lattices<br />

because all the structure parameters are included in the terms<br />

cEn_m(()0). From Mieher's calculated values of E+1(co) and E+2(oo)<br />

an isotropic relaxation time is predicted, which is given by<br />

where<br />

T=<br />

A<br />

1r<br />

Af (I)<br />

e2 YQ ZT*2E (T*)<br />

3305c 1983<br />

40<br />

71d2v 3 a2<br />

The term (e2yQ/r5) is a measure of the strength of the electric<br />

quadrupole interaction between nuclei, r being the nearest-neighbour<br />

separation and ya scalar.<br />

The weakness of the above expression is that any indirect<br />

contributions to the nulcear quadrupole coupling are included only<br />

through the multiplying factor y. In ionic crystals the electron<br />

charge cloud surrounding each nucleus is distorted from spherical<br />

symmetry by the electric field gradient arising from the other ions.<br />

This leads to an additional contribution to the nuclear quadrupole<br />

coupling, the magnitude of which can be estimated from the value<br />

of the Sternheimer anti-shielding factor<br />

(3,24)<br />

for the particular<br />

ion. However, compounds with a zinc blende type lattice structure<br />

(2.29)

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