10. Appendix
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676 <strong>Appendix</strong> C<br />
from the slopes of these plots are 0.33 eV and 0.26 eV, respectively. Notice<br />
that the emission activation energy Eem is not the same as the capture activation<br />
energy Ecap. Their difference Eem Ecap is equal to the thermal ionization<br />
energy which is defined as the energy required to thermally ionize carriers out<br />
of the deep center. The relation between the three energies will become clear<br />
when we discuss the large lattice relaxation model.<br />
ELECTRON EMISSION OR CAPTURE RATE (sec -1)<br />
10 7<br />
10<br />
10<br />
10<br />
10<br />
10<br />
5<br />
3<br />
10<br />
-1<br />
-3<br />
-5<br />
0.33 eV<br />
0.26 eV<br />
Al Ga As(Te)<br />
0.36 0.64<br />
ELECTRON EMISSION<br />
RATE<br />
ELECTRON CAPTURE<br />
RATE<br />
THERMAL<br />
QUENCHING OF<br />
PHOTOCONDUCTIVITY<br />
0.18 eV<br />
5 7 9 11 13 15 17<br />
1000/T (1/K)<br />
Fig. A4.2 The Arrhenius plots<br />
for the emission and capture<br />
rates of the deep centers in Al-<br />
GaAs:Te obtained by Lang et al.<br />
Reproduced from [Lang79a].<br />
In the TSCAP measurement shown in Fig. A4.1(b) the total capacitance (as<br />
distinct from the capacitance difference measured in DLTS) is measured as a<br />
function of temperature. An increase in capacitance indicates that a smaller<br />
number of electrons are trapped at the deep centers. The curve labeled as (1)<br />
is the steady-state state zero-bias capacitance curve. This curve is reversible for<br />
increasing and decreasing temperatures. Curves labeled as (2) and (3) are irreversible<br />
with respect to temperature cycling. Curve (2) is obtained by first<br />
cooling the sample in the dark from about 200 K to 50 K with a bias of<br />
1 V. This positive bias causes electrons to be trapped on the deep centers<br />
thus returning them to the neutral charged state. At the lowest temperature<br />
the bias voltage is set to zero so that the electrons want to escape from the<br />
deep centers. However, the emission rate at low temperature is very slow and,<br />
therefore, the deep centers remain in a non-equilibrium state. As the sample<br />
is warmed above 100 K the emission process is thermally activated and be-