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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-

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