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emission intensity.<br />

ˆ It is found that signicant PL intensities can be obtained by annealing un<strong>de</strong>r<br />

forming gas at temperatures as low as 380-500°C during 0.5h.<br />

4.12 Conclusion<br />

tel-00916300, version 1 - 10 Dec 2013<br />

A thorough investigation of <strong>Si</strong>N x materials indicated that the refractive in<strong>de</strong>x of<br />

the layer is the most important indicator of the material properties. It is possible<br />

to obtain similar structural and optical properties with the two kinds of <strong>de</strong>position<br />

approaches for silicon nitri<strong>de</strong> layers investigated here (reactive sputtering and<br />

co-sputtering). <strong>Si</strong>gnicant emission intensities were obtained by using SRSN in a<br />

multilayer structure. A short time annealing treatment un<strong>de</strong>r nitrogen ow (STA,<br />

1min-1000°C) on SRSO/SRSN MLs results in the highest emission intensities which<br />

is attributed the high <strong>de</strong>nsity <strong>Si</strong>-np. The presence of <strong>Si</strong>-np and therefore emission<br />

after STA in SRSO/SRSN MLs contrary to SRSO/<strong>Si</strong>O 2 MLs reect the advantages<br />

of SRSN in favouring the <strong>Si</strong>-np formation in SRSO sublayers with a faster kinetics.<br />

<strong>Si</strong>milarly, it is shown in this chapter that annealing un<strong>de</strong>r forming gas even at<br />

low temperatures enhances emission intensity of the ML. Enhancing the emission<br />

intensity of the SRSO/SRSN MLs either by STA or by FG annealing reects the<br />

advantages of this material over SRSO/<strong>Si</strong>O 2 which requires 1h-900-1100°C for <strong>Si</strong>-np<br />

formation leading to emission, with regard to thermal budget for photovoltaics or<br />

even photonic applications. The <strong>de</strong>nsity of <strong>Si</strong>-np after STA in SRSO/SRSN ML (almost<br />

10 20 np/cm 3 ) is higher than the <strong>Si</strong>-np <strong>de</strong>nsity achieved after CA in SRSO/<strong>Si</strong>O 2<br />

ML.<br />

Hence, a preliminary experiment to test these two samples for electrical conductivity<br />

was ma<strong>de</strong>. Figure 4.46 compares the dark current curves of (3.5 nm SRSO/5<br />

nm SRSN) with our (3.5 nm SRSO/3.5 nm <strong>Si</strong>O 2 ) MLs.<br />

The resistivity was calculated to be 2.15 and 214 MW·cm in the SRSO/SRSN and<br />

SRSO/<strong>Si</strong>O 2 MLs, respectively at 7.5 V. <strong>Si</strong>nce the thickness of the SRSO sublayer is<br />

the same in both cases (3.5 nm), this <strong>de</strong>crease in the resistivity of the SRSO/SRSN<br />

MLs can be ascribed to the substitution of <strong>Si</strong>O 2 by SRSN sublayers. This two-fold<br />

enhanced conductivity paves the way for further improvement of the SRSO/SRSN<br />

MLs' conductivity, for example, by <strong>de</strong>creasing the thickness of this SRSN sublayer.<br />

Thus, this chapter successfully <strong>de</strong>monstrates the advantages of SRSO/SRSN over<br />

SRSO/<strong>Si</strong>O 2 MLs with a control over thermal budget for <strong>de</strong>vice applications.<br />

134

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