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volume of SRSN in the material and was seen only in 100(3.5/5) ML (Ref. Fig.<br />

4.35b) or 50(3.5/t SRSN>5nm ) after gaussian curve tting (not shown here). In or<strong>de</strong>r<br />

to verify the inuence of annealing un<strong>de</strong>r FG and SRSN volume on this PL peak<br />

intensity, SRSN/<strong>Si</strong>O 2 ML was also subjected to FG annealing (Fig. 4.44). The<br />

SRSN sublayer thickness in this ML is lower (=3.5 nm) than in SRSO/SRSN MLs<br />

investigated above in section 4.6 and still the peak around 1.9 eV is present.<br />

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

Figure 4.44: PL spectra obtained from FG<br />

annealed 50(3.5/5) SRSN/<strong>Si</strong>O 2 .<br />

In both gures 4.43 and 4.44, 1.9<br />

eV peak is present in SRSN/<strong>Si</strong>O 2 MLs<br />

<strong>de</strong>spite the two dierent annealing processes<br />

employed. In the case of N 2<br />

annealing, since the <strong>Si</strong>O 2 <strong>de</strong>fects are<br />

mostly passivated after CA, we can reasonably<br />

assume that the dominant contribution<br />

of this emission is from SRSN<br />

sublayers which also to emit in the same<br />

energy range as <strong>Si</strong>O 2 . In the case of FG<br />

annealed samples the dominant contribution<br />

of luminescence comes from <strong>de</strong>fects<br />

in <strong>Si</strong>O 2 , since the temperature is<br />

lower for <strong>de</strong>fect passivation. These observations help us to attribute the peak (3) of<br />

SRSO/SRSN PL spectra to be the contribution of SRSN sublayer.<br />

The presence of nanocrystals were found neither in XRD spectra of SRSN/<strong>Si</strong>O 2<br />

[Nalini 12] nor in the TEM images of SRSO/SRSN thereby indicating the emission<br />

from SRSN sublayer is not from <strong>Si</strong>-np. It can be seen that there is a blueshift in<br />

the central peak position from 1.57 eV after STA to 1.75 eV after FG annealing in<br />

50(3.5/5) SRSO/SRSN ML (Ref. Fig. 4.39a), whereas for the two dierent annealing<br />

processes un<strong>de</strong>r N 2 or FG ow employed on SRSN/<strong>Si</strong>O 2 MLs there is no change in<br />

the peak intensity and the position remains xed around 1.9 eV. Theoretical mo<strong>de</strong>l<br />

has predicted that for a given <strong>de</strong>fect, the peak position is xed and cannot be<br />

controlled with ease [Kim 05]. This peak position around 1.9 eV can therefore be<br />

ascribed to the <strong>de</strong>fects in SRSN sublayers.<br />

Besi<strong>de</strong>s these <strong>de</strong>fect related PL, it can be said that in a SRSO <strong>base</strong>d ML, replacing<br />

<strong>Si</strong>O 2 by SRSN sublayers favours <strong>Si</strong>-np emission also, at a reduced thermal budget<br />

(STA in SRSO/SRSN versus CA in SRSO/<strong>Si</strong>O 2 MLs). Thus, SRSN sublayers contribute<br />

signicantly towards emission around 1.9 eV (peak 3) and between 1.5-1.7<br />

eV (peak 2) due to <strong>de</strong>fects in the matrix, and by favouring the <strong>Si</strong>-np formation<br />

respectively.<br />

130

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