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Films minces à base de Si nanostructuré pour des cellules ...

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Aim of the study<br />

To see the inuence of<br />

hydrogen plasma<br />

Deposition / placing<br />

in hydrogen- rich<br />

plasma<br />

3h <strong>de</strong>position<br />

(continuous)<br />

3h <strong>de</strong>position + 1h<br />

placing in plasma<br />

without <strong>de</strong>position<br />

t(nm)<br />

n 1.95eV<br />

236 1.76<br />

236 1.76<br />

Table 3.7:<br />

samples.<br />

Role of hydrogen plasma on the growth of reactively co-sputtered SRSO<br />

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

During multilayer fabrication we expect to alternate between hydrogen-rich plasma<br />

(Ar+H 2 ) and pure Ar plasma. Hence the residual hydrogen in the plasma might<br />

etch the next forming sublayers. Therefore, this study was ma<strong>de</strong> to get a <strong>de</strong>eper<br />

insight on the role of hydrogen plasma on the material growth. Table 3.7 shows the<br />

thickness and refractive in<strong>de</strong>x obtained on two samples: (i) SRSO layer <strong>de</strong>posited<br />

during 3h, and (ii) SRSO layer placed 1h in Ar+H 2 plasma after 3h <strong>de</strong>position.<br />

It can be seen that there is no change in the thickness or the refractive in<strong>de</strong>x<br />

of the samples after 3h continuous <strong>de</strong>position or 3h <strong>de</strong>position + 1h placing in<br />

the hydrogen plasma without <strong>de</strong>position. This implies that the hydrogen does not<br />

participate in etching if <strong>Si</strong> and <strong>Si</strong>O 2 catho<strong>de</strong>s are closed, and plays a role on the<br />

material growth only if the <strong>de</strong>position process is ongoing. The latter was conrmed<br />

by observing an increase in refractive in<strong>de</strong>x (1.82) and thickness (308 nm) when<br />

3h <strong>de</strong>posited SRSO is placed 1h in plasma activating the <strong>Si</strong> catho<strong>de</strong> (i.e) <strong>de</strong>posited<br />

for an additional 1h. Therefore, during the multilayer growth it is wise to allow<br />

sucient time to evacuate hydrogen before the <strong>de</strong>position of next sublayer since <strong>Si</strong><br />

catho<strong>de</strong> is active (open) during both SRSO and <strong>Si</strong>O 2 sublayer growth.<br />

3.7 SRSO-P15 in a multilayer system: SRSO/<strong>Si</strong>O 2<br />

The goal behind fabricating SRSO/<strong>Si</strong>O 2 multilayer conguration is to control the<br />

size and <strong>de</strong>nsity of the <strong>Si</strong>-np within SRSO layer in accordance with the quantum<br />

connement eect. PL measurements are indicative of the presence of <strong>Si</strong>-np (exciton)<br />

which are required for <strong>de</strong>sirable absorption and carrier generation in a third<br />

generation PV <strong>de</strong>vice. Reducing the <strong>Si</strong> excess to attain smaller crystals signicantly<br />

<strong>de</strong>creases the <strong>Si</strong>-np <strong>de</strong>nsity in a monolayer. But in a multilayer (ML), the SRSO<br />

sublayer thickness controls the <strong>Si</strong>-np size without reducing their <strong>de</strong>nsity and the<br />

<strong>Si</strong>O 2 barrier between the two consecutive SRSO sublayers prevent the overgrowth of<br />

81

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