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maximum power into the plasma.<br />

(a) Reactive sputtering : The principle of introducing a reactive gas (g) such<br />

as H 2 , N 2 , O 2 into the chamber and forming a thin lm through chemical reactions<br />

between the sputtered species and gaseous plasma is known as reactive sputtering.<br />

Oxi<strong>de</strong> and nitri<strong>de</strong> lms are often formed by reactive sputtering and the stochiometry<br />

of the lm can be tuned by controlling the relative ow rates of the inert and reactive<br />

gases. The <strong>de</strong>sired compound is formed at the substrate, <strong>de</strong>pending on the power<br />

and the surface reactivity. In this thesis, the total gas ow was xed at 10 standard<br />

cubic cm/min (sccm) while changing the ratio of the gas ow (in sccm) between<br />

the reactive gas and Ar. The equivalent partial pressure (mTorr) in the chamber<br />

displayed by the pressure indicator for a given gas ow (sccm) was used to calculate<br />

the reactive gas rate (r g %) in percentage by,<br />

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

r g (%) = [P g /(P g + P Ar )] ∗ 100 Eqn (2.1)<br />

where P g represents the partial pressure of reactive gas, g (g may be H 2 , N 2 or<br />

O 2 <strong>de</strong>pending on the process) and P Ar represents the partial pressure of Argon.<br />

(b) Eect of magnetron : Magnetron sputtering uses the principle of applying<br />

a magnetic eld to the conventional sputtering target in or<strong>de</strong>r to obtain more<br />

ecient ionization of the plasma even at low pressures. The magnets placed behind<br />

and sometimes at the si<strong>de</strong> of the target capture the escaping electron and conne<br />

them to the immediate vicinity of the target. This connement provi<strong>de</strong>d by the<br />

magnet is illustrated in the sputter process shown in gure 2.1. Due to the increased<br />

connement as compared to a conventional DC system, the plasma <strong>de</strong>nsity<br />

often increases at least by an or<strong>de</strong>r of magnitu<strong>de</strong>. This results in fast <strong>de</strong>position<br />

rates at low pressures. However the major limitation of using magnetron is that the<br />

target ero<strong>de</strong>s inhomogeneously due to the non-uniform magnetic eld.<br />

Experimental set-up and working<br />

The samples for this work were <strong>de</strong>posited using AJA Orion 5 UHV sputtering unit<br />

from AJA international [AJA 1] which has multiple magnetron sources aimed at a<br />

common focal point (Confocal sputtering). The substrate is placed in the vicinity<br />

of this focal point and is kept un<strong>de</strong>r rotation to ensure uniform <strong>de</strong>position of the<br />

lm. The sputtering chamber was maintained un<strong>de</strong>r vacuum of 10 −7 - 10 −8 mTorr<br />

using a turbo-molecular pump coupled to the primary pump. The substrate and the<br />

target which function as the ano<strong>de</strong> and the catho<strong>de</strong> repectively, are placed facing<br />

each other in the sputtering chamber and an inert gas (Ar) is introduced. Applying<br />

the RF power and introducing a pressure controlled gas ow leads to the presence<br />

31

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