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DESIGN CONCEPTS OF TF-SI SOLAR CELLS 347<br />

800<br />

600<br />

(a) Before<br />

processing<br />

Al<br />

Si (220)<br />

Intensity<br />

[CPS]<br />

400<br />

200<br />

0<br />

Al<br />

2500<br />

2000<br />

0 20 40 60 80 100 120 140<br />

2 q<br />

[deg]<br />

(b) After<br />

processing<br />

Si (220)<br />

1500<br />

Intensity<br />

[CPS]<br />

1000<br />

500<br />

Si (111)<br />

Al<br />

Al<br />

0<br />

0 20 40 60 80 100 120 140<br />

2 q<br />

[deg]<br />

Figure 8.27 XRD spectrum of a 2-µm-thick HWCVD Si film, deposited on Al/Cr/glass at about<br />

500 ◦ C (a) before optical processing; and (b) after optical processing at ∼480 ◦ C for 3 min. A significant<br />

increase in Si (220) compared to Si (111) orientation can be seen in (b)<br />

toward a-Si. From this figure, it is clear that 3 min of optical processing time was not<br />

sufficient to crystallize the entire film at 460 ◦ C. Figure 8.29(b) is a TEM plan view of<br />

the film showing distribution of grain sizes near the Si–Al interface.<br />

Detailed profiling of Al across the crystallized films, done by SIMS (secondary<br />

ion mass spectroscopy) and micro-X-ray, showed that in optically crystallized films the<br />

Al concentration dropped by several orders of magnitude within about 1 µm from the<br />

Al-Si interface [81, 83]. These results indicate that Al is required only for the initiation<br />

of crystallization. After the nucleation, the crystallization front propagates into a-Si while<br />

grain enhancement occurs in the crystallized film. It is believed that vacancy injection<br />

from Al-Si interface is responsible for grain enhancement.<br />

Investigation of the possibility of applying optically assisted MIC showed that<br />

crystallization of a-Si can start at about 200 ◦ C in less than 3 min. This crystallization

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