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Amorphous/Microcrystalline Phase Control in Silicon Film Deposition for Improved Solar Cell Performance

Published online by Cambridge University Press:  09 August 2011

Joohyun Koh
Affiliation:
Center for Thin Film Devices, The Pennsylvania State University, University Park, PA 16802.
H. Fujiwara
Affiliation:
Electrotechnical Laboratory, 1-1-4 Umezono, Tsukuba-shi, Ibaraki 305-8568, Japan.
Yeeheng Lee
Affiliation:
Center for Thin Film Devices, The Pennsylvania State University, University Park, PA 16802.
C. R. Wronski
Affiliation:
Center for Thin Film Devices, The Pennsylvania State University, University Park, PA 16802.
R. W. Collins
Affiliation:
Center for Thin Film Devices, The Pennsylvania State University, University Park, PA 16802.
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Abstract

Real time optical studies have provided insights into the growth of hydrogenated amorphous silicon (a-Si:H) and microcrystalline silicon (μc-Si:H) thin films by plasma-enhanced chemical vapor deposition as a function of the H2-dilution gas flow ratio Research-article=[H2]/[SiH4], the accumulated film thickness db, and the substrate material. Results pertinent to the optimization of a-Si:H-based solar cells have been obtained in studies of Si film growth at moderate to high R on dense amorphous semiconductor film surfaces. For depositions with 15≤Research-article≤80 on freshly-deposited a-Si:H, initial film growth occurs in the amorphous phase. Upon continued growth, however, a transition is observed as crystallites begin to nucleate from the amorphous film. The thickness at which this amorphous-to-microcrystalline (a→μc) transition occurs is found to decrease with increasing R.Based on these results, a deposition phase diagram has been proposed that describes the a–gc transition as a continuous function of R and db. We find that the optimum stabilized a-Si:H p-i-n solar cell performance is obtained in an i-layer growth process that is maintained as close as possible to the phase boundary (but on the amorphous side) versus film thickness.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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