Solid-Phase Epitaxy Emitter for Silicon Solar Cells
- Authors
- Kim, Hyunho; Park, Sungeun; Ji, Kwang-Sun; Lee, Kyung Dong; Kim, Seongtak; Bae, Soohyun; Ahn, Seh-Won; Lee, Heon-Min; Kang, Yoonmook; Lee, Hae-Seok; Kim, Donghwan
- Issue Date
- 10월-2016
- Publisher
- AMER SCIENTIFIC PUBLISHERS
- Keywords
- Solid-Phase Epitaxy; Solar Cells; Solid-Phase Epitaxy Emitter (SEE); Crystallization
- Citation
- JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, v.16, no.10, pp.10702 - 10706
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
- Volume
- 16
- Number
- 10
- Start Page
- 10702
- End Page
- 10706
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/87317
- DOI
- 10.1166/jnn.2016.13222
- ISSN
- 1533-4880
- Abstract
- This paper presents a new emitter formation method, "solid-phase epitaxy emitter," that involves an applied solid-phase epitaxial growth based on the rapid thermal processing of a-Si:H thin films. We describe the solid-phase epitaxial growth of intrinsic and phosphorous-doped a-Si: H thin films through rapid thermal processing using radio-frequency plasma-enhanced chemical vapor deposition. The phase transition of these films results from heat treatment above 600 degrees C. We examined the defects in the epitaxially grown silicon that formed at the phase interfaces. Phosphorous-doped a-Si: H produced using phosphine gas (PH3, diluted H-2) exhibited a diminished crystallinity compared with intrinsic a-Si: H because of the disturbance of dopant atoms. Based on this formation method, we fabricated a solid-phase epitaxy emitter cell with an efficiency of 16.7%. In addition, this method is expected to be simpler and more cost effective than the conventional method.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School of Energy and Environment (KU-KIST GREEN SCHOOL) > Department of Energy and Environment > 1. Journal Articles
- College of Engineering > Department of Materials Science and Engineering > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.