論文

査読有り
2014年4月

Epitaxial growth of Si-1 (-) Ge-x(x) alloys and Ge on Si(100) by electron-cyclotron-resonance Ar plasma chemical vapor deposition without substrate heating

THIN SOLID FILMS
  • Naofumi Ueno
  • ,
  • Masao Sakuraba
  • ,
  • Junichi Murota
  • ,
  • Shigeo Sato

557
開始ページ
31
終了ページ
35
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.tsf.2013.11.023
出版者・発行元
ELSEVIER SCIENCE SA

By using electron-cyclotron-resonance (ECR) Ar-plasma chemical vapor deposition (CVD) without substrate heating, the epitaxial growth process of Si1-xGex alloy and Ge films deposited directly on dilute-HF-treated Si(100) was investigated. From the reflection high energy electron diffraction patterns of the deposited Si1-xGex alloy (x-0.50, 0.75) and Ge films on Si(100), it is confirmed that epitaxial growth can be realized without substrate heating, and that crystallinity degradation at larger film thickness is observed. The X-ray diffraction peak of the epitaxial films reveals the existence of large compressive strain, which is induced by lattice matching with the Si(100) substrate at smaller film thicknesses, as well as strain relaxation behavior at larger film thicknesses. The Ge fraction of Si1-xGex thin film is in good agreementwith the normalized GeH4 partial pressure. The Si1-xGex deposition rate increases with an increase of GeH4 partial pressure. The GeH4 partial pressure dependence of partial deposition rates [(Si or Ge fraction) x (Si1-xGex thickness)/(deposition time)] shows that the Si partial deposition rate is slightly enhanced by the existence of Ge. From these results, it is proposed that the ECR-plasma CVD process can be utilized for Ge fraction control in highly-strained heterostructure formation of group IV semiconductors. (C) 2013 Elsevier B.V. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.tsf.2013.11.023
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000333968300007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.tsf.2013.11.023
  • ISSN : 0040-6090
  • Web of Science ID : WOS:000333968300007

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