Confined High-Pressure Chemical Deposition of Hydrogenated Amorphous Silicon

Neil F. Baril, Rongrui He, Todd D. Day, Justin R. Sparks, Banafsheh Keshavarzi, Mahesh Krishnamurthi§, Ali Borhan, Venkatraman Gopalan§, Anna C. Peacock#, Noel Healy#, Pier J. A. Sazio#, and John V. Badding*
Department of Chemistry, Department of Chemical Engineering, §Department of Materials Science and Engineering, and Materials Research Institute, Pennsylvania State University, University Park, Pennsylvania 16802, United States
# Optoelectronics Research Centre, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom
J. Am. Chem. Soc., 2012, 134 (1), pp 19–22
DOI: 10.1021/ja2067862
Publication Date (Web): December 8, 2011
Copyright © 2011 American Chemical Society

Abstract

Abstract Image

Hydrogenated amorphous silicon (a-Si:H) is one of the most technologically important semiconductors. The challenge in producing it from SiH4 precursor is to overcome a significant kinetic barrier to decomposition at a low enough temperature to allow for hydrogen incorporation into a deposited film. The use of high precursor concentrations is one possible means to increase reaction rates at low enough temperatures, but in conventional reactors such an approach produces large numbers of homogeneously nucleated particles in the gas phase, rather than the desired heterogeneous deposition on a surface. We report that deposition in confined micro-/nanoreactors overcomes this difficulty, allowing for the use of silane concentrations many orders of magnitude higher than conventionally employed while still realizing well-developed films. a-Si:H micro-/nanowires can be deposited in this way in extreme aspect ratio, small-diameter optical fiber capillary templates. The semiconductor materials deposited have 0.5 atom% hydrogen with passivated dangling bonds and good electronic properties. They should be suitable for a wide range of photonic and electronic applications such as nonlinear optical fibers and solar cells.

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History

  • Published In Issue January 11, 2012
  • Article ASAPDecember 13, 2011
  • Just Accepted ManuscriptDecember 08, 2011
  • Received: July 20, 2011

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