24
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

Thermal modification of wide-bandgap hydrogenated amorphous silicon-carbon alloy films grown by plasma-enhanced chemical vapour deposition from C2H2+SiH4 mixtures

, &
Pages 485-496 | Received 07 Jun 1996, Accepted 12 Sep 1996, Published online: 20 Aug 2006
 

Abstract

The thermal stability of hydrogenated amorphous silicon-carbon (a-Si1−xCx: H) alloy films grown by plasma-enhanced chemical vapour deposition from C2H2+SiH4 mixtures was characterized by means of infrared spectroscopy, electron spin resonance, transmittance-reflectance spectroscopy and photoluminescence (PL) spectroscopy. It is demonstrated that the network undergoes relaxation and reconstruction under the condition of low-temperature annealing. Weak C-C, Si-Si and C-Si bonds will be broken, and a new stage of hydrogen effusion and structural rearrangement will occur under the condition of high-temperature annealing. The thermal stability a-Si1−xCx:H of films increases with increase in carbon content. In carbon-poor a-Si1−xCx:H networks, the dangling bonds are the main non-radiative recombination channel, which causes a strong correlation of the PL signal with defect density. In carbon-rich a-Si1−xCx:H networks, π-bonded clusters play an important role in the luminescence process. The PL intensity has little dependence on defects in carbon-rich a-Si1−xCx:H.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.