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Photoluminescence of plasma enhanced chemical vapor deposition amorphous silicon oxide with silicon nanocrystals grown at different fluence ratios and substrate temperatures
Journal article   Peer reviewed

Photoluminescence of plasma enhanced chemical vapor deposition amorphous silicon oxide with silicon nanocrystals grown at different fluence ratios and substrate temperatures

Chun-Jung Lin, Chi-Kuan Lin, Chih-Wei Chang, Yu-Lun Chueh, Hao-Chung Kuo, Eric Wei-Guang Diau, Li-Jen Chou and Gong-Ru Lin
Japanese Journal of Applied Physics, Part 1: Regular Papers and Short Notes and Review Papers, Vol.45(2 A), pp.1040-1043
08/02/2006

Abstract

Lifetime Photoluminescence Plasma enhanced chemical vapor deposition Si-rich silicon dioxide Silicon nanocrystals
Near-infrared photoluminescent dynamics of thermally annealed Si-rich SiO x films grown by plasma enhanced chemical vapor deposition at different substrate temperatures and N 2 O/SiH 4 fluence ratios are studied. The size of nanocrystallite Si (nc-Si) critically depends on the density of oxygen atoms in a Si-rich layer when the N 2 O/SiH 4 ratio is smaller than 4; that is, it significantly increases at low N 2 O/SiH 4 ratios. Deposition at a high N 2 O/SiH 4 ratio strongly reduces the density of nc-Si and degrades the luminescence at 700-800 nm since the density of oxygen atoms is sufficient in the reaction of nc-Si with silicon atoms and formation of a stoichiometric SiO 2 matrix. Under a high RF power condition, the increasing substrate temperature usually inhibits the precipitation of nc-Si since high-temperature growth facilitates stochiometric SiO 2 deposition. The disappearance of visible PL reveals the complete regrowth of a stoichiometric SiO 2 matrix around a nanocrystallite Si cluster after annealing. The results of the transient luminescent analysis of Si-rich SiO x samples corroborate well with the observed values and reveal a lifetime of 43 μs under an optimized nc-Si precipitation condition of 1100°C annealing for 3 h. ©2006 The Japan Society of Applied Physics.

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