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The Effect of UV Light on IR Absorption in Chemically Vapor Deposited a-SiNx:H Films

Published online by Cambridge University Press:  22 February 2011

C. H. Seager
Affiliation:
Sandia National Laboratories, Albuquerque, N. M. 87185
J. Kanicki
Affiliation:
IBM Research Division, T. J. Watson Research Center, Yorktown Heights, N. Y. 0598
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Abstract

We have measured the optical absorption properties of Plasma Enhanced Chemically Vapor Deposited (PECVD) films of hydrogenated amorphous silicon nitride (a-SiNx:H) over the energy range from 0.54 to 2 eV using Photothermal Deflection Spectroscopy (PDS). The near-infrared absorption properties of these films provide a quantitative estimate of the amount of H bonded to Si or N as well as a measure of the the density of electronic gap states due to species like Si dangling bonds. Typical PDS spectra obtained on as-deposited films show a broad absorption tail with a large number of narrow absorption peaks. Using the phase sensitive feature of this spectroscopy we are able to separate nitride-related absorption from that arising from the fused quartz substrates. In addition to the broad, featureless band tail, whose magnitude is quite sensitive to optical excitation with light above ̃3.9 eV, we observe a number of narrow absorption peaks which we identify as overtones of localized vibrational modes. Specifically, we see peaks at 0.82 and 1.20 eV which we identify as the 1st and second harmonics of N-H stretching vibrations, and several other peaks whose origins remain undetermined. Prolonged UV excitation produces no detectable change in these vibrational modes, although large changes are seen in the underlying absorption tail. This reinforces previous suggestions that photoinduced changes in these films do not arise from rearrangement of the bonded hydrogen.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

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