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Nmr Study of Ortho-Molecular Hydrogen in Hydrogenated Amorphous Silicon

Published online by Cambridge University Press:  15 February 2011

Tining Su
Affiliation:
University of Utah, Department of Physics, Salt Lake City, Utah
P.C. Taylor
Affiliation:
University of Utah, Department of Physics, Salt Lake City, Utah
Shenlin Chen
Affiliation:
University of Utah, Department of Physics, Salt Lake City, Utah
R.S. Crandall
Affiliation:
National Renewable Energy Laboratory, Golden, Colorado.
A.H. Mahan
Affiliation:
National Renewable Energy Laboratory, Golden, Colorado.
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Abstract

A Jeener-Broekaert three-pulse sequence is used to investigate ortho-molecular hydrogen (o-H2) in device quality amorphous silicon films prepared by plasma enhanced chemical vapor deposition (PECVD) and hot wire CVD (HWCVD). For the PECVD sample, the concentration of hydrogen molecules is ~ 11% of the total hydrogen concentration, one order of magnitude larger than that inferred from spin-lattice relaxation time measurements (~1%). Hence, most of the hydrogen molecules do not serve as effective relaxation centers. For HWCVD samples with ~3 to 4% hydrogen and very low void densities, the concentrations of hydrogen molecules are ~1% of the total hydrogen concentration. In these samples, spin-lattice relaxation measurements for bonded hydrogen indicate that the concentration of hydrogen molecules that contribute to spin-lattice relaxation is at most 0.1% of the total hydrogen concentration. Spin-lattice relaxation time (T1) measurements of ortho-molecular hydrogen indicate two very different T1's. The longer T1 is ~ 0.6 s, possibly due to an electric quadrupole-quadrupole (EQQ) interaction between o-H2 molecules and, the shorter T1 is ~ 3 ms, very close to that calculated for a two-phonon Raman process for rotating o-H2.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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