Abstract
Hydrogen interactions with microscopic cavities in Si were quantitatively characterized in thermal-release experiments. Closed internal cavities were formed by He-ion implantation and annealing and were characterized by transmission-electron microscopy. The isotopes protium ${(}^{1}$H) and deuterium (D) were introduced by ion implantation or heating in ${\mathrm{H}}_{2}$ gas. During temperature ramping the redistribution and release of D were monitored by nuclear-reaction profiling, and the bonding of $^{1}\mathrm{H}$ was selectively examined by infrared absorption spectroscopy. By exploiting the properties of closed internal surfaces this study determined the Si-H bond energy for surface monohydrides, the result being 2.5\ifmmode\pm\else\textpm\fi{}0.2 eV. Hydrogen bonded to the internal surfaces was found to lie several tenths of an eV lower in energy than ${\mathrm{H}}_{2}$ gas and H trapped at lattice defects. The oxidized external surface of the Si specimens did not detectably impede H release, implying an efficient recombination process at the Si-${\mathrm{SiO}}_{2}$ interface for which possible mechanisms are considered.
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