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Hydrogen Manipulated Below Surface of Palladium
Scientists at Penn State University in University
Park, Pennsylvania, have manipulated hydrogen
atoms into stable sites beneath the surface of
a palladium crystal, creating a structure predicted
to be important in metal catalysts, hydrogen storage
and fuel cells.
Observations of the effects of the resulting subsurface
hydrides hydrogen atoms with a partial
negative charge confirmed the existence
of the stable sites, which had been predicted
but previously had neither been deliberately assembled
nor directly observed. The research was led by
Paul S. Weiss, distinguished professor of chemistry
and physics at Penn State.
After moving absorbed hydrogen atoms to just below
the crystal surface, the researchers were able
to observe how the presence of the hydride in
specific sites within a metal crystal affects
the chemical, physical and electronic properties
of the metal. Understanding these effects could
advance efforts to improve chemical reactions
involving metal catalysts. In addition, the subsurface
hydride may provide a model material for application
in hydrogen storage and fuel cells. The ability
to prepare the subsurface hydride provides a research
tool for these applications.
The researchers carried out the experiments in
a low-temperature scanning tunneling microscope
(STM) under ultrahigh vacuum by exposing the crystal
to a hydrogen atmosphere. They removed excess
hydrogen from the surface by cycles of exposure
to heat and oxygen. After the surface had been
cleaned, the researchers were able to use electrons
from the STM tip to move hydrogen atoms that had
been absorbed into the bulk metal up into the
stable subsurface sites. As the hydride formed
underneath the surface of the material, Weiss
and his team observed that the surface of the
crystal distorted, the positive charge of palladium
atoms above them increased, and interactions occurred
with hydrogen atoms on the surface of the palladium
crystal.
This research was funded by the Air Force Office
of Scientific Research, with additional support
from the Army Research Office, the National Science
Foundation and the Office of Naval Research.
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