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https://hdl.handle.net/2142/18878
Description
Title
Hydrogen in thin film niobium
Author(s)
Reimer, Paul Meyer
Issue Date
1993
Doctoral Committee Chair(s)
Zabel, Hartmut
Department of Study
Physics
Discipline
Physics
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
hydrogen
Thin films
niobium
x-ray diffraction
ion-beam
hydrogen profiling
Language
en
Abstract
"An experimental study of hydrogen dissolved in thin films of niobium is presented.
The chief techniques used were x-ray diffraction and ion-beam hydrogen profiling.
Niobium was grown on sapphire substrates by molecular beam epitaxy, resulting
in high quality films. It has previously been shown that such films are clamped by
the sapphire substrate: On hydrogen uptake they expand only in the out-of-plane
direction.
Transverse scans of these Nb films show evidence for a novel ordering, long-range
orientational ordering (LROO): For a portion of the film, the crystallographic planes
are oriented over in-plane length scales larger than the in-plane atomic correlation
length. The well-oriented planes are exactly parallel to the crystallographic planes of
the sapphire substrate.
The concept of lattice roughness is introduced-this is the root mean square deviation
in the out-of-plane direction, modulo the lattice parameter, of the atoms in
each crystallographic plane. It is shown that lattice roughness leads to a Q dependent
damping factor, similar to a Debye-Waller factor, which affects LROO peaks. This
explains, qualitatively, the radial dependence seen in the transverse scans. A method
is illustrated to quantitatively measure the lattice roughness and the fraction of the
sample which is well-oriented (in the sense of LROO).
A Nb sample with an initially broad LROO peak showed marked narrowing of the
peak on loading with hydrogen. This effect is ascribed to hydrogen-enhanced defect
mobility. This leads to a new means of improving metal film quality: ""cold-annealing""
by introducing hydrogen to sweep defects out to the sample boundary. A promising
preliminary trial of hydrogen defect annealing in the growth chamber resulted in a
sample with a larger portion in the LROO state. X-ray reflectivity measurements
which support this picture are shown.
A direct determination of the hydrogen-induced volume expansion as a function
of hydrogen concentration in Nb films, and gold-capped Nb films has been made.
Hydrogen concentration was measured by using 15N ion bombardment and lattice
parameter were measured with x-ray diffraction. The volume change in a clamped
film per unit hydrogen concentration, is found to be approximately three times that .
of bulk Nb.
It is shown that the hydrogen-induced volume depends on the derivative of of the
hydrogen heat of solution, !1H, with respect to the logarithm of the volume. It is
argued that the factor three enhancement may be largely explained by the strong
dependence of !1H on band parameters which have the necessary volume dependence
to reproduce the effect found. A supporting measurement on a partially-clamped
polycrystalline film is shown.
Ion bombardment yields a profile of hydrogen concentration as a function of depth
below the film surface. The H profiles indicate significant hydrogen gradients in thin
Nb films, with H concentration increasing with increasing depth. A concentration
gradient should lead to a lattice parameter gradient, observable with X-ray diffraction.
While the best thin films fail to show lattice parameter gradients, thicker and poorer
quality (polycrystalline) films do show gradients. These observations are reconciled
by assuming that there is a metastable, non-homogeneous, hydrogen concentration
mode (or resonance) in thin films. Supporting evidence is shown, and the conditions
for instability of the mode are discussed."
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