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Hydriding Reaction of LaNi5: Correlations between Thermodynamic States and Sorption Kinetics during Activation
Ist Teil von
Physical Chemistry, 2011, p.105-113
Ort / Verlag
Canada: Apple Academic Press
Erscheinungsjahr
2011
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Introduction
Metal-hydride systems are increasingly studied for hydrogen-storage applications.
In particular, many intermetallic compounds (IMCs) such as the Haucke (AB5)
phases oer several interesting features, in terms of specic energy, volumetric
energy, and kinetics. Practical applications require the determination of both thermodynamic and kinetic properties which are, in general, measured separately.
Pneumatochemical impedance spectroscopy (PIS) [1] now oers the possibility
of analyzing hydriding/dehydriding reaction mechanisms, raw kinetic data being measured using a classical Sieverts experimental setup [2]. Using PIS, kinetic
information is not only a measure of a global reaction rate (limited by any ratedetermining step): the dierent steps involved in the sorption reaction are put
into evidence and the values of individual rate parameters are inferred. Results obtained so far on various IMCs indicate that most hydriding mechanisms involve
two microscopic reaction steps: (i) the surface chemisorption of molecular hydrogen which is dissociated into two surface ad-atoms; (ii) the diusion-controlled
transport of hydrogen atoms to bulk regions where they can either accumulate (in
solid-solution domains) or precipitate to form metal hydrides (in two-phase domains). PIS is therefore an in situ spectroscopic tool which can be used to analyze
surface and bulk processes in solid-gas systems.