Abstract :
Hydrogen interaction with defects in thin niobium (Nb) films was investigated using slow positron implantation spectroscopy
(SPIS) combined with X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thin Nb films on Si substrates
were prepared using cathode beam sputtering at room temperature. Initially, the microstructure of the virgin (hydrogen-free)
films was characterized. Subsequently, the films were step-by-step electrochemically charged with hydrogen and the evolution
of the microstructure with increasing hydrogen concentration was monitored. Hydrogen loading leads to a significant lattice
expansion which was measured by XRD. Contrary to free-standing bulk metals, thin films are highly anisotropic. The in-plane
expansion is prevented because the films are clamped on the elastically hard substrate. On the other hand, the out-of-plane
expansion is substantially higher than in the bulk samples. Moreover, an enhanced hydrogen solubility in the a-phase was found
in nanocrystalline Nb films. It was found that most of positrons in the films are trapped at open-volume defects at grain
boundaries (GBs). These defects represent trapping sites also for hydrogen atoms. Hydrogen trapping at vacancy-like defects
like GBs leads to a local increase of the electron density and is reflected by a pronounced decrease of the S parameter in the
hydrogen-loaded samples. In addition, it was found that new defects are introduced at higher concentrations of hydrogen due to
the formation of NbH (b-phase) particles
Keywords :
Niobium films , hydrogen , Doppler broadening , X-ray diffraction , Slow positron implantation spectroscopy