English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Finite-size effects in the nuclear magnetic resonance of epitaxial palladium thin films

MPS-Authors
/persons/resource/persons280261

MacFarlane,  W. A.
Department Solid State Spectroscopy (Bernhard Keimer), Max Planck Institute for Solid State Research, Max Planck Society;

Larkin,  T. I.
Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

MacFarlane, W. A., Parolin, T. J., Larkin, T. I., Richter, G., Chow, K. H., Hossain, M. D., et al. (2013). Finite-size effects in the nuclear magnetic resonance of epitaxial palladium thin films. Physical Review B, 88(14): 144424.


Cite as: https://hdl.handle.net/21.11116/0000-000E-C7A7-5
Abstract
We have measured the NMR of Li-8(+) implanted in a set of thin epitaxial films of Pd. We find a large, negative, strongly temperature-dependent Knight shift K consistent with previous measurements on polycrystalline films. The temperature dependence of the shift exhibits a characteristic deviation from the susceptibility chi(T). In particular, at low temperature, K(T) continues to follow a simple Curie-Weiss dependence. This result provides important insight into the origin of the low-temperature behavior of chi(T) in strongly paramagnetic metals. In addition, we find the room temperature shift depends on film thickness, with changes on the order of 20% between films 100 nm and 30 nm thick. We also observe a surface-related resonance in both Au-capped and uncapped films with a small positive shift. These features bear a striking similarity to the Pt NMR line shapes in much smaller Pt particles. However, they seem to originate, not from adsorbed species, but rather in confinement effects on the highly exhange-enhanced Pd d band.