Bulk band structure and Fermi surface of nickel: A soft x-ray angle-resolved photoemission study

N. Kamakura, Y. Takata, T. Tokushima, Y. Harada, A. Chainani, K. Kobayashi, S. Shin

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)


We study the bulk band structure and Fermi surface of nickel metal by soft x-ray angle-resolved photoemission spectroscopy (SX ARPES). SX ARPES, using tunable photons from hν∼300 to 800 eV, facilitates depth-sensitive in-plane band mapping of Ni(100). Horizontal- and vertical-polarization- dependent studies are used to selectively enhance dipole-allowed transitions. While low-temperature (50 K) results provide band dispersions consistent with the direct transition model, room-temperature (300 K) studies confirm and quantify significant intensity loss due to nondirect transitions. The band maps provide band dispersions and identify all the bands in the Γ-X-W-W-X- Γ quadrant in momentum space. In particular, the results show that a hole pocket derived from the X2↓ down-spin band exists in bulk Ni. This is in contrast to results of surface-sensitive ultraviolet ARPES studies but consistent with other bulk-sensitive measurements. The Z1↓ band is also shown to have depth-sensitive band dispersion and Fermi surface crossings. In addition, the magnetically active Z2↓ down-spin band shows nearly flatband behavior. The Fermi surface and band dispersions determined by the present ARPES measurements are in good agreement with local density approximation band structure calculations. SX ARPES is thus a valuable probe of the intrinsic momentum-resolved electronic structure of solids.

Original languageEnglish
Article number045127
JournalPhysical Review B - Condensed Matter and Materials Physics
Issue number4
Publication statusPublished - 2006

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics


Dive into the research topics of 'Bulk band structure and Fermi surface of nickel: A soft x-ray angle-resolved photoemission study'. Together they form a unique fingerprint.

Cite this