Interplay of Chemical Bonding and Magnetism in Fe_4N, Fe_3N, Fe_2N

Physics – Condensed Matter – Materials Science

Scientific paper

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

16 pages, 15 figures

Scientific paper

10.1016/S0304-8853(99)00296-6

Using spin density functional theory we have carried out a comparative study of chemical bonding and magnetism in Fe_4N, Fe_3N and Fe_2N. All of these compounds form close packed Fe lattices, while N occupies octahedral interstitial positions. High spin fcc Fe and hypothetical FeN with rock salt structure have been included in our study as reference systems. We find strong, covalent Fe-N bonds as a result of a substantial \sigma-type p-d hybridisation, with some charge transfer to N. Those Fe d orbitals which contribute to the p-d bonds, do no longer participate in the exchange splitting of the Fe d bands. Because of the large exchange fields, the majority spin d bands are always fully occupied, while the minority spin d bands are close to half-filling, thus optimizing the Fe d-d covalent bonding. As a consequence, in good approximation the individual Fe moments decrease in steps of 0.5 \mu_B from fcc iron (2.7 \mu_B) via Fe_4N (2.7 and 1.97 mu_B}), \chem{Fe_3N} (1.99 \mu_B) to \zeta - Fe_2N (1.43 \mu_B).

No associations

LandOfFree

Say what you really think

Search LandOfFree.com for scientists and scientific papers. Rate them and share your experience with other people.

Rating

Interplay of Chemical Bonding and Magnetism in Fe_4N, Fe_3N, Fe_2N does not yet have a rating. At this time, there are no reviews or comments for this scientific paper.

If you have personal experience with Interplay of Chemical Bonding and Magnetism in Fe_4N, Fe_3N, Fe_2N, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Interplay of Chemical Bonding and Magnetism in Fe_4N, Fe_3N, Fe_2N will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFWR-SCP-O-542915

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.