Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Sulfur- and Oxygen-Induced Alterations of the Iron (001) Surface Magnetism and Work Function: A Theoretical Study
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.ORCID iD: 0000-0001-8748-3890
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering. (SeRC)ORCID iD: 0000-0001-7788-6127
2013 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 117, no 12, 6161-6171 p.Article in journal (Refereed) Published
Abstract [en]

The electronic structure and magnetic properties of atomic sulfur and oxygen adsorbed on the iron (001) surface are examined using density functional theory (DFT). The sulfur/oxygen coverage is considered from a quarter of one monolayer (ML) to a full monolayer. The work function change, magnetic properties, and density of states are determined and compared. We find that the work function increases with sulfur coverage in agreement with experiment. We also find that sulfur interacts strongly with the surface layer and that the magnetic moment of the Fe surface decreases as the sulfur coverage increases. In the case of oxygen adsorption, we find that the magnetic moment of the surface Fe atoms instead increases. We show that the difference in surface magnetic moment between sulfur adsorption and oxygen adsorption can be simply explained combining the Slater-Pauling rigid band model linking d-occupation and magnetic moment with an electronegativity argument. Moreover, the work function of the Fe surface as a function of oxygen coverage is found to be very sensitive to overlayer arrangement, here seen in the cases of 0.5 ML c(2 x 2) and 0.5 ML p(2 x 1). This is shown to result from large differences in the surface dipole moment change induced by the oxygen adsorption in the two different overlayer arrangements.

Place, publisher, year, edition, pages
2013. Vol. 117, no 12, 6161-6171 p.
Keyword [en]
Density functional theories (DFT), Oxygen adsorption, Sulfur adsorption, Surface dipole moment, Surface magnetic moments, Surface magnetism, Theoretical study, Work function change
National Category
Physical Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-122527DOI: 10.1021/jp3102496ISI: 000317032100019Scopus ID: 2-s2.0-84875743327OAI: oai:DiVA.org:kth-122527DiVA: diva2:623041
Funder
Knut and Alice Wallenberg FoundationSwedish Research CouncilSwedish e‐Science Research Center
Note

QC 20130524

Available from: 2013-05-24 Created: 2013-05-23 Last updated: 2017-12-06Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full textScopus

Authority records BETA

Hugosson, Håkan WilhelmDelin, Anna

Search in DiVA

By author/editor
Hugosson, Håkan WilhelmCao, WeiminSeetharaman, SeshadriDelin, Anna
By organisation
Materials Science and Engineering
In the same journal
The Journal of Physical Chemistry C
Physical Chemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 42 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf