uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • 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
Magnetic and electronic structure of the TlCo2S2
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Materials Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics.
Show others and affiliations
2004 (English)In: Journal of Solid State Chemistry, ISSN 0022-4596, E-ISSN 1095-726X, Vol. 177, no 9, 2977-2984 p.Article in journal (Refereed) Published
Abstract [en]

An extensive investigation of the ferromagnetic compound TlCo2S2 has resulted in new information on the electronic and magnetic structure. Electronic structure calculations showed that magnetic ordering is energetically favorable with a clear driving force for ferromagnetic coupling within the cobalt layers. TlCo2S2 is metallic and the conductivity is due to holes in the valence band. XPS single crystal measurements did not show evidence of mixed oxidation states of cobalt. Neutron powder diffraction resulted in a ferromagnetic structure with the magnetic moment in the ab-plane. The derived magnetic moment of the cobalt atom is at 10 K and is in very good agreement with the value, at 10 K, inferred from the magnetic hysteresis curve.

Place, publisher, year, edition, pages
2004. Vol. 177, no 9, 2977-2984 p.
National Category
Engineering and Technology Natural Sciences
Identifiers
URN: urn:nbn:se:uu:diva-93540DOI: 10.1016/j.jssc.2004.04.057OAI: oai:DiVA.org:uu-93540DiVA: diva2:167048
Available from: 2005-10-07 Created: 2005-10-07 Last updated: 2017-12-14Bibliographically approved
In thesis
1. Chemical Tuning of the Magnetic Interactions in Layer Structures
Open this publication in new window or tab >>Chemical Tuning of the Magnetic Interactions in Layer Structures
2005 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Thin metal films have found their use in many magnetic devices. They form pseudo two-dimensional systems, where the mechanisms for the magnetic interactions between the layers are not completely understood. Layered crystal structures have an advantage over such artificial systems, since the layers can be strictly mono-atomic without any unwanted admixture. In this study, some model systems of layered magnetic crystal structures and their solid solutions have been investigated by x-ray and neutron diffraction, Mössbauer and electron spectroscopy, heat-capacity and magnetic measurements, and first-principle electronic structure calculations, with the goal of deepening our understanding through controlled chemical synthesis.

The compounds TlCo2S2, TlCo2Se2 and their solid solution TlCo2Se2-xSx, all containing well separated cobalt atom sheets, order with the moments ferromagnetically aligned within the sheets. In TlCo2S2, the net result is ferromagnetism, while TlCo2Se2 exhibits antiferromagnetism. The inter-layer distance is crucial for the long-range coupling, and it was varied systematically through Se-S substitution. The incommensurate helical magnetic structure found for TlCo2Se2 (x = 0) prevails in the composition range 0 ≤ x ≤ 1.5 but the pitch of the helix changes. The accompanying reduction in inter-layer distance on sulphur substitution varies almost linearly with the coupling angle of the helix. An additional competing commensurate helix (90°) appears in the medium composition range (found for x = 0.5 and 1.0).

The systems TlCo2-xMexSe2 show helical magnetic ordering for Me = Fe or Cu, while a collinear antiferromagnetic structure occurs for Me = Ni. Magnetic order is created by iron substitution for copper in the Pauli paramagnetic TlCu2Se2, but now with the moments perpendicular to the metal sheets.

TlCrTe2 forms a quite different crystal structure, with intra-layer ferromagnetic alignment and net collinear antiferromagnetism. In contrast to the other phases, the values of the moments conform well to a localised model for Cr3+.

Place, publisher, year, edition, pages
Uppsala: Institutionen för materialkemi, 2005. 63 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 97
Keyword
Inorganic chemistry, neutron powder diffraction, magnetometry, layered magnetic structure, incommensurate helical structure, ThCr2Si2 type structure, antiferromagnetism, ferromagnetism, electronic structure calculations, Oorganisk kemi
National Category
Inorganic Chemistry
Identifiers
urn:nbn:se:uu:diva-5973 (URN)91-554-6357-6 (ISBN)
Public defence
2005-10-28, Häggsalen, Ångström Laboratory, Lägerhyddsvägen 1, Uppsala, 10:15
Opponent
Supervisors
Available from: 2005-10-07 Created: 2005-10-07 Last updated: 2013-09-13Bibliographically approved
2. Tunable Magnetic Properties of Transition Metal Compounds
Open this publication in new window or tab >>Tunable Magnetic Properties of Transition Metal Compounds
2005 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The magnetic properties of transition metal compounds have been studied using SQUID-magnetometry, magnetic force microscopy and Lorentz transmission electron microscopy. New magnetic materials have been found and their magnetic properties have been determined. How the magnetic properties of a material can be changed through e.g. chemical substitution of magnetic and nonmagnetic atoms and shape and size effects have also been studied. Three different sets of samples have been investigated: three new Mn-compounds, two substitution series of layered magnetic structures and ferromagnetic micronsized thin film elements.

The three Mn-compounds, Mn3IrSi, IrMnSi and Mn8Pd15Si7, show different magnetic ordering. Mn3IrSi orders 'antiferromagnetically' at 210 K. IrMnSi forms a double cycloidal spin spiral below 460 K. Mn8Pd15Si7 only shows short-range magnetic ordering.

Substituting Se with S in TlCo2Se2-xSx changes the magnetic order from a spin spiral to a colinear ferromagnet for a composition of x=1.75. An intermediate region exists where the compound is neither a pure ferromagnet, nor purely a spin spiral, as evidenced by the magnetization versus field measurements for the x=1.3 and 1.5 samples. This is also seen in the temperature dependent susceptibility measurements. For the TlCu2-xFexSe2 compounds it was found that the ordering temperature and saturation magnetic moment per Fe-atom changed with composition x.

Ferromagnetic micronsized thin film elements in permalloy, Fe20Ni80, and epitaxial Fe/Co multilayers were studied. For the Fe/Co multilayer thin film elements it was found that it is possible to change the magnetization reversal process, by aligning the easy shape anisotropy axis with either the easy or the hard magnetocrystalline anisotropy axis. In the permalloy elements the effect of inter-elemental distance was found to determine the interval of fields where multidomain states were stable, so that for shorter inter-elemental distances multidomain states were stable for a shorter interval of fields. The domain structure of permalloy elements in rotating magnetic fields was also studied. Higher applied fields led to a broader interval of angles in which saturated states were stable.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2005. viii, 58 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 95
Keyword
Magnetic properties, Transition metal compounds, Magnetic structure, Domain structure, SQUID-magnetometry, MFM
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-5939 (URN)91-554-6346 (ISBN)
Public defence
2005-10-14, Polhemsalen, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 10:00
Opponent
Supervisors
Available from: 2005-09-22 Created: 2005-09-22 Last updated: 2015-09-14Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full text

Authority records BETA

Berger, RolfNordblad, Per

Search in DiVA

By author/editor
Berger, RolfNordblad, Per
By organisation
Department of Materials ChemistryDepartment of PhysicsDepartment of Materials Science
In the same journal
Journal of Solid State Chemistry
Engineering and TechnologyNatural Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 1089 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • 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