Magnetic ordering in the rutile molecular magnets MII[N(CN)2]2 (M = Ni, Co, Fe, Mn, Ni0.5Co0.5, and Ni0.5Fe0.5)

Alexandros Lappas, Andrew S. Wills, Mark A. Green, Kosmas Prassides, Mohamedally Kurmoo

研究成果: Article査読

33 被引用数 (Scopus)

抄録

Rietveld refinement of powder neutron diffraction data, combined with group theory considerations, is used to determine the magnetic structures of the binary metal dicyanamide, MII[N(CN)2]2 where M = Ni, Co, Fe, Mn, Ni0.5Co0.5, and Ni0.5Fe0.5. Compounds with M = Mn or Fe show a canted antiferromagnetic arrangement of spin oriented in the ab crystallographic plane, with antiparallel components of the two sublattices along the a axis and parallel along the b axis. Symmetry considerations forbid an additional moment, whether compensated or not, to be present along the c axis. The compounds with fewer unpaired electrons (Co and Ni) are ferromagnets, with all moments oriented along the c axis. The mixed composition of Ni0.5Co0.5 displays the same collinear ferromagnetic structure as its parent compounds. However, the composition with M = Ni0.5Fe0.5, whose parent compounds show different magnetic behavior, does not exhibit long-range magnetic ordering down to 1.7 K. Magnetostriction was observed for the ferromagnets for which we investigated the variable temperature powder neutron diffraction. The cobalt-rich compounds show more pronounced effects, consistent with their increasing magnetocrystalline anisotropy.

本文言語English
論文番号144406
ページ(範囲)1444061-1444068
ページ数8
ジャーナルPhysical Review B - Condensed Matter and Materials Physics
67
14
出版ステータスPublished - 2003 4月

ASJC Scopus subject areas

  • 電子材料、光学材料、および磁性材料
  • 凝縮系物理学

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