کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1333429 979077 2007 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Structure and magnetism of rare-earth-substituted Ca3Co2O6
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Structure and magnetism of rare-earth-substituted Ca3Co2O6
چکیده انگلیسی

Yttrium- and rare-earth-substituted derivatives of Ca3−vRvCo2O6 (RY, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Yb, and Lu) have been synthesized and structurally characterized by powder X-ray and neutron diffraction. All phases adopt the K4CdCl6-type structure with space group R3¯c), in which the trivalent R3+ substituents randomly occupy the Ca2+ site. The homogeneity range of Ca3−vRvCo2O6 extends to v≈0.90 for the substituents concerned. A significant increase in the Co2–O distances within the trigonal-prismatic Co2O6 co-ordination polyhedra upon introduction of R3+ confirms that extra electrons from the R3+-for-Ca2+ substitution exclusively enter the Co2 site of the quasi-one-dimensional Ca3−vRvCo2O6 structure, thereby formally reducing its oxidation state. This is furthermore supported by magnetic susceptibility and low-temperature neutron diffraction measurements. The long-range ferrimagnetic ordering temperature is reduced upon R substitution and appears to vanish for v>∼0.30.

Yttrium- and rare-earth-substituted derivatives of Ca3−vRvCo2O6 have been synthesized. A significant increase in the Co2–O distances within the trigonal-prismatic Co2O6 coordination polyhedra confirms that extra electrons from the R3+-for-Ca2+ substitution enter the Co2 site, thereby formally reducing its valence state. The long-range ferrimagnetic ordering of the parent Ca3Co2O6 phase vanishes at v>∼0.30 in Ca3−vRvCo2O6.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Solid State Chemistry - Volume 180, Issue 2, February 2007, Pages 628–635
نویسندگان
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