2005
DOI: 10.1016/j.jssc.2004.10.026
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Synthesis, structure, and magnetism of Tb4PdGa12 and Tb4PtGa12

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Cited by 13 publications
(23 citation statements)
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“…So far, the magnetic properties of 4:1:12 compounds are only known for Tb 4 PdGa 12 and Tb 4 PtGa 12 that both order antiferromagnetically at T N = 16 and 12 K and display metamagnetic transitions at 0 H c ≈ 5 and 0.3 T, respectively [24,25]. Similarly, U 4 PdGa 12 also orders antiferromagnetically, at T N = 43 K, but does not show any metamagnetic transitions up to μ 0 H c = 9 T.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…So far, the magnetic properties of 4:1:12 compounds are only known for Tb 4 PdGa 12 and Tb 4 PtGa 12 that both order antiferromagnetically at T N = 16 and 12 K and display metamagnetic transitions at 0 H c ≈ 5 and 0.3 T, respectively [24,25]. Similarly, U 4 PdGa 12 also orders antiferromagnetically, at T N = 43 K, but does not show any metamagnetic transitions up to μ 0 H c = 9 T.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, the first physical measurements of 4:1:12 compounds were reported on two isotype compounds, Tb 4 PdGa 12 and Tb 4 PtGa 12 . They both order antiferromagnetically at T N = 16 and 12 K and present metamagnetic transitions at μ 0 H c ≈ 5 and 0.3 T, respectively [24,25].…”
Section: Introductionmentioning
confidence: 99%
“…Alternatively to the above method, the ternary phase can also be synthesized following the published heating profile for Tb 4 PdGa 12 . 42 Yttrium (0.068 g, 1 mmol), manganese (0.041 g, 1 mmol), and excess gallium (1.0532 g, 20 mmol) were combined in an alumina crucible and sealed in the same manner as mentioned above. The tube was heated to 1150 °C over 7 h, slowly cooled to 530 °C over 41 h, then cooled down to 300 °C in 2 h, inverted, and centrifuged to remove excess Ga flux.…”
Section: Methodsmentioning
confidence: 99%
“…Clues to how atomic sizes may influence the favorability of the HoCoGa 5 type can be found in our earlier CP analysis of the Y 4 PdGa 12 structure type, which can accommodate larger transition metal atoms into the octahedral holes of a AuCu 3 -like YGa 3 network (Figure a). A hypothetical “YGa 3 ” phase was found to be destabilized by the stretching of the Ga–Ga interactions due to the relatively large size of the Y atoms. Filling 1/4 of the octahedral holes with a transition metal atom was found to relieve this situation in two ways: (1) the presence on the T atoms replaced the overly long the Ga–Ga contacts in their Ga 6 environment with nearly ideal T–Ga ones, and (2) the expansion of the stuffed Ga 6 octahedron compresses the Ga–Ga distances in neighboring unstuffed octahedra.…”
Section: Results and Discussionmentioning
confidence: 91%