2016
DOI: 10.1103/physrevb.94.134414
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Magnetic properties of the covalent chain antiferromagnetRbFeSe2

Abstract: Single crystals of the ternary iron selenide RbFeSe 2 have been investigated by means of x-ray diffraction, magnetic susceptibility, magnetization, and specific-heat measurements as well as by Mössbauer spectroscopy. Built up from linear chains of edge-sharing FeSe 4 tetrahedra, RbFeSe 2 represents a quasi-one-dimensional antiferromagnet. Below T N = 248 K three-dimensional antiferromagnetic collinear magnetic order sets in, with the magnetic moments oriented perpendicularly to the chain direction. The hyperfi… Show more

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Cited by 29 publications
(42 citation statements)
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“…The most closely-related compounds to the K 2 MnS 2 structure type are the family of AFeX 2 (A = K, Rb, Cs, Tl; X = S, Se) compounds, which can be divided into three groups based on their crystal and magnetic structures. [13] All AFeX 2 compounds have tetrahedrally co-arXiv:1905.03318v1 [cond-mat.mtrl-sci] 8 May 2019 ordinated Fe 3+ chains along c, but many of these have an additional degree of structural freedom, manifested as a monoclinic distortion (TlFeS 2 , TlFeSe 2 , KFeSe 2 , and RbFeSe 2 with the magnetic moments ordered perpendicular to the chains; and KFeS 2 , RbFeS 2 with the ordered moments slightly tilted from the chain axis). [14,15] Only CsFeS 2 is orthorhombic, but it further distorts martensitically at its magnetic transition at 70 K, with moments slightly tilted off the chain direction.…”
Section: Introductionmentioning
confidence: 99%
“…The most closely-related compounds to the K 2 MnS 2 structure type are the family of AFeX 2 (A = K, Rb, Cs, Tl; X = S, Se) compounds, which can be divided into three groups based on their crystal and magnetic structures. [13] All AFeX 2 compounds have tetrahedrally co-arXiv:1905.03318v1 [cond-mat.mtrl-sci] 8 May 2019 ordinated Fe 3+ chains along c, but many of these have an additional degree of structural freedom, manifested as a monoclinic distortion (TlFeS 2 , TlFeSe 2 , KFeSe 2 , and RbFeSe 2 with the magnetic moments ordered perpendicular to the chains; and KFeS 2 , RbFeS 2 with the ordered moments slightly tilted from the chain axis). [14,15] Only CsFeS 2 is orthorhombic, but it further distorts martensitically at its magnetic transition at 70 K, with moments slightly tilted off the chain direction.…”
Section: Introductionmentioning
confidence: 99%
“…in the Cs salts) as well as in Na[FeS 2 ] (I222) the parallel Q2 edges of all linear chains are at equal heights (Figure 3a, c, and d), whereas the edge positions of neighboring chains differ in the K and Rb phases of the KFeS 2 -type structure (C2/c, Figure 3b). In the latter structure, a nearly regular eight-coordination of A + is achieved, the effective coordination numbers ( 1 ECoN, [37,38] ), which are used throughout this work to quantify and compare the cation coordination, are also close to 8 Table 3). The Fe-Fe distances are also very similar, with values close to 270 pm for the sulfido and 280 to 283 pm for the selenido compounds (Reports on strongly alternating Fe-Fe distance along the chains, which still appear in recent works, [8] are not based on reliable crystal data).…”
Section: Articlementioning
confidence: 79%
“…In the latter structure, a nearly regular eight-coordination of A + is achieved, the effective coordination numbers ( 1 ECoN, [37,38] ), which are used throughout this work to quantify and compare the cation coordination, are also close to 8 Table 3). The Fe-Fe distances are also very similar, with values close to 270 pm for the sulfido and 280 to 283 pm for the selenido compounds (Reports on strongly alternating Fe-Fe distance along the chains, which still appear in recent works, [8] are not based on reliable crystal data). As expected, the coordination number of the A cations increases continuously from four (Na) via eight (K/Rb) to finally nine for the Cs title compound.…”
Section: Articlementioning
confidence: 79%
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