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Fe5O5[B6O10(OH)3]·nH2O: Wave-layered Iron Borate and Frustrated Antiferromagnetism

Yang, T (author)
Sun, Junliang (author)
Stockholms universitet,Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi
Li, G (author)
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Wang, Y (author)
Christensen, J (author)
He, Z (author)
Christensen, K-E (author)
Zou, Xiaodong (author)
Stockholms universitet,Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi
Liao, F (author)
Lin, J (author)
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 (creator_code:org_t)
2009-10-26
2009
English.
In: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 48:23, s. 11209-11214
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The first layered iron borate, Fe5O5[B6O10(OH)3]·nH2O, has been prepared by the boric acid flux method. Its structure, determined by single crystal X-ray diffraction, contains a double FeO6-octahedral layer and an unusual [B6O13] chain. The rigid and cambered [B6O13] chains bend the octahedral layers, resulting in a wave-like and sandwiched structure. Crystallographic study indicates the structural modulation is mainly from the [B6O13] chains because of the insertion of water molecules in between. Nevertheless, FeO6 layers in the average structure, which are well separated by borate chains, is still a reasonable model to understand the two-dimensional magnetism. The strong antiferromagnetic interactions and the complex Fe3+-net suggest a possible geometrically magnetic frustration, which may be the reason for the second-order temperature-induced magnetic transition at 125 K. The condensed Fe3+ layers and the relatively low redox potential at about 1.25 V versus Li+/Li show its potentials as an anodic material.

Keyword

low-dimensional structure
disorder
superstructure
electron diffraction

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art (subject category)

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