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Synthesis, thermal stability, and structure of (V[sub. 13]Mo[sub. 87])O[sub 2. 935]: A new oxide with the open [open quotes]Hexagonal MoO[sub 3][close quotes] structure

Journal Article · · Journal of Solid State Chemistry; (United States)
;  [1]
  1. Univ. of Pennsylvania, Philadelphia, PA (United States)
New oxides with the stoichiometry (Li[sub x]H[sub .13[minus]x])(V[sub .13]Mo[sub .87])O[sub 3][center dot]0.26H[sub 2]O and the structure of [open quotes]hexagonal MoO[sub 3][close quotes] have been precipitated directly from Li-V-Mo aqueous solutions. At room temperature in dilute HCl, these precipitates undergo a rapid ion-exchange reaction to give the pure protonic form of vanadium-stabilized hexagonal MoO[sub 3], H[sub .13](V[sub .13]Mo[sub .87])O[sub 3][center dot]0.26H[sub 2]O. Complete dehydration of this solid acid yields a new oxide (V[sub .13]Mo[sub .87])O[sub 2.935] which retains the structure of hexagonal MoO[sub 3] up to 460[degrees]C. Whereas all the previously reported compounds with the hexagonal MoO[sub 3] framework have contained large stabilizing cations in the one dimensional channels of the structure, (V[sub .13]Mo[sub .87])O[sub 2.935] represents the open form of hexagonal MoO[sub 3] and has empty channels with free diameters approaching 3.3 [angstrom]. Powder neutron diffraction was used to confirm the structure of (V[sub .13]Mo[sub .87])O[sub 2.935] which was refined in space group P6[sub 3] with final lattice parameters of a = 10.593(1), c = 3.6944(4) [angstrom]; V = 359.01 [angstrom][sup 3]. The [open quotes]porosity[close quotes] of this structure is significantly, [approx] 12-18%, greater than the [alpha], [beta], and [beta][prime] polymorphs of MoO[sub 3].
OSTI ID:
7284154
Journal Information:
Journal of Solid State Chemistry; (United States), Journal Name: Journal of Solid State Chemistry; (United States) Vol. 105:2; ISSN 0022-4596; ISSN JSSCBI
Country of Publication:
United States
Language:
English