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Title: Structure and bonding in Li/sub 2/MoO/sub 3/ and Li/sub 2-x/MoO/sub 3/ (0 less than or equal to x less than or equal to 1. 7)

Journal Article · · J. Solid State Chem.; (United States)

Li/sub 2/MoO/sub 3/ prepared by hydrogen reduction of Li/sub 2/MoO/sub 4/ was studied by X-ray and neutron diffraction. The results imply that the previous assignment of a ..beta..-Li/sub 2/SnO/sub 3/ structure to this material (C2/c; a = 4.97 A, b = 8.61 A, c = 10.10 A, ..beta.. = 99.5/sup 0/) is inappropriate. Li/sub 2/MoO/sub 3/ has a novel, disordered ..cap alpha..-NaFeO/sub 2/ structure (R anti 3m; a = 2.884 A, c = 14.834 A) with the molybdenum present as Mo/sub 3/O/sub 3/ clusters. This structural model is consistent with the diamagnetism and low electrical conductivity of Li/sub 2/MoO/sub 3/ and accounts for certain features of the Li/sub 2/O-MoO/sub 2/ phase diagram. The presence of Mo/sub 3/O/sub 13/ clusters in Li/sub 2/MoO/sub 3/ was confirmed by comparison of the He-I photoelectron spectra of Li/sub 2/MoO/sub 3/ and Zn/sub 2/Mo/sub 38/; the latter compound is known from single-crystal X-ray diffraction to contain Mo/sub 3/O/sub 13/ clusters. Oxidative extraction of us to 85% of the lithium from Li/sub 2/MoO/sub 3/ was achieved at ambient temperature with mild oxidizing agents and electrochemically. Crystallographic studies of Li/sub 2-x/MoO/sub 3/ by X-ray and neutron powder diffraction show that lithium extraction is accompanied by migration of some molybdenum ions to sites in the lattice previously occupied by lithium ions. Electrochemical delithiation of Li/sub 2/MoO/sub 3/ is kinetically slow and not fully reversible.

Research Organization:
Univ. of Texas, Austin (USA)
OSTI ID:
6809566
Journal Information:
J. Solid State Chem.; (United States), Vol. 76:1
Country of Publication:
United States
Language:
English