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LiMo 8 O 10 : Polar Crystal Structure with Infinite Edge-Sharing Molybdenum Octahedra.
- Source :
-
Inorganic chemistry [Inorg Chem] 2022 Sep 05; Vol. 61 (35), pp. 13924-13932. Date of Electronic Publication: 2022 Aug 22. - Publication Year :
- 2022
-
Abstract
- Polycrystalline LiMo <subscript>8</subscript> O <subscript>10</subscript> was prepared in a sealed Mo crucible at 1380 °C for 48 h using the conventional high-temperature solid-state method. The polar tetragonal crystal structure (space group I 4 <subscript>1</subscript> md ) is confirmed based on the Rietveld refinement of powder neutron diffraction and <superscript>7</superscript> Li/ <superscript>6</superscript> Li solid-state NMR. The crystal structure features infinite chains of Mo <subscript>4</subscript> O <subscript>5</subscript> (i.e., Mo <subscript>2</subscript> Mo <subscript>4/2</subscript> O <subscript>6/2</subscript> O <subscript>6/3</subscript> ) as a repeat unit containing edge-sharing Mo <subscript>6</subscript> octahedra with strong Mo-Mo metal bonding along the chain. X-ray absorption near-edge spectroscopy of the Mo-L <subscript>3</subscript> edge is consistent with the formal Mo valence/configuration. Magnetic measurements reveal that LiMo <subscript>8</subscript> O <subscript>10</subscript> is paramagnetic down to 1.8 K. Temperature-dependent resistivity [ρ(T)] measurement indicates a semiconducting behavior that can be fitted with Mott's variable range hopping conduction mechanism in the temperature range of 215 and 45 K. The ρ(T) curve exhibits an exponential increase below 5 K with a large ratio of ρ <subscript>1.8</subscript> /ρ <subscript>300</subscript> = 435. LiMo <subscript>8</subscript> O <subscript>10</subscript> shows a negative field-dependent magnetoresistance between 2 and 25 K. Heat capacity measurement fitted with the modified Debye model yields the Debye temperature of 365 K.
Details
- Language :
- English
- ISSN :
- 1520-510X
- Volume :
- 61
- Issue :
- 35
- Database :
- MEDLINE
- Journal :
- Inorganic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 35993886
- Full Text :
- https://doi.org/10.1021/acs.inorgchem.2c01917