Lithium molybdenum purple bronze

Preparation

The compound was first obtained by Martha Greenblatt and others by a temperature gradient flux technique. In a typical preparation, a stoichometric melt of Li
2MoO
4, MoO
2 and MoO
3 is maintained in a temperature gradient from 490 to 640 °C over 15 cm in vacuum over several days. Excess reagents are dissolved with a hot potassium carbonate solution releasing metallic-purple plate-like crystals, a couple mm wide and less than a mm thick.

Structure

The crystal structure of Li
0.9Mo
6O
17 was determined by Onoda and others through single-crystal X-ray diffraction. The crystal system is monoclinic, with approximate unit cell dimensions a = 1.2762 nm, b = 0.5523 nm, and c = 0.9499 nm, with angle β = 90.61°, volume V = 0.6695 nm³ and Z = 2. In typical crystals, a is the shortest dimension (perpendicular to the plates) and b the longest. The density is 4.24 g/cm³. The structure is rather different from that of potassium molybdenum purple bronze K
0.9Mo
6O
17, except that both are organized in layers. The difference may be explained by the relative sizes of the K+
and Li+
ions.

The unit cell contains six crystallographically independent molybdenum sites. One-third of the molybdenum atoms are surrounded by four oxygens, two thirds are surrounded by six oxygens. The crystal is a stack of slabs; each slab consists of three layers of distorted MoO
6 octahedra sharing corners. The lithium ions are inserted in the large vacant sites between the slabs. There are zigzag chains of alternating molybdenum and oxygen atoms extending along the b axis.

Properties

Lithium molybdenum purple bronze is quite different than the sodium, potassium and thallium analogs. It has a three-dimensional crystal structure, but a pseudo-one-dimensional (1D) metallic character, eventually becoming a superconductor at about 2 K Its properties are most spectacular below 5 meV. The Tomonaga-Luttinger liquid theory has been invoked to explain its anomalous behavior.

Electrical conductivity

At room temperature, Greenblatt and others (in 1984) measured the resistivity of lithium purple bronze along the a, b and c axes as 2.47 Ω cm, 0.0095 Ω cm, and on the order of 0.25 Ω cm, respectively. The conductivities would be in the ratio 1:250:10, which would make this compound an almost one-dimensional conductor. However, Da Luz and others (2007) measured 0.079, 0.018, and 0.050 Ω cm, respectively, which corresponds to conductivity ratios 1:6:2.4 for a:b:c; whereas H. Chen and others (2010) measured 0.854, 0.016, and 0.0645 Ω cm, respectively, which correspond to conductivity ratios of 1:53:13.

This anisotropy has been attributed to the crystal structure, specifically to the zig-zag chains of molybdenum and oxygen atoms

Resistivity and temperature

The resistivity along all three axes increases linearly with temperature from about 30 K to 300 K, as in a metal. This is anomalous since such a law is expected above the Debye temperature (= 400 K for this compound) The resistivity ratios along the three axes are preserved in that range.

Metal-insulator transition

As the lithium purple bronze is cooled from 30 K to 20, it changes abruptly to an insulator. After reaching a minimum at about 24 K, the resistivity increases 10-fold and becomes somewhat more isotropic, with conductivities 1:25:14. The anisotropy is partially restored if a magnetic field is applied perpendicular to the b axis. The transition may be related to the onset of a charge density wave. Santos and others have observed that the thermal expansion coefficient is largest along the a axis, so cooling will bring the conducting chains closer together, leading to a dimensional cross-over. The theory of Luttinger liquids then predicts such behavior. Anyway, as of 2010 there was no consensus explanation for this transition.

Superconducting state

Lithium molybdenum purple bronze becomes superconductor between 1 and 2 K.

Magnetoresistance

The magnetoresistance of lithium purple bronze is negative when the magnetic field is applied along the b-axis, but large and positive when the field is applied along the a-axis and the c-axis.