Osmium-containing
oxides are rare due to the difficulty in stabilizing
complex structures with a fixed stoichiometry and metastability of the phases. Bismuth-substituted
thallium osmate pyrochlore samples, Tl2–x
Bi
x
Os2O7–y
, were synthesized using solid-state reactions where
the solubility limit was found to be approximately x = 1.4. Members of this solid solution were characterized by their
structural, electronic, magnetic, and thermal properties to understand
the influence of Bi3+ substitution on the ground state.
The Os-containing pyrochlores crystallize in the ideal cubic pyrochlore
structure (Fd
m), and the lattice parameter a was found to slightly
increase as a function of Bi content. A possible interplay between
structure and cation valence states was explored using both neutron
powder diffraction and X-ray absorption spectroscopy, suggesting that
a combination of Os4+/Os5+ and Tl1+/Tl3+ mixed valency throughout the solid solution allows
for the stabilization of the pyrochlore structure. The system is metallic
for the entire solid solution and predominantly exhibits temperature-independent
paramagnetism. Specific heat measurements show an enhanced Sommerfeld
coefficient, a possible flat-band signature. This system gave insight
into the bonding preferences of Os, indicating a dependence on high
oxidation states and mixed valence for the stability of complex structures.