Transition elements (Co²⁺, Ni²⁺, and Cu²⁺ ions) were substituted in place of tetrahedral Zn²⁺ ions in the tetragonal non-centrosymmetric spinel LiZnNbO₄ (LZN) and LiZnNb_0.5Sb_0.5O₄ (LZSN) compounds to form new colored compounds. The dielectric studies indicated reasonable values with low loss. The compounds were SHG-active. Magnetic studies reveal the Co²⁺ substituted Li(Zn_0.25Co_0.75)NbO₄ compound to be antiferromagnetic in nature.

Abstract

The non - centrosymmetric tetragonal inverse spinel structure of LiZnNbO₄ has been explored with a view to prepare new colored compounds. The substitution of Co²⁺, Ni²⁺, Fe²⁺, Mn²⁺, and Cu²⁺ ions were attempted in the place of Zn²⁺ ions and Sb⁵⁺ ions in place of Nb⁵⁺ ions. The studies indicated that 0.75 Zn²⁺ ions in LiZnNbO₄ can be replaced by Co²⁺ ions and 0.5 Zn²⁺ ions in LiZnNb_0.5Sb_0.5O₄ compound. The substitution of Co²⁺ ions gives rise to different shades of blue color in Li(Zn_1-xCo_x)NbO₄ compounds and from ink blue to blue-green color in Li(Zn_1-xCo_x)(Nb_0.5Sb_0.5)O₄ compounds. The different colors observed in the present study were explained by the traditional allowed d-d transitions as well as the metal-to-metal charge transfer (MMCT) transitions involving Nb⁵⁺ (4d ⁰) ions and partially filled 3d electrons. The SHG studies indicate that the prepared compounds are SHG active. All the compounds exhibit reasonable dielectric behavior with low loss. The XPS studies confirm the oxidation states of the different substituted ions. Raman studies indicate variations in the bands due to the substitutions in the parent LiZnNbO₄ phase. Magnetic studies on the Co²⁺ ions substituted compounds suggest antiferromagnetic behavior.