Abstract

We report the solid-state synthesis of all eighteen layered oxide chalcogenides in the structural family AM2Q2O (A = K/Rb/Cs; M = Ti/V; Q = S/Se/Te), allowing the determination of trends in composition and reactivity within the series. All materials are isostructural, crystallising in the primitive tetragonal space group P4/mmm as reported previously for five compounds in the series. The titanium or vanadium ions have intermediate valency on a single crystallographic site, leading to temperature-independent paramagnetism and correlated electronic behaviour which is influenced by the compositional variation. Furthermore, the alkali metal ions in ▪ and ▪ can be removed by oxidative deintercalation using ▪ at room temperature to produce a new metastable van der Waals layered phase, ▪. During the deintercalation reaction the oxide chalcogenide layers undergo a relative shift by (0.5,0.5) in the ab plane such that ▪ is body-centered with space group I4/mmm.

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