Synthesis, crystal structure and electronic structure of AgxZrTe2

A systematic study of the crystal and electronic structure of the intercalation compound AgxZrTe2 in the Ag concentration range of x = 0–0.37 has been performed. It was found that the Ag atoms occupy the sites in the interlayer gap that are tetrahedrally coordinated by the Te atoms. The chemical bon...

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Bibliographic Details
Published in:Journal of alloys and compounds Vol. 906; p. 164269
Main Authors: Shkvarina, E.G., Merentsov, A.I., Shkvarin, A.S., Postnikov, M.S., Titov, A.A., Tsud, N., Yarmoshenko, Yu.M., Patrakov, E.I., Titov, A.N.
Format: Journal Article
Language:English
Published: Lausanne Elsevier B.V 15-06-2022
Elsevier BV
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Summary:A systematic study of the crystal and electronic structure of the intercalation compound AgxZrTe2 in the Ag concentration range of x = 0–0.37 has been performed. It was found that the Ag atoms occupy the sites in the interlayer gap that are tetrahedrally coordinated by the Te atoms. The chemical bond is provided by the Ag 4d/Te 5p hybridization. The comparison of the studied electronic structure with the available data on the electrochemical measurements of AgxZrTe2 in the temperature range of 200–400 °C indicates the formation of covalent centers accompanied by the formation of the half-filled band of Ag 4d/Te 5p hybridized states. The shape of the phase diagram in the region of low Ag concentrations coincides with that observed for AgxTiTe2, in which the stability of the covalent centers is confirmed by the Ag 5s/Ti 3d hybridization. This indicates the universal character of the influence of the localized or extended states of conduction electrons on the phase diagram of intercalation compounds. •The crystal structure of low-temperature and high-temperature synthesized AgxZrTe2 (x = 0–0.37) was studied using XRD.•Single crystals of AgxZrTe2 were studied using electron spectroscopic methods.•The electronic structure and electric resistivity were studied.•The data obtained suggest the Te 5p/Ag 4d hybridization.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2022.164269