Quasimolecular complexes in the CuxTiSe2−ySy intercalation compound. Issue 46 (8th November 2018)

• Record Type: Journal Article
• Authors: Shkvarin, A. S.; Merentsov, A. I.; Titov, A. A.; Yarmoshenko, Yu. M.; Shkvarina, E. G.; Píš, I.; Nappini, S.; Titov, A. N.
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 46(2018)
• Page Start: 12592
• Page End: 12600
• Publication Date: 2018-11-08
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8tc04115f
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : The Cu intercalation into Ti(Se1− y Sy)2 leads to the formation of the Cu–S quasimolecules, which are responsible for the charge-density-wave state suppression. Abstract : TiSe2 is a member of the layered transition metal dichalcogenides and displays a transition into the charge density wave (CDW) state upon cooling. The intercalation of copper into TiSe2 leads to a superconducting state transition. However, these electronic states are suppressed when both Cu and S are introduced into the TiSe2 crystal structure. The electronic structures of the copper intercalated Cu x TiSe2− y S y (0 < y < 0.3) compounds have been studied using XPS, XAS and ResPES spectroscopic techniques and theoretical calculations. We show evidence suggesting that the copper atoms occupy sulfur coordinated tetrahedral sites in the interlayer space. This is accompanied by the formation of the Cu–S chemical bonds involving Ti 3d-orbitals and S 3d-orbitals. The suppression mechanism of the CDW and superconducting states in Cu x TiSe2− y S y due to the sulfur for selenium substitution has been proposed considering that sulfur acts as a trap for copper atoms and does not allow Cu–TiSe2 bond formation.