XAFS studies of soft-heavy-metal-ion-intercalated MxMoS2 (M = Hg2+, Ag+) solids

Citation
Pg. Allen et al., XAFS studies of soft-heavy-metal-ion-intercalated MxMoS2 (M = Hg2+, Ag+) solids, CHEM MATER, 13(7), 2001, pp. 2257-2265
Citations number
48
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
CHEMISTRY OF MATERIALS
ISSN journal
08974756 → ACNP
Volume
13
Issue
7
Year of publication
2001
Pages
2257 - 2265
Database
ISI
SICI code
0897-4756(200107)13:7<2257:XSOSM(>2.0.ZU;2-O
Abstract
XAFS studies were performed on two new soft-heavy-metal-ion-intercalated ma terials MxMoS2 (M = Hg2+, Ag+). For the compound Hg0.32MoS2, EXAFS results show an average Hg coordination environment consisting of approximate to2 S atoms at 2.38 Angstrom and approximate to0.2 (+/- 35%) Kg atoms at 2.55 An gstrom. Along with Hg XANES analysis, these data indicate that the Hg atoms in this compound are present as a mixture of mercuric and mercurous ions. Ag EXAFS analysis of the compound Ag0.61MoS2 indicates a Ag coordination en vironment consisting of approximate to2 S atoms at 2.43 Angstrom. Ag EXAFS and XANES results for heat-treated Ag0.61MoS2 indicate that the Ag coordina tion environment has changed to that nearly identical for silver metal with several Ag-Ag interactions detected. The results suggest that heat treatme nt of Ag0.61MoS2 facilitates the chemical reduction of the intercalated sil ver ions to elemental silver. In addition, Mo EXAFS and XANES analyses indi cate that both the Hg- and Ag-intercalated compounds have significant amoun ts of the 1T-phase of MoS2 in them. Prolonged exposure of both of these mat erials to an aerobic atmosphere does not affect their Mo EXAFS. Comparison of these results with those for exfoliated and restacked MoS2 suggests that different intercalated guest ions afford different oxidative stabilities t o the host MoS2 layers. This hypothesis is used to rationalize some inconsi stencies in previous reports of MxMoS2 XAFS studies.