skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Soft-hard acid-base interactions: probing coordination preferences of sulfur an selenium in mixed chalcophosphates in the family APbPS{sub 4-x}Se{sub x} (A = K, Rb, cs; x = 0-4).

Journal Article · · Inorg. Chem.
DOI:https://doi.org/10.1021/ic901283k· OSTI ID:966350

The synthesis and structures of the three new compounds, KPbPS{sub 1.84}Se{sub 2.16} (1), RbPbPS{sub 1.56}Se{sub 2.43} (2), and CsPbPS{sub 3.46}Se{sub 0.54} (3), are reported. The solid state structures of 1-3 consist of two-dimensional layers of [PbP(S/Se){sub 4}] separated by alkali metal ions. The structure of 1 was solved in the orthorhombic space group Pna2{sub 1}. Compounds 2 and 3 possess the CsSmGeS{sub 4} structure type, crystallizing in the orthorhombic space group P2{sub 1}2{sub 1}2{sub 1}. All compounds were refined as racemic twins. All chalcogen sites around the tetrahedrally coordinated P atoms show mixed S/Se occupancy; however, there is a preference for Se binding to Pb ions and S binding to alkali ions. A {sup 31}P magic angle spinning NMR study on 1 suggests that, in mixed seleno-/thiophosphates, all of the anions [PS{sub x}Se{sub 4-x}]{sup 3-} (x = 0, 1, 2, 3, 4) are present. The different amount of sulfur and selenium present in KPbPS{sub 1.84}Se{sub 2.16} (1), RbPbPS{sub 1.56}Se{sub 2.43} (2), and CsPbPS{sub 3.46}Se{sub 0.54} (3) is reflected in the solid state absorption spectra from which bandgaps of 2.2 eV were determined for 1 and 2, and a blue-shift to 2.5 eV was observed because of the higher sulfur-content in 3. Thermogravimetric analysis experiments indicated that, upon heating, compound 1 decomposes forming PbSe and sulfur together with other unidentified products. A Raman spectrum of compound 1 showed more bands than are usually observed in seleno- or thiophosphate salts and is another indicator of the mixed seleno-/thiophosphate anions found in 1.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC); National Science Foundation (NSF)
DOE Contract Number:
DE-AC02-06CH11357
OSTI ID:
966350
Report Number(s):
ANL/MSD/JA-65426; INOCAJ; TRN: US200921%%275
Journal Information:
Inorg. Chem., Vol. 48, Issue 18 ; 2009; ISSN 0020-1669
Country of Publication:
United States
Language:
ENGLISH