Control of Metal-Ion Composition in the Synthesis of Ternary II-II′-VI Nanoparticles by Using a Mixed-Metal Cluster Precursor Approach

• Published in: Chemistry : a European journal Vol. 12; no. 5; pp. 1547 - 1554
• Main Authors: DeGroot, Marty W., Rösner, Harald, Corrigan, John F.
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01.02.2006; WILEY‐VCH Verlag
• Subjects: cadmium; chalcogens; cluster compounds; nanostructures; zinc
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.200501081

The ternary molecular nanoclusters [ZnxCd10−xSe4(SePh)12(PnPr3)4] (x=1.8, 1 a; x=2.6, 1 b) were employed as single‐source precursors for the synthesis of high‐quality hexagonal ZnxCd1−xSe nanocrystals. The tellurium clusters [ZnxCd10−xTe4(TePh)12(PnPr3)4] (x=1.8, 2 a; x=2.6, 2 b) are equally convenient precursors for the synthesis cubic ZnxCd1−xE nanoparticles. The thermolysis of the cluster molecules in hexadecylamine provides an efficient system in which the inherent metal‐ion stoichiometry of the clusters is retained in the nanocrystalline products, whilst also affording control of particle size within the 2–5 nm range. In all cases, the nanoparticles are monodisperse, and luminescence spectra exhibit emission energies close to the absorption edge. Analysis of the optical spectra and X‐ray diffraction patterns of these materials indicates a metal‐ion concentration gradient within the structures of the nanocrystals, with ZnII ions predominantly located near the surface of the particles. Zinc into it! Ternary Zn‐Cd‐Se and Zn‐Cd‐Te molecular nanoclusters have been employed as single‐source precursors for the synthesis of high‐quality ZnxCd1−xSe and ZnxCd1−xTe (illustrated) nanocrystals, respectively. The thermolysis of the molecular precursors in hexadecylamine solvent provides a route in which the inherent metal‐ion stoichiometry of the clusters is retained in the nanocrystalline materials.