Hybrid crystalline organic-inorganic quantum confined systems are disclosed, which contain alternating layers of a bifunctional organic ligand and a II-VI semiconducting chalcogenide, wherein the semiconducting chalcogenide layers contain chalcogenides have the formula MQ, in which M is independently selected from II-VI semiconductor cationic species and Q is independently selected from S, Se and Te; and the bifunctional organic ligands of each organic ligand layer are bonded by a first functional group to an element M of an adjacent II-VI semiconducting chalcogenide layer and by a second functional group to an element M from the adjacent opposing II-VI semiconducting chalcogenide layer, so that the adjacent opposing II-VI semiconducting chalcogenide layers are linked by the bifunctional organic ligands of the organic ligand layers. Optical absorption experiments show that these systems produce a significant blue shift in their optical absorption edges, 1. 2-1. 5 eV, compared to a shift of 1.
Hybrid Nanostructured Materials Based On Ii-Vi Semiconductors
Jing Li - Cherry Hill NJ, US Xiaoying Huang - Camden NJ, US
International Classification:
H01L031/00
US Classification:
257/442000
Abstract:
Hybrid crystalline organic-inorganic quantum confined systems are disclosed, which contain alternating layers of a bifunctional organic ligand and a II-VI semiconducting chalcogenide, wherein the semiconducting chalcogenide layers contain chalcogenides have the formula MQ, in which M is independently selected from II-VI semiconductor cationic species and Q is independently selected from S, Se and Te; and the bifunctional organic ligands of each organic ligand layer are bonded by a first functional group to an element M of an adjacent II-VI semiconducting chalcogenide layer and by a second functional group to an element M from the adjacent opposing II-VI semiconducting chalcogenide layer, so that the adjacent opposing II-VI semiconducting chalcogenide layers are linked by the bifunctional organic ligands of the organic ligand layers. Optical absorption experiments show that these systems produce a significant blue shift in their optical absorption edges, 1.2-1.5 eV, compared to a shift of 1.0 electron volt by the best grown II-VI or II-V semiconducting quantum colloidal dots. In addition, the II-VI confined layers in these systems possess a perfectly periodic arrangement.
Jing Li - Cranbury NJ, US Long Pan - Westmont NJ, US Xiaoying Huang - Piscataway NJ, US
International Classification:
C07F015/00
US Classification:
546/002000
Abstract:
The present invention describes three-dimensional porous coordination compounds, a method of making the compounds, and a method of using the compounds to contain reactants in a reaction, said compounds characterized by a plurality of sheets comprising a two-dimensional array of repeating structural units comprising at least one transition metal, one polyfunctional ligand and one exodentate ligand wherein: (1) at least one binding member of each said polyfunctional ligand is coordinated to transition metal atoms in two different repeating structural units within one sheet; (2) said binding sites of each exodentate bridging ligand are coordinated to transition metal atoms in a each of two adjacent sheets, and (3) the ligands of the three-dimensional polymeric compound define channels and pores of molecular size throughout the structure of the compound.