Solution synthesis of optoelectronic components has the advantages of processability, bandgap tuning, and large-scale manufacturing potential. The synthesis of monodispersed rhombs in solution, however, has rarely been reported, even though rhombs are promising for realizing unique optical functions in integrated optoelectronics. We present in this article our success in developing a facile chemical method that used two polyols to generate nearly monodispersed metal-organic rhombic platelets. The success lies on the careful selection of precursors of proper oxidation states and the optimization of both the thermodynamic and the kinetic conditions for synthesis. Cuprous acetate, which acted as a heterogeneous nucleation agent, was dispersed in ethylene glycol, which acted as a stabilizer, a ligand, and a monomer for the formation of polymeric glycolates. By adjusting the volume ratio of polyethylene glycol (PEG) to ethylene glycol and the polymer size of PEG, rhombic platelets of 200-580 nm in side length and 170-240 nm in thickness were synthesized with aid of suitable structure-directing and dispersing agents. Energy-dispersive X-ray spectroscopy and FT-IR analyses revealed that the rhombic platelets were mainly composed of copper glycolate polymer chains. Knowledge obtained from this study can be expected to be applied to and to shed light on broad research topics concerning novel metal-organic nanostructure syntheses.
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http://dx.doi.org/10.1166/jnn.2012.6694 | DOI Listing |
Gels
September 2022
Chair of Food Process Engineering, Technische Universität Berlin, 10623 Berlin, Germany.
Wax esters are considered to have a dominant contribution in the gelling properties of wax-based oleogels. To understand their gelling behavior, oleogels of seven different wax esters (total carbon number from 30 to 46; c = 10% [/]) in medium-chain triglycerides oil were characterized. Scanning electron microscopy revealed that wax esters crystallize in rhombic platelets with a thickness of 80 to 115 monomolecular layers.
View Article and Find Full Text PDFJ Am Chem Soc
December 2020
School of Materials Sciences, Indian Association for the Cultivation of Science, Kolkata 700032 India.
Bright lead halide perovskite nanocrystals, which have been extensively studied in the past 5 years, are mostly confined to a six faceted hexahedron (cube/platelet) shape. With variations of ligand, precursor, reaction temperature, and surface modification, their brightness has been enhanced and phase became stable, but ultimate nanocrystals still retained the hexahedron cube or platelet shape in most of the hot injection reactions. In contrast, by exploration of α-halo ketone in amine as a halide precursor, different shaped nanocrystals without compromising the photoluminescence quantum yield (PLQY) are reported.
View Article and Find Full Text PDFInt J Mol Sci
November 2020
Institut für Theoretische Physik, TU Wien, Wiedner Hauptstraße 8-10, A-1040 Wien, Austria.
Non-spherical colloids provided with well-defined bonding sites-often referred to as patches-are increasingly attracting the attention of materials scientists due to their ability to spontaneously assemble into tunable surface structures. The emergence of two-dimensional patterns with well-defined architectures is often controlled by the properties of the self-assembling building blocks, which can be either colloidal particles at the nano- and micro-scale or even molecules and macromolecules. In particular, the interplay between the particle shape and the patch topology gives rise to a plethora of tilings, from close-packed to porous monolayers with pores of tunable shapes and sizes.
View Article and Find Full Text PDFSoft Matter
March 2020
Institut für Theoretische Physik, TU Wien, Wiedner Hauptstraße 8-10, A-1040 Wien, Austria. and CNR-ISC, Uos Sapienza, Piazzale A. Moro 2, 00185 Roma, Italy.
Anisotropy at the level of the inter-particle interaction provides the particles with specific instructions for the self-assembly of target structures. The ability to synthesize non-spherical colloids, together with the possibility of controlling the particle bonding pattern via suitably placed interaction sites, is nowadays enlarging the playing field for materials design. We consider a model of anisotropic colloidal platelets with regular rhombic shape and two attractive sites placed along adjacent edges and we run Monte Carlo simulations in two-dimensions to investigate the two-stage assembly of these units into clusters with well-defined symmetries and, subsequently, into extended lattices.
View Article and Find Full Text PDFJ Phys Condens Matter
May 2020
Faculty of Physics, University of Vienna, Boltzmanngasse 5, A-1090, Vienna, Austria. Institut für Theoretische Physik, TU Wien, Wiedner Hauptstraße 8-10, A-1040 Wien, Austria.
Patchy colloidal platelets with non-spherical shapes have been realized with different materials at length scales ranging from nanometers to microns. While the assembly of these hard shapes tends to maximize edge-to-edge contacts, as soon as a directional attraction is added-by means of, e.g.
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