88 research outputs found
Toward efficient synthesis of porous all-carbon-based nanocomposites for enantiospecific separation
Chiral separation and asymmetric synthesis and catalysis are crucial processes for obtaining enantiopure compounds, which are especially important in the pharmaceutical industry. The efficiency of the separation processes is readily increased by using porous materials as the active material can interact with a larger surface area. Silica, metalâorganic frameworks, or chiral polymers are versatile porous materials that are established in chiral applications, but their instability under certain conditions in some cases requires the use of more stable porous materials such as carbons. In addition to their stability, porous carbon materials can be tailored for their ability to adsorb and catalytically activate different chemical compounds from the liquid and the gas phase. The difficulties imposed by the functionalization of carbons with chiral species were tackled in the past by carbonizing chiral ionic liquids (CILs) together with a template to create pores, which results in the entire body of a material that is built up from the precursor. To increase the atomic efficiency of ionic liquids for better economic utilization of CILs, the approach presented here is based on the formation of a composite between CIL-derived chiral carbon and a pristine carbon material obtained from carbohydrate precursors. Two novel enantioselective carbon composite materials are applied for the chiral recognition of molecules in the gas phase, as well as in solution. The enantiomeric ratio of the l-composite for phenylalanine from the solution was (L/D) = 8.4, and for 2-butanol from the gas phase, it was (S/R) = 1.3. The d-composite showed an opposite behavior, where the enantiomeric ratio for phenylalanine was (D/L) = 2.7, and for 2-butanol from the gas phase, it was (R/S) = 1.3
Photoluminescence Stokes shift and exciton fine structure in CdTe nanocrystals
The photoluminescence spectra of spherical CdTe nanocrystals with zincblende
structure are studied by size-selective spectroscopic techniques. We observe a
resonant Stokes shift of 15 meV when the excitation laser energy is tuned to
the red side of the absorption band at 2.236 eV. The experimental data are
analyzed within a symmetry-based tight-binding theory of the exciton spectrum,
which is first shown to account for the size dependence of the fundamental gap
reported previously in the literature. The theoretical Stokes shift presented
as a function of the gap shows a good agreement with the experimental data,
indicating that the measured Stokes shift indeed arises from the electron-hole
exchange interaction.Comment: 8 pages, 4 figures, LaTe
Evolution of the electronic structure with size in II-VI semiconductor nanocrystals
In order to provide a quantitatively accurate description of the band gap
variation with sizes in various II-VI semiconductor nanocrystals, we make use
of the recently reported tight-binding parametrization of the corresponding
bulk systems. Using the same tight-binding scheme and parameters, we calculate
the electronic structure of II-VI nanocrystals in real space with sizes ranging
between 5 and 80 {\AA} in diameter. A comparison with available experimental
results from the literature shows an excellent agreement over the entire range
of sizes.Comment: 17 pages, 4 figures, accepted in Phys. Rev.
Silica-carbon nanocomposites: A new concept for the design of solar absorbers
To create materials that are composites or hybrids structured on the nanometer scale or the meso-domain, respectively, is one of the major tasks in modern materials science. In this paper, we demonstrate general strategies on how to obtain these nanocomposites founded on the knowledge about ordered mesoporous materials. One strategy involves the formation of the composite by performing a chemical reaction in the pores of a pre-formed ordered mesoporous silica while the other strategy uses compounds that first mold their porous environment in the silica and in a succeeding step react to the final composite. As a model system, here, we present the formation of porous silica-carbon hybrid materials. Besides this more general question, we also tackle the task of finding a suitable application for the obtained nanocomposites. We chose an application as selective solar-absorber materials
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