RESUMEN
The assembly of colloidal semiconductive nanocrystals into highly ordered superlattices predicts novel structure-related properties by design. However, those structure-property relationships, such as charge transport depending on the structure or even directions of the superlattice, have remained unrevealed so far. Here, electric transport measurements and X-ray nanodiffraction are performed on self-assembled lead sulfide nanocrystal superlattices to investigate direction-dependent charge carrier transport in microscopic domains of these materials. By angular X-ray cross-correlation analysis, the structure and orientation of individual superlattices is determined, which are directly correlated with the electronic properties of the same microdomains. By that, strong evidence for the effect of superlattice crystallinity on the electric conductivity is found. Further, anisotropic charge transport in highly ordered monocrystalline domains is revealed, which is attributed to the dominant effect of shortest interparticle distance. This implies that transport anisotropy should be a general feature of weakly coupled nanocrystal superlattices.
RESUMEN
We report a high-throughput and easy-to-implement approach to fabricate microchannels of nanocrystal superlattices with dimensions of â¼4 µm2, thus approaching the size of typical single-crystalline domains. By means of microcontact printing, highly ordered superlattices with microscale dimensions are transferred onto photolithographically prepatterned microelectrodes, obtaining well-defined superlattice microchannels. We present step-by-step guidelines for microfabrication, nanocrystal self-assembly and patterning to archive large quantities of up to 330 microchannels per device for statistically meaningful investigations of charge transport in single-crystalline superlattice domains. As proof-of-concept, we perform conductivity and field-effect transistor measurements on microchannels of PbS nanocrystal superlattices. We find that the electric transport within microchannel superlattices is orders of magnitude more efficient than within conventional large-scale channels, highlighting the advantage of the near single-crystalline microchannels presented in this paper.
RESUMEN
The successful fabrication of monolithic capillary columns for enantiomer separations was achieved within vinylized fused silica capillaries via fast "one-pot" photo-initiated free radical polymerization reaction. A mixture consisting of polyhedral oligomeric silsesquioxane, O-[2-(methacryloyloxy)ethylcarbamoyl]-10,11-dihydroquinidine was copolymerized in the presence of n-butanol, ethylene glycol and photo-initiator 2,2-dimethoxy-2-phenylacetophenone. The morphology of the resultant polymeric hybrid inorganic-organic material and its permeability as well as porosity can be controlled by adjusting the composition of the monomers and binary porogenic solvent. The chromatographic characteristics of the columns have been investigated. Separation factors of N-acetyl-phenylalanine (Ac-Phe) and dichlorprop dropped with decrease of chiral functional monomer. Permeability was better when the macroporogen ethyleneglycol was present at higher concentrations during the polymerization. In general, the chiral compounds were well separated (dichlorprop: α = 1.53, Rs up to 4.14; Ac-Phe: α = 1.36, Rs up to 2.69) by nano-HPLC with an optimized enantioselective monolithic capillary column which can be prepared within a few minutes.
