ABSTRACT
The critical terrace width λ for 2D island nucleation and growth (2DNG) on large-scale atomically flat terraces of a step-bunched Si(111)-(7×7) surface has been studied by in situ ultrahigh vacuum reflection electron microscopy as a function of the substrate temperature T and Si deposition rate R. The dependence of λ(2)(R) is characterized by a power law with scaling exponent χ=1.36-1.46, validating an attachment limited (AL) growth kinetics up to 720 °C. At this temperature, the Arrhenius dependencies lnλ(2)(1/T) change their slope, so that the effective 2DNG activation energy E(2D) drops from 2.4 eV down to 0.5 eV at T>720 °C. We first show that the E(2D) change is caused by a transition between AL and DL (diffusion limited) growth kinetics accompanied by a step shape transformation. The AL growth mode is characterized by kinetic length d(-)~10(5)a and the preferential step-down attachment of atoms to steps limited by an energy barrier E(ES)(-)≈0.9 eV.
ABSTRACT
A convenient and simple approach for the preparation of molecularly imprinted polymers (MIPs) based on polyamide (nylon-6) was developed. The polymer matrix formation occurred during the transition of nylon from dissolved to solid state in the presence of template molecules in the initial solution. 2,2,2-Trifluoroethanol (TFE) was chosen as a main solvent for the polyamide. It provides a high solubility of nylon and does not significantly change the structure of biopolymers. The alteration of the polymer matrix structure after the addition of different types of porogens in the nylon/TFE solution was investigated. The structured polymers in the form of films and microparticles were prepared in the chosen optimal conditions. Different model biomolecular templates (of low- and high-molecular weight) were used for the preparation of MIPs, which were shown to specifically recognize these molecules upon binding experiments. The binding of the template molecules to MIPs was monitored using spectrophotometric, radioisotopic, or fluorometric detection. The selectivity coefficients of the MIPs were estimated to be 1.4-4.6 depending on the type of templates and conditions of the polymer matrix formation.
