The adsorption and desorption behavior of poly(amido amine) (PAMAM) dendrimers at the water-silica interface was investigated by optical reflectometry. Polymer desorption upon dilution was studied as a function of generation (i.e., molecular mass), solution pH, and ionic strength. Three distinct adsorption regimes upon flushing with dendrimer-free solutions were identified. (i) Completely reversible adsorption refers to rapid and complete desorption. (ii) Partially reversible adsorption is characterized by rapid but partial desorption and a remaining irreversibly bound fraction. (iii) Irreversible adsorption refers to the case where there is no detectable change in the adsorbed mass. The system tends to be completely reversible for low generations, low pH values, and high ionic strengths, while it tends to be irreversible for high generations, high pH values, and low ionic strengths. The parameters for which these regimes are found are summarized in corresponding adsorption maps.
A CO2 laser (lambda = 10.6 microm) was used to heat a solution of water and alcohol saturated by Zn(AcAc)2 on a fused quartz substrate in open air. After only a few seconds of irradiation, various zinc oxide (ZnO) nanostructures including nanorods and nanowires are formed near the center of the irradiated zone, surrounded by a porous thin film of ZnO nanoparticles. The type of structures produced and their localization on the substrate can be varied by selecting adequate irradiation time and laser power ranges. The deposits have been analyzed using SEM, TEM, EDS, XRD, and Raman spectroscopy, revealing that the nanorods (aspect ratio ~6) and nanowires (aspect ratio ~94) are single-crystalline structures which grow along the c axis of wurtzite ZnO. The nanoparticles are also single-crystalline and have an average diameter of 16 nm. A qualitative model for nanostructure growth is proposed, based on previous studies of aqueous solution and hydrothermal processing.
We report a new methodology based on glancing angle deposition (GLAD) of an organic molecule in combination with perpendicular growth of a second inorganic material. The resulting thin films retain a very well-defined tilted columnar microstructure characteristic of GLAD with the inorganic material embedded inside the columns. We refer to this new methodology as growth assisted by glancing angle deposition or GAGLAD, since the material of interest (here, the inorganic) grows in the form of tilted columns, though it is deposited under a nonglancing configuration. As a "proof of concept", we have used silver and zinc oxide as the perpendicularly deposited material since they usually form ill-defined columnar microstructures at room temperature by GLAD. By means of our GAGLAD methodology, the typical tilted columnar microstructure can be developed for materials that otherwise do not form ordered structures under conventional GLAD. This simple methodology broadens significantly the range of materials where control of the microstructure can be achieved by tuning the geometrical deposition parameters. The two examples presented here, Ag/Alq3 and ZnO/Alq3, have been deposited by physical vapor deposition (PVD) and plasma enhanced chemical vapor deposition (PECVD), respectively: two different vacuum techniques that illustrate the generality of the proposed technique. The two type of hybrid samples present very interesting properties that demonstrate the potentiality of GAGLAD. On one hand, the Ag/Alq3 samples present highly optical anisotropic properties when they are analyzed with linearly polarized light. To our knowledge, these Ag/Alq3 samples present the highest angular selectivity reported in the visible range. On the other hand, ZnO/Alq3 samples are used to develop highly porous ZnO thin films by using Alq3 as sacrificial material. In this way, antireflective ZnO samples with very low refractive index and extinction coefficient have been obtained.
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