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Adam J Nolte

Publications and source records attributed to Adam J Nolte.

3 recordsLinked to original sources

pH-induced hysteretic gating of track-etched polycarbonate membranes: swelling/deswelling behavior of polyelectrolyte multilayers in confined geometry.

pH-induced hysteretic gating of track-etched polycarbonate membranes (TEPC) has been achieved by depositing layer-by-layer assembled polyelectrolyte multilayers comprising poly(allylamine hydrochloride) (PAH) and poly(sodium 4-styrenesulfonate) (PSS) at a high pH condition (pH > 9.0). Scanning electron microscopy and transmission electron microscopy showed that the average bilayer thickness of multilayers was greater within the cylindrical pores of track-etched polycarbonate membranes compared to the multilayers on planar substrates (e.g., Si wafers and the face of TEPC membranes). Swelling/deswelling properties of multilayers and gating properties of the multilayer-modified TEPC membranes were studied by measuring the flux of pH-adjusted deionized water. Large discontinuous changes in the transmembrane flux were observed, indicating that the multilayers within the cylindrical pores of TEPC membranes exhibit the discontinuous swelling/deswelling behavior observed previously for planar systems. The degree of swelling as estimated by simple models, however, showed that (PAH/PSS) multilayers in the confined geometry swelled to smaller extents compared to the same multilayers on planar substrates under the same conditions. Multilayer-modified membranes showed reversible gating properties as the pH condition of feed solution was alternated between pH 2.5 and 10.5. In situ atomic force microscopy (AFM) was used to visualize the closing of the pores as a function of time. The hysteretic gating property of the multilayer-modified TEPC membrane was utilized to achieve either a "closed" or "open" state at one pH condition depending on the pretreatment history, thereby enabling either the retention or passage of high-molecular weight polymers by varying the membrane pretreatment condition.

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Photo-cross-linkable polyelectrolyte multilayers for 2-D and 3-D patterning.

We report the synthesis of poly(acrylic acid-ran-vinylbenzyl acrylate) (PAArVBA), a photo-cross-linkable weak polyelectrolyte, and its incorporation into polyelectrolyte multilayer (PEM) films. PEM films assembled from PAArVBA and poly(allylamine hydrochloride) (PAH) are found to exhibit similar thickness trends with assembly pH as those previously reported for poly(acrylic acid) (PAA)/PAH multilayers. Swelling properties of the as-built and photo-cross-linked films are studied by in situ ellipsometry. Two-dimensional masking techniques are used to pattern regions of high and low swelling, as confirmed by atomic force microscopy (AFM), and to provide spatial control over the low-pH-induced microporosity transition exhibited by PAH/PAA PEMs. Films containing alternating blocks of PAH/PAArVBA bilayers and PAH/PAA bilayers were assembled, laterally photopatterned, and exposed to low-pH solution to generate nanoporosity leading to patterned Bragg reflectors, thereby demonstrating three-dimensional control over film structure in these weak PEM assemblies.

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Creating effective refractive index gradients within polyelectrolyte multilayer films: molecularly assembled rugate filters.

We demonstrate the use of aqueous-based layer-by-layer (LbL) processing and in situ nanoreactor chemistry for creating polyelectrolyte multilayer (PEM) nanocomposites in which the concentration of a nanoparticle species is modulated throughout the depth of the film in a complex way. Using the in situ growth of silver nanoparticles to selectively increase the refractive index of precisely defined regions of the PEM film, we have produced a digitized rugate filter, a special type of dielectric mirror possessing many thin layers that approximate a continuous, periodic refractive index profile. The design of the digital rugate from an initial smooth index profile was aided by a computer, and construction of the device was accomplished entirely by automated means. Poly(allylamine hydrochloride) (PAH) and poly(acrylic acid) (PAA) bilayer regions within the film supported subsequent nanoreactor chemistry and created the high refractive index regions of the film, while PAH and poly(styrenesulfonate) (PSS) bilayer regions remained unmodified and served as the low index regions. Spectroscopic results obtained from the assembled device confirm the presence of a reflection band that grows in amplitude with increasing silver incorporation, reaching a peak reflectance of 75% after five silver loading and exchange cycles. The rugate structure suppresses reflection sidebands, features common to Bragg reflectors and simpler dielectric mirror designs. Cross-sectional TEM reveals nanoscale control of the size and location of silver-containing domains within the PEM film. The ability of this method to control the placement of nanoparticles within PEMs enables the inexpensive, easy production of conformable optical coatings with tunable properties. In addition, these nanocomposite films may have applications in a number of other fields where precise control of effective gradients in physical properties throughout thin films has been shown to affect the overall performance in a desirable way.

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