Lay-Theng Lee

Synthesis of a covalent monolayer sheet by photochemical anthracene dimerization at the air/water interface and its mechanical characterization by AFM indentation

Covalent monolayer sheets in 2 hours: spreading of threefold anthracene-equipped shape-persistent and amphiphilic monomers at the air/water interface followed by a short photochemical treatment provides access to infinitely sized, strictly monolayered, covalent sheets with in-plane elastic modulus in the range of 19 N/m.

Synthesis of two-dimensional analogues of copolymers by site-to-site transmetalation of organometallic monolayer sheets

Monolayer sheets have gained attention due to the unique properties derived from their two-dimensional structure. One of the key challenges in sheet modification/synthesis is to exchange integral parts while keeping them intact. We describe site-to-site transmetalation of Zn(2+) in the netpoints of cm(2)-sized, metal-organic sheets by Fe(2+), Co(2+), and Pb(2+). This novel transformation was done both randomly and at predetermined patterns defined by photolithography to create monolayer sheets composed of different netpoints. All transmetalated sheets are mechanically strong enough to be spanned over 20 × 20 μm(2) sized holes. Density functional theory calculations provide both a model for the molecular structure of an Fe(2+)-based sheet and first insights into how transmetalation proceeds. Such transmetalated sheets with random and patterned netpoints can be considered as two-dimensional analogues of linear copolymers. Their nanoscale synthesis presents an advance in monolayer/polymer chemistry with applications in fields such as surface coating, molecular electronics, device fabrication, imaging, and sensing.

Properties of surfactant monolayers in relation to microemulsion phase behaviour

Abstract The relationship between the properties of surfactant monolayers at oil-water interfaces and the phase behaviour in bulk of mixtures of oil + water + surfactant is discussed. Such monolayer properties include the spontaneous curvature, c o the interfacial tension, I γ, the elasticity K (or rigidity) associated with the mean curvature, and the elasticity K associated with the Gaussian curvature. The model system chosen for investigation is the anionic surfactant AOT + aqueous NaCl + n-alkane at 20°C. In such systems, inversion of microemulsion type from oil-in-water (o/w) to water-in-oil (w/o) is possible with increasing electrolyte concentration. The tension, γ, passes through an ultralow minimum value at conditions corresponding to the formation of three phases. Using small angle neutron scattering, we have determined the structure of surfactant-rich third phases (c o ~ 0) formed with the different alkanes. Lamellar phases consisting of surfactant monolayers separated alternately by oil and water appear with short alkanes, whereas L 3 and bicontinuous phases form in systems containing longer alkanes. The bending elasticity K has been measured for planar monolayers at the oil-water interface by ellipsometry. K is independent of salt concentration but depends markedly on alkane chain length N, falling from ~ 1 k B T for N B T for N = 14. This is discussed in terms of the differing extents of oil penetration into the surfactant chains. Higher rigidities favouring lamellar phases and lower rigidities favouring bicontinuous microemulsions are in line with the theoretical predictions of de Gennes and Taupin. Estimates of the constant K have been obtained in droplet microemulsions (w/o) from a knowledge of their size, K and γ. The sign of the constant is in agreement with the geometry of the phases formed in three phase systems. Finally, the ideas and concepts developed in the oil-water systems described above are used to explain the wetting behaviour by alkanes of AOT monolayers at the air-water surface.

Surface Mechanical Properties of Thin Polymer Films Investigated by AFM in Pulsed Force Mode

Atomic force microscopy in the pulsed force mode (PFM) is applied in this work to the study of thin dewetting patterns formed by drying an aqueous solution of poly(N-isopropylacrylamide) (PNIPAM) and sodium dodecyl sulfate (SDS) on mica. This technique allows the automated acquisition of typically 4 x 10(6) force-distance curves on the sample surface together with maps showing nanodomains differentiated by their stiffness and adhesion to the tip. Topography images of dry films revealed a morphology formed by droplets distributed on the substrate. Adhesion and stiffness images with good lateral resolution show droplets containing polymer and surfactant contrasting with the substrate and also nanosized heterogeneities inside these droplets. They also revealed very small dewetted structures which could not be observed in the topography map by noncontact AFM. Adhesion interactions between the AFM tip and the polymer or the dewetted mica substrate were measured in terms of adhesion force and detachment energy, and can be used as new information to understand dewetting patterns containing silica particles, PNIPAM, and SDS. Other surface mechanical parameters such as stiffness, maximum indentation, hardness, compliance, hysteresis, and Youngs modulus were obtained by sampling many points and used to characterize the PNIPAM/SDS films formed in the dewetting process.

Polymer–surfactant interactions: neutron scattering and reflectivity

Abstract Recent studies of bulk and interfacial properties of polymer–surfactant systems using neutron scattering and neutron reflectivity are presented, with some discussions on a few selected systems. In bulk, the principal interests are centred on thermosensitive and hydrophobically modified associative polymers, where structural information has been used to interpret the effects of surfactants on the solubilization behavior, phase separation and gelation processes of these polymers. Conversely, the effects of polymers anchored in surfactant layers and membranes and the resulting phase changes in microemulsion systems have also received much interest. At the interface, information obtained on the structure and composition of mixed polymer–surfactant layers is discussed in relation to the surface tension and stability of these layers.

Tuning the Structure of Thermosensitive Gold Nanoparticle Monolayers

Gold nanoparticles grafted with poly(N-isopropylacrylamide) (PNIPAM) are rendered amphiphilic and thermosensitive. When spread on the surface of water, they form stable Langmuir monolayers that exhibit surface plasmon resonance. Using Langmuir balance and contrast-matched neutron reflectivity, the detailed structural properties of these nanocomposite monolayers are revealed. At low surface coverage, the gold nanoparticles are anchored to the interface by an adsorbed PNIPAM layer that forms a thin and compact pancake structure. Upon isothermal compression (T=20 degrees C), the adsorbed layer thickens with partial desorption of polymer chains to form brush structures. Two distinct polymer conformations thus coexist: an adsorbed conformation that assures stability of the monolayer, and brush structures that dangle in the subphase. An increase in temperature to 30 degrees C results in contractions of both adsorbed and brush layers with a concomitant decrease in interparticle distance, indicating vertical as well as lateral contractions of the graft polymer layer. The reversibility of this thermal response is also shown by the contraction-expansion of the polymer layers in heating-cooling cycles. The structure of the monolayer can thus be tuned by compression and reversibly by temperature. These compression and thermally induced conformational changes are discussed in relation to optical properties.

Interactions between a lipase and charged surfactants – a comparison between bulk and interfaces

The interaction between a charged surfactant and a lipase has been investigated by several methods. Interactions in aqueous bulk phase was studied by NMR and by microcalorimetry. Surface tension and neutron reflectivity were used for studies at the air-water interface. Interactions at the interface between a hydrophobic solid surface and water was investigated by ellipsometry. The results obtained are as follows. The cationic surfactant, tetradecyltrimethylammonium bromide (iodide in the NMR experiments), showed strong interaction at the air-water and the hydrophobic solid-water interfaces but no clear indication of an interaction in bulk phase was seen. The anionic surfactant showed no interaction with the lipase neither at the interfaces, nor in bulk. The difference in behavior of the system cationic surfactant-lipase in bulk and at the interfaces may be due to the change in enzyme conformation that is known to occur at interfaces between water and an apolar phase.

Interparticle distance in monolayers controlled by soft spacers

This paper addresses the use of graft polymer layers as spacers to control interparticle distance in 2-dimensional monolayers. Gold nanoparticles grafted with thermosensitive PNIPAM-based polymers with a large range of molecular mass and different degrees of hydrophobicity have been studied. The hydrophobicity of the polymer is adjusted by incorporation of a comonomer n-propylamine. The resulting copolymer, PNIPAM-co-NPAM, exhibits lower collapse transition temperature and increased cooperativity in the collapse process with n ≈ 150 compared to n ≈ 100 for PNIPAM, n being the number of monomers per collapse domain. Langmuir isotherms of these polymers under moderate compression follow closely a π ≈ c3 behavior with corresponding critical exponent ν = 3/4 as predicted for 2-dimensional polymer conformation in good solvent. Nanoparticles grafted with these polymers form stable Langmuir monolayers where the graft polymer chains adopt a 2-D stretched conformation that tethers the nanoparticles to the interface. The nanoparticle cores are thus isolated by the polymer shells resulting in nanoparticle areas that increase with polymer chain length. Correspondingly, the interparticle distance is found to vary with chain length as Dp ≈ N0.8. For the Au-PNIPAM-NPAM, a moderate increase in temperature to near-θ conditions decreases the nanoparticle area by about 30% through lateral collapse of the polymer layer. This thermally induced molecular collapse in a 2-D monolayer is an unusual and novel observation that may be attributed to cooperative effects of the collapse transition of the new copolymer PNIPAM-co-NPAM.

Silica Nanoparticles at Interfaces Modulated by Amphiphilic Polymer and Surfactant

The interfacial behavior of silica nanoparticles in the presence of an amphiphilic polymer poly( N-isopropylacrylamide) (PNIPAM) and an anionic surfactant sodium dodecyl sulfate (SDS) is studied using neutron reflectivity. While the nanoparticles do not show any attraction to hydrophilic and hydrophobic surfaces in pure water, presence of the amphiphilic polymer induces significant adsorption of the nanoparticles at the hydrophobic surface. This interfacial behavior is activated due to interaction of the nanoparticles with PNIPAM, the amphiphilic nature of which leads to strong adsorption at a hydrophobic surface but only weak interaction with a hydrophilic surface. The presence of SDS competes with nanoparticle-PNIPAM interaction and in turn modulates the interfacial properties of the nanoparticles. These adsorption results are discussed in relation to nanoparticle organization templated by dewetting of charged polymer solutions on a solid substrate. Our previous studies showed that nanoparticle assembly can be induced to form complex morphologies produced by dewetting of the polymer solutions, such as a polygonal network and long-chain structures. This approach, however, works on a hydrophilic substrate but not on a hydrophobic substrate. These observations can be explained in part by particle-substrate interactions revealed in the present study.

A Study of Phase Change in Langmuir-Blodgett Films of Mesomorphic Side-Chains Polymers

Abstract Langmuir-Blodgett films of mesomorphic side-chain polymethacrylates are investigated from the point of view of their phase change versus temperature via X-ray and neutron reflectivity. Upon heating, “thick” films undergo an irreversible transition towards the well known smectic Al lamellar phase. In contrast a bilayer deposited onto a solid substrate appears to be very stable upon annealing. Such a behaviour is believed to induce an epitaxial mechanism when cooling “thick” Rims from the isotropic melt phase.