Exceptionally Stable Dimers and Trimers of Au25 Clusters Linked with a Bidentate Dithiol: Synthesis, Structure and Chirality Study.

A bidentate chiral dithiol (diBINAS) is utilised to bridge Au25 nanoclusters to form oligomers. Separation by size allows the isolation of fractions that are stable thanks to the bidentate nature of the linker. The structure of the products is elucidated by small-angle X-ray scattering and calculated using density functional theory. Additional structural details are studied by diffusion-ordered nuclear magnetic resonance spectroscopy, transmission electron microscopy and matrix-assisted laser desorption/ionization time of flight mass spectrometry. Significant changes in the optical properties are analysed by UV/Vis and fluorescence spectroscopies, with the latter demonstrating a strong emission enhancement. Furthermore, the emergent chiral characteristics are studied by circular dichroism. Due to the geometry constraints of the nanocluster assemblies, diBINAS can be regarded as a templating molecule, taking a step towards the directed self-assembly of metal clusters.

Nanomechanical and structural study of Au38 nanocluster Langmuir-Blodgett films using bimodal atomic force microscopy and X-ray reflectivity.

HYPOTHESIS: Langmuir-Blodgett (LB) technique allows the deposition of gold nanoparticles and nanoclusters (atomically precise nanoparticles below 2 nm in diameter) onto solid substrates with an unprecedented degree of control and high transfer ratios. Nanoclusters are expected to follow the crinkle folding mechanism, which promotes the formation of trilayers of nanoparticles but kinetically disfavors the formation of the fourth layer. EXPERIMENTS: LB films of Au38(SC2H4Ph)24 nanocluster were prepared at a range of surface pressures in the bilayer/trilayer regime and their internal structure was analyzed with X-ray Reflectivity (XRR) and Grazing-Incidence Wide-Angle X-ray Scattering (GIWAXS). Bimodal atomic force microscopy (AFM) imaging was used to quantify the elastic modulus, which can be correlated with the topography at the same point on the surface. FINDINGS: Nanocluster bilayers and trilayers exhibited the elastic moduli of ca. 1.2 GPa and 0.9 GPa respectively. Films transferred in the 20-25 mN/m surface pressure regime displayed a particular propensity to form highly vertically organized trilayers. Further compression resulted in disorganization of the layers. Crucially, the use of two cantilevers of contrasting stiffness for bimodal AFM measurements has demonstrated a new approach to quantify the mechanical properties of ultrathin films without the use of deconvolution algorithms to remove the substrate contribution.

Protein Transport upon Advection at the Air/Water Interface: When Charge Matters.

The formation of dense protein interfacial layers at a free air-water interface is known to result from both diffusion and advection. Furthermore, protein interactions in concentrated phases are strongly dependent on their overall positive or negative net charge, which is controlled by the solution pH. As a consequence, an interesting question is whether the presence of an advection flow of water toward the interface during protein adsorption produces different kinetics and interfacial structure of the adsorbed layer, depending on the net charge of the involved proteins and, possibly, on the sign of this charge. Here we test a combination of the following parameters using ovalbumin and lysozyme as model proteins: positive or negative net charge and the presence or absence of advection flow. The formation and the organization of the interfacial layers are studied by neutron reflectivity and null-ellipsometry measurements. We show that the combined effect of a positive charge of lysozyme and ovalbumin and the presence of advection flow does induce the formation of interfacial multilayers. Conversely, negatively charged ovalbumin forms monolayers, whether advection flow is present or not. We show that an advection/diffusion model cannot correctly describe the adsorption kinetics of multilayers, even in the hypothesis of a concentration-dependent diffusion coefficient as in colloidal filtration, for instance. Still, it is clear that advection is a necessary condition for making multilayers through a mechanism that remains to be determined, which paves the way for future research.

Deposition of Extended Ordered Ultrathin Films of Au38 (SC2 H4 Ph)24 Nanocluster using Langmuir-Blodgett Technique.

Langmuir-Blodgett technique is utilized to deposit ultrathin films of Au38 (SC2 H4 Ph)24 nanocluster onto solid surfaces such as mica and silicon. The morphologies of the films transferred at various surface pressures within the mono/bi/trilayer regime are studied by atomic force microscopy (AFM). The time spent on the water surface before the deposition has a decisive effect on the final ordering of nanoclusters within the network and is studied by fast AFM, X-ray reflectivity, and grazing-incidence wide-angle X-ray scattering.

Imbibition and structure of silica nanoporous media characterized by neutron imaging.

HYPOTHESIS: Colloidal silica dispersions dried under controlled conditions form solid gels that display mechanical properties similar to those observed in several practical processes. An understanding of their structural characteristics and liquid flow properties can therefore help establish these gels as an alternative family of model materials to study practical porous systems. EXPERIMENTS: Neutron radiography is a non-destructive technique well-adapted to study hydrogen-rich domains in porous materials due to the high attenuation power of hydrogen. We apply this technique to study gels prepared from silica nanoparticles of radii 5-40 nm. FINDINGS: The water content in the gels have been quantified and different types of porosities have been determined: total porosity, effective porosity that contributes to liquid flow, and residual porosity that contains bound residual water. This residual water increases with decrease in particle size and constitutes an important fraction of the gel. The dynamics of water imbibition follows a √t law, from which the effective pore size and permeability are evaluated. We highlight the role of particle size on water retention, on particle organization and its impact on mechanical resistance. Quantitative analysis of the propagating liquid front shows front broadening that suggests elongated pores with reduced correlated liquid menisci.

Equilibrium Protein Adsorption on Nanometric Vegetable Oil Hybrid Film/Water Interface Using Neutron Reflectometry.

Nanofilms of about 2 nm thickness have been formed at the air-water interface using functionalized castor oil (ICO) with cross-linkable silylated groups. These hybrid films represent excellent candidates for replacing conventional polymeric materials in biomedical applications, but they need to be optimized in terms of biocompatibility, which is highly related to protein adsorption. Neutron reflectivity has been used to study the adsorption of two model proteins, bovine serum albumin and lysozyme, at the silylated oil (ICO)-water interface in the absence and presence of salt at physiologic ionic strength and pH and at different protein concentrations. These measurements are compared to adsorption at the air-water interface. While salt enhances adsorption by a similar degree at the air-water and oil-water interfaces, the impact of the oil film is significant with adsorption at the oil-water interface 3-4-fold higher compared to that at the air-water interface. Under these conditions, the concentration profiles of the adsorbed layers for both proteins indicate multilayer adsorption. The thickness of the outer layer (oil side) is close to the dimension of the minor axis of the protein molecule, ∼30 Å, suggesting a sideway orientation with the long axis parallel to the interface. The inner layer extends to 55-60 Å. Interestingly, in all cases, the composition of the oil film remains intact without significant protein penetration into the film. The optimal adsorption on these nanofilms, 1.7-2.0 mg·m-2, is comparable to the results obtained recently on thick solid cross-linked films using a quartz crystal microbalance and atomic force microscopy, showing in particular that adsorption at these ICO film interfaces under standard physiological conditions is nonspecific. These results furnish useful information toward the elaboration of vegetable oil-based nanofilms in direct nanoscale applications or as precursor films in the fabrication of thicker macroscopic films for biomedical applications.

Imbibition on a porous layer: dynamical and mechanical characterization.

Solvent penetration in porous layers was analyzed using dynamical and mechanical characterization. Spreading dynamics of a solvent drop in a porous substrate provided parameters of the porous medium such as permeability and porosity. These measurements are relevant for many porous systems, for example paintings or porous varnishes and resins… We present direct visualizations of the drop as well as of the wet zone during the imbibition process and we evidence three distinct regimes. Experiments performed with various porous systems and different solvents highlight a universal behavior. The mechanical properties during the imbibition process are deduced through indentation testing measurements. We show that solvent penetration is responsible for the appearance of a viscous component in the system. A characteristic time depending on the solvent and on the porous medium is then deduced. The system recovers its initial mechanical properties and no swelling nor cracking is observed contrary to the case of paintings. This result tends to prove that visco-plastic properties are required to observe swelling or cracking.

Structuration of the Surface Layer during Drying of Colloidal Dispersions.

During evaporative drying of a colloidal dispersion, the structural behavior at the air-dispersion interface is of particular relevance to the understanding of the consolidation mechanism and the final structural and mechanical properties of the porous media. The drying interface constitutes the region of initial drying stress that, when accumulated over a critical thickness, leads to crack formation. This work presents an experimental study of top-down drying of colloidal silica dispersions with three different sizes (radius 5, 8, and 13 nm). Using specular neutron reflectivity, we focus on the structural evolution at the free drying front of the dispersion with a macroscopic drying surface and demonstrate the existence of a thick concentrated surface layer induced by heterogeneous evaporation. The reflectivity profile contains a strong structure peak due to scattering from particles in the interfacial region, from which the interparticle distance is deduced. A notable advantage of these measurements is the direct extraction of the corresponding dispersion concentration from the critical total reflection edge, providing a straightforward access to a structure-concentration relation during the drying process. The bulk reservoir of this experimental configuration renders it possible to verify the evaporation-diffusion balance to construct the surface layer and also to check reversibility of particle ordering. We follow the structural evolution of this surface layer from a sol to a soft wet-gel that is the precursor of a fragile skin and the onset of significant particle aggregation that precedes formation of the wet-crust. Separate complementary measurements on the structural evolution in the bulk dispersion are also carried out by small-angle neutron scattering, where the particle concentration is also extracted directly from the experimental curves. The two sets of data reveal similar structural evolution with concentration at the interface and in the bulk and an increase in the degree of ordering with the particle size.

Covalently bonded multimers of Au25(SBut)18 as a conjugated system.

Aromatic dithiol linkers were used to prepare aggregates of Au25(SR)18 clusters (SR: thiolate) via ligand exchange reactions. Fractions of different aggregate sizes were separated by size exclusion chromatography (SEC). The aggregates were characterized by UV-vis absorption spectroscopy, matrix assisted laser desorption ionization (MALDI) mass spectrometry, nuclear magnetic resonance (NMR) spectroscopy (including diffusion-ordered spectroscopy, DOSY) and small angle X-ray scattering (SAXS). At a 2 : 1 cluster : dithiol ratio, small aggregates (dimers, trimers) and also larger aggregates consisting of 10-20 Au25 clusters were formed, according to DOSY, besides unreacted (monomeric) Au25(SR)18. MALDI mass spectrometry shows signals consistent with dimers and trimers (doubly charged). The SAXS curves for the small aggregates can be well fitted by a pearl-necklace model. For the bigger aggregates the SAXS curves evidence a characteristic separation distance between the clusters within the aggregates, which is imposed by the length of the linker. The SAXS curves of these larger aggregates can be well fitted with a core-shell sphere model with a sticky hard-sphere structure factor, in agreement with closely packed aggregates. The absorption spectra of smaller aggregates resemble those of individual Au25(SR)18 clusters; however, and most importantly, the larger aggregates show completely different, less structured spectra with a new band emerging at 840 nm. We assign this drastic change in the absorption spectra and the new band to the electronic coupling between the clusters through the all aromatic linker. In accordance with this view, the aggregates formed with a linker containing methylene groups, thus breaking conjugation, do not show the band at 840 nm. By the addition of monothiols to the larger aggregates their size can be reduced through an "unlinking" reaction. This reaction also affects the band at 840 nm, which moves to higher energy when reducing the aggregate size, as would be expected within a particle in a box model. The electronic coupling between the clusters through the linker is the basis for future applications in nanoelectronics.

Crack opening: from colloidal systems to paintings.

Shrinkage cracks are observed in many materials, particularly in paintings where great interest lies in deducing quantitative information on the material with the aim of proposing authentication methods. We present experimental measurements on the crack opening induced by the drying of colloidal layers and compare these results to the case of a pictorial layer. We propose a simple model to predict the crack width as a function of the thickness of the drying layer, based on the balance between the drying stress buildup and the shear frictional stress with the substrate. Key parameters of the model include the mechanical properties that are measured experimentally using micro-indentation testing. A good agreement between theory and experimental data for both colloidal layers and the real painting is found. These results, by comparing the shrinkage cracks in model layers and in pictorial layers, validate the method based on the use of colloidal systems to simulate and to reproduce drying cracks in paintings.

Three-Legged 2,2'-Bipyridine Monomer at the Air/Water Interface: Monolayer Structure and Reactions with Ni(II) Ions from the Subphase.

The behavior of compound 2 [1,3,5-tri(2,2'-bipyridin-5-yl)benzene] with three bipyridine units arranged in a star geometry is investigated in the presence and absence of Ni(ClO4)2. Its properties at the air-water interface as well as after transfer onto a solid substrate are studied by several techniques including Brewster angle microscopy, X-ray reflectivity, neutron reflectivity, X-ray photoelectron spectroscopy, Rutherford backscattering spectrometry, and atomic force microscopy combined with optical microscopy. It is found that compound 2 within the monolayers formed stays almost vertical at the interface and that at high Ni2+/2 (Ni2+/2 = 4000, 20'000) ratios two of the three bipyridine units of 2 are complexed, resulting in supramolecular sheets that are likely composed of arrays of linear metal-organic complexation polymers.

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.

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.

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 Young's modulus were obtained by sampling many points and used to characterize the PNIPAM/SDS films formed in the dewetting process.

Foam films from thermosensitive PNIPAM and SDS solutions.

Thin liquid foam films stabilized with the addition of a temperature-sensitive neutral polymer, poly(N-isopropylacrylamide) (PNIPAM), in the presence of varying amounts of an anionic surfactant, SDS, were investigated using the thin-film balance. Data were analyzed in light of new and previously reported neutron reflectivity data describing the adsorption behavior of PNIPAM/SDS mixtures at the single air-water interface. In the case of thin films prepared from pure polymer solutions, unexpectedly thick and stable films were observed, and increases in solution temperature or polymer molecular weight induce corresponding increases in the thin-film thickness. This behavior is attributed to a stabilization of the films by repulsive entropic forces between long dangling polymer tails adsorbed at the interfaces. The addition of SDS causes a striking decrease in the thin-film thickness that is very well correlated with the desorption of polymer chains from the interface resulting from polymer-surfactant interactions in the bulk. Upon SDS introduction, repulsive forces stabilizing the films vary from purely entropic forces for small amounts of surfactant to supramolecular oscillatory forces at high SDS concentrations, whereas a combination of electrostatic and entropic forces is expected in intermediate concentration regions. Properties of thin films made from PNIPAM and SDS are thus highly sensitive to parameters such as the polymer-surfactant ratio, temperature, and molecular weight, offering precise control of the thin-film thickness that could be used to tailor foam characteristics.

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.

Effect of hydrogen-bonding complexation on the interfacial behavior of poly(isoprene)-b-poly(ethylene oxide) and poly(isoprene)-b-poly(acrylic acid) Langmuir monolayers.

The effect of hydrogen-bonding complexation on the interfacial behavior of poly(isoprene)-b-poly(ethylene oxide) (PI-b-PEO) diblock copolymer at the air-water interface has been investigated by Langmuir balance and neutron reflectivity. PI-b-PEO forms Langmuir monolayers with PI as the anchoring block. Introduction of a second diblock, poly(isoprene)-b-poly(acrylic acid) (PI-b-PAA) yields PI-b-PEO/PI-b-PAA mixed layers with interfacial behavior that is pH-dependent. At pH 10.0 and 5.7, the compression (pi-A) isotherms exhibit three regions that are characteristic of PEO-type tethered layers, (i) a low-pressure 2-D "pancake" region (region I), (ii) a pseudoplateau where PEO segments desorb and are immerse in the subphase (region II), and (iii) a steep pressure rise region commonly considered as the "brush" regime (region III). At pH 2.5, on the other hand, the pi-A isotherm shows only two regions, (I) and (III). This novel behavior is attributed to hydrogen-bonding complexation between the undissociated carboxylic acids and the PEO, forming very compact layers. It appears that desorption of PEO segments is hindered as a consequence of this complexation. Furthermore, no brush-like structure is observed in region III of the isotherml; thus, the steep rise in surface pressure in this case arises primarily from interactions of the anchoring block. The hydrogen-bonded complex of PI-b-PEO/PI-b-PAA monolayers thus shows enhanced surface stability.

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.

Liquid templating for nanoparticle organization into complex patterns.

Dewetting of thin films of charged polymer solutions produces complex patterns that can be applied to direct nanoparticle organization on solid substrates. The morphology produced by dewetting can be controlled by the solution properties, temperature, and substrate wetting. In this work, new results on this liquid-template self-assembly system are presented, with special emphasis on producing large arrays of organized nanoparticles. On a hydrophilic substrate with complete wetting, the patterns include polygonal networks and parallel-track arrays that extend over several hundreds of microns. These large structures are formed under well-controlled drying conditions and characterized by scanning electron microscopy, which is better suited for the examination of large as well as small areas than atomic force microscopy. On partial wetting substrates, new patterns are observed, including a complex set of parallel curved bands with variable particle number densities.

Gas permeability in polymer- and surfactant-stabilized bubble films.

The gas permeabilities of thin liquid films stabilized by poly(N-isopropylacrylamide) (PNIPAM) and PNIPAM-SDS (sodium dodecyl sulfate) mixtures are studied using the "diminishing bubble" method. The method consists of forming a microbubble on the surface of the polymer solution and measuring the shrinking rates of the bubble and the bubble film as the gas diffuses from the interior to the exterior of the bubble. PNIPAM-stabilized films exhibit variable thicknesses and homogeneities. Interestingly, despite these variable features, the gas permeability of the film is determined principally by the structure of the adsorbed polymer layer that provides an efficient gas barrier with a value of gas permeability coefficient that is comparable to that of an SDS Newton black film. In the presence of SDS, both the film homogeneity and the gas permeability coefficient increase. These changes are related to interactions of PNIPAM with SDS in the solution and at the interface, where coadsorption of the two species forms mixed layers that are stable but that are more porous to gas transfer. The mixed PNIPAM-SDS layers, studied previously for a single water-air interface by neutron reflectivity, are further characterized here in a vertical free-draining film using X-ray reflectivity.