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We demonstrate how gold nanoparticle monolayers can be curled up into hollow scrolls that make it possible to extract both bending and stretching moduli from indentation by atomic force microscopy. We find a bending modulus that is 2 orders of magnitude larger than predicted by standard continuum elasticity, an enhancement we associate with nonlocal microstructural constraints. This finding opens up new opportunities for independent control of resistance to bending and stretching at the nanoscale.

Self-assembly of nanoparticles at fluid interfaces has emerged as a simple yet efficient way to create two-dimensional membranes with tunable properties. In these membranes, inorganic nanoparticles are coated with a shell of organic ligands that interlock as spacers and provide tensile strength. Although curvature due to gradients in lipid-bilayer composition and protein scaffolding is a key feature of many biological membranes, creating gradients in nanoparticle membranes has been difficult. Here, we show by X-ray scattering that nanoparticle membranes formed at air/water interfaces exhibit a small but significant ∼6 Å difference in average ligand-shell thickness between their two sides. This affects surface-enhanced Raman scattering and can be used to fold detached free-standing membranes into tubes by exposure to electron beams. Molecular dynamics simulations elucidate the roles of ligand coverage and mobility in producing and maintaining this asymmetry. Understanding this Janus-like membrane asymmetry opens up new avenues for designing nanoparticle superstructures.

Monolayers composed of colloidal nanoparticles, with a thickness of less than ten nanometers, have remarkable mechanical strength and can suspend over micron-sized holes to form free-standing membranes. We discuss experiments probing the tensile strength and bending stiffness of these self-assembled nanoparticle sheets. The fracture behavior of monolayers and multilayers is investigated by attaching them to elastomer substrates which are then stretched. For different applied strain, the fracture patterns are imaged down to the scale of single particles. The resulting detailed information about the crack width distribution allows us to relate the measured overall tensile strength to the distribution of local bond strengths within a layer. We then introduce two methods by which freestanding nanoparticle monolayers can be rolled up into hollow, tubular “nano-scrolls”, either by electron beam irradiation during imaging with a scanning electron microscope or by spontaneous self-rolling. Indentation measurements on the nano-scrolls yield values for the bending stiffness that are significantly larger than expected from the response to stretching. The ability to stretch, bend, and roll up nanoparticle sheets offers new possibilities for a variety of applications, including sensors and mechanical transducers.

Monolayers composed of colloidal nanoparticles, with a thickness of less than 10 nm, have remarkable mechanical moduli and can suspend over micrometer-sized holes to form free-standing membranes. In this paper, we discuss experiments and coarse-grained molecular dynamics simulations characterizing the thermomechanical properties of these self-assembled nanoparticle membranes. These membranes remain strong and resilient up to temperatures much higher than previous simulation predictions and exhibit an unexpected hysteretic behavior during the first heating–cooling cycle. We show this hysteretic behavior can be explained by an asymmetric ligand configuration from the self-assembly process and can be controlled by changing the ligand coverage or cross-linking the ligand molecules. Finally, we show the screening effect of water molecules on the ligand interactions can strongly affect the moduli and thermomechanical behavior.

Thin-film membranes consisting of nanoparticles are of interest in applications ranging from nanosieves to electric, magnetic, or photonic devices and sensors. However, the fabrication of large-scale membranes in a simple but controlled way has remained a challenge, due to the limited understanding of their mechanical properties. Systematic experiments on ultrathin, freestanding nanoparticle membranes of different core materials, core sizes, and capping ligands are reported. The results demonstrate that a drying-mediated self-assembly process can be used to create close-packed monolayer membranes that span holes tens of micrometers in diameter. Containing up to approximately 10(7) particles, these freely suspended layers exhibit remarkable mechanical properties with Young's moduli of the order of several GPa, independent of membrane size. Comparison of three different core-ligand combinations suggests that the membrane's elastic response is set by how tightly the ligands are bound to the particle cores and by the ligand-ligand interactions.

Critical photonic, electronic, and magnetic applications of two-dimensional nanocrystal superlattices often require nanostructures in perfect single-crystal phases with long-range order and limited defects. Here we discovered a crystalline phase with quasi-long-range positional order for two-dimensional nanocrystal superlattice domains self-assembled at the liquid-air interface during droplet evaporation, using in situ time-resolved X-ray scattering along with rigorous theories on two dimensional crystal structures. Surprisingly, it was observed that drying these superlattice domains preserved only an orientational order but not a long-range positional order, also supported by quantitative analysis of transmission electron microscopy images.

We report an experimental study of Langmuir monolayers of dodecanethiol-ligated gold nanoparticles with in situ optical microscopy and X-ray scattering. The particle spacing increases with thiol concentration but does not depend on surface pressure. Compression beyond the full coverage of the monolayers causes the monolayers to wrinkle. With the presence of excess thiol molecules, the wrinkles unfold back to monolayer upon the expansion of the surface area. A theoretical model based on van der Waals' attraction and tunable steric repulsion is adopted to explain this reversibility.

The assembly of nanoparticles into large, two-dimensional structures provides a route for the exploration of collective phenomena among mesoscopic building blocks. We characterize the structure of Langmuir monolayers of dodecanethiol-ligated gold nanoparticles with in situ optical microscopy and X-ray scattering. The interparticle spacing increases with thiol concentration and does not depend on surface pressure. The correlation lengths of the Langmuir monolayer crystalline domains are on the order of five to six particle diameters. Further compression of the monolayers causes wrinkling; however, we find that wrinkled monolayers with excess thiol can relax to an unwrinkled state following a reduction of surface pressure. A theoretical model based on van der Waals attraction and tunable steric repulsion is adopted to explain this reversibility.

When a drop of a colloidal solution of nanoparticles dries on a surface, it leaves behind coffee-stain-like rings of material with lace-like patterns or clumps of particles in the interior. These non-uniform mass distributions are manifestations of far-from-equilibrium effects, such as fluid flows and solvent fluctuations during late-stage drying. However, recently a strikingly different drying regime promising highly uniform, long-range-ordered nanocrystal monolayers has been found. Here we make direct, real-time and real-space observations of nanocrystal self-assembly to reveal the mechanism. We show how the morphology of drop-deposited nanoparticle films is controlled by evaporation kinetics and particle interactions with the liquid-air interface. In the presence of an attractive particle-interface interaction, rapid early-stage evaporation dynamically produces a two-dimensional solution of nanoparticles at the liquid-air interface, from which nanoparticle islands nucleate and grow. This self-assembly mechanism produces monolayers with exceptional long-range ordering that are compact over macroscopic areas, despite the far-from-equilibrium evaporation process. This new drop-drying regime is simple, robust and scalable, is insensitive to the substrate material and topography, and has a strong preference for forming monolayer films. As such, it stands out as an excellent candidate for the fabrication of technologically important ultra thin film materials for sensors, optical devices and magnetic storage media.

From proton exchange membranes in fuel cells to ion channels in biological membranes, the well-specified control of ionic interactions in confined geometries profoundly influences the transport and selectivity of porous materials. Here we outline a versatile new approach to control a membrane's electrostatic interactions with ions by depositing ligand-coated nanoparticles around the pore entrances. Leveraging the flexibility and control by which ligated nanoparticles can be synthesized, we demonstrate how ligand terminal groups such as methyl, carboxyl and amine can be used to tune the membrane charge density and control ion transport. Further functionality, exploiting the ligands as binding sites, is demonstrated for sulfonate groups resulting in an enhancement of the membrane charge density. We then extend these results to smaller dimensions by systematically varying the underlying pore diameter. As a whole, these results outline a previously unexplored method for the nanoparticle functionalization of membranes using ligated nanoparticles to control ion transport.

Particle−particle and particle−substrate interactions cause nanocrystals to self-assemble into superlattice structures upon drying from a colloidal suspension on a solid surface. Rapid dewetting of a volatile solvent, however, can significantly undermine the degree of ordering. We demonstrate here that by increasing the concentration of the nonvolatile dodecanethiol ligand, dewetting can be controlled and gold nanocrystal superlattices can be formed on silicon nitride substrates with long range ordering over several microns. Monolayer and bilayer superlattices can be produced by adjusting the nanocrystal concentration. The superlattice structures are robust and are not perturbed by the final dewetting of the solvent.

A novel digestive ripening process is shown to narrow the particle size distribution from a highly polydisperse dodecanethiol ligated gold colloid. Unlike the Ostwald ripening process, the digestion occurs through transferring materials from large particles to small particles. Temperature-induced size segregation can further select the particle sizes. By using these two methods, highly ordered superlattices using nanocrystals as building blocks can be synthesized directly from a polydisperse colloid.

Anisotropic Pb nanoprisms were synthesized using high-temperature polyol reduction of lead acetylacetonate through a kinetically controlled synthesis. Transmission electron microscopy showed that the majority of the prisms grows along {111} planes. Selected area electron diffraction (SAED) on single prism revealed that the anisotropic growth is due to twinning in the growing nuclei. Magnetic measurements on a colloidal deposited film exhibited a large magnetic hysteresis that is due to the penetration and pinning of magnetic flux. This flux trapping behavior could be due to a possible transition from type I to type II superconductor given the finite thickness of the prisms (

The self-assembly of nanoscale structures from functional nanoparticles has provided a powerful path to developing devices with emergent properties from the bottom-up. Here we demonstrate that freestanding sheets self-assembled from various nanoparticles form versatile nanomechanical resonators in the megahertz frequency range. Using spatially resolved laser-interferometry to measure thermal vibrational spectra and image vibration modes, we show that their dynamic behavior is in excellent agreement with linear elastic response for prestressed drumheads of negligible bending stiffness. Fabricated in a simple one-step drying-mediated process, these resonators are highly robust and their inorganic–organic hybrid nature offers an extremely low mass, low stiffness, and the potential to couple the intrinsic functionality of the nanoparticle building blocks to nanomechanical motion.

A new, versatile substrate design for surface-enhanced Raman spectroscopy (SERS) is introduced that provides better illumination and collection efficiency than other solid substrates. It uses sheets of 5 nm diameter gold nanoparticles that are draped by drying-mediated self-assembly onto 100 nm thick silicon nitride membranes. During laser illumination, partial in-situ sintering of the nanoparticles into larger structures with tiny gaps (≈2 nm) greatly increases the SERS enhancement factor. The detection of 1 pM of p-mercaptoaniline and 1 fg of 2,4-dinitrotoluene is demonstrated. The use of self-assembled nanoparticle sheets furthermore makes it possible to perform SERS detection in situ on top of a probe solution droplet.

Close-packed monolayers self-assembled from ligated nanoparticles can form 10 nm thin sheets that stretch over micrometer-wide holes. Employing electron and focused ion beams, we show that one can locally tailor the strain in such sheets while they remain clamped around their perimeter, making it possible to imprint strain fields by design. Furthermore, using the nanoparticles themselves to track imposed strain gradients allows for the first direct measurement of Poisson’s ratio in these two-dimensional materials.

Close-packed nanoparticle monolayers have recently been shown to form mechanically robust, free-standing membranes. We report the first measurements of molecular transport through such ultrathin sheets, self-assembled from dodecanethiol-ligated gold nanocrystals. For aqueous solutions we find filtration coefficients 2 orders of magnitude larger than those observed in polymer-based filters, sieving of large solutes, and for smaller solutes a pronounced dependence of rejection on being charged. These results open up new possibilities for controlled delivery and separation of nano-objects.

We demonstrate a method for laterally patterning metal nanocrystal monolayers. Extended monolayers are first self-assembled onto a solid substrate. Direct electron-beam exposure is then used to strip the dodecanethiol ligand coating from the nanocrystal cores, enabling the cores to stick to the underlying substrate. During a subsequent washing step in a solvent mixture, nanocrystals from the unexposed regions are removed and floated off, leaving behind the desired pattern.

We report a facile one-step approach which involves no flammable gas, no catalyst, and no in situ polymerization for the preparation of well-aligned carbon nanotube array. A polymer precursor is placed on top of an anodized aluminum oxide (AAO) membrane containing regular nanopore arrays, and slow heating under Ar flow allows the molten polymer to wet the template through adhesive force. The polymer spread into the nanopores of the template to form polymer nanotubes. Upon carbonization the resulting multi-walled carbon nanotubes duplicate the nanopores morphology precisely. The process is demonstrated for 230, 50, and 20 nm pore membranes. The synthesized carbon nanotubes are characterized with scanning/transmission electron microscopies, Raman spectroscopy, and resistive measurements. Convenient functionalization of the nanotubes with this method is demonstrated through premixing CoPt nanoparticles in the polymer precursors.

Nanoparticle superlattices are hybrid materials composed of close-packed inorganic particles separated by short organic spacers. Most work so far has concentrated on the unique electronic, optical and magnetic behaviour of these systems. Here, we demonstrate that they also possess remarkable mechanical properties. We focus on two-dimensional arrays of close-packed nanoparticles and show that they can be stretched across micrometre-size holes. The resulting free-standing monolayer membranes extend over hundreds of particle diameters without crosslinking of the ligands or further embedding in polymer. To characterize the membranes we measured elastic properties with force microscopy and determined the array structure using transmission electron microscopy. For dodecanethiol-ligated 6-nm-diameter gold nanocrystal monolayers, we find a Young's modulus of the order of several GPa. This remarkable strength is coupled with high flexibility, enabling the membranes to bend easily while draping over edges. The arrays remain intact and able to withstand tensile stresses up to temperatures around 370 K. The purely elastic response of these ultrathin membranes, coupled with exceptional robustness and resilience at high temperatures should make them excellent candidates for a wide range of sensor applications.

Compared with the top-down lithographic techniques, bottom-up chemical synthesis and self-assembly approaches offer much more flexibilities in creating magnetic nanostructures with controlled size, shape, composition and physical properties. This review summarizes some of the latest developments in this field, with emphasis mainly on transition metals, their alloys and metal oxide nanoparticles. The focus is directed towards the conditions of individual particles as well as large assemblies of particles through colloidal chemistry. Furthermore, some of the future directions in nanomagnetism from the perspective of physical chemists is also presented.