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The perception of organic crystals being rigid static entities is quickly eroding, and molecular crystals are now matching a number of properties previously thought to be unique to soft materials. Here, we present crystals of a boronate ester that encompass many of the elastic and plastic mechanical properties of polymers such as bending, twisting, coiling and highly efficient self-healing of up to 67%, while they maintain their long-range structural order. The approach utilizes the concept of dynamic covalent chemistry and proves it can be applied towards ordered materials. This work expands our current understanding of the properties of crystalline molecular materials, and it could have implications towards the development of mechanically robust organic crystals that are capable of self-repair for durable all-organic electronics and soft robotics., Organic crystal is described that can be bent plastically and twisted elastically, and can self-heal to 67%, an efficiency that is an order-of-magnitude higher compared to the only previously reported example.

Simple surfactants have proven to be some of the most effective agents to mitigate the deposition of asphaltenes on pipeline walls; however, the best practices for their application are often empir...

Understanding of polymorphism of organic semiconducting materials is the key to structural control of their electrical and mechanical properties. Motivated by the ambipolar n-type charge transport and electroluminescence of thienopyrrolyldione end-capped oligothiophenes, here we studied the propensity of one representative to crystallize as different polymorphs which display distinctly different mechanically properties. The crystal structures of the two polymorphs (denoted "α" and "β") of the material, 2,2′-(2,2′-thiophene-5,5′-diyl)bis(5-butyl-5H-thieno[2,3-c]pyrrole-4,6)-dione (C4-NT3N), were determined. In the α phase, the molecules interact strongly by Ï-stacking, forming columns which are bonded via C-H-O and chalcogen bonds, and this packing is consistent with the elastic behavior observed with the crystals. Instead, the β phase has the molecules aligned along their core forming layers. While the molecules interact strongly within the layers, they are practically unbound between the layers. The presence of slip planes in this form explains the plastic deformation induced by applying a force perpendicular to the (001). The thermal behavior and the enantiotropic relationship of the polymorphs are reported.

A bioinspired fluorophore that is analogous to the substrate in the bioluminescence of fireflies was prepared and reacts when exposed to weak blue LED light. Upon excitation, this material is photodecarboxylated with a nearly 81-fold enhancement of the solid-state emission, the fluorescence quantum yield of the product in solution is approximately 90 %, and violent disintegrative effects occur as a result of the release of carbon dioxide. Crystallographic and computational results, together with global spectral analysis of the kinetics, confirmed that most of the emission observed in the decay-associated spectra is intrinsic to the product molecule, with only a minor contribution from an excimer through π-π stacking of the molecules in the crystal.

Photoexcitation can lead to either homogeneous or heterogeneous transformations of a reactive surface. Homogeneous transformations result in a statistical mixture of reactants and products, whereas the outcome of heterogeneous transformations is a coexistence of macroscopic reactant and product domains, separated by a phase boundary. Heterogeneous photoinduced changes are also typically restricted to the surface, have individual phase structures that are inaccessible with classical diffraction methods, and possess surface properties that cannot readily be measured by the traditional wetting (water contact angle) technique. In this study, we demonstrate application of Atomic Force Microscopy (AFM) to obtain high spatial resolution surface energy distribution in the trans and cis domains on the surface of azobenzene single crystal. UV excitation of single crystals of 3′,4′-dimethyl-4-(dimethylamino)azobenzene results in domino-like trans-to-cis isomerization on their surface. In the AFM phase channel, this ...

Plastic bending of organic crystals is a well-known, yet mechanistically poorly understood phenomenon. On three structurally related epimers, derivatives of galactose, glucose, and mannose, it is demonstrated here that small changes in the molecular structure can have a profound effect on the mechanical properties. While the galactose derivative affords crystals which can be easily bent, the crystals of the derivatives of glucose and mannose are brittle and do not bend. Structural, microscopic, and mechanical evidence is provided showing that hydrogen bonding of water molecules is the key element for sliding over the slip planes in the crystal and accounts for the plastic bending.

Peak Force Tapping-mode AFM is used to investigate the three-dimensional morphology of RuO 2 nanoparticles supported on a solid surface, with sub-nanometer spatial resolution. Samples were prepared by spin coating (i) a drop of RuO 2 colloidal suspension onto a mica sheet, followed by further treatments (drying, calcination and/or reduction), and (ii) a second drop of colloidal suspension on fresh, dried or calcined RuO 2 -mica. RuO 2 crystallites are supported with a certain distribution of sizes, and this heterogeneity is essentially maintained after high-temperature treatments. After calcination, single coated RuO 2 -mica samples present small RuO 2 crystallites (4.5 nm height) as well as nanorod-like assemblies (14 nm height). A disaggregation of particles occurs during the reduction treatment. Double coating RuO 2 over non-calcined RuO 2 -mica samples involves mechanical effects causing re-dispersion of supported clusters. An intermediate drying step is unable to prevent re-dispersion of particles and even leads to repulsion between dehydrate RuO 2 supported particles and hydrated particles in suspension. Meanwhile, a calcination step prevents re-dispersion and promotes growth of supported crystallites. Nanorods formed by single RuO 2 deposition exhibit mostly regular flat surfaces, while a second RuO 2 deposition on calcined RuO 2 -mica samples leads to larger nanorods with stepped surfaces (terraces), a favourable geometry for ammonia synthesis reaction.

Ischemic heart disease often leads to myocardial infarction and remains the most common cause for death in humans. Although the exact impetus for the infarction remains elusive, a mechanism has been proposed that relates the disease to the observed high cholesterol levels in the body. The mechanism claims that cholesterol crystallizes inside the arterial plaque into needle-shaped crystals. The crystals puncture the fibrous cap of the plaque, whereby the necrotic contents of the plaque are spilled, subsequently clotting the blood vessels. This hypothesis has not been given sufficient attention partly due to the purported softness of the organic crystals and the common platy habit of the known crystal forms of cholesterol. In this work it is shown that, from hydrophobic solutions that attempt to emulate the plaque contents, a new solid form of cholesterol crystallizes as prisms with mucronate tips, and they are sufficiently strong to puncture a lamb pericardium, which mimics the plaque cap. The properties of the crystals were assessed by mechanical, structural, and crystallographic analyses. The results support the hypothesis that the cholesterol crystals can be considered, at least within the framework of the proposed mechanism, a possible cause of myocardial infarction.

Protein fibrillation is involved in many serious diseases, and protein oligomers are proved to be precursors of amyloid fibrils. NMR and QCMD experiments allowed us to establish that the interaction between citrate-stabilized gold nanoparticles and a paradigmatic amyloidogenic protein, β2-microglobulin, is able to interfere with protein association into oligomers.

Hybridization of polyoxometalates (POMs) via an organic-inorganic association constitutes a new route to develop heterogeneous POM catalysts with tunable supramolecular architecture. As the structural stability of POMs is strongly influenced by the pH conditions, a quantitative understanding of the POMs-polymer association is important in practical applications. Herein, we use Quartz Crystal Microbalance (QCM) to systematically investigate the interactions of Keggin phosphotungstic acid POM with a polyampholyte polymer-coated QCM sensor as a function of pH. The mass of adsorbed POMs increases when pH decreases from 5.6 to 2, indicating that electrostatic forces play a major role in the formation of POM-polymer hybrids. This finding is complemented by AFM images that show an increase in the size of the hybrid entities from 5 to 12 nm as the pH decreases from 5.6 to 2. The POM adsorbed amount at a particular pH value reaches an equilibrium level with time. The hybrids further gain in adsorbed mass only when lowering the pH value of the POM solution. The hybrid structure formed above pH 2 shows resistance to leaching as indicated by the steady level of the adsorbed mass during a rinsing step with water. However, at pH 2, the rinsing step causes desorption of some weakly adsorbed POMs. It is shown that leached POMs can be re-adsorbed back into the polymer matrix during a second contact with a POM solution at pH 2. This adsorption-desorption cycles of POMs were successfully repeated. Our experiments shed light into the coexistence of tightly as well as loosely bound POMs in hybrid catalyst formed at pH 2. The loosely bound POMs can potentially act as homogeneous catalysts when desorbed. However, these leached POMs can be re-adsorbed back into the matrix, preserving the heterogeneous state of the catalyst. Our results show that QCM is a powerful technique to study in situ the dynamics of the adsorption of POMs on a polymer matrix under different pH conditions.

The concept of biomineralization and encapsulation of organic molecules into inorganic matrices to alter and enhance their physical properties has been evolved and perfected in natural systems. Being inspired by the natural biomineralization of foreign components into calcite, here the inclusion of a plant virus, cowpea mosaic virus (CPMV) of 5.4% by mass into crystals of calcite is reported. The viral particles are labeled with a fluorescent tag (Alexa Fluor 532), and are observed within the calcite matrix using confocal fluorescence microscopy. Upon encapsulation, the calcite crystals exhibit an irregular and aggregated morphology, as visualized with atomic force and electron microscopy. The viral particles protected inside the calcite crystals are able to resist harsh chemical agents. While spherical viral particles such as CPMV can be easily included in calcite, viruses such as the tobacco mosaic virus are not compatible with the host, presumably due to their high aspect ratio. The results provide a simple and scalable method to incorporate viral particles into inorganic matrix, and could prove useful in thermal stabilization of sensitive viral biological agents such as vaccines in the future.

The propensity for adherence to solid surfaces of asphaltenes, a complex solubility class of heteropolycyclic aromatic compounds from the heavy fraction of crude oil, has long been the root cause of scale deposition and remains an intractable problem in the petroleum industry. Although the adhesion is essential to understanding the process of asphaltene deposition, the relationship between the conformation of asphaltene molecules on mineral substrates and its impact on adhesion and mechanical properties of the deposits is not completely understood. To rationalize the primary processes in the process of organic scale deposition, here we use atomic force microscopy (AFM) to visualize the morphology of petroleum asphaltenes deposited on model mineral substrates. High imaging contrast was achieved by the differential adhesion of the tip between asphaltenes and the mineral substrate. While asphaltenes form smooth continuous films on all substrates at higher concentrations, they deposit as individual nanoparticles at lower concentrations. The size, shape, and spatial distribution of the nanoaggregates are strongly affected by the nature of the substrate; while uniformly distributed spherical particles are formed on highly polar and hydrophilic substrates (mica), irregular islands and thicker patches are observed with substrates of lower polarity (silica and calcite). Asphaltene nanoparticles flatten when adsorbed on highly oriented pyrolytic graphite due to π-π interactions with the polycyclic core. Force-distance profiles provide direct evidence of the conformational changes of asphaltene molecules on hydrophilic/hydrophobic substrates that result in dramatic changes in adhesion and mechanical properties of asphaltene deposits. Such an understanding of the nature of adhesion and mechanical properties tuned by surface properties, on the level of asphaltene nanoaggregates, would contribute to the design of efficient asphaltene inhibitors for preventing asphaltene fouling on targeted surfaces. Unlike flat surfaces, the AFM phase contrast images of defected calcite surfaces show that asphaltenes form continuous deposits to fill the recesses, and this process could trigger the onset for asphaltene deposition.

International audience; Insulated molecular wires formed from organic molecules may have promising applications in organic and flexible electronic devices. Here, the authors provide compelling evidence of the formation of insulated molecular wires by sheathing conducting regioregular poly(3-butylthiophene-2,5-diyl) (P3BT) fibrils with insulating nanotubes from 3,5-bis-(5-hexylcarbamoylpentyloxy)-benzoic acid decyl ester molecules through a nucleation and growth process. For dilute systems, conducting atomic force microscopy together with force-distance curves and current-voltage spectroscopy are concomitantly performed to sense current from the topmost surface to the core of the composite fibrils at controlled tip indentation depths. Results show that current is sensed only when the core of the nanocomposite fibrils is reached which indicates the presence of an insulating layer around the semiconducting P3BT fibrils. The existence of this molecular nanocomposite is further supported by neutron scattering experiments carried out on more concentrated systems at different temperatures.

The hybridization of polyoxometalates (POMs) through an organic–inorganic association offers several processing advantages in the design of heterogeneous catalysts. A clear understanding of the organization of these hybrid materials on solid surfaces is necessary to optimise their properties. Herein, we report for the first time the organization of Keggin phosphotungstic [PW12O40]3− and Wells–Dawson (WD) phosphomolybdic [P2Mo18O62]6− anions deposited on mica (hydrophilic), and highly oriented pyrolytic graphite (HOPG) (hydrophobic) surfaces. Next, the supramolecular organization of the organic–inorganic hybrid materials formed from the association of POM anions and dimethyldioctadecylammonium bromide (DODA) is investigated as a function of the hydrophilic or hydrophobic nature of the surfaces. The height of the Keggin-POM anions, measured with tapping mode (TM-AFM) is always in good agreement with the molecular dimension of symmetric Keggin-POM anions (ca. 1 nm). However, the asymmetric WD-POM anions form monolayer assemblies on the surfaces with the orientation of their long molecular axis (ca. 1.6 nm) depending on the hydrophilic or hydrophobic properties of the substrate. Namely, the long axis is parallel on mica, and perpendicular on HOPG. When hybridized with DODA, the organization of the hybrid material is dictated by the interaction of the alkyl side chains of DODA with the substrate surface. On HOPG, the DODA–POM hybrid forms small domains of epitaxially arranged straight nanorod structures with their orientation parallel to each other. Conversely, randomly distributed nanospheres are formed when the hybrid material is deposited on freshly cleaved mica. Finally, a UV–ozone treatment of the hybrid material allows one to obtain highly dispersed isolated POM entities on both hydrophilic and hydrophobic surfaces. The hybridization strategy to prevent the clustering of POMs on various supports would enable to develop highly dispersed POM-based heterogeneous catalysts with enhanced functionalities.

CdS quantum dots were grown on mesoporous TiO2 films by successive ionic layer adsorption and reaction processes in order to obtain CdS particles of various sizes. AFM analysis shows that the growth of the CdS particles is a two-step process. The first step is the formation of new crystallites at each deposition cycle. In the next step the pre-deposited crystallites grow to form larger aggregates. Special attention is paid to the estimation of the CdS particle size by X-ray photoelectron spectroscopy (XPS). Among the classical methods of characterization the XPS model is described in detail. In order to make an attempt to validate the XPS model, the results are compared to those obtained from AFM analysis and to the evolution of the band gap energy of the CdS nanoparticles as obtained by UV–vis spectroscopy. The results showed that XPS technique is a powerful tool in the estimation of the CdS particle size. In conjunction with these results, a very good correlation has been found between the number of deposition cycles and the particle size.

Hybridization of polyoxometalates (POMs) via the formation of an organic-inorganic association constitutes a new route to develop a heterogeneous POM catalyst with tunable functionality imparted through supramolecular assembly. Herein, we report on strategies to obtain tunable well-defined supramolecular architectures of an organic-inorganic heterogeneous hybrid catalyst formed by the association of a hydrophobically substituted polyampholyte copolymer (poly N, N-diallyl-N-hexylamine-alt-maleic acid) and phosphotungstic acid (H3PW12O40) POMs. The self-assembling property of the initial polyampholyte copolymer matrix is modulated by controlling the pH of the hybridization solution. When deposited on a mica surface, isolated, long and extended polymer chains are formed under basic conditions (pH 7.9), while globular or coiled structures are formed under acidic conditions (pH 2). The supramolecular assembly of the POM-polymer hybrid is found to be directed by the type and quantities of charges present on the polyampholyte copolymer, which themselves depend on the pH conditions. The hypothesis is that the Keggin type [PW12O40](3-) anions, which have a size of ~1 nm, electrostatically bind to the positive charge sites of the polymer backbone. The hybrid material stabilized at pH 5.3 consists of POM-decorated polymer chains. Statistical analysis of distances between pairs of POM entities show narrow density distributions, suggesting that POM entities are attached to the polymer chains with a high level of order. Conversely, under acidic conditions (pH 2), the hybrid shows the formation of a core-shell type of structure. The strategies reported here, to tune the supramolecular assembly of organic-inorganic hybrid materials, are highly valuable for the design and a more rational utilization of POM heterogeneous catalysts in several chemical transformations.

Over the last few years, intensive research has been devoted to the exploitation of vegetal fibres in composite reinforcements. The mechanical properties of the natural fibre reinforced composite materials are largely dependant on the adhesion between the fibre and the polymer matrix. To improve the interfacial adhesion, raw flax fibres were chemically modified using an alkali and an eco-friendly enzymatic treatment. Atomic force microscopy (AFM) was used to probe the surface properties of the raw, alkali and enzyme treated flax fibres. First, topography images of the treated flax fibres, as investigated by AFM-Tapping mode, reveals the removal of pectin polysaccharides from the primary cell wall and allows for visualisation underneath the oriented cellulose microfibrils with a typical diameter of 25–30 nm. The removal of pectin polysccharides was also confirmed by the Infra-red spectroscopy analysis. Secondly, the lateral distribution of local adhesion properties of the fibres, as investigated using the AFM Force-Volume (FV) imaging mode, showed a heterogeneous distribution of adhesion forces on raw flax fibres in comparison with treated ones. The variation in adhesion forces was explained in terms of local changes in the hydrophilic properties of the raw flax fibre, due to the presence of some amorphous hydrophilic pectins. Furthermore, the difference in adhesion correlated well with the principal effect of the treatments which was mainly as the removal of the pectin materials on the primary cell wall of the fibre.

International audience

International audience; Natural fiber-reinforced polymers or biocomposites are becoming increasingly popular as an environment friendly alternative to traditional glass fiber-reinforced thermoplastics. The mechanical properties of reinforced biocomposites, such as flax/polylactic acid (PLA), are largely governed by the level of interfacial interactions between the two constituents apart from their intrinsic properties. The hierarchical organization of various polysaccharides present in natural fibers results in complex mechanisms at the interface which are still poorly understood and difficult to analyze through a traditional approach that rely on indirect assessments. The possibility of measuring direct adhesion force between individual particles using the colloidal force microscopy has been exploited here by developing an experimental set-up in which a micrometer colloidal PLA bead is brought into close contact with molecularly smooth polysaccharide surfaces that mimic the main constituents of flax fibers, cellulose, hemicellulose, and pectins. Adhesion force measurements performed under ambient and low relative humidity conditions indicate that cellulose/PLA is the weakest interface in the biocomposite. Moreover, the results emphasize the important role of water molecules for the more hydrophilic polymers in flax fibers that takes place in the fundamental forces involved in the adhesion phenomena at the biocomposite interface.

The effect of alkali and enzymatic treatments on flax fibre morphology, mechanical, and adhesion properties was investigated. The multilength scale analysis allows for the correlation of the fibre's morphological changes induced by the treatments with mechanical properties to better explain the adherence properties between flax and PLA. The atomic force microscopy (AFM) images revealed the removal of primary layers, upon treatments, down to cellulose microfibrils present in the secondary layers. The variation in mechanical properties was found to be dependent, apart from the crystalline content, on interaction between cellulose microfibrils and encrusting polysaccharides, pectins and hemicelluloses, in the secondary layers. Finally, microbond tests between the modified fibres and PLA emphasize the important role of the outer fibre's surface on the overall composite properties. It was observed here that gentle treatments of the fibres, down to the oriented microfibrils, are favourable to a better adherence with a PLA drop. This paper highlights the important role of amorphous polymers, hemicellulose and pectin, in the optimisation of the adhesion and mechanical properties of flax fibres in the biocomposite.

Over the last few years, intensive research has been devoted to the exploitation of “green products” based on natural resources for both matrices and as reinforcements in composite systems. The mechanical properties of reinforced biocomposites, such as flax/polylactic acid (PLA), are largely governed by interfacial properties between the two constituents apart from their intrinsic properties. Although many papers indirectly demonstrate the importance of optimising the interface between these two polymers, the exact nature of the interaction between the natural fibre and the polymeric matrix has not been clearly investigated on a fundamental level and is presently a major technological limitation of these materials. This work presents the first direct study of adhesion forces, by colloidal force microscopy, between smooth PLA films representing the polymer matrix, and a microbead of cellulose that mimic the cellulose material in flax fibres. Normalised adhesion force measurements have shown the importance of capillary forces when experiments were carried out under ambient conditions. Experiments, conducted under dry air, allowed for the deduction of the contribution of pure van der Waals forces, and our results, through the calculation of the Hamaker constant, show that these forces, for the PLA/cellulose/air system, were lower than those obtained for the cellulose/cellulose/air system and hence underlined the importance of optimising the interface among these materials. This study demonstrates the capacity of AFM to probe direct interactions in complex systems by adjusting the nature of the surface and the probe to mimic the materials in contact. Furthermore, the technique can be operated in a variety of environments, consistent with composite making and provides particular opportunity for testing and improving the properties of these new classes of composite materials.

Vegetable fibers have several positive aspects, such as low production costs, biodegradability and good mechanical properties, which make them very attractive in the field of composite reinforcement. The aim of this study is to introduce into a l -poly-(lactic-acid) (PLLA) – hemp biocomposite a new compatibilizer, inspired from the mussels' adhesive capacity, to improve the fiber-matrix bonding. As a first step, we carried out atomic force microscopy (AFM) and surface energy measurements in order to prove the compatibilizer's presence. Secondly, tensile tests were performed. The results show a significant increase of Young's modulus and the breaking strength when using polydopamine. Observations made through scanning electronic microscopy (SEM) confirmed an improvement of the fiber-matrix coupling in the presence of poly-(dopamine).