The integration of metal atoms and clusters in well-defined dielectric cavities is a powerful strategy to impart new properties to them that depend on the size and geometry of the confined space as well as on metal-host electrostatic interactions. Here, we unravel the dependence of the electronic properties of metal clusters on space confinement by studying the ionization potential of silver clusters embedded in four different zeolite environments over a range of silver concentrations. Extensive characterization reveals a strong influence of silver loading and host environment on the cluster ionization potential, which is also correlated to the cluster's optical and structural properties. Through fine-tuning of the zeolite host environment, we demonstrate photoluminescence quantum yields approaching unity. This work extends our understanding of structure-property relationships of small metal clusters and applies this understanding to develop highly photoluminescent materials with potential applications in optoelectronics and bioimaging.

Despite the intensive research efforts devoted to graphene fabrication over the past decade, the production of high-quality graphene on a large scale, at an affordable cost, and in a reproducible manner still represents a great challenge. Here, we report a novel method based on the controlled electrochemical exfoliation of graphite in aqueous ammonium sulfate electrolyte to produce graphene in large quantities and with outstanding quality. Because the radicals (e.g., HO(•)) generated from water electrolysis are responsible for defect formation on graphene during electrochemical exfoliation, a series of reducing agents as additives (e.g., (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO), ascorbic acid, and sodium borohydride) have been investigated to eliminate these radicals and thus control the exfoliation process. Remarkably, TEMPO-assisted exfoliation results in large graphene sheets (5-10 μm on average), which exhibit outstanding hole mobilities (∼405 cm(2) V(-1) s(-1)), very low Raman I(D)/I(G) ratios (below 0.1), and extremely high carbon to oxygen (C/O) ratios (∼25.3). Moreover, the graphene ink prepared in dimethylformamide can exhibit concentrations as high as 6 mg mL(-1), thus qualifying this material for intriguing applications such as transparent conductive films and flexible supercapacitors. In general, this robust method for electrochemical exfoliation of graphite offers great promise for the preparation of graphene that can be utilized in industrial applications to create integrated nanocomposites, conductive or mechanical additives, as well as energy storage and conversion devices.

International audienceA new polymer blend formed by poly(3-hexylthiophene)-poly(4-vinylpyridine) (P3HT-P4VP) block copolymers and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is reported. The P4VP and PCBM are mixed together by weak supramolecular interactions, and the resulting materials exhibit microphase separated morphologies of electron-donor and electron-acceptor rich domains. The properties of the blend, used in photovoltaic devices as active layers, are also discussed

Fullerene-grafted rod−coil block copolymers, designed for being used as active polymer layers in donor–acceptor bulk heterojunction photovoltaic devices, have been synthesized. The copolymer synthesis was monitored by 1H nuclear magnetic resonance, size exclusion chromatography and infrared absorption spectroscopy, while the material properties were explored by X-ray diffraction, atomic force microscopy, UV–vis absorption, and photoluminescence spectroscopy. Structural properties of bulk materials and thin films were investigated to study the influence of the coil block molecular weight as well as that of the grafted fullerenes on the molecular self-assembling process. The results show that the rod homopolymer is in the crystalline state at ambient temperature and undergoes a phase transition into a smectic-type liquid-crystalline phase at 55 °C. The rod−coil microphase separation enhances interlamellar ordering but destabilizes the intralamellar order, leading to the appearance of a liquid-crystalline phase for the non-fullerene-grafted copolymer at ambient temperature. Adding the fullerene moieties considerably affects the polymer assembling through the growth of fullerene nanocrystals. The latter hinder the formation of the lamellar phase by pinning the coil segments. The identification of the major driving forces that control the molecular self-assembling process allows us to suggest different alternative strategies that can be used as guidelines for the design of new photovoltaic polymer self-assembling materials.

Achieving the full control over the production as well as processability of high-quality graphene represents a major challenge with potential interest in the field of fabrication of multifunctional devices. The outstanding effort dedicated to tackle this challenge in the last decade revealed that certain organic molecules are capable of leveraging the exfoliation of graphite with different efficiencies. Here, a fundamental understanding on a straightforward supramolecular approach for producing homogenous dispersions of unfunctionalized and non-oxidized graphene nanosheets in four different solvents is attained, namely N-methyl-2-pyrrolidinone, N,N-dimethylformamide, ortho-dichlorobenzene, and 1,2,4-trichlorobenzene. In particular, a comparative study on the liquid-phase exfoliation of graphene in the presence of linear alkanes of different lengths terminated by a carboxylic-acid head group is performed. These molecules act as graphene dispersion-stabilizing agents during the exfoliation process. The efficiency of the exfoliation in terms of concentration of exfoliated graphene is found to be proportional to the length of the employed fatty acid. Importantly, a high percentage of single-layer graphene flakes is revealed by high-resolution transmission electron microscopy and Raman spectroscopy analyses. A simple yet effective thermodynamic model is developed to interpret the chain-length dependence of the exfoliation yield. This approach relying on the synergistic effect of a ad-hoc solvent and molecules to promote the exfoliation of graphene in liquid media represents a promising and modular strategy towards the rational design of improved dispersion-stabilizing agents.

Multifunctional materials can be engineered by combining multiple chemical components, each conferring a well-defined function to the ensemble. Graphene is at the centre of an ever-growing research effort due to its combination of unique properties. Here we show that the large conformational change associated with the trans–cis photochemical isomerization of alkyl-substituted azobenzenes can be used to improve the efficiency of liquid-phase exfoliation of graphite, with the photochromic molecules acting as dispersion-stabilizing agents. We also demonstrate reversible photo-modulated current in two-terminal devices based on graphene–azobenzene composites. We assign this tuneable electrical characteristics to the intercalation of the azobenzene between adjacent graphene layers and the resulting increase in the interlayer distance on (photo)switching from the linear trans-form to the bulky cis-form of the photochromes. These findings pave the way to the development of new optically controlled memories for light-assisted programming and high-sensitive photosensors.

Metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) have attracted enormous attention in recent years.R ecently,M OF@COF are emerging as hybrid architectures combining the unique features of the individual components to enable the generation of materials displaying novel physicochemical properties.Herein we report an unprecedented use of aza-Diels-Alder cycloaddition reaction as post-synthetic modification of MOF@COF-LZU1, to generate aza-MOFs@COFs hybrid porous materials with extended p-delocalization. Aaproof-of-concept, the obtained aza-MOFs@COFs is used as electrode in supercapacitors displaying specific capacitance of 20.35 mFcm À2 and high volumetric energy density of 1.16 Fcm À3 .O ur approach of post-synthetic modification of MOFs@COFs hybrids implement rational design for the synthesis of functional porous materials and expands the plethora of promising application of MOFs@COFs hybrid porous materials in energy storage applications.

Novel fullerene‐grafted poly(3‐hexylthiophene) (P3HT)‐based rod‐coil block copolymers have been synthesized. The regioregular P3HT rod block has been synthesized by a modified Grignard metathesis reaction (GRIM). An original in situ end‐capping reaction has been developed in order to convert the P3HT block into an efficient macro‐initiator for the nitroxide‐mediated radical polymerization (NMRP) of the coil block. Controlled radical polymerization of the second poly(butylacrylate‐stat‐chloromethylstyrene) [P(BA‐stat‐CMS)] block has been done through various conditions leading to different coil block lengths. The final electron donor‐acceptor block copolymer has been obtained after C60 grafting in soft conditions. Copolymers have been characterized by 1H NMR and size exclusion chromatography. Optical characterizations, before and after C60 grafting, are reported.magnified image