Long-range selective transport of anions and cations in graphene oxide membranes, causing selective crystallization on the macroscale

Monoatomic nanosheets can form 2-dimensional channels with tunable chemical properties, for ion storage and filtering applications. Here, we demonstrate transport of K+, Na+, and Li+ cations and F- and Cl- anions on the centimeter scale in graphene oxide membranes (GOMs), triggered by an electric bias. Besides ion transport, the GOM channels foster also the aggregation of the selected ions in salt crystals, whose composition is not the same as that of the pristine salt present in solution, highlighting the difference between the chemical environment in the 2D channels and in bulk solutions

Indium-modified copper nanocubes for syngas production by aqueous CO2 electroreduction

Electroreduction of carbon dioxide represents an appealing strategy to rethink a waste product as a valuable feedstock for the formation of value-added compounds. Among the metal electrodes able to catalyze such processes, copper plays a central role due to its rich chemistry. Strategies aimed at tuning Cu selectivity comprise nanostructuring and alloying/post-functionalization with heterometals. In this contribution, we report on straightforward electrochemical methods for the formation of nanostructured Cu-In interfaces. The latter were fully characterized and then used as cathodes for CO2 electroreduction in aqueous environment, leading to the selective production of syngas, whose composition varies upon changing the applied bias and indium content. In particular, gaseous mixtures compatible with the synthesis of methanol or aldehydes (i.e. respectively with 1 : 2 and 1 : 1 CO/H2 ratios) are produced at low (i.e. −0.62 V vs. RHE) applied bias with >3.5 mA cm−2 current densities (in absolute value). Even if the proposed cathodes undergo structural modifications upon prolonged exposure to CO2 reduction conditions, their catalytic activity can be restored by introducing an additional In(iii) precursor to the electrolytic solution

Carbon nanotube - Based cold cathodes: Field emission angular properties and temporal stability

The field emission (FE) properties of carbon nanotube (CNT)-based cathodes have been investigated on nanostructured surfaces grown by plasma enhanced chemical vapor deposition. The FE angular properties and temporal stability of the emergent electron beam have been determined using a dedicated apparatus for cathodes of various architectures and geometries, characterized by scanning electron microscopy and I-V measurements. The angular electron beam divergence and time instability at the extraction stage, which are crucial parameters in order to obtain high brilliance of FE-based-cathode electron sources, have been measured for electrons emitted by several regular architectures of vertically aligned arrays and critically compared to conventional disordered cathodes. The measured divergences strongly depend on the grid mesh. For regular arrays of individual CNT, divergences from 2° to 5° have been obtained; in this specific case, measurements together with ray-tracing simulations suggest that the maximum emission angle is of the order of ±30° about the tube main axis. Larger divergences have been measured for electron beams emitted from honeycomb-structured cathodes (6°) and significantly broader angle distributions (10°) from disordered CNT surfaces. Emission current instabilities of the order of 1% for temporal stability studies conducted across a medium time scale (hours) have been noted for all cathodes consisting of a high number (10$^{4}$ and larger) of aligned CNTs, with the degree of stability being largely independent of the architecture.The European AXIS project (FP7-SME-1-2007) is acknowledged for financial support

Light-induced reversible modification of the work function of a new perfluorinated biphenyl azobenzene chemisorbed on Au (111)

This work was financially supported by EC through the Marie-Curie ITN SUPERIOR (PITN-GA-2009-238177) and IEF MULTITUDES (PIEF-GA-2012-326666), the ERC project SUPRAFUNCTION (GA-257305), the Agence Nationale de la Recherche through the LabEx project Chemistry of Complex Systems (ANR-10-LABX-0026_CSC), and the International Center for Frontier Research in Chemistry (icFRC). The work in Mons is further supported by the Interuniversity Attraction Poles Programme (P7/05) initiated by the Belgian Science Policy Office, and by the Belgian National Fund for Scientific Research (FNRS). J.C. is an FNRS research director. The synthesis team in Switzerland acknowledges financial support by the Swiss National Science Foundation (SNF) and the Swiss Nanoscience Institute (SNI)

Mesoscopic 3D Charge Transport in Solution-Processed Graphene-Based Thin Films: A Multiscale Analysis

Graphene and related 2D material (GRM) thin films consist of 3D assembly of billions of 2D nanosheets randomly distributed and interacting via van der Waals forces. Their complexity and the multiscale nature yield a wide variety of electrical characteristics ranging from doped semiconductor to glassy metals depending on the crystalline quality of the nanosheets, their specific structural organization ant the operating temperature. Here, the charge transport (CT) mechanisms are studied that are occurring in GRM thin films near the metal-insulator transition (MIT) highlighting the role of defect density and local arrangement of the nanosheets. Two prototypical nanosheet types are compared, i.e., 2D reduced graphene oxide and few-layer-thick electrochemically exfoliated graphene flakes, forming thin films with comparable composition, morphology and room temperature conductivity, but different defect density and crystallinity. By investigating their structure, morphology, and the dependence of their electrical conductivity on temperature, noise and magnetic-field, a general model is developed describing the multiscale nature of CT in GRM thin films in terms of hopping among mesoscopic bricks, i.e., grains. The results suggest a general approach to describe disordered van der Waals thin films

Semicrystalline Polythiophene-Based Nanoparticles Deposited from Water on Flexible PET/ITO Substrates as a Sustainable Approach toward Long-Lasting Solid-State Electrochromic Devices

info:eu-repo/grantAgreement/EC/H2020/734834/EU FCT/MEC (UIDB/50006/2020). PhD grant SFRH/BD/139171/2018 from FCT/MCTES. We are very grateful to Dr. Carlos Pinheiro and Ynvisible company for discussions and assistance in the assembly of the electrochromic devices.We report the use of films of poly(3-hexylthiophene-2,5-diyl) nanoparticles (P3HT-NPs) prepared with the reprecipitation method employing water as solvent in the absence of surfactants for solid-state electrochromic devices (ECDs) and prove that these displays present enhanced properties when compared to similar ECDs with thin films deposited from chloroform. Films of differently sized nanoparticles (100 to 400 nm) were prepared and spray-coated on flexible PET-ITO substrates and tested for electrochromic properties. ECDs with switching times (t(90)) of 4 s were obtained using P3HT-NPs with a diameter of 100 nm, while those built using P3HT thin film presented longer switching speeds over 13 s for reduction (bleached to colored state). Additionally, the devices were subjected to 1000 cycles using -1.5 V/1.5 V, and the displays using P3HT 100 nm NPs presented higher transmittances (Delta(T) = +/- 20%) when compared with devices with P3HT thin film due to a more efficient oxidation step. Our data show that the availability of colloidal nanoparticles made of conjugated polymers deposited from water is an environmentally sustainable strategy leading to electrochromic devices with improved properties.authorsversionpublishe

Structure and dynamics of pentacene on SiO2: From monolayer to bulk structure

We have used confocal micro Raman spectroscopy, atomic force microscopy (AFM), and x-ray diffraction (XRD) to investigate pentacene films obtained by vacuum deposition on SiO2 substrates. These methods allow us to follow the evolution of lattice structure, vibrational dynamics, and crystal morphology during the growth from monolayer, to TF, and, finally, to bulk crystal. The Raman measurements, supported by the AFM and XRD data, indicate that the film morphology depends on the deposition rate. High deposition rates yield two-dimensional nucleation and quasi-layer-by-layer growth of the T-F form only. Low rates yield three-dimensional nucleation and growth, with phase mixing occurring in sufficiently thick films, where the T-F form is accompanied by the "high-temperature" bulk phase. Our general findings are consistent with those of previous work. However, the Raman measurements, supported by lattice dynamics calculations, provide additional insight into the nature of the TFs, showing that their characteristic spectra originate from a loss of dynamical correlation between adjacent layers

Graphene oxide–polysulfone filters for tap water purification, obtained by fast microwave oven treatment

The availability of clean, pure water is a major challenge for the future of our society. 2-Dimensional nanosheets of GO seem promising as nanoporous adsorbent or filters for water purification; however, their processing in macroscopic filters is challenging, and their cost\ua0vs.\ua0standard polymer filters is too high. Here, we describe a novel approach to combine graphene oxide (GO) sheets with commercial polysulfone (PSU) membranes for improved removal of organic contaminants from water. The adsorption physics of contaminants on the PSU-GO composite follows Langmuir and Brunauer–Emmett–Teller (BET) models, with partial swelling and intercalation of molecules in between the GO layers. Such a mechanism, well-known in layered clays, has not been reported previously for graphene or GO. Our approach requires minimal amounts of GO, deposited directly on the surface of the polymer, followed by stabilization using microwaves or heat. The purification efficiency of the PSU-GO composites is significantly improved\ua0vs.\ua0benchmark commercial PSU, as demonstrated by the removal of two model contaminants, rhodamine B and ofloxacin. The excellent stability of the composite is confirmed by extensive (100 hours) filtration tests in commercial water cartridges

Benchmarking of graphene-based materials: Real commercial products versus ideal graphene

There are tens of industrial producers claiming to sell graphene and related materials (GRM), mostly as solid powders. Recently the quality of commercial GRM has been questioned, and procedures for GRM quality control were suggested using Raman Spectroscopy or Atomic Force Microscopy. Such techniques require dissolving the sample in solvents, possibly introducing artefacts. A more pragmatic approach is needed, based on fast measurements and not requiring any assumption on GRM solubility. To this aim, we report here an overview of the properties of commercial GRM produced by selected companies in Europe, USA and Asia. We benchmark: (A) size, (B) exfoliation grade and (C) oxidation grade of each GRM versus the ones of \u27ideal\u27 graphene and, most importantly, versus what reported by the producer. In contrast to previous works, we report explicitly the names of the GRM producers and we do not re-dissolve the GRM in solvents, but only use techniques compatible with industrial powder metrology. A general common trend is observed: Products having low defectivity (%sp 2 bonds >95%) feature low surface area (<200 m 2 g -1 ), while highly exfoliated GRM show a lower sp 2 content, demonstrating that it is still challenging to exfoliate GRM at industrial level without adding defects