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Liquid-phase exfoliation (LPE) has been shown to be capable of producing large quantities of high-quality dispersions suitable for processing into subsequent applications. LPE typically requires surfactants for aqueous dispersions or organic solvents with high boiling point. However, they have major drawbacks such as toxicity, aggregation during solvent evaporation or the presence of residues. Here, dispersions of molybdenum disulfide in acetone are prepared and show much higher concentration and stability than predicted by Hansen parameter analysis. Aiming to understand these enhanced properties, the nanosheets were characterised using UV-visible spectroscopy, zeta potential measurements, atomic force microscopy, Raman spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and scanning transmission microscopy combined with spatially-resolved electron energy loss spectroscopy. Also, the performance of the MoS2 nanosheets exfoliated in acetone was compared to that of those exfoliated in isopropanol as a catalyst for the hydrogen evolution reaction. The conclusion from the chemical characterisation was that MoS2 nanosheets exfoliated in acetone have an oxygen edge functionalisation, in the form of molybdenum oxides, changing its interaction with solvents and explaining the observed high-quality and stability of the resulting dispersion in a low boiling point solvent. Exfoliation in acetone could potentially be applied as a pretreatment to modify the solubility of MoS2 by edge functionalisation., The SR-EELS studies were conducted at the Laboratorio de Microscopias Avanzadas (LMA) at the Instituto de Nanociencia de Aragon (INA) – Universidad de Zaragoza (Spain). This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement no. 642742 and under the “Graphene Flagship” project grant agreement no. 785219. R. A. also acknowledges the support from the Spanish Ministerio de Economia y Competitividad (MAT2016-79776-P), from the Government of Aragon and the European Social Fund under the project “Construyendo Europa desde Aragon” 2014-2020 (grant number E13_17R). VN wishes to thank the support of SFI (AMBER and I-Form centres, PIYRA and US-Ireland grants) and the ERC CoG (3D2DPrint).

Hybrid nanomaterials fabricated by the heterogeneous integration of 1D (carbon nanotubes) and 2D (graphene oxide) nanomaterials showed synergy in electrical and mechanical properties. Here, we reported the infiltration of carboxylic functionalized single-walled carbon nanotubes (C-SWNT) into free-standing graphene oxide (GO) paper for better electrical and mechanical properties than native GO. The stacking arrangement of GO sheets and its alteration in the presence of C-SWNT were comprehensively explored through scanning electron microscopy, X-ray photoelectron spectroscopy (XPS) and X-ray diffraction. The C-SWNTs bridges between different GO sheets produce a pathway for the flow of electrical charges and provide a tougher hybrid system. The nanoscopic surface potential map reveals a higher work function of the individual functionalised SWNTs than surrounded GO sheets showing efficient charge exchange. We observed the enhanced conductivity up to 50 times and capacitance up to 3.5 times of the hybrid structure than the GO-paper. The laminate of polystyrene composites provided higher elastic modulus and mechanical strength when hybrid paper is used, thus paving the way for the exploitation of hybrid filler formulation in designing polymer composites.

Nanohybrid materials based on nanoparticles of the intrinsically microporous polymer PIM-1 and graphene oxide (GO) are prepared from aqueous dispersions with a re-precipitation method, resulting in the surface of the GO sheets being decorated with nanoparticles of PIM-1. The significant blueshift in fluorescence signals for the GO/PIM-1 nanohybrids indicates modification of the optoelectronic properties of the PIM-1 in the presence of the GO due to their strong interactions. The stiffening in the Raman G peak of GO (by nearly 6 cm^{-1}) further indicates p-doping of the GO in the presence of PIM. Kelvin probe force microscopy (KPFM) and electrochemical reduction measurements of the nanohybrids provide direct evidence for charge transfer between the PIM-1 nanoparticles and the GO nanosheets. These observations will be of importance for future applications of GO-PIM-1 nanohybrids as substrates and promoters in catalysis and sensing.

There remains a major materials challenge in maintaining the performance of platinum (Pt) anode catalysts in fuel cells due to corrosion and blocking of active sites. Herein, we report a new materials strategy for improving anode catalyst stability based on a protective microporous coating with an inert and highly rigid (non-blocking) polymer of intrinsic microporosity (PIM-EA-TB). The "anti-corrosion" effect of the PIM-EA-TB coating is demonstrated with a commercial Pt catalyst (3-5 nm diameter, 40 wt% Pt on Vulcan-72) and for three important fuel cell anode reactions: (i) methanol oxidation, (ii) ethanol oxidation, and (iii) formic acid oxidation.

A film of the polymer of intrinsic microporosity PIM-7 is coated onto a glassy carbon electrode and the resulting effects on electron transfer reactions are studied for three different types of processes: (i) aqueous solution based, (ii) solid state surface immobilised, and (iii) electrocatalytic processes on electrodeposited palladium. The effects on reactivity for hydroquinone oxidation in aqueous phosphate buffer are shown to be linked to microporosity causing a slightly lower rate of mass transport without detrimental effects on electron transfer and reaction kinetics. Next, water-insoluble microcrystalline anthraquinone is immobilised directly into the PIM-7 film and shown to give a chemically reversible reduction process, which is enhanced in the presence of PIM-7, when compared to the case of anthraquinone immobilised directly onto bare glassy carbon. Electrodeposition of a film of nano-palladium is demonstrated to give catalytically active electrodes for the reduction/oxidation of protons/hydrogen, the reduction of oxygen, and for the oxidation of formic acid and methanol. With the PIM-7 film applied onto palladium, a mechanical stabilisation effect occurs. In addition, both the hydrogen insertion and the hydrogen evolution reactions as well as formic acid oxidation are enhanced. Effects are discussed in terms of PIM-7 beneficially affecting the interfacial reaction under triphasic conditions. The microporous polymer acts as an interfacial “gas management” layer.

The one-step vacuum carbonization synthesis of a platinum nano-catalyst embedded in a microporous heterocarbon (Pt@cPIM) is demonstrated. A nitrogen-rich polymer of an intrinsic microporosity (PIM) precursor is impregnated with PtCl62&minus, to give (after vacuum carbonization at 700 &deg, C) a nitrogen-containing heterocarbon with embedded Pt nanoparticles of typically 1&ndash, 4 nm diameter (with some particles up to 20 nm diameter). The Brunauer-Emmett-Teller (BET) surface area of this hybrid material is 518 m2 g&minus, 1 (with a cumulative pore volume of 1.1 cm3 g&minus, 1) consistent with the surface area of the corresponding platinum-free heterocarbon. In electrochemical experiments, the heterocarbon-embedded nano-platinum is observed as reactive towards hydrogen oxidation, but essentially non-reactive towards bigger molecules during methanol oxidation or during oxygen reduction. Therefore, oxygen reduction under electrochemical conditions is suggested to occur mainly via a 2-electron pathway on the outer carbon shell to give H2O2. Kinetic selectivity is confirmed in exploratory catalysis experiments in the presence of H2 gas (which is oxidized on Pt) and O2 gas (which is reduced on the heterocarbon surface) to result in the direct formation of H2O2.

A water-insoluble Polymer with Intrinsic Microporosity (or PIM, here for the particular case of the Tröger Base system PIM-EA-TB, BET area ca. 103 m2 g−1) is demonstrated to act as a rigid host environment for highly water-insoluble molecular catalysts, here tetraphenylporphyrinato-iron (FeTPP), surrounded by aqueous solution-filled micropores. A PIM-EA-TB film containing catalyst is deposited onto the electrode and immersed for voltammetry (i) with 4-(3-phenyl-propyl)-pyridine to give an organogel, or (ii) bare directly into aqueous solution. The porous host allows processes to be optimised as a function of solution phase, composition, and catalyst loading. Effective electron transfer as well as effective electrocatalysis is reported for aqueous oxygen and peroxide reduction. Given the use of completely water-insoluble catalyst systems, the methodology offers potential for application with a wide range of hitherto unexplored molecular electrocatalysts and catalyst combinations in aqueous media. Keywords: Electrocatalysis, Ion transfer, Peroxide, Oxygen, Fuel cell, Sensing

The enzymeless glucose oxidation process readily occurs on nano-gold electrocatalyst at pH7, but it is highly susceptible to poisoning (competitive binding), for example from protein or chloride. Is it shown here that gold nanoparticle catalyst can be protected against poisoning by a polymer of intrinsic microporosity (PIM-EA-TB with BET surface area 1027m2g-1). This PIM material when protonated, achieves a triple catalyst protection effect by (i) size selective repulsion of larger protein molecules (albumins) and (ii) membrane ion selection effects, and (iii) membrane ion activity effects. PIM materials allow "environmental control" to be introduced in electrocatalytic processes.

“Ionic diode” (or current rectification) effects are potentially important for a range of applications including water purification. In this preliminary report, we observe novel ionic diode behaviour of thin (300 nm) membranes based on a polymer of intrinsic microporosity (PIM-EA-TB) supported on a poly-ethylene-terephthalate (PET) film with a 20 μm diameter microhole, and immersed in aqueous electrolyte media. Current rectification effects are observed for half-cells with the same electrolyte solution on both sides of the membrane for cases where cation and anion mobility differ (HCl, other acids, NaOH, etc.) but not for cases where cation and anion mobility are more alike (LiCl, NaCl, KCl, etc.). A pH-dependent reversal of the ionic diode effect is observed and discussed in terms of tentatively assigned mechanisms based on both (i) ion mobility within the PIM-EA-TB nano-membrane and (ii) a possible “mechanical valve effect” linked to membrane potential and electrokinetic movement of the membrane as well as hydrostatic pressure effects. Keywords: Electrokinetic effects, Salt separation, Membrane potential, Nanofluidics, Iontronics, Electrophysiology

Anion uptake and charge transport in a polymer of intrinsic microporosity (here PIM-EA-TB) is investigated for three cases: (i) the oxidation of ferrocene embedded into a thin film of PIM-EA-TB on a glassy carbon electrode, (ii) the reduction of protons absorbed into a thin film of PIM-EA-TB on a platinum electrode, and (iii) the potential-driven transport of anions and protons in an asymmetrically deposited free-standing PIM-EA-TB membrane working as a current rectifier or "ionic diode". In all three cases the competing effects of the diameter and hydrophobicity (size and hydration energy) of the anion are important. For free-standing membranes very high ionic diode rectification ratios (>10(3) at +/- 1 V) are observed in particular for thicker deposits of PIM-EA-TB and for chloride or perchlorate containing electrolyte. (C) 2015 Elsevier B.V. All rights reserved.

We describe ion current rectification using a Polymer of Intrinsic Microporosity (PIM) based on Tröger's base (PIM-EA-TB). When deposited asymmetrically over one (or more) 20 μm diameter hole(s) in 6 μm thick poly(ethylene terephthalate) and investigated in a two-compartment electrochemical cell with acidified aqueous NaCl on both sides, novel ionic diode effects are observed.

Vacuum carbonization of organic precursors usually causes considerable structural damage and collapse of morphological features. However, for a polymer with intrinsic microporosity (PIM-EA-TB with a Brunauer-Emmet-Teller (BET) surface area of 1027 m(2)g(-1)), it is shown here that the rigidity of the molecular backbone is retained even during 500 °C vacuum carbonization, yielding a novel type of microporous heterocarbon (either as powder or as thin film membrane) with properties between those of a conducting polymer and those of a carbon. After carbonization, the scanning electron microscopy (SEM) morphology and the small-angle X-ray scattering (SAXS) Guinier radius remain largely unchanged as does the cumulative pore volume. However, the BET surface area is decreased to 242 m(2)g(-1), but microporosity is considerably increased. The new material is shown to exhibit noticeable electrochemical features including two pH-dependent capacitance domains switching from ca. 33 Fg(-1) (when oxidized) to ca. 147 Fg(-1) (when reduced), a low electron transfer reactivity toward oxygen and hydrogen peroxide, and a four-point-probe resistivity (dry) of approximately 40 MΩ/square for a 1-2 μm thick film.

A highly rigid amine-based polymer of intrinsic microporosity (PIM), prepared by a polymerization reaction involving the formation of Tröger's base, is demonstrated to act as an ionic diode with electrolyte-dependent bistable switchable states.

Polymers of intrinsic microporosity (PIM or here PIM-EA-TB) offer a highly rigid host environment into which hexachloroplatinate(IV) anions are readily adsorbed and vacuum carbonised (at 500 °C) to form active embedded platinum nanoparticles. This process is characterised by electron and optical microscopy, atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and electrochemical methods, which reveal that the PIM microporosity facilitates the assembly of nanoparticles of typically 1.0 to 2.5-nm diameter. It is demonstrated that the resulting carbonised “Pt@cPIM” from drop-cast films of ca. 550-nm average thickness, when prepared on tin-doped indium oxide (ITO), contain not only fully encapsulated but also fully active platinum nanoparticles in an electrically conducting hetero-carbon host. Alternatively, for thinner films (50–250 nm) prepared by spin coating, the particles become more exposed due to additional loss of the carbon host. In contrast to catalyst materials prepared by vacuum-thermolysed hexachloroplatinate(IV) precursor, the platinum nanoparticles within Pt@cPIM retain high surface area, electrochemical activity and high catalyst efficiency due to the molecular rigidity of the host. Data are presented for oxygen reduction, methanol oxidation and glucose oxidation, and in all cases, the high catalyst surface area is linked to excellent catalyst utilisation. Robust transparent platinum-coated electrodes are obtained with reactivity equivalent to bare platinum but with only 1 μg Pt cm−2 (i.e. ~100% active Pt nanoparticle surface is maintained in the carbonised microporous host). [Figure not available: see fulltext.]