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Nickel nanoparticle electrodeposition is studied on flat glassy carbon (GC) or on nitrogen‐doped reduced graphene oxide (rGO‐N) substrates. The effects of a very thin (nominally 16 nm) layer polymer of intrinsic microporosity (PIM‐1) are investigated (i) on enhancing nickel nanoparticle nucleation and growth during electrodeposition and (ii) on enhancing hydrogen evolution electrocatalysis. Beneficial effects are tentatively assigned to PIM‐1 suppressing blocking effects from interfacial hydrogen bubble formation. Exploratory data suggest that in aqueous 0.5 M NaCl solution (artificial seawater) nickel nanoparticles grown into a thin film of PIM‐1 could be a viable electrocatalyst with an onset of hydrogen evolution only slightly negative compared to that observed for platinum nanoparticles. [ABSTRACT FROM AUTHOR]

Ionic diodes are components in ionic circuits for AC‐electricity driven desalination and ion extraction processes. Independent of the ionic diode type/mechanism, achieving ionic current rectification at high ionic strengths is challenging but important, for example in seawater desalination and treatment of brine. Here, the butylation of a molecularly rigid (glassy) polymer of intrinsic microporosity (PIM‐EA‐TB) is shown to give anionic diodes with ultrahigh rectification effects (associated with interfacial resistivity) even in high ionic strength aqueous 2 M NaCl solution. The effect is rationalised based on polymer structure affecting ion transport. [ABSTRACT FROM AUTHOR]

In this work, a new polymeric binder (polymer of intrinsic microporosity, PIM‐1) has been investigated and discussed to prepare and characterize composite materials for the cathodic oxygen reduction reaction. The new binder is a polymer of intrinsic microporosity, a family of organic compounds with molecularly rigid (glassy) structure, good mechanical and chemical stability. Their influence on the electrocatalytic behaviour of a commercial electrocatalyst during the oxygen reduction reaction in acidic and alkaline media has been investigated, discussed and compared to the behaviour of common cationic and anionic polymer binders, using rotating disk electrode (RDE) techniques. Polymers of intrinsic microporosity perform similarly well, and sometimes better (due to rigidity and gas permeation) when compared to commercial binders. Thus, herein, we showed that PIMs do represent a very promising and versatile alternative as binders in electrocatalysis. [ABSTRACT FROM AUTHOR]

Redox flow batteries (RFBs) are promising for large‐scale long‐duration energy storage owing to their inherent safety, decoupled power and energy, high efficiency, and longevity. Membranes constitute an important component that affects mass transport processes in RFBs, including ion transport, redox‐species crossover, and the net volumetric transfer of supporting electrolytes. Hydrophilic microporous polymers, such as polymers of intrinsic microporosity (PIM), are demonstrated as next‐generation ion‐selective membranes in RFBs. However, the crossover of redox species and water migration through membranes are remaining challenges for battery longevity. Here, a facile strategy is reported for regulating mass transport and enhancing battery cycling stability by employing thin film composite (TFC) membranes prepared from a PIM polymer with optimized selective‐layer thickness. Integration of these PIM‐based TFC membranes with a variety of redox chemistries allows for the screening of suitable RFB systems that display high compatibility between membrane and redox couples, affording long‐life operation with minimal capacity fade. Thickness optimization of TFC membranes further improves cycling performance and significantly restricts water transfer in selected RFB systems. [ABSTRACT FROM AUTHOR]

Dibenzomethanopentacene (DBMP) is shown to be a useful structural component for making Polymers of Intrinsic Microporosity (PIMs) with promise for making efficient membranes for gas separations. DBMP‐based monomers for PIMs are readily prepared using a Diels–Alder reaction between 2,3‐dimethoxyanthracene and norbornadiene as the key synthetic step. Compared to date for the archetypal PIM‐1, the incorporation of DBMP simultaneously enhances both gas permeability and the ideal selectivity for one gas over another. Hence, both ideal and mixed gas permeability data for DBMP‐rich co‐polymers and an amidoxime modified PIM are close to the current Robeson upper bounds, which define the state‐of‐the‐art for the trade‐off between permeability and selectivity, for several important gas pairs. Furthermore, long‐term studies (over ≈3 years) reveal that the reduction in gas permeabilities on ageing is less for DBMP‐containing PIMs relative to that for other high performing PIMs, which is an attractive property for the fabrication of membranes for efficient gas separations. [ABSTRACT FROM AUTHOR]

Organic solvent nanofiltration (OSN) is an emerging membrane separation technology, which urgently requires robust, easily processed, OSN membranes possessing high permeance and small solutes‐selectivity to facilitate enhanced industrial uptake. Herein, we describe the use of two 2,2′‐biphenol (BIPOL) derivatives to fabricate hyper‐crosslinked, microporous polymer nanofilms through IP. Ultra‐thin, defect‐free polyesteramide/polyester nanofilms (≈5 nm) could be obtained readily due to the relatively large molecular size and ionized nature of the BIPOL monomers retarding the rate of the IP. The enhanced microporosity arises from the hyper‐crosslinked network structure and monomer rigidity. Specifically, the amino‐BIPOL/PAN membrane exhibits extraordinary permselectivity performances with molecular weight cut‐off as low as 233 Da and MeOH permeance of ≈13 LMH/bar. Precise separation of small dye mixtures with similar M.W. based on both their charge and molecular size are achieved. [ABSTRACT FROM AUTHOR]

Redox flow batteries (RFBs) based on aqueous organic electrolytes are a promising technology for safe and cost‐effective large‐scale electrical energy storage. Membrane separators are a key component in RFBs, allowing fast conduction of charge‐carrier ions but minimizing the cross‐over of redox‐active species. Here, we report the molecular engineering of amidoxime‐functionalized Polymers of Intrinsic Microporosity (AO‐PIMs) by tuning their polymer chain topology and pore architecture to optimize membrane ion transport functions. AO‐PIM membranes are integrated with three emerging aqueous organic flow battery chemistries, and the synergetic integration of ion‐selective membranes with molecular engineered organic molecules in neutral‐pH electrolytes leads to significantly enhanced cycling stability. [ABSTRACT FROM AUTHOR]

Graphitic carbon nitride (g‐C3N4) with photo‐attached platinum (Pt@g‐C3N4) is known to generate hydrogen under illumination in aqueous environments in the presence of carbohydrate hole quenchers. Here, Pt@g‐C3N4 is embedded into a polymer of intrinsic microporosity (PIM‐1) host material with a molecularly rigid structure to maintain active unblocked catalyst surfaces and to control transport to/from the photocatalyst. A Clark‐type oxygen/hydrogen sensor is employed with Pt@g‐C3N4 embedded into PIM‐1 applied as a film to be the gas‐permeable sensor membrane. Oxygen reduction and hydrogen production are observed in situ as a function of light exposure and quencher concentration. Significant size‐selectivity favouring smaller more flexible saccharides or carbohydrate/ hydrocarbon quenchers is observed and attributed to rate limiting PIM‐1 micropore transport. Effective hydrogen production through a Teflon membrane is demonstrated. The underlying hydrogen production/ photocurrent enhancing effects of the microporous PIM‐1 film on the photochemical process are revealed. [ABSTRACT FROM AUTHOR]

Polymers of intrinsic microporosity (PIMs), such as the archetypal spirobisindane‐based PIM‐1, are among the most promising new materials for making gas separation membranes with high permeance for potential use in high‐throughput applications. Here it is shown that ultrapermeable PIMs can be prepared by fusing rigid and bulky triptycene (Trip) to the spirobisindane (SBI) unit. PIM‐SBI‐Trip and its copolymer with PIM‐1 (PIM‐1/SBI‐Trip) are both ultrapermeable after methanol treatment (PCO2 > 20 000 Barrer). Old films, although less permeable, are more selective and therefore provide data that are close to the recently redefined Robeson upper bounds for the important CO2/CH4, CO2/N2, and O2/N2 gas pairs. Temperature‐dependent permeation measurements and analysis of the entropic and energetic contributions of the gas transport parameters show that the enhanced performance of these polymers is governed by strong size‐sieving character, mainly due to the energetic term of the diffusivity, and related to their high rigidity. Both polymers show a relatively weak pressure‐dependence in mixed gas permeability experiments up to 6 bar, suggesting a potential use for CO2 capture from flue gas or for the upgrading of biogas. [ABSTRACT FROM AUTHOR]

The polymer of intrinsic microporosity PIM‐EA‐TB provides a molecularly rigid micropore structure containing tertiary amine sites and is shown here to interact with hydrogen bonding guest molecules such as caffeic acid. Voltammetric data with a PIM‐EA‐TB film on glassy carbon electrodes show that in both acidic solution (pH 2; PIM‐EA‐TB is protonated) and in neutral solution (pH 6; PIM‐EA‐TB is not protonated) caffeic acid is slowly accumulated into the microporous host. Binding constants are estimated and suggested to be linked to hydrogen bonding causing accumulation of caffeic acid. When employing PIM‐EA‐TB as an asymmetric membrane coated onto a 5 μm thick Teflon support film with 10 μm diameter microholes (using either a single microhole or a 10×10 array of microholes), binding of caffeic acid is shown to cause a modulation of the ionic current without affecting the pH‐dependent ionic diode behaviour. Two complementary types of effects of caffeic acid guests are discussed based on blocking anion diffusion pathways and based on removal of positive charges. The caffeic acid transport mechanism/efficiency is investigated in view of selective molecular pumping. [ABSTRACT FROM AUTHOR]

The polymer of intrinsic microporosity PIM‐1 is employed to disperse and deposit a Pt@titanate nanosheet photocatalyst film. The resulting microporous films allow electrolyte and oxygen permeation to give conventional oxygen reduction voltammetric responses on glassy carbon or on platinum disk electrodes in the dark. Preliminary data are presented showing that with pulsed light from a blue LED (385 nm) oxygen reduction at the electrode is effectively "switched off". A mechanism is tentatively assigned as photocatalytic depletion of oxygen near the electrode. Photoelectrochemical current responses are observed in aqueous NaOH, NaCl, Na2HPO4 and shown to be light intensity and oxygen concentration dependent. Electroanalytical applications are suggested. [ABSTRACT FROM AUTHOR]

Hybrid electrodes with improved O2 tolerance and capability of CO2 conversion into liquid products in the presence of O2 are presented. Aniline molecules are introduced into the pore structure of a polymer of intrinsic microporosity to expand its gas separation functionality beyond pure physical sieving. The chemical interaction between the acidic CO2 molecule and the basic amino group of aniline renders enhanced CO2 separation from O2. Loaded with a cobalt phthalocyanine‐based cathode catalyst, the hybrid electrode achieves a CO Faradaic efficiency of 71 % with 10 % O2 in the CO2 feed gas. The electrode can still produce CO at an O2/CO2 ratio as high as 9:1. Switching to a Sn‐based catalyst, for the first time O2‐tolerant CO2 electroreduction to liquid products is realized, generating formate with nearly 100 % selectivity and a current density of 56.7 mA cm−2 in the presence of 5 % O2. [ABSTRACT FROM AUTHOR]

Membranes which allow fast and selective transport of protons and cations are required for a wide range of electrochemical energy conversion and storage devices, such as proton‐exchange membrane (PEM) fuel cells (PEMFCs) and redox flow batteries (RFBs). Herein we report a new approach to designing solution‐processable ion‐selective polymer membranes with both intrinsic microporosity and ion‐conductive functionality. Polymers are synthesized with rigid and contorted backbones, which incorporate hydrophobic fluorinated and hydrophilic sulfonic acid functional groups, to produce membranes with negatively charged subnanometer‐sized confined ionic channels. The ready transport of protons and cations through these membranes, and the high selectivity towards nanometer‐sized redox‐active molecules, enable efficient and stable operation of an aqueous alkaline quinone redox flow battery and a hydrogen PEM fuel cell. [ABSTRACT FROM AUTHOR]

The performance and safety of lithium (Li) metal batteries can be compromised owing to the formation of Li dendrites. Here, the use of a polymer of intrinsic microporosity (PIM) is reported as a feasible and robust interfacial layer that inhibits dendrite growth. The PIM demonstrates excellent film‐forming ability, electrochemical stability, strong adhesion to a copper metal electrode, and outstanding mechanical flexibility so that it relieves the stress of structural changes produced by reversible lithiation. Importantly, the porous structure of the PIM, which guides Li flux to obtain uniform deposition, and its strong mechanical strength combine to suppress dendrite growth. Hence, the electrochemical performance of the anode is significantly enhanced, promising excellent performance and extended cycle lifetime for Li metal batteries. [ABSTRACT FROM AUTHOR]

Polymers of intrinsic microporosity (PIMs) as molecularly rigid polymers have emerged as a new class of gas‐permeable glassy materials. They offer excellent processability and a range of potential applications also in electrochemical processes. Particularly interesting is the ability of some PIM films to remain gas‐permeable/binding even in the presence of (aqueous) liquid electrolyte to give triphasic interfacial reactivity. Gaseous reagents or products (such as hydrogen or oxygen) are bound probably into hydrophobic regions in the wet PIM film to avoid macroscopic bubble formation and to enhance both the surface reactivity and the apparent activity of the gas solute close to the electrode/catalyst surface. The photoelectrochemical formation of hydrogen gas close to a platinum electrode is enhanced by PIM‐1, which is presented as an example of energy harvesting through molecular H2 "energy carrier" transport. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Hydrogen oxidation and oxygen reduction are two crucial energy conversion reactions, which are shown to be both strongly affected by the presence of intrinsically microporous polymer coatings on electrodes. Polymers of intrinsic microporosity (PIMs) are known to possess extremely high internal surface area and ability to bind gases under dry conditions. It is shown here that both, hydrogen‐ and oxygen gas binding into PIMs, also occurs under wet or "triphasic" conditions in aqueous electrolyte environments (when immersed in 0.01 M phosphate buffer at pH 7). For two known PIM materials (PIM‐1 and PIM‐PY), nanoparticles are formed by an anti‐solvent precipitation protocol and then cast as a film onto platinum or glassy carbon electrodes. Voltammetry experiments reveal evidence for hydrogen and oxygen binding. Both, PIM‐1 and PIM‐PY, locally store hydrogen or oxygen gas at the electrode surface and thereby significantly affect electrocatalytic reactivity. The onset of oxygen reduction on glassy carbon is shifted by 0.15 V in the positive direction. One for three: Due to their hydrophobic and molecularly rigid nature, intrinsically microporous polymers affect the conditions for gas|liquid electrolyte|solid electrode triphasic reactions. [ABSTRACT FROM AUTHOR]

Abstract: Membrane separation for gas purification is an energy‐efficient and environment‐friendly technology. However, the development of high performance membranes is still a great challenge. In principle, mixed matrix membranes (MMMs) have the potential to overcome current materials limitations, but in practice there is no straightforward method to match the properties of fillers and polymers (the main components of MMMs) in such a way that the final membrane performance reflects the high performance of the microporous filler and the processability of the continuous polymer phase. This issue is especially important when high flux polymers are utilized. In this work, we demonstrate that the use of small amounts of a glassy polymer in combination with high performance PIM‐1 allow for the preparation of metal–organic framework (MOF)‐based MMMs with superior separation properties and low aging rates under humid conditions, meeting the commercial target for post‐combustion CO2 capture. [ABSTRACT FROM AUTHOR]

The use of ultrathin films as selective layers in composite membranes offers significant advantages in gas separation for increasing productivity while reducing the membrane size and energy costs. In this contribution, composite membranes have been obtained by the successive deposition of approximately 1 nm thick monolayers of a polymer of intrinsic microporosity (PIM) on top of dense membranes of the ultra-permeable poly[1-(trimethylsilyl)-1-propyne] (PTMSP). The ultrathin PIM films (30 nm in thickness) demonstrate CO2 permeance up to seven times higher than dense PIM membranes using only 0.04 % of the mass of PIM without a significant decrease in CO2/N2 selectivity. [ABSTRACT FROM AUTHOR]

Ionic diode phenomena occur at asymmetric ionomer | aqueous electrolyte microhole interfaces. Depending on the applied potential, either an 'open' or a 'closed' diode state is observed switching between a high ion flow rate and a low ion flow rate. Physically, the 'open' state is associated mainly with conductivity towards the microhole within the ionomer layer and the 'closed' state is dominated by restricted diffusion-migration access to the microhole interface opposite to the ionomer. In this report we explore a 'heterojunction' based on an asymmetric polymer of intrinsic microporosity (PIM) | Nafion ionomer microhole interface. Improved diode characteristics and current rectification are observed in aqueous NaCl. The effects of creating the PIM | Nafion micro-interface are investigated and suggested to lead to novel sensor architectures. [ABSTRACT FROM AUTHOR]

In contrast to most common electrochemiluminescence (ECL) techniques that require either an additional reagent or continuous pulsing between oxidative and reductive potentials, here a fluorescent polymer of intrinsic microporosity (PIM-1) is shown to exhibit intrinsic ECL without the need for a co-reactant at positive applied potentials and as a function of pH. PIM-1 is known to possess high microporosity (based on its rigid and contorted molecular structure) and excellent fluorescence properties. By depositing a nanoparticulate form of the PIM-1 material onto tin-doped indium oxide, we achieve a hierarchically porous deposit with good sustained ECL activity in aqueous media. The mechanism for this reagentless ECL is suggested to be linked to reactive oxygen species produced at positive potentials and discussed in terms of potential analytical applications. [ABSTRACT FROM AUTHOR]

The development of polymeric anion-exchange membranes (AEMs) combining high ion conductivity and long-term stability is a major challenge for materials chemistry. AEMs with regularly distributed fixed cationic groups, based on the formation of microporous polymers containing the V-shape rigid Tröger's base units, are reported for the first time. Despite their simple preparation, which involves only two synthetic steps using commercially available precursors, the polymers provide AEMs with exceptional hydroxide conductivity at relatively low ion-exchange capacity, as well as a high swelling resistance and chemical stability. An unprecedented hydroxide conductivity of 164.4 mS cm−1 is obtained at a relatively a low ion-exchange capacity of 0.82 mmol g−1 under optimal operating conditions. The exceptional anion conductivity appears related to the intrinsic microporosity of the charged polymer matrix, which facilitates rapid anion transport. [ABSTRACT FROM AUTHOR]

Efficient reactions between fluorine-functionalised biphenyl and terphenyl derivatives with catechol-functionalised terminal groups provide a route to large, discrete organic molecules of intrinsic microporosity (OMIMs) that provide porous solids solely by their inefficient packing. By altering the size and substituent bulk of the terminal groups, a number of soluble compounds with apparent BET surface areas in excess of 600 m2 g−1 are produced. The efficiency of OMIM structural units for generating microporosity is in the order: propellane>triptycene>hexaphenylbenzene>spirobifluorene>naphthyl=phenyl. The introduction of bulky hydrocarbon substituents significantly enhances microporosity by further reducing packing efficiency. These results are consistent with findings from previously reported packing simulation studies. The introduction of methyl groups at the bridgehead position of triptycene units reduces intrinsic microporosity. This is presumably due to their internal position within the OMIM structure so that they occupy space, but unlike peripheral substituents they do not contribute to the generation of free volume by inefficient packing. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The enzymeless glucose oxidation process readily occurs on nano-gold electrocatalyst at pH 7, 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 1027 m2 g−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. [ABSTRACT FROM AUTHOR]

A key challenge in efficient molecular separation is fabricating large‐scale, highly selective polymeric membranes with precise pore control at the molecular scale. Herein, a new contorted monomer 6,6′‐dihydroxy‐2,2′‐biphenyldiamine (DHBIPDA) is introduced as a building block to generate cross‐linked, ultra‐thin microporous nanofilms (sub‐10 nm) via interfacial polymerization, enabling rapid, and precise molecular nanofiltration. Using diacyl chloride (TPC) as the cross‐linker instead of trimesoyl chloride (TMC) significantly reduces the pore sizes within the membranes and achieves a narrower pore distribution due to a semi‐crystalline structure. The film structures are confirmed using comprehensive characterization techniques including wide‐angle X‐ray scattering (WAXS), X‐ray diffraction (XRD), positron annihilation lifetime spectroscopy (PALS), CO2 adsorption analysis, and molecular‐scale simulation. The DHBIPDA/TPC and DHBIPDA/TMC membranes achieve methanol permeance values of up to 16.4 and 15.1 LMH bar−1 coupled with molecular weight cutoffs (MWCOs) as low as 283 and 306 Da, respectively. The DHBIPDA/TPC membrane demonstrates both higher permeance and higher selectivity compared to its relatively disordered counterpart DHBIPDA/TMC, consistent with characterization data. The DHBIPDA‐derived membrane efficiently separates dye mixtures with similar molecular weights and enables effective recycling of organometallic homogeneous catalysts, suggesting its potential for industrial applications. [ABSTRACT FROM AUTHOR]

Microporous polymer nanosheets with thicknesses in the range 3–5 nm and with high apparent surface area (Brunauer–Emmett–Teller surface area 940 m2 g−1) are formed when the effectively bifunctional (tetrafluoro) monomer used in the preparation of the prototypical polymer of intrinsic microporosity PIM‐1 is replaced with an effectively tetrafunctional (octafluoro) monomer to give a tightly crosslinked network structure. When employed as a filler in mixed‐matrix membranes based on PIM‐1, a low loading of 0.5 wt% network‐PIM‐1 nanosheets gives rise to enhanced CO2 permeability and CO2/CH4 selectivity, compared to pure PIM‐1. [ABSTRACT FROM AUTHOR]

Keywords: modified electrodes; triphasic catalysis; ion conductivity; ionic diodes; gas diffusion electrodes Modified electrodes, triphasic catalysis, ion conductivity, ionic diodes, gas diffusion electrodes. [Extracted from the article]