with Nafi on/SiO 2 hybrid membrane at the current density, 10 mA cm −2 . [ 10 ] Apart from the modifi cation of Nafi on membrane, the enhanced performances of VRB were recently also achieved with several kinds of sulfonated aromatic polymers in terms of the minimized hydrophilic domains. [11][12][13] Therefore, it is understood that the control of hydrophobic nature seems to be a common way to reduce the vanadium cross-over.More recently, Zhang et al. reported a VRB with a nanofi ltration type porous membrane that achieved competitive performances, a CE up to 95% and an EE of 76%. [ 14 ] The working principle has been based on the size sieving separation owing to the quite different size of proton and vanadium ions. [ 15 ] This strategy offers not only tremendously decreased cost owing to the already commercialized product, but also an ultimate insight toward maximizing H + /V selectivity. If the pore size of the membrane only enables protons (or water) transfer, the maximized performances could be achieved through the maximized H + /V selectivity. Thus, the subnano-sieving membrane for proton permselective transport is challenging. Here we report a fundamentally new concept to realize such proton/ vanadium selectivity. The concept is unprecedented as the material is hydrophobic, does not swell in water, contains micro porosity hosting water molecules along which protons can migrate and does not allow any other (vanadium) whatsoever. The proposed working principle of such hydrophobic polymers with intrinsic microporosity is disclosed in Scheme 1 .PIM-1 is the fi rst generation polymer having an intrinsic microporosity. We hypothesize that these materials can transport protons preferentially in VRBs because of its hydrophobic molecular structure, limited swelling in aqueous solution, inherent microporous structure with a pore diameter less than 2 nm, high free volume fraction above 20%, good solution processability, and relatively slow physical ageing compared to other high free volume polymers. [16][17][18] Even though hydrophobic, its microporosity is suspected to transport water molecules at high rates: Kentish and co-workers demonstrated water vapor permeation through PIM-1 at no fewer than 30 000 Barrer (1 Barrer = 10 −10 cm 3 (STP) cm (cm 2 s cm Hg) −1 ) above a water activity of 0.7. [ 19 ] Yet, little is known about the state of water inside such microporous polymers: one may anticipate the water being preferentially partitioned in the free-volume forming the microporosity rather than being absorbed into the polymer matrix. This could imply that a certain degree of proton transfer could occur by water molecules inside PIM-1. Meanwhile, the partitioning of hydro-solvated vanadium ions is expected to be limited by both the small radius of its pores and the difference of dielectric property, as illustrated in Scheme 1 .Recent increasing interest in the integration of renewable energy sources has accelerated efforts to develop electric energy storage (EES). [ 1,2 ] Among many approaches for EES, the allvanad...

Tetracyanchinodimethan (TCNQ) auf Silbernanopartikeln (AgNPs) induziert hohe positive Oberflächenladungen, die einen Grenzflächendipol erzeugen, über den sich die Energieniveaus der AgNPs einstellen lassen (siehe Bild). Poly(vinylpyrrolidon)‐Membranen, die dispergierte AgNPs mit TCNQ enthalten, zeigen eine hohe Selektivität bei der Trennung gasförmiger Olefin‐Paraffin‐Gemische.

Calling the tune: High positive surface charges induced by tetracyanoquinodimethane (TCNQ) allow tuning of the energy levels of silver nanoparticles (AgNPs) through an interface dipole (see picture). Facilitated transport membranes containing AgNPs with TCNQ dispersed in poly(vinylpyrrolidone) show high mixed‐gas selectivity for the separation of olefin/paraffin mixtures.

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The unique pore structure of PIM-1 as a solid interphase can suppress transport of solvent and consequently unwanted chemical reactions at the interface of anodes.

Charge transfer and dipole formation at silver nanoparticle–tetracyanoquinoid takes place in the solid-state membrane, forming an unprecedented, highly olefin permselective facilitated transport membrane with a mixed gas selectivity of over 100 for a propylene–propane mixture. This provides a potential alternative to the highly energy-intensive cryogenic distillation process for olefin/paraffin separation.

In search of small dielectric constant (D k) and low-dissipation (D f) energy substrates for high-frequency appliances, a benzoate-group-substituted bisphenol A based resin was synthesized from bisphenol A dibenzolate and bisphenol A diglycidyl ether. Compared to the common bisphenol A diglycidyl ether epoxy resin, introduction of the benzoate group was considered to lead to increased hydrophobic character, which was supported by water absorption investigation as well as absorption peak investigation of the OH region via Fourier transform infrared spectra. The cured resin with few water molecules exhibited restricted motion of the segment, and, consequently, thermally stable properties (coefficient of thermal expansion and thermogravimetric analysis) were achieved. Ultimately, the developed epoxy resin showed dramatically reduced D k (3.05 at 1 GHz) and D f (0.016 at 1 GHz) values as well as enhanced adhesive properties. The excellent overall properties lead to its promising use in various fields involving electrical devices.