Hui Na

From metal–organic framework (MOF) to MOF–polymer composite membrane: enhancement of low-humidity proton conductivity

A chiral two-dimensional MOF, {[Ca(D-Hpmpc)(H2O)2]·2HO0.5}n (1, D-H3pmpc = D-1-(phosphonomethyl) piperidine-3-carboxylic acid), with intrinsic proton conductivity has been synthesized and characterized. Structure analysis shows that compound 1 possesses protonated tertiary amines as proton carriers and hydrogen-bonding chains served as proton-conducting pathways. Further, MOF–polymer composite membranes have been fabricated via assembling polymer PVP with different contents of rod-like 1 submicrometer crystals. Interestingly, the proton conductivity of this composite membrane containing 50 wt% 1 is rapidly increased, compared with that of pure submicrometer crystals at 298 K and ∼53% RH. Therefore, it is feasible to introduce humidification of PVP into composite membranes to enhance low-humidity proton conductivity; and humidified PVP with adsorbed water molecules plays an important role in proton conduction indicated by the results of water physical sorption and TG/DTG analyses. This study may offer a facile strategy to prepare a variety of solid electrolyte materials with distinctive proton-conducting properties under a low humidity.

Cross-linked polybenzimidazole with enhanced stability for high temperature proton exchange membrane fuel cells

Cross-linked polybenzimidazole membranes were obtained by heating at 160 °C, using 4,4′-diglycidyl(3,3′,5,5′-tetramethylbiphenyl) epoxy resin (TMBP) as the cross-linker. The cross-linking reaction temperature was determined by DSC and the successful completion of the cross-linking reaction was shown by FTIR and solubility tests. The cross-linked membranes showed high proton conductivity and strong mechanical properties, as well as low swelling after immersion in 85% phosphoric acid at 90 °C. For instance, the membrane with a cross-linker content weight percent of 20% (PBI-TMBP 20%) with a PA doping level of 4.1 exhibited a proton conductivity of 0.010 S cm−1 and a low swelling volume of 50%. Moreover, the cross-linked membranes showed excellent oxidative stability. The PBI-TMBP 20% cross-linked membrane tested in Fentons reagent (3% H2O2 solution, 4 ppm Fe2+, 70 °C) kept its shape for more than 480 h and did not break. In particular, the proton conductivity of the PA-PBI-TMBP 20% membrane after Fentons test (30% H2O2, 20 ppm Fe2+, 85 °C) remained at a high level of 0.009 S cm−1. This investigation proved that cross-linking is a very effective approach for improving the performance of proton exchange membranes.

Anion‐Conductive Membranes with Ultralow Vanadium Permeability and Excellent Performance in Vanadium Flow Batteries

Anion exchange membranes prepared from quaternized poly(tetramethyl diphenyl ether sulfone) (QAPES) were first investigated in the context of vanadium flow battery (VFB) applications. The membranes showed an impressive suppression effect on vanadium ions. The recorded vanadium permeability was 0.02×10(-7)-0.09×10(-7) cm(2) min(-1), which was two orders of magnitude lower than that of Nafion 115. The self-discharge duration of a VFB single cell with a QAPES membrane is four times longer than that of Nafion 115. The morphological difference in hydrophilic domains between QAPES and Nafion was confirmed by TEM. After soaking the membranes in VO(2)(+) solution, adsorbed vanadium ions can barely be found in QAPES, whereas the hydrophilic domains of Nafion were stained. In the ex situ chemical stability test, QAPES showed a high tolerance to VO(2)(+) and remained intact after immersion in VO(2)(+) solution for over 250 h. The performance of a VFB single cell assembled with QAPES membranes is equal to or even better than that of Nafion 115 and remains stable in a long-term cycle test. These results indicate that QAPES membranes can be an ideal option in the fabrication of high-performance VFBs with low electric capacity loss.

Silane-cross-linked polybenzimidazole with improved conductivity for high temperature proton exchange membrane fuel cells

Silane-cross-linked polybenzimidazole (PBI) membranes with high proton conductivity and excellent mechanical properties were successfully prepared by using a silane monomer, γ-(2,3-epoxypropoxy)propyltrimethoxysilane (KH560), as a cross-linker. Fourier transform infrared spectroscopy and solubility tests were used to characterize and confirm the cross-linked structure in the membranes. The silane-cross-linked membranes displayed excellent chemical stability and improved mechanical strength. Especially at high temperature (130 °C), where the tensile strength value was in the range of 68.6 to 99.3 MPa, while that of the pristine PBI was 61.7 MPa. Moreover, the proton conductivity was significantly enhanced because the silane-cross-linked structure in the membranes could absorb more phosphoric acid. Considering the tradeoff of mechanical properties and proton conductivity, 3% KH560 in weight was demonstrated to be the optimum content in the membranes, for instance, the SCPBI-3/7.95 PA (the cross-linker content was 3 wt% and the PA doping level was 7.95) had a proton conductivity of 0.081 S cm−1 and that of the SCPBI-3/9.07 PA was 0.114 S cm−1 at 200 °C, while that of pristine PBI was 0.015 S cm−1 at 200 °C.

Cross-linked hydroxide conductive membranes with side chains for direct methanol fuel cell applications

A series of novel poly(ether ether ketone) copolymers containing methyl groups on the side chain were prepared based on a new monomer (3,4-dimethyl)phenylhydroquinone. Then a series of hydroxide exchange membranes with different IEC values were obtained through bromination and quaternary amination of the copolymers. By adjusting the contents of methyl groups in the copolymers, we could control the final structures of the membranes. The chemical structures of the monomers and copolymers were analyzed by 1H NMR spectroscopy. After that, for the purpose of enhancing the dimensional stability and methanol resistance of the membrane, we prepared cross-linked membranes through a Friedel–Crafts reaction between bromomethyl groups and aromatic rings. The properties of the membranes related to fuel cell application were evaluated in detail. All the membranes showed good thermal and mechanical stabilities and conductivities. Moreover, the cross-linked membranes exhibit better dimensional stabilities and selectivities. Among those membranes, xPEEK–Q-100 showed a high conductivity (0.036 S cm−1 at 80 °C), a low swelling ratio of 6.6% and a methanol permeation coefficient of 2.9 × 10−7 cm2 s−1. The outstanding properties indicated that the application of PEEK–Q-xx membranes in fuel cells was promising.

Surface modification of heteropoly acid/SPEEK membranes by polypyrrole with a sandwich structure for direct methanol fuel cells

A series of SPEEK/HPW/Ppy-n composite membranes with a sandwich structure were successfully prepared by surface modification with polypyrrole (Ppy) in order to stabilize phosphotungstic acid (HPW) in poly(ether ether ketone)s (SPEEKs) and reduce the methanol crossover. Ppy coatings with a large number of secondary ammonium groups (NH2+) interact with anions of HPW to decrease HPW leaching from the membrane. In addition, the hydrophobic Ppy layers allow for little methanol transport, which leads to a significant decline in methanol crossover with reasonable levels of proton conductivity. The properties of the membranes were investigated in detail by UV, SEM, ac impedance, and TGA. As observed, Ppy-modified membranes were better at immobilizing HPW and exhibited higher selectivities than previously reported SPEEK/HPW composite membranes. All the results indicate that the SPEEK/HPW/Ppy-n composite membranes are excellent candidates for direct methanol fuel cells.

Cross-linked aromatic cationic polymer electrolytes with enhanced stability for high temperature fuel cell applications

Diamine-cross-linked membranes were prepared from cross-linkable poly(arylene ether ketone) containing pendant cationic quaternary ammonium group (QPAEK) solution by a facile and general thermal curing method using 4,4′-diaminodiphenylmethane with rigid framework and 1,6-diaminohexane with flexible framework as cross-linker, respectively. Self-cross-linked cationic polymer electrolytes membranes were also prepared for comparison. The diamines were advantageously distributed within the polymeric matrix and its amine function groups interacted with the benzyl bromide of QPAEK, resulting in a double anchoring of the molecule. Combining the excellent thermal stability, the addition of a small amount of diamines enhanced both the chemical and mechanical stability and the phosphoric acid doping (PA) ability of membranes. Fuel cell performance based on impregnated cross-linked membranes have been successfully operated at temperatures up to 120 °C and 180 °C with unhumidified hydrogen and air under ambient pressure, the maximum performance of diamine-cross-linked membrane is observed at 180 °C with a current density of 1.06 A cm−2 and the peak power density of 323 mW cm−2. The results also indicate that the diamine-cross-linked membranes using the rigid cross-linker show much improved properties than that using the flexible cross-linker. More properties relating to the feasibility in high temperature proton exchange membrane fuel cell applications were investigated in detail.

Carboxyl-terminated benzimidazole-assisted cross-linked sulfonated poly(ether ether ketone)s for highly conductive PEM with low water uptake and methanol permeability

A carboxyl-terminated benzimidazole trimer was synthesized as a crosslinker by controlling the ratio of 3,3′-diaminobenzidine and isophthalic acid. Composite membranes were obtained by mixing the benzimidazole trimer and sulfonated poly(ether ether ketone) (SPEEK) together. Cross-linked membranes were obtained by heating the composite membranes at 160 °C. All of the properties of the cross-linked membranes were significantly increased, including proton conductivity, methanol permeability and water uptake due to the more compact structure compared to the non-cross-linked membranes. The cross-linked SPEEK-BI7 and cross-linked SPEEK-BI11 had excellent proton conductivities (0.22 and 0.19 S cm−1) at 80 °C, which were higher than that of Nafion 117 (0.125 S cm−1). Transmission electron microscopy (TEM) analysis revealed a clear microphase separated structure of cross-linked membranes. Other properties, such as thermal and mechanical stability, required for use as a proton exchange membrane (PEM) have been investigated. The cross-linked membranes showed improved properties over membranes without crosslinking.

Flammability properties and electromagnetic interference shielding of PVC/graphene composites containing Fe3O4 nanoparticles

The effects of combined graphene/Fe3O4 nanoparticles on the flame retardancy and smoke suppression of PVC were studied. The dispersion state of graphene in the PVC matrix was improved with the help of Fe3O4 nanoparticles. As a result, the peak values of heat release rate and smoke production rate measured by cone calorimetry were obviously decreased in the PVC/graphene/Fe3O4 composites. According to the results from TGA tests and structural characterization of residual char, the improved flame retardancy was partially attributed to the formation of a network-like structure due to the good dispersion state of graphene in the PVC matrix, and partially to the carbonization of degradation products of PVC catalyzed by Fe3O4 nanoparticles. In addition, ternary PVC composites showed higher mechanical properties than pure PVC. More importantly, the resulting material possessed both electrical and magnetic properties. As a result, the ternary composites showed favorable electromagnetic shielding efficiency in the X-band frequency region (8–12 GHz), due to the formation of conducting interconnected graphene-based networks in the insulating PVC matrix and the magnetic properties.

One-Step Microfluidic Fabrication of Polyelectrolyte Microcapsules in Aqueous Conditions for Protein Release.

We report a microfluidic approach for one-step fabrication of polyelectrolyte microcapsules in aqueous conditions. Using two immiscible aqueous polymer solutions, we generate transient water-in-water-in-water double emulsion droplets and use them as templates to fabricate polyelectrolyte microcapsules. The capsule shell is formed by the complexation of oppositely charged polyelectrolytes at the immiscible interface. We find that attractive electrostatic interactions can significantly prolong the release of charged molecules. Moreover, we demonstrate the application of these microcapsules in encapsulation and release of proteins without impairing their biological activities. Our platform should benefit a wide range of applications that require encapsulation and sustained release of molecules in aqueous environments.