Study of high-temperature proton exchange membrane through one-step encapsulation of ionic liquid in sulfonated poly(ether ether ketone)

The proton exchange membrane (PEM) is the core component of a high-performance proton exchange membrane fuel cell (PEMFC). Since the traditional PEM has the disadvantages of poor cell performance and high cost, a new kind of PEM with good proton conductivity, low cost and simple preparation should be explored. In this paper, several different binary hybrid membranes were successfully prepared through one-step encapsulation of different ionic liquids (ILs) in sulfonated poly(ether ether ketone) (SPEEK). The prepared membranes were characterized by scanning electron microscope (SEM), thermogravimetric analysis (TG), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), proton conductivity measurements and dynamic mechanical analysis (DMA). SEM images showed that ILs were fully doped into SPEEK. FT-IR and XPS proved that SPEEK and IL formed a new chemical bond combined with intermolecular hydrogen bonds. The TG results showed that the binary hybrid membranes could maintain stability even at 300°C. The water uptake and swelling ratio showed that the water absorption capacity of the binary composite membrane played a vital role in improving proton conductivity. The proton conductivity study showed that ILs doping also helped to improve the proton conductivity of the SPEEK membrane. When the doping amount of IL was maintained at 30 wt.%, it has the highest proton conductivity, 25 mS cm⁻¹ at 120°C. It was proved that anhydrous hybrid membrane tetraphenyl imidazole sulfate/SPEEK ([IM2][H₂PO₄]/SPEEK) could be used in PEMFC at medium temperature.     

Blend membranes based on disulfonated poly(aryl ether ether ketone)s (SPEEK) and poly(amide imide) (PAI) for direct methanol fuel cell usages

Highly disulfonated poly(aryl ether ether ketone)s (SPEEK-70) copolymer was synthesized via direct polymerization to precisely control the degree of sulfonation (D_s = 1.40), which was confirmed and estimated by ¹H NMR. As expected, the proton conductivity of SPEEK-70 membrane is 0.084 S/cm at 25 °C and increases to 0.167 S/cm at 80 °C, surpassing that of Nafion^® 117. However, the relatively high methanol crossover and excessively swelling properties limited its usage in DMFC. Poly(amide imide) was blended with SPEEK-70 to improve the methanol resistance and mechanical properties. These blend membranes were characterized as a function of weight fraction of PAI in terms of ion exchange capacity (IEC), water uptake, water desorption, proton conductivity and methanol permeability in detail. Although the proton conductivities decreased upon the addition of PAI, higher selectivity values defined as the ratio of proton conductivity to methanol permeability were found for the blend membranes. Therefore, the SPEEK/PAI blend membranes are promising for usage in DMFC.     

Hydrophilic TiO2 decorated carbon nanotubes/sulfonated poly(ether ether ketone) composite proton exchange membranes for fuel cells

Sulfonated poly(ether ether ketone) (SPEEK) is currently considered to be one of the most potential candidates of commercial perfluorinated sulfonic acid proton exchange membranes. To balance the proton conductivity and mechanical properties of SPEEK, nano TiO₂ coated carbon nanotubes (TiO₂@CNTs) were prepared using a benzyl alcohol-assisted sol-gel method and then used as a new nanofiller to modify SPEEK to prepare SPEEK/TiO₂@CNTs composite membranes. The thick insulated TiO₂ coating layer can effectively avoid the risk of electronic short-circuiting formed by CNTs, while the hydrophilicity of TiO₂ can also reduce the polar difference between CNTs and SPEEK matrix, thus promoting the homogeneous dispersion of CNTs in the composites. As a result, the composite membranes demonstrated simultaneously improved strength and proton conductivity. Incorporating 5 wt% of TiO₂@CNTs exhibited 31% growth in mechanical strength when compared with pure SPEEK. Moreover, the maximum conductivity was 0.104 S cm⁻¹ (80°C) for the composite membrane with 5 wt% of TiO₂@CNTs, which was nearly twice as high as that of SPEEK membrane (0.052 S cm⁻¹).     

Inorganic-organic hybrid membranes with anhydrous proton conduction prepared from tetramethoxysilane/methyl-trimethoxysilane/trimethylphosphate and 1-ethyl-3-methylimidazolium-bis (trifluoromethanesulfonyl) imide for H2/O2 fuel cells

Anhydrous proton-conducting inorganic-organic hybrid membranes were prepared by sol-gel process with tetramethoxysilane/methyl-trimethoxysilane/trimethylphosphate and 1-ethyl-3-methylimidazolium-bis (trifluoromethanesulfonyl) imide [EMI][TFSI] ionic liquid as precursors. These hybrid membranes were studied with respect to their structural, thermal, proton conductivity, and hydrogen permeability properties. The Fourier transform infrared spectroscopy (FT-IR) and ³¹P, ¹H, and ¹³C nuclear magnetic resonance (NMR) measurements have shown good chemical stability, and complexation of PO(OCH₃)₃ with [EMI][TFSI] ionic liquid in the studied hybrid membranes. Thermal analysis including TG and DTA confirmed that the membranes were thermally stable up to 330 °C. Thermal stability of the hybrid membranes was significantly enhanced by the presence of inorganic SiO₂ framework and high stability of [TFSI] anion. The effect of [EMI][TFSI] ionic liquid addition on the microstructure of the membranes was studied by scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDX) micrographs and no phase separation at the surfaces of the prepared membranes was observed and also homogeneous distribution of all elements was confirmed. Proton conductivity of all the prepared membranes was measured from −20 °C to 150 °C, and high conductivity of 5.4 × 10⁻³ S/cm was obtained for 40 wt% [EMI][TFSI] doped 40TMOS-50MTMOS-10PO(OCH₃)₃ (mol%) hybrid membrane, at 150 °C under anhydrous conditions. The hydrogen permeability was found to decrease from 1.61 × 10⁻¹¹ to 1.39 × 10⁻¹² mol/cm s Pa for 40 wt% [EMI][TFSI] doped hybrid membrane as the temperature increases from 20 °C to 150 °C. For 40 wt% [EMI][TFSI] doped hybrid membrane, membrane electrode assemblies were prepared and a maximum power density value of 0.22 mW/cm² at 0.47 mA/cm² as well as a current density of 0.76 mA/cm² were obtained at 150 °C under non-humidified conditions when utilized in a H₂/O₂ fuel cell.     

Fast proton conductor under anhydrous condition synthesized from 12-phosphotungstic acid and ionic liquid

In this study, we synthesized a molecular hybrid conductor electrolyte using PWA ([H₃PW₁₂O₄₀·nH₂O]) and [1-butyl-3-methylimidazole][bis-(fluoromethanesulfonyl) amide] ([BMIM][TFSI]) ionic liquid. The [BMIM][TFSI] ionic liquid can interact with the strongly acidic PWA. The hybrids were hydrophilic, and included some water molecules in the structure of the hybrids. The water molecules remained up to 80 °C, contributing to improve conductivity under an anhydrous N₂ atmosphere. The conductivity of PWA-[BMIM][TFSI] hybrid under anhydrous conditions increased from 10⁻⁴ S/cm to 0.04 S/cm at 60 °C. The conductivity of the hybrids at each temperature was higher than that of pure PWA and [BMIM][TFSI] under anhydrous condition. It can be due to the protonic carriers.     

Sulfonated poly(ether ether ketone)/zirconium tricarboxybutylphosphonate composite proton-exchange membranes for direct methanol fuel cells

Sulfonated poly(ether ether ketone) (SPEEK) is a very promising alternative membrane material for direct methanol fuel cells. However, with a fairly high degree of sulfonation (DS), SPEEK membranes can swell excessively and even dissolve at high temperature. This restricts membranes from working above a high tolerable temperature to get high proton conductivity. To deal with this contradictory situation, insolvable zirconium tricarboxybutylphosphonate (Zr(PBTC)) powder was employed to make a composite with SPEEK polymer in an attempt to improve temperature tolerance of the membranes. SPEEK/Zr(PBTC) composite membranes were obtained by casting a homogeneous mixture of Zr(PBTC) and SPEEK in N,N-dimethylacetamide on a glass plate and then evaporating the solvent at 60°C. Many characteristics were investigated, including thermal stability, liquid uptake, methanol permeability and proton conductivity. Results showed significant improvement not only in temperature tolerance, but also in methanol resistance of the SPEEK/Zr(PBTC) composite membranes. The membranes containing 30 wt-% ∼ 40 wt-% of Zr(PBTC) had their methanol permeability around 10⁻⁷ cm²·s⁻¹ at room temperature to 80°C, which was one order of magnitude lower than that of Nafion?115. High proton conductivity of the composite membranes, however, could also be achieved from higher temperature applied. At 100% relative humidity, above 90°C the conductivity of the composite membrane containing 40 wt-% of Zr(PBTC) exceeded that of the Nafion?115 membrane and even reached a high value of 0.36 S·cm⁻¹ at 160°C. Improved applicable temperature and high conductivity of the compositemembrane indicated its promising application inDMFC operations at high temperature. __________ Translated from Acta Polymerica Sinica, 2007, (4): 337–342 [译自:高分子学报]     

Synthesis and characterization of poly(aryl ether ketone) copolymers containing (hexafluoroisopropylidene)-diphenol moiety as proton exchange membrane materials

Sulfonated poly(aryl ether ketone)s (SPAEK) copolymers were synthesized by aromatic nucleophilic polycondensation from 4,4′-(hexafluoroisopropylidene)-diphenol, 1,3-bis(4-fluorobenzoyl)benzene and di-sulfonated difluorobenzophenone. The copolymers exhibited good thermal and oxidative stability. The SPAEK membranes with sulfonic acid content (SC) ranging from 0.6 to 1.16 maintained adequate mechanical strength after immersion in water at 80 °C for 24 h. The proton conductivities of the SPAEK films increased with SC and temperature, reaching values above 3.3×10⁻² S/cm at 80 °C for SC≥0.76. Tensile strength measurement indicated that SPAEK membranes with SC 0.76, 0.98 and 1.16 are tough and strong at ambient conditions. Consequently, these materials are promising as proton exchange membranes (PEM) for fuel cells operated at medium temperatures.     

A new anhydrous proton conductor based on polybenzimidazole and tridecyl phosphate

Most of the anhydrous proton conducting membranes are based on inorganic or partially inorganic materials, like SrCeO₃ membranes or polybenzimidazole (PBI)/H₃PO₄ composite membranes. In present work, a new kind of anhydrous proton conducting membrane based on fully organic components of PBI and tridecyl phosphate (TP) was prepared. The interaction between PBI and TP is discussed. The temperature dependence of the proton conductivity of the composite membranes can be modeled by an Arrhenius relation. Thermogravimetric analysis (TGA) illustrates that these composite membranes are chemically stable up to 145 °C. The weight loss appearing at 145 °C is attributed to the selfcondensation of phosphate, which results in the proton conductivity drop of the membranes occurring at the same temperature. The DC conductivity of the composite membranes can reach ∼10⁻⁴ S/cm for PBI/1.8TP at 140 °C and increases with increasing TP content. The proton conductivity of PBI/TP and PBI/H₃PO₄ composite membranes is compared. The former have higher proton conductivity, however, the proton conductivity of the PBI/H₃PO₄ membranes increases with temperature more significantly. Compared with PBI/H₃PO₄ membranes, the migration stability of TP in PBI/TP membranes is improved significantly.     

Enhanced high-temperature polymer electrolyte membrane for fuel cells based on polybenzimidazole and ionic liquids

Polybenzimidazole (PBI)/ionic liquid (IL) composite membranes were prepared from an organosoluble, fluorine-containing PBI with ionic liquid, 1-hexyl-3-methylimidazolium tri?uoromethanesulfonate (HMI-Tf). PBI/HMI-Tf composite membranes with different HMI-Tf concentrations have been prepared. The ionic conductivity of the PBI/HMI-Tf composite membranes increased with both the temperature and the HMI-Tf content. The composite membranes achieve high ionic conductivity (1.6 × 10⁻² S/cm) at 250 °C under anhydrous conditions. Although the addition of HMI-Tf resulted in a slight decrease in the methanol barrier ability and mechanical properties of the PBI membranes, the PBI/HMI-Tf composite membranes have demonstrated high thermal stability up to 300 °C, which is attractive for high-temperature (>200 °C) polymer electrolyte membrane fuel cells.     

Proton conducting membranes based on semi-interpenetrating polymer network of Nafion and polybenzimidazole

A new strategy to prepare the reinforced composite membranes for polymer electrolyte membrane fuel cells (PEMFCs), which can work both in humidified and anhydrous state, was proposed via constructing semi-interpenetrating polymer network (semi-IPN) structure from polybenzimidazole (PBI) and Nafion^®212, with N-vinylimidazole as the crosslinker. The crosslinkable PBI was synthesized from poly(2,2′-(m-phenylene)-5,5′-bibenzimidazole) and p-vinylbenzyl chloride. The semi-IPN structure was formed during the membrane preparation. The composite membranes exhibit excellent thermal stability, high-dimensional stability, and significantly improved mechanical properties compared with Nafion^®212. The proton transport in the hydrated composite membranes is mainly contributed by the vehicle mechanism, with proton conductivity from ∼10⁻² S/cm to ∼10⁻¹ S/cm. When the temperature exceeds 100 °C, the proton conductivity of the semi-IPN membranes decreases quickly due to the dehydration of the membranes. Under anhydrous condition, the proton conductivity of the membranes will drop to ∼10⁻⁴ S/cm, which is also useful for intermediate temperature (100-200 °C) PEMFCs. The benzimidazole structure of PBI and the acidic component of Nafion^® provide the possibility for the proton mobility via structure diffusion involving proton transfer between the heterocycles with a corresponding reorganization of the hydrogen bonded network.     

Physicochemical characterization of low sulfonated polyether ether ketone/Smectite clay composite for proton exchange membrane fuel cells

Polyether ether ketone (PEEK) with a low sulfonation degree was blended using different proportions of sodium rich Smectite clay (3 and 6 wt%) to use as an electrolyte membrane for fuel cell application. The structural functionalities, surface morphologies, and the thermal stability of the resultant composite membranes were characterized using Fourier-transform infrared spectroscopy, X-ray diffraction (XRD), scanning electron microscopy, atom force microscopy, and thermo-gravimetric analysis. FT-IR showed that no chemical reactions take place between the sulfonated polyether ether ketone (SPEEK) and the clay with different ratios. XRD diffractograms illustrated a lower degree of crystallinity of the blended SPEEK than pristine SPEEK. The elaborated composite membranes proved to have a higher thermal stability than SPEEK. Furthermore, the SPEEK/clay composite membranes with 3 and 6 wt% in clay loading had higher water uptake and lower methanol uptake than those in pristine SPEEK It was also shown that, the incorporation of sodium ions rich Smectite clay layers between the clusters in SPEEK improved the conductivity to 2 × 10⁻² S/cm at 140°C (for 6 wt% in clay) without compromising the dimensional stability of the composite membranes. These results propose the composite membranes as a potential candidate for methanol fuel cells at temperatures above 120°C making SPEEK composite membrane competitive to that of Nafion membrane.     

Anhydrous proton conducting polymer electrolytes based on poly(vinylphosphonic acid)-heterocycle composite material

The development of anhydrous proton conducting membrane is important for the operation of polymer electrolyte membrane fuel cell (PEMFC) at intermediate temperature (100-200 °C). In this study, we have investigated the acid-base hybrid materials by mixing of strong phosphonic acid polymer of poly(vinylphosphonic acid) (PVPA) with the high proton-exchange capacity and organic base of heterocycle, such as imidazole (Im), pyrazole (Py), or 1-methylimidazole (MeIm). As a result, PVPA-heterocycle composite material showed the high proton conductivity of approximately 10⁻³ S cm⁻¹ at 150 °C under anhydrous condition. In particular, PVPA-89 mol% Im composite material showed the highest proton conductivity of 7×10⁻³ S cm⁻¹ at 150 °C under anhydrous condition. Additionally, the fuel cell test of PVPA-89 mol% Im composite material using a dry H₂/O₂ showed the power density of approximately 10 mW cm⁻² at 80 °C under anhydrous conditions. These acid-base anhydrous proton conducting materials without the existence of water molecules might be possibly used for a polymer electrolyte membrane at intermediate temperature operations under anhydrous or extremely low humidity conditions.     

Low-swelling proton-conducting copoly(aryl ether nitrile)s containing naphthalene structure with sulfonic acid groups meta to the ether linkage

Wholly aromatic poly(aryl ether ether nitrile)s containing naphthalene structure with sulfonic acid groups meta to ether linkage (m-SPAEEN), intended for fuel cells applications as proton conducting membrane materials, were prepared via nucleophilic substitution polycondensation reactions. The incorporation of rigid naphthalene structure with meta-sulfonic acid groups was with the intent of improving the aggregation of hydrophilic and hydrophobic domains and to increase the acidity and conductivities. m-SPAEEN copolymers were readily synthesized by potassium carbonate mediated nucleophilic polycondensation reactions of commercially available monomers: 2,6-difluorobenzonitrile (2,6-DFBN), 2,8-dihydroxynaphthalene-6-sulfonate sodium salt (2,8-DHNS-6), and 4,4′-biphenol (4,4′-BP) in dimethylsulfoxide (DMSO) at 160-170 °C. The sulfonic acid group content (SC), expressed as a number per repeat unit of polymer, ranged from 0 to 0.6 and was readily controlled by changing the feed ratio of 2,8-DHNS-6 to 2,6-DFBN. High thermal stability of m-SPAEEN copolymers was indicated by observed glass transition temperatures (T_gs) ranging from 223 to 335 °C in sodium salt form and from 230 to 260 °C in acid form (m-SPAEENH) and decomposition temperatures (T_d)s over 250 °C in acid form and over 350 °C in sodium form in both nitrogen and air. All m-SPAEENH copolymers exhibited reasonable flexibility and tensile strength in the range of 39-78 MPa, indicating they were mechanically stronger than Nafion^®117, which had an approximate value of 10 MPa under the same test conditions. As expected, m-SPAEENH copolymers showed considerably reduced moisture absorption compared to previously prepared sulfonated hydroquinone based poly(aryl ether nitrile). m-SPAEENH copolymers also showed improved proton conductivities. Proton conductivity curves parallel to that of Nafion 117 were obtained with proton conductivity of 10⁻¹ S/cm at equivalent ion exchange capacities (IEC) of 1.6 and 1.9, comparable to Nafion^®117. The best compromise combining PEM mechanical strength, water swelling and proton conductivity, was achieved at SC of 0.5 and 0.6.     

Direct synthesis of sulfonated poly(ether ether ketone ketone)s (SPEEKKs) proton exchange membranes for fuel cell application

A series of sulfonated poly(ether ether ketone ketone)s (SPEEKK)s based membranes have been prepared and evaluated for proton exchange membranes (PEM). The membranes show very good thermal and mechanical stabilities. The structures of membranes were studied with AFM. The membranes show very good proton conductive ability (25 °C: 0.007-0.04 s/cm) and methanol resistance (25 °C: 7.68×10⁻⁸ to 5.75×10⁻⁷ cm²/s). The methanol diffusion coefficients of membranes are much lower than that of Nafion (2×10⁻⁶ cm²/s). The SPEEKKs membranes show very good respective in direct methanol fuel cells (DMFC) usages.     

Effect of ionic strength on the foam fractionation of BSA with existence of antifoaming agent

Foam fractionation is an economical and effective technology for protein concentration and separation. However, the presence of antifoaming agent in the fermentation broth restricts the application of this technology. In this paper surfactant-assisted foam process was conducted with a mimic system using bovine serum albumin (BSA) as target protein, polyoxypropylene polyoxyethylene glylerin ether (PGE) as antifoaming agent and cetyltrimethyl ammonium bromide (CTAB) as surfactant, putting emphasis on study of the effect of ionic strength on the separation process. The experimental results showed that with ionic strength increasing, the mixed-system foaming ability gradually increased. Under the conditions of C_BSA 100 mg/L, C_CTAB 20 mg/L, C_PGE 8 mg/L and pH 7.4, feed liquid 250 mL, air flow rate 100 mL/min at 25 °C, the maximum enrichment ratio of BSA reached 27 when the ionic strength was 0.0500 mol/kg and the maximum recovery of BSA reached 80.5% when the ionic strength was 0.1696 mol/kg. Furthermore, K⁺ had better separate efficiency than Na⁺ under the same ionic strength.     

The Preparation of Metal–Organic-Framework/Boron Phosphate Hybrid Materials for Improved Performances in Proton Exchange Membranes

New types of metal–organic framework based hybrid materials are designed and prepared, which involving the hybridization of various content of boron phosphate (BPO₄) with the precursor of HKUST-1. The structure of obtained HKUST-1/BPO₄ hybrid materials (HB) is fully investigated, and then applied to construct sulfonated poly (ether ether ketone) (SPEEK) based proton exchange membranes (SPEEK/HB). Owing to effective interactions between hybrid materials and SPEEK matrix, the achieved composite membranes reflect a considerable improvement in mechanical and thermal stability, oxidative stability, methanol permeation, and proton conductivity. In particular, the tensile strength of SPEEK/HB-20 composite membrane is 41.3 MPa, which is 1.5 times higher than pristine SPEEK, and the methanol permeability reduced to one-third of SPEEK at the same time. The SPEEK/HB-10 displays the highest proton conductivity of 37.4 mS cm⁻¹ at 80 °C, which is obviously higher than pristine SPEEK. These results reveal that the hybridization of HKUST-1 with BPO₄ provide a promising candidate in the modification of proton exchange membranes (PEMs), and this strategy also possess great application potential in other types of MOFs-based hybrid materials.     

Imidazole/(HPO3)3‐doped sulfonated poly (ether ether ketone) composite membrane for fuel cells

A novel gel of imidazole/(HPO₃)₃ was synthesized and incorporated into sulfonated poly (ether ether ketone) (SPEEK) to fabricate composite proton exchange membranes. The composite membranes were characterized by alternating current impedance (AC), thermogravimetry (TG), differential scanning calorimetry (DSC), X‐ray diffraction (XRD), scanning electron microscope (SEM) and mechanical property test. Based on the electrochemical performance investigation, the proton conductivity of the membrane is intimately correlated with the temperature and the mass ratio of imidazole/(HPO₃)₃ in the composite. The SPEEK/imidazole/(HPO₃)₃?4 composite membrane (with 44.4 wt % of imidazole/(HPO₃)₃) has the optimized performance at 135°C. Mover, the strength of the composite membranes is almost comparable to that of Nafion membrane. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41946.     

Polymer electrolytes based on poly(ethylene glycol) dimethyl ether and the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate: Preparation, physico-chemical characterization, and theoretical study

Polymer electrolytes based on poly(ethylene glycol) dimethyl ether (PEGdME) and the ionic liquid (IL) 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF₆) have been prepared and characterized by different techniques. Coordination of the IL by the polymer occurs mainly in the amorphous phase. This finding was correlated with previous theoretical investigations of a similar model for polymer electrolytes based on poly(ethylene oxide), PEO, and IL. It has been obtained ionic conductivity σ ∼ 10⁻³ S cm⁻¹ for the polymer electrolyte with 35 wt% of IL at 100 °C. The same order of magnitude for σ was obtained by molecular dynamics simulation of PEO/IL. This work demonstrates consistency between experimental and theoretical results for polymer electrolytes containing ionic liquids.     

Synthesis and NMR studies of the polymer membranes based on poly(4-vinylbenzylboronic acid) and phosphoric acid

Proton conduction in novel anhydrous membranes based on host polymer, poly(4-vinylbenzylboronic acid), (P4VBBA) and phosphoric acid, (H₃PO₄) as proton solvent was studied. The materials were prepared by the insertion of the proton solvent into P4VBBA at different stoichiometric ratios to get P4VBBA·xH₃PO₄ composite electrolytes. Homopolymer and the composite materials were characterized by FT-IR, ¹¹B MAS NMR and ³¹P MAS NMR. ¹¹B MAS NMR results suggested that acid doping favors or leads to a four-coordinated boron arrangement. ³¹P MAS NMR results illustrated the immobilization of phosphoric acid to the polymer through condensation with boron functional groups (B-O-P and/or B-O-P-O-B). Thermogravimetric analysis (TGA) showed that the condensation of composite materials starts approximately at 140 °C. An exponential weight loss above this temperature was attributed to intermolecular condensation of acidic units forming cross-linked polymer. The insertion of phosphoric acid into the matrix softened the materials shifting T_g to lower temperatures. The temperature dependence of the proton conductivity was modeled with Arrhenius relation. P4VBBA·2H₃PO₄ has a maximum proton conductivity of 0.0013 S/cm at RT and 0.005 S/cm at 80 °C.     

Zirconium phosphate sulfonated poly (fluorinated arylene ether)s composite membranes for PEMFCs at 100-140 °C

Organic-inorganic hybrid composite membranes have been prepared and evaluated for polymer electrolyte membrane fuel cells (PEMFCs) at 100-140 °C. A series of synthesized poly (fluorinated arylene ether)s was sulfonated by fuming sulfuric acid (20% SO₃). The zirconium phosphate composite membrane was prepared by soaking the sulfonated poly (fluorinated arylene ether)s stepwise in 1 M zirconyl chloride solution and 1 M phosphoric acid solution. The chemical, thermal, and electrochemical properties of the composite membrane were investigated by thermogravimetric analysis (TGA), field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and unit cell test. The cell performance of the zirconium phosphate sulfonated poly (fluorinated arylene ether)s composite membrane was superior to that of the starting membrane at intermediate temperature, 100-140 °C. And the cell performance with composite membrane indicated stable behavior during experimentation when operating temperature maintained at 120 °C, whereas sulfonated poly (fluorinated arylene ether)s membrane was irreversible degradation under the same condition.