Preparation and Characterization of Tetra-imidazolium Hydroxide Polyphenylene Membranes via Nickel Catalyzed C–c Coupling Polymerization

Imidazolium hydroxide anion exchange membranes functionalized with conjugated tetraphenylethylene moieties were synthesized via Ni(0) catalyzed polymerization by sequential chloromethylation, substitution with imidazoliums and ion exchange. Moreover, with their pendant benzoyl groups the copolymers showed high molecular weight, durability, thermo-oxidative stability, high solubility in polar aprotic solvents and strong chemical and thermal stability in comparison to alkyl quaternary ammonium-functionalized polymers. The proposed polymer membranes, without ether linkages, demonstrated improved performance in ion exchange capacity, water uptake, ion conductivity, and thermal stability. The polymer membranes were studied by 1 H-NMR (Nuclear Magnetic Resonance) spectroscopy, thermogravimetric analysis, water uptake, ion exchange capacity and ion conductivity. Surface morphologies were assessed by atomic force microscope (AFM). The synthesized polymers may have applications as fuel cell membranes because of their excellent ion conductivity.


Introduction
Fuel cells are eco-friendly power sources having high energy density.Compared to other types of polymer electrolyte membranes, perfluorosulfonic acid polymers are more effective [1,2] but in the same time they tend to be expensive.To overcome these demerits, alkaline anion exchange membranes (AAEMs) are being developed [3][4][5].They employ electrode catalysts (Fe/Co/Ni/Ag) and show better cathode kinetics than other fuel cells [6][7][8][9].Quaternary ammonium functionalized anion exchange membranes (QAAEM) have been developed and many researchers have revealed that the QAAEMs possess low conductivity and poor stability [10][11][12][13][14][15].The common possible degradation pathways of quaternary ammonium species associated with OH ´ions include Hoffman (E2) elimination, direct nucleophilic substitution (SN2) and also ylide formation [3,4,[16][17][18].Recently, imidazolium-based AEMs have stood out in this aspect.These membranes have five-membered heterocyclic rings and conjugated imidazolium cation structures, which are expected to display good stability under alkaline conditions [19][20][21].Therefore, our aim was to prepare AEM materials with a resonance stabilized cationic group, like an imidazolium cation.The membranes containing conjugated imidazole rings are chemically more stable at high pH than ones with quaternary ammonium species, showing no apparent loss of ionic conductivity [3,22].We synthesized polymers without ethers linkage in the polymer main chain by carbon-carbon coupling reactions because polymer ether linkages are easily degraded by nucleophiles.There are three kinds of method to accomplish this: the Ni/Zn method, the superacid method, and the Diels-Alder method.Among them the Ni/Zn method is easy to use to obtain high molecular weights and useful to form a variety of monomer structures [23][24][25][26][27][28].
This work reports the fabrication of a series of anion exchange membranes containing poly(phenylene) units with four imidazolium functionalized ionic groups on the main polymer chain.The membranes were synthesized by nickel-catalyzed polymerization, chloromethylation using chloro methyl methyl ether, anhydrous zinc chloride as a Lewis acid catalyst and treatment with 1-methylimidazole.The tetraphenylene monomer consisted of a 4:6 ratio of cis and trans forms.With this conjugated cis/trans isomer basis it has a non-planar conformation containing the peripheral four aromatic rings.The alkaline tetra-imidazolium functionalized membranes were characterized by 1 H-NMR (Nuclear Magnetic Resonance) spectroscopy, thermogravimetric analysis, water uptake, ion exchange capacity assessment and by the investigation of atomic force microscopic (AFM) images.

Preparation of 1,4-Dichloro-2,5-Dibenzoylbenzene (PBP)
A mixture of 2,5-dichloro-p-xylene (2.6 g, 11.5 mmol), potassium permanganate (13.6 g, 88.5 mmol), and pyridine (40.5 mL, 512 mmol) in distilled water (12.5 mL) was placed in a 250 mL round bottom flask.The mixture was stirred for 12 h at a temperature of 100 ˝C.The reaction mixture was cooled to room temperature and filtered.The filtrate was evaporated to remove pyridine and water.The solid was dissolved in water and acidified with hydrochloric acid to a pH of 1.The resulting white solid was filtered and dried in an oven at 60 ˝C.Dichloroterephthalic acid (2.15 g, 9.25 mmol) was stirred at reflux condition for 24 h with thionyl chloride (7.5 mL, 9.75 mmol) and pyridine (0.09 mL, 0.9 mmol).The solution was evaporated and a yellow solid obtained.Immediately, the yellow solid was dissolved in carbon disulfide and added dropwise into benzene (2.45 mL, 27.75 mmol), and aluminum chloride (6.17 g, 46.25 mmol) in carbon disulfide (50 mL) over 30 min.The mixture was stirred at 40 ˝C for 24 h and the residue was poured into ice water with hydrochloric acid.The product was filtered and washed twice with water and also recrystallized using ethanol before drying in an oven at 60 ˝C [30].

Preparation of Poly(tetraphenylethylene)-co-(dibenzoylphenylene) (PTPEDBP)
The polymerization was conducted in a 100 mL three-neck flask containing nickel bromide (0.11 g, 0.51 mmol), zinc powder (2 g, 30.71 mmol), and triphenylphosphine (1.07 g, 4.09 mmol) with a nitrogen inlet.In another one-neck round-flask, bis(4-chlorophenyl)-1,2-diphenylethylene (0.45 g, 1.12 mmol) and 1,4-dichloro-2,5-dibenzoylbenzene (1.6 g, 4.48 mmol) were taken.The mixture of catalysts and monomers were prepared in glove box under a nitrogen atmosphere.DMAc was added via syringe into the catalyst flask and stirred at 80 ˝C for 10 min.The monomers were dissolved in DMAc and injected slowly by syringe into the catalyst flask, whereby the solution of catalyst changed color to deep red.The reaction was allowed to proceed for 24 h at 100 ˝C.After that the polymer was poured into water with 30% hydrochloric acid.The resulting bright yellow solid was filtered and washed with methanol and water.After drying in an oven at 60 ˝C, the polymer was dissolved in DMAc and reprecipitated in 10% HCl aqueous solution before drying in an oven at 60 ˝C.

Preparation of Chloromethylated Polymer (PTPEDBP-Cl)
PTPEDBP-Cl was prepared by the chloromethylation of PTPEDBP (1.0 g, 1.84 mmol) in 1,1,2,2-tetrachloroethane (15.0 mL) in a 100 mL three neck round-bottom flask, fitted with a condenser, a nitrogen inlet/outlet and a magnetic stirrer.Zinc chloride (0.25 g, 1.84 mmol) was added at room temperature and chloro methyl methyl ether (3.65 mL) was then added dropwise.The reaction mixture was stirred for 12 h at room temperature.It was precipitated using mixture of methanol and water (50:50) and repeatedly washed with methanol and deionized water, individually.The light brown polymer was collected by filtration and dried in a vacuum oven for 24 h at 80 ˝C.

Preparation of Tetra-Imidazolium Chloride Polymer (PTPEDBP-I/Cl)
PTPEDBP-I/Cl was prepared from a solution of PTPEDBP-Cl (0.5 g, 0.81 mmol) in DMAc (8.0 mL).Firstly, 1-methylimidazole (0.81 mL, 7.14 mmol) was added dropwise.The mixture was stirred for 24 h at 55 ˝C, cooled to room temperature and decanted into ethyl acetate for precipitation.The light yellow solid was collected by filtration and repeatedly washed with ethyl acetate to remove any remaining 1-methylimidazole.The solid polymer was dried in a vacuum oven at 80 ˝C for 24 h.

Preparation of Tetra-Imidazolium Hydroxide Polymer (PTPEDBP-I/OH)
PTPEDBP-I/OH was prepared from 10 wt% PTPEDBP-I/Cl dissolved in dimethylsulfoxide.The membrane was prepared by casting this solution to 25 µm thickness on a flat glass plate (5 cm ˆ5 cm) [4,10].The membrane's thickness was controlled by using a polymer wt% solution.It was then dried at 80 ˝C for 24 h in a vacuum oven.The chloride anions (Cl ´) were converted to OH ´by immersing the membrane in 1.0 M KOH solution for 48 h.It was then repeatedly washed with deionized water until the pH of the residual water was neutral.

Characterization of Membranes
The copolymer structure was confirmed by 1 H-NMR spectra, which were recorded on a DRX (400 MHz) spectrometer (Bruker, Billerica, MA, USA) using CDCl 3 and deuterated dimethylsulfoxide (DMSO-d 6 ) solvents and tetramethylsilane (TMS) as an internal standard.Thermogravimetric analysis was performed using a TGA-7 analyzer (Perkin-Elmer, Waltham, MA, USA).Water uptake, the percentage mass change of the dry membrane was assessed from the mass difference of the membrane vacuum dried at 100 ˝C for 24 h before and after immersion in deionized water at 80 ˝C for 24 h.The wet membrane was wiped dry before weighing.Membrane swelling degree was calculated as the percentage length change of each dry membrane after immersion in water at 80 ˝C for 24 h.Membrane ion exchange capacity was determined by back titration.A membrane in the OH ´form was immersed in a standard hydrochloric acid solution (0.1 M, 30.0 mL) for 48 h.The solution was then titrated with a standard solution of potassium hydroxide (0.1 M) using phenolphthalein as an indicator.The membrane was washed and immersed in deionized water for 24 h to remove any remaining HCl and then dried under vacuum at 60 ˝C for 24 h.Its dry mass was measured.The membrane's ion exchange capacity (IEC/mmol g ´1) was calculated as the ratio of the amount of protons lost from the HCl solution determined by titration to the mass of dry membrane.Ionic conductivities in hydroxide (OH ´) form of the fully hydrated membranes were determined from their resistance measured by electrochemical impedance spectroscopy using a membrane testing system (MTS-740, Scribner Associates Inc., Southern Pines, NC, USA) with an impedance analysis interface (PSM 1735, Newton's 4th Ltd., Leicester, UK) at 80 ˝C under 100% relative humidity.Evaluation of ionic conductivity under fully hydrated conditions was performed with the cell immersed in deionized water at room temperature.All the prepared samples were equilibrated in pure water for at least 24 h prior to conductivity estimation.The samples were brought into equilibrium with the given temperature for at least 30 min before any measurement.Assessment was conducted under open circuit conditions by applying a small alternating voltage (10 mV) with frequency varied from 1 ˆ10 5 to 1 Hz.Ion conductivity was calculated as: where L is the membrane thickness in cm, A is the electrode area in cm 2 , and R mem is ohmic resistance measured by four-point probe alternating current electrochemical impedance spectroscopy.The surface morphologies of the anionic polymer membranes were observed by atomic force microscope (AFM).
Tapping mode atomic force microscopic observations were performed with a Nanoscope (R) IIIA device (Digital Instrument, Milano, Italy), using microfabricated cantilevers with an amplitude set point 0.7785 V.All samples were cast on a flat glass plates and heated at 60 ˝C (3 h), 80 ˝C (3 h), 100 ˝C (3 h), and 120 ˝C for 1 h to form around 25 µm.The resulting films were allowed to stand under 100% relative humidity at room temperature prior to investigation.The chemical stability of the alkaline polymer membranes were assessed by measuring the weight change in each day after immersion the sample in 1.0 M KOH solution at 60 ˝C.

Preparation of Polymers
The polymers were synthesized via nickel-catalyzed carbon-carbon coupling polymerization of bis(4-chlorophenyl)-1,2-diphenylethylene and 1,4-dichloro-2,5-dibenzoylbenzene (Figure 1).Sulfonation was then performed to introduce sulfonic acid groups in the polymer.The number of sulfonic acid groups was controlled by varying the mole ratio of BCD monomer.A series of sulfonated polymers were prepared by controlling the mole ratios of BCD at 10%, 15% and 20%. Figure 2 shows the chemical structure of PTPEDBP polymer by 1 H-NMR.The protons of phenyl groups appeared at 6.76-8.00ppm.
testing system (MTS-740, Scribner Associates Inc., Southern Pines, NC, USA) with an impedance analysis interface (PSM 1735, Newton's 4th Ltd., Leicester, UK) at 80 °C under 100% relative humidity.Evaluation of ionic conductivity under fully hydrated conditions was performed with the cell immersed in deionized water at room temperature.All the prepared samples were equilibrated in pure water for at least 24 h prior to conductivity estimation.The samples were brought into equilibrium with the given temperature for at least 30 min before any measurement.Assessment was conducted under open circuit conditions by applying a small alternating voltage (10 mV) with frequency varied from 1 × 10 5 to 1 Hz.Ion conductivity was calculated as: where L is the membrane thickness in cm, A is the electrode area in cm 2 , and Rmem is ohmic resistance measured by four-point probe alternating current electrochemical impedance spectroscopy.The surface morphologies of the anionic polymer membranes were observed by atomic force microscope (AFM).Tapping mode atomic force microscopic observations were performed with a Nanoscope (R) IIIA device (Digital Instrument, Milano, Italy), using microfabricated cantilevers with an amplitude set point 0.7785 V.All samples were cast on a flat glass plates and heated at 60 °C (3 h), 80 °C (3 h), 100 °C (3 h), and 120 °C for 1 h to form around 25 μm.The resulting films were allowed to stand under 100% relative humidity at room temperature prior to investigation.The chemical stability of the alkaline polymer membranes were assessed by measuring the weight change in each day after immersion the sample in 1.0 M KOH solution at 60 °C .

Preparation of Polymers
The polymers were synthesized via nickel-catalyzed carbon-carbon coupling polymerization of bis(4-chlorophenyl)-1,2-diphenylethylene and 1,4-dichloro-2,5-dibenzoylbenzene (Figure 1).Sulfonation was then performed to introduce sulfonic acid groups in the polymer.The number of sulfonic acid groups was controlled by varying the mole ratio of BCD monomer.A series of sulfonated polymers were prepared by controlling the mole ratios of BCD at 10%, 15% and 20%. Figure 2 shows the chemical structure of PTPEDBP polymer by 1 H-NMR.The protons of phenyl groups appeared at 6.76-8.00ppm.Chloromethylated polyphenylene (PTPEDBP-Cl) was prepared by Friedel-Crafts reaction with chloromethyl methyl ether and a Lewis acid catalyst, ZnCl2 (Figure 1).Reaction time, the ratio of chloromethyl methyl ether and amount of ZnCl2 are important to control the molecular weight of the resulting polymer.A 1:30 mole ratio of ZnCl2 and chloro methyl methyl ether (CMME) represents effective chloromethylation conditions to avoid any degradation of the polymer and achieve 100% substitution.The PTPEDBP-Cl structure was confirmed by 1 H-NMR.The methylene protons of the chloromethyl groups appeared at 4.5 ppm (Figure 2).Chloromethylation yield (100%) was estimated from the integral ratio of methylene protons to the total phenyl protons at 6.72-7.78ppm.
PTPEDBP-I/Cl was prepared using 1-methylimidazole in 1,1,2,2-tetrachloroethane at 70 °C for 24 h (Figure 1).Conversion of chloromethyl groups to imidazolium was achieved by controlling the molar ratio of PTPEDBP-Cl and 1-methylimidazole.It was observed that the 1:12.5 mole ratio of PTPEDBP-Cl and 1-methylimidazole gave imidazolium chloride polymer without any polymer backbone degradation, whose structure was identified by the characteristic downfield peak at 5.41, 9.48 ppm (Figure 2) which indicated the imidazolium cation-essentially an electron withdrawing group [31].NMR data showed that 100% conversion to imidazolium groups occurred.This membrane's thickness was controlled by using polymer wt% solution to a thickness of 25 μm [4,32].Usually, membranes thicker than 50 μm show poor uptake of hydroxide ions.

Properties of Anion Exchange Membrane
Thermal stability is required for anion exchange membranes at high temperatures to control thermodynamic voltage losses during the membranes' use in fuel cells [33].The thermooxidative stabilities of membranes were investigated by themogravimetric analysis.Figure 3 reveals that PTPEDBP is thermally stable up to 520 °C in air.The weight loss of PTPEDBP-Cl at around 200-400 °C corresponds to the decomposition of chloromethyl groups.The weight loss of PTPEDBP-I/OH shown at 250 °C probably corresponds to the decomposition of the imidazolium cation.However, membranes bearing imidazolium cations were more thermally stable than those containing ammonium groups in the anion exchange membrane [33] because of the higher decomposition temperature of the imidazolium groups [3,31].Chloromethylated polyphenylene (PTPEDBP-Cl) was prepared by Friedel-Crafts reaction with chloromethyl methyl ether and a Lewis acid catalyst, ZnCl 2 (Figure 1).Reaction time, the ratio of chloromethyl methyl ether and amount of ZnCl 2 are important to control the molecular weight of the resulting polymer.A 1:30 mole ratio of ZnCl 2 and chloro methyl methyl ether (CMME) represents effective chloromethylation conditions to avoid any degradation of the polymer and achieve 100% substitution.The PTPEDBP-Cl structure was confirmed by 1 H-NMR.The methylene protons of the chloromethyl groups appeared at 4.5 ppm (Figure 2).Chloromethylation yield (100%) was estimated from the integral ratio of methylene protons to the total phenyl protons at 6.72-7.78ppm.
PTPEDBP-I/Cl was prepared using 1-methylimidazole in 1,1,2,2-tetrachloroethane at 70 ˝C for 24 h (Figure 1).Conversion of chloromethyl groups to imidazolium was achieved by controlling the molar ratio of PTPEDBP-Cl and 1-methylimidazole.It was observed that the 1:12.5 mole ratio of PTPEDBP-Cl and 1-methylimidazole gave imidazolium chloride polymer without any polymer backbone degradation, whose structure was identified by the characteristic downfield peak at 5.41, 9.48 ppm (Figure 2) which indicated the imidazolium cation-essentially an electron withdrawing group [31].NMR data showed that 100% conversion to imidazolium groups occurred.This membrane's thickness was controlled by using polymer wt% solution to a thickness of 25 µm [4,32].Usually, membranes thicker than 50 µm show poor uptake of hydroxide ions.

Properties of Anion Exchange Membrane
Thermal stability is required for anion exchange membranes at high temperatures to control thermodynamic voltage losses during the membranes' use in fuel cells [33].The thermooxidative stabilities of membranes were investigated by themogravimetric analysis.Figure 3 reveals that PTPEDBP is thermally stable up to 520 ˝C in air.The weight loss of PTPEDBP-Cl at around 200-400 ˝C corresponds to the decomposition of chloromethyl groups.The weight loss of PTPEDBP-I/OH shown at 250 ˝C probably corresponds to the decomposition of the imidazolium cation.However, membranes bearing imidazolium cations were more thermally stable than those containing ammonium groups in the anion exchange membrane [33] because of the higher decomposition temperature of the imidazolium groups [3,31].Membranes suitable for alkaline fuel cells require sufficient imidazolium groups to provide ionic conductivity while maintaining mechanical integrity.The ion exchange capacities of the PTPEDBP-I/OH membranes increased as 1.14, 1.67, and 2.08 mmol g −1 with the increasing numbers of imidazolium hydroxide groups-the theoretical and the experimental (titrated) capacities were in reasonably good agreement (Table 1).Membranes' water uptakes varied from 12.7% to 31.2% at 30 °C and from 25.4% to 64.5% at 80 °C with increasing numbers of imidazolium hydroxide groups (Table 1).In Figure 4 shows increase of water uptake for the PTPEDBP-I/OH membranes as IEC increases.The hydrophilic properties of the membranes become better with increasing IEC values.Therefore, the polyphenylene membranes become more hydrophilic and absorb more water with the increases of IEC from 1.14 to 2.08.Water uptake is low like in other imidazolium-based systems (24.76% at 60 °C and <31%) [3,34].Membranes suitable for alkaline fuel cells require sufficient imidazolium groups to provide ionic conductivity while maintaining mechanical integrity.The ion exchange capacities of the PTPEDBP-I/OH membranes increased as 1.14, 1.67, and 2.08 mmol g ´1 with the increasing numbers of imidazolium hydroxide groups-the theoretical and the experimental (titrated) capacities were in reasonably good agreement (Table 1).Membranes' water uptakes varied from 12.7% to 31.2% at 30 ˝C and from 25.4% to 64.5% at 80 ˝C with increasing numbers of imidazolium hydroxide groups (Table 1).In Figure 4 shows increase of water uptake for the PTPEDBP-I/OH membranes as IEC increases.The hydrophilic properties of the membranes become better with increasing IEC values.Therefore, the polyphenylene membranes become more hydrophilic and absorb more water with the increases of IEC from 1.14 to 2.08.Water uptake is low like in other imidazolium-based systems (24.76% at 60 ˝C and <31%) [3,34].Membranes suitable for alkaline fuel cells require sufficient imidazolium groups to provide ionic conductivity while maintaining mechanical integrity.The ion exchange capacities of the PTPEDBP-I/OH membranes increased as 1.14, 1.67, and 2.08 mmol g −1 with the increasing numbers of imidazolium hydroxide groups-the theoretical and the experimental (titrated) capacities were in reasonably good agreement (Table 1).Membranes' water uptakes varied from 12.7% to 31.2% at 30 °C and from 25.4% to 64.5% at 80 °C with increasing numbers of imidazolium hydroxide groups (Table 1).In Figure 4 shows increase of water uptake for the PTPEDBP-I/OH membranes as IEC increases.The hydrophilic properties of the membranes become better with increasing IEC values.Therefore, the polyphenylene membranes become more hydrophilic and absorb more water with the increases of IEC from 1.14 to 2.08.Water uptake is low like in other imidazolium-based systems (24.76% at 60 °C and <31%) [3,34].Compared to the ammonium hydroxide membranes of the IEC values of 1.88 and 2.54 mmol g ´1 and water uptakes 95% and 160%) [10], our imidazolium-based polyphenylene membrane showed very low water uptakes.This is possibly due to the presence of conjugated imidazole rings which weakens the interaction with water molecules.In Table 1, the imidazolium-containing membranes showed less swelling than other reported anion exchange membranes containing ammonium groups (26.8%-58.8%)[32], demonstrating their high dimensional stability due to both the resonance stabilized conjugated imidazolium cations and rigid backbone.Ion conductivities of 16.8 to 30.5 mS cm ´1 were observed at 80 ˝C and 100% relative humidity.Conductivity values increased as ion exchange capacity and temperatures increased (Figure 5 and Table 1).
Energies 2016, 9, 271 7 of 10 Compared to the ammonium hydroxide membranes of the IEC values of 1.88 and 2.54 mmol g −1 and water uptakes 95% and 160%) [10], our imidazolium-based polyphenylene membrane showed very low water uptakes.This is possibly due to the presence of conjugated imidazole rings which weakens the interaction with water molecules.In Table 1, the imidazolium-containing membranes showed less swelling than other reported anion exchange membranes containing ammonium groups (26.8%-58.8%)[32], demonstrating their high dimensional stability due to both the resonance stabilized conjugated imidazolium cations and rigid backbone.Ion conductivities of 16.8 to 30.5 mS cm −1 were observed at 80 °C and 100% relative humidity.Conductivity values increased as ion exchange capacity and temperatures increased (Figure 5 and Table 1).At higher temperatures, the membranes showed high water affinity and led to faster migration of ions and high ionic conductivity [3].The developed AEMs (Tokuyama Co., Tokyo, Japan) are hydrocarbon polymers which consist of hydrocarbon main chains and quaternary ammonium salts.The OH − conductivities of Tokuyama membrane are around 38-42 mS cm −1 , and our membranes shows a little low value of 31 mS cm −1 [35].The PTPEDBP-I/OH membranes show low ion conductivities, despite their higher ion exchange capacities like typical hydrocarbon membranes (10-22 mS cm −1 and 18-46 mS cm −1 ) [36].This was possibly due to low water absorption caused by resonance effects.The polymers' surface morphologies were assessed on a 1 μm × 1 μm scale by atomic force microscopy in tapping mode under ambient conditions (Figure 6).Several worm-shaped domains are better observed in PTPEDBP-I/OH.The swollen hydrophilic domains were assumed to be more connected to the bulk membrane, rather remaining isolated from each other.The hydrophilic domain with microstructure is distinctive with disordered ionic At higher temperatures, the membranes showed high water affinity and led to faster migration of ions and high ionic conductivity [3].The developed AEMs (Tokuyama Co., Tokyo, Japan) are hydrocarbon polymers which consist of hydrocarbon main chains and quaternary ammonium salts.The OH ´conductivities of Tokuyama membrane are around 38-42 mS cm ´1, and our membranes shows a little low value of 31 mS cm ´1 [35].The PTPEDBP-I/OH membranes show low ion conductivities, despite their higher ion exchange capacities like typical hydrocarbon membranes (10-22 mS cm ´1 and 18-46 mS cm ´1) [36].This was possibly due to low water absorption caused by resonance effects.The polymers' surface morphologies were assessed on a 1 µm ˆ1 µm scale by atomic force microscopy in tapping mode under ambient conditions (Figure 6).Compared to the ammonium hydroxide membranes of the IEC values of 1.88 and 2.54 mmol g −1 and water uptakes 95% and 160%) [10], our imidazolium-based polyphenylene membrane showed very low water uptakes.This is possibly due to the presence of conjugated imidazole rings which weakens the interaction with water molecules.In Table 1, the imidazolium-containing membranes showed less swelling than other reported anion exchange membranes containing ammonium groups (26.8%-58.8%)[32], demonstrating their high dimensional stability due to both the resonance stabilized conjugated imidazolium cations and rigid backbone.Ion conductivities of 16.8 to 30.5 mS cm −1 were observed at 80 °C and 100% relative humidity.Conductivity values increased as ion exchange capacity and temperatures increased (Figure 5 and Table 1).At higher temperatures, the membranes showed high water affinity and led to faster migration of ions and high ionic conductivity [3].The developed AEMs (Tokuyama Co., Tokyo, Japan) are hydrocarbon polymers which consist of hydrocarbon main chains and quaternary ammonium salts.The OH − conductivities of Tokuyama membrane are around 38-42 mS cm −1 , and our membranes shows a little low value of 31 mS cm −1 [35].The PTPEDBP-I/OH membranes show low ion conductivities, despite their higher ion exchange capacities like typical hydrocarbon membranes (10-22 mS cm −1 and 18-46 mS cm −1 ) [36].This was possibly due to low water absorption caused by resonance effects.The polymers' surface morphologies were assessed on a 1 μm × 1 μm scale by atomic force microscopy in tapping mode under ambient conditions (Figure 6).Several worm-shaped domains are better observed in PTPEDBP-I/OH.The swollen hydrophilic domains were assumed to be more connected to the bulk membrane, rather remaining isolated from each other.The hydrophilic domain with microstructure is distinctive with disordered ionic Several worm-shaped domains are better observed in PTPEDBP-I/OH.The swollen hydrophilic domains were assumed to be more connected to the bulk membrane, rather remaining isolated from Energies 2016, 9, 271 8 of 10 each other.The hydrophilic domain with microstructure is distinctive with disordered ionic channels.The membrane provided the required ionic conductivity for fuel cell applications owing to the larger number of interconnects of the hydrophilic domains in the disordered morphology [31].Anion exchange membranes in alkaline fuel cells require chemical stability against nucleophilic attack by OH ´ions.The PTPEDBP-I/OH membranes' stabilities were investigated in 1.0 M KOH at 60 ˝C over 5 days [3,9,31].Ion conductivity was measured each day after free KOH had been removed through washing in deionized water.
The membranes showed relatively better chemical stability (Figure 7) than the quaternary ammonium functionalized polymers [36]; the quaternary ammonium polymers suffer from nucleophilic substitution or elimination reactions [4,35], The strong chemical stability aspect of the imidazolium hydroxide polymers is largely affected by the steric hindrance that demonstrates the good competing deprotonation reaction [37] and the presence of conjugated imidazolium cation that could reduce the SN2 substitution and Hofmann (E2) elimination reactions by the aggressive hydroxide nucleophile [3,35].Overall, the imidazolium functionalized polycarbonate anion exchange membranes are stable in alkaline conditions.
Energies 2016, 9, 271 8 of 10 channels.The membrane provided the required ionic conductivity for fuel cell applications owing to the larger number of interconnects of the hydrophilic domains in the disordered morphology [31].Anion exchange membranes in alkaline fuel cells require chemical stability against nucleophilic attack by OH − ions.The PTPEDBP-I/OH membranes' stabilities were investigated in 1.0 M KOH at 60 °C over 5 days [3,9,31].Ion conductivity was measured each day after free KOH had been removed through washing in deionized water.The membranes showed relatively better chemical stability (Figure 7) than the quaternary ammonium functionalized polymers [36]; the quaternary ammonium polymers suffer from nucleophilic substitution or elimination reactions [4,35], The strong chemical stability aspect of the imidazolium hydroxide polymers is largely affected by the steric hindrance that demonstrates the good competing deprotonation reaction [37] and the presence of conjugated imidazolium cation that could reduce the SN2 substitution and Hofmann (E2) elimination reactions by the aggressive hydroxide nucleophile [3,35].Overall, the imidazolium functionalized polycarbonate anion exchange membranes are stable in alkaline conditions.

Conclusions
A series of anion conductive membranes were synthesized by successive chloromethylation, substitution with 1-methylimidazole and ion exchange reactions of bisphenol polycarbonate.Chloromethylation was important in giving quantitative imidazolium substitution and also the subsequent ion exchange reactions.The PTPEDBP-I/OH membranes showed high ionic conductivity 16.8-30.5mS cm −1 at 80 °C and 100% relative humidity.The prepared AEMs bearing imidazolium cation are flexible and show enough good dimensional stability for use as novel potential alkaline fuel cell material candidates.Additionally, alkaline imidazolium membranes exhibit good stability in alkaline conditions that could overcome the known limitations of quaternary ammonium hydroxide polymers.Therefore, the imidazolium-functionalized membranes can contribute to improvements of fuel cell performance because they show relatively better conductivity and chemical stability than ammonium anion membranes, and similar results compared to imidazolium anion membranes.(NRF-2014H1C1A1066447) and Basic Science Research Program through the National Research Foundation of

Conclusions
A series of anion conductive membranes were synthesized by successive chloromethylation, substitution with 1-methylimidazole and ion exchange reactions of bisphenol polycarbonate.Chloromethylation was important in giving quantitative imidazolium substitution and also the subsequent ion exchange reactions.The PTPEDBP-I/OH membranes showed high ionic conductivity 16.8-30.5mS cm ´1 at 80 ˝C and 100% relative humidity.The prepared AEMs bearing imidazolium cation are flexible and show enough good dimensional stability for use as novel potential alkaline fuel cell material candidates.Additionally, alkaline imidazolium membranes exhibit good stability in alkaline conditions that could overcome the known limitations of quaternary ammonium hydroxide polymers.Therefore, the imidazolium-functionalized membranes can contribute to improvements of fuel cell performance because they show relatively better conductivity and chemical stability than ammonium anion membranes, and similar results compared to imidazolium anion membranes.

Figure 7 .
Figure 7.The chemical stability of tetra-imidazolium hydroxide polymer membranes PTPEDBP-I/OH 10 and PTPEDBP-I/OH 20 after immersion in 1.0 M KOH solution at 60 °C : ion conductivity at 80 °C and 100% relative humidity.

Figure 7 .
Figure 7.The chemical stability of tetra-imidazolium hydroxide polymer membranes PTPEDBP-I/OH 10 and PTPEDBP-I/OH 20 after immersion in 1.0 M KOH solution at 60 ˝C: ion conductivity at 80˝C