The effective methanol-blocking and proton conductivity membranes based on sulfonated poly (ether ether ketone ketone) and polyorganosilicon with functional groups

To solve the conflict between high proton conductivity and low methanol crossover of pristine sulfonated aromatic polymer membranes, the polyorganosilicon doped sulfonated poly (ether ether ketone ketone) (SPEEKK) composite membranes were prepared by introducing polyorganosilicon additive with various functional groups into SPEEKK in this study. Scanning electron microcopy (SEM) images showed the obtained membranes were compact. No apparent agglomerations, cracks and pinholes were observed in the SEM images of composite membranes. The good compatibility between polymer and additive led to the interconnection, thus producing new materials with great characteristics and enhanced performance. Besides, the dual crosslinked structure could be formed in composite membranes through the condensation of silanols and the strong interaction between matrix and additive. The formation of dual crosslinked structure optimized the water absorption, enhanced the hydrolytic stability and oxidative stability of membranes. Especially, the incorporation of additive improved the strength and flexibility of composite membranes at the same time, meaning that the life of the composite membranes might be extended during the fuel cell operation. Meanwhile, the proton conductivity improved with increasing additive content due to the loading of more available acidic groups. It is noteworthy that at 25% additive loading, the proton conductivity reached a maximum value of 5.4 × 10⁻² S cm⁻¹ at 25 °C, which exceeded the corresponding value of Nafion^@ 117 (5.0 × 10⁻² S cm⁻¹) under same experimental conditions. The composite membrane with 20 wt% additive was found to produce the highest selectivity (1.22 × 10⁵ S cm⁻³) with proton conductivity of 4.70 × 10⁻² S cm⁻¹ and methanol diffusion coefficient of 3.85 × 10⁻⁷ cm² s⁻¹, suggesting its best potential as proton exchange membrane for direct methanol fuel cell application. The main novelty of our work is providing a feasible and environment-friendly way to prepare the self-made polyorganosilicon with various functional groups and introducing it into SPEEKK to fabricate the dual crosslinked membranes. This design produces new materials with outstanding performance.     

A facile,effective thermal crosslinking to balance stability and proton conduction for proton exchange membranes based on blend sulfonated poly(ether ether ketone)/sulfonated poly(arylene ether sulfone)

The development of hydrocarbon polymer electrolyte membranes with high proton conductivities and good stability as alternatives to perfluorosulfonic acid membranes is an ongoing research effort. A facile and effective thermal crosslinking method was carried out on the blended sulfonated poly (ether ether ketone)/poly (aryl ether sulfone) (SPEEK/SPAES) system. Two SPEEK polymers with ion exchange capacities (IECs) of 1.6 and 2.0 mmol g^?1 and one SPAES polymer (2.0 mmol g^?1) were selected to create different blends. The effect of thermal crosslinking on the fundamental properties of the membranes, especially their physicochemical stability and electrochemical performance, were investigated in detail. The homogeneous and flexible thermally-crosslinked SPEEK/SPAES membranes displayed excellent mechanical toughness (27–46 Mpa), suitable water uptake (<60%), high dimensional stability (swelling ratio < 15%) and large proton conductivity (>120 mS cm^?1) at 80 °C. The thermal crosslinking membranes also show significantly enhanced hydrolytic (<2.5%) and oxidative stability (<2%). Fuel cell with t-SPEEK/SPAES (1:2:2) membrane achieves a power density of 665 mW cm^?2 at 80 °C.     

Novel sulfonated poly(ether ether ketone ketone)s for direct methanol fuel cells usage: Synthesis,water uptake,methanol diffusion coefficient and proton conductivity

A novel series of sulfonated poly(ether ether ketone ketone)s (SPEEKKs) with different degrees of sulfonation (Ds) were synthesized from 1,3-bis(3-sodium sulfonate-4-fluorobenzoyl)benzene (1,3-SFBB-Na), 1,3-bis(4-fluorobenzoyl)benzene (1,3-FBB) and 3,3′,5,5′-tetramethyl-4,4′-biphenol (TMBP) by aromatic nucleophilic polycondensation. The chemical structures of SPEEKKs were confirmed by FT-IR spectroscopy and the Ds values of the polymers were calculated by ¹H NMR and titration methods, respectively. The thermal stabilities of the SPEEKKs in acid and sodium forms were characterized by thermogravimetric analysis (TGA), which showed that SPEEKKs had excellent thermal properties at high temperatures. All the SPEEKK polymers were easily solution cast into tough membranes. Water uptakes, proton conductivities and methanol diffusion coefficients of the SPEEKK membranes were measured. Water uptake increased with Ds and temperature. Compared to Nafion, the SPEEKK-60, -70 and -80 membranes showed higher proton conductivities at 80 °C, while the other SPEEKK membranes showed relatively lower proton conductivities. This may be due to the different distribution of ion-conducting domains in membrane. However, these membranes showed lower methanol diffusions in the range of 8.32 × 10⁻⁹ to 1.14 × 10⁻⁷ cm² s⁻¹ compared with that of Nafion (2 × 10⁻⁶ cm² s⁻¹) at the same temperature. The membranes also showed excellent mechanical properties (with a Young's modulus > 1 GPa and a tensile strength > 40 MPa). These results indicate that the SPEEKK membranes are promising materials for use in direct methanol fuel cell (DMFC) applications.     

Molecular structure and transport dynamics in Nafion and sulfonated poly(ether ether ketone ketone) membranes

An atomistic simulation technique is performed to investigate the molecular structure and transport dynamics inside a hydrated Nafion membrane and a hydrated sulfonated poly(ether ether ketone ketone) (SPEEKK) membrane. The simulation system consists of the representative fragments of the polymer electrolytes, hydronium ions and solvent molecules, such as water plus methanol molecules. Simulation results show that the hydrated SPEEKK has less phase separation among hydrophobic and hydrophilic regions in comparison with the Nafion. Those water channels formed in the SPEEKK are much narrower compared to those in the Nafion. These characteristics lead to a lower mobility of hydronium ions and water molecules and hence relatively lower diffusion coefficient of methanol in the SPEEKK. It results in the reduction of the methanol permeation problem in direct methanol fuel cells.     

Enhanced proton conductivity of poly (arylene ether ketone sulfone) containing uneven sulfonic acid side chains by incorporating imidazole functionalized metal-organic framework

In this study, the side-chain type hybrid proton exchange membranes which based on metal-organic frameworks (MOFs) and organic matrix of sulfonated poly (arylene ether ketone sulfone) containing both long and short sulfonic acid side chains (S-C-SPAEKS) were prepared. MOF-801 was used as a template and then imidazole was encapsulated into MOF-801 as additional proton carriers. In imidazole -MOF-801, imidazole was used as a functional group to coordinate with the zirconium metal site of the functional group. Imidazole-MOF-801 and hybrid membranes were characterized by XRD, ¹H NMR and FT-IR. These hybrid membranes exhibited excellent proton conductivities and good thermal stabilities. Compared to pure S-C-SPAEKS (0.0487 S cm^?1 at 30 °C, 0.0809 S cm^?1 at 80 °C), S-C-SPAEKS/0.5% Im-MOF-801 showed a great improvement (0.1205 S cm^?1 at 30 °C, 0.1992 S cm^?1 at 80 °C), which was about 2.5 times higher than that of pure S-C-SPAEKS and 2 times higher than that of commercial Nafion117 (0.1003 S cm^?1 at 80 °C). The results indicated that imidazole functionalized MOFs and uneven side chain structure synergistically made an important contribution to proton transport. This series of hybrid membranes have the potential to be used as alternative proton exchange membranes.     

Improving the proton conductivity of sulfonated poly (ether ether ketone) membranes by incorporating a crystalline nanoassembly of trimesic acid and melamine

A novel proton exchange membrane was synthesized by embedding a crystalline which was nano-assembled through trimesic acid and melamine (TMA·M) into the matrix of the sulfonated poly (ether ether ketone) (SPEEK) to enhance the proton conductivity of the SPEEK membrane. Fourier transform infrared indicated that hydrogen bonds existed between SPEEK and TMA·M. XRD and SEM indicated that TMA·M was uniformly distributed within the matrix of SPEEK, and no phase separation occurred. Thermogravimetric analysis showed that this membrane could be applied as high temperature proton exchange membrane until 250 °C. The dimensional stability and mechanical properties of the composite membranes showed that the performance of the composite membranes is superior to that of the pristine SPEEK. Since TMA·M had a highly ordered nanostructure, and contained lots of hydrogen bonds and water molecules, the proton conductivity of the SPEEK/TMA·M-20% reached 0.00513 S cm⁻¹ at 25 °C and relative humidity 100%, which was 3 times more than the pristine SPEEK membrane, and achieved 0.00994 S cm⁻¹ at 120 °C.     

Anion exchange membranes based on poly (ether ether ketone) containing N-spirocyclic quaternary ammonium cations in phenyl side chain

It was reported that the existence of N-spirocyclic quaternary ammonium (QA) cation could improve alkaline stability of anion exchange membrane materials (AEM). Therefore, the cyclo-quaternization reaction with pyrrolidine (Pyr) and piperidine (Pip) was carried out to prepare quaternized poly (ether ether ketone)s bearing five-membered and six-membered N-spirocyclic quaternary ammonium (QA) groups in the phenyl side chains (QPEEK-spiro-pyr and QPEEK-spiro-pip), respectively. From the transmission electron microscope, the hydrophilic-hydrophobic phase-separated morphology was formed in QPEEK-spiro membranes after incorporating N-spirocyclic QA cations and bulky spacer simultaneously in the phenyl side chain. The effect of N-spirocyclic QA groups on performance of resulted AEMs was then studied in detail. The anion conductivities of QPEEK-spiro-pyr and QPEEK-spiro-pip in OH^? form at 80 °C were 49.6 and 30.9 S cm^?1, respectively. The remaining proportions of hydroxide conductivity for QPEEK-spiro-pyr and QPEEK-spiro-pip membranes after immersing in 1 M NaOH at 60 °C were 81.0% and 74.7%, respectively, which were higher than that of 62.3% for QPEEK-TMA containing conventional QA groups in the phenyl side chain. Fuel cell assembled with QPEEK-spiro-pyr achieves a peak power density of 90 mW cm^?2. These results indicate the strategy of simultaneously introducing N-spirocyclic QA cations and bulky spacers can improve the performance of AEM to a certain extent. There are some other factors that influence the alkaline stability of the prepared AEMs, such as the existence of ether bonds in the main chain. However, this work still provides a valuable reference towards the molecular design of AEMs with improved performance.     

Dielectric behaviour of UV-crosslinked sulfonated poly (ether ether ketone) with methyl cellulose (SPEEK-MC) as proton exchange membrane

Proton exchange membrane materials based on sulfonated poly ether ether ketone (SPEEK) with Methyl Cellulose (MC) are developed by solution cast technique and exposed to UV radiation with Bezoin Ethyl Ether (BEE) as photoinitiator. The addition of MC into SPEEK polymer enhances the conductivity up to 8.7 × 10^?3 Scm^?1 at 30 °C temperature and 80% relative humidity. This new crosslinked hybrid membrane shows good prospect for the use as proton exchange membrane in fuel cell.     

Novel branched sulfonated poly(ether ether ketone)s membranes for direct methanol fuel cells

In this article, novel branched sulfonated poly(ether ether ketone)s (Br-SPEEK) containing various amounts of 1,3,5-tris(4-fluorobenzoyl)benzene as the branching agent have been successfully prepared. Compared with the traditional linear polymer membranes, the membranes prepared by Br-SPEEK showed improved mechanical strength, excellent dimensional stability and superior oxidative stability with similar proton conductivity. Notably, the Br-SPEEK-10 membrane began to break after 267 min in Fenton's reagent at 80 °C, which was 4 times longer than that of the L-SPEEK. Although the proton conductivity decreased with the addition of the branching agent, satisfying methanol permeability value was observed (down to 6.3 × 10⁻⁷ cm² s⁻¹), which was much lower than Nafion 117 (15.5 × 10⁻⁷ cm² s⁻¹). All the results indicated that the novel branched sulfonated poly(ether ether ketone)s membrane was potential candidate as proton conductive membranes for application in fuel cells.     

High alkaline stability and long-term durability of imidazole functionalized poly(ether ether ketone) by incorporating graphene oxide/metal-organic framework complex

The poly(ether ether ketone) (PEEK) was prepared as organic matrix. ZIF-8 and GO/ZIF-8 were used as fillers. A series of novel new anion exchange membranes (AEMs) were fabricated with imidazole functionalized PEEK and GO/ZIF-8. The structure of ZIF-8, GO/ZIF-8 and polymers are verified by ¹H NMR, FT-IR and SEM. This series of hybrid membranes showed good thermal stability, mechanical properties and alkaline stability. The ionic conductivities of hybrid membranes are in the range of 39.38 mS cm^?1–43.64 mS cm^?1 at 30 °C, 100% RH and 59.21 mS cm^?1–86.87 mS cm^?1 at 80 °C, 100% RH, respectively. Im-PEEK/GO/ZIF-8-1% which means the mass percent of GO/ZIF-8 compound in Im-PEEK polymers is 1%, showed the higher ionic conductivity of 86.87 mS cm^?1 at 80 °C and tensile strength (38.21 MPa) than that of pure membrane (59.21 mS cm^?1 at 80 °C and 19.47 MPa). After alkaline treatment (in 2 M NaOH solution at 60 °C for 400 h), the ionic conductivity of Im-PEEK/GO/ZIF-8-1% could also maintain 92.01% of the original ionic conductivity. The results show that hybrid membranes possess the ability to coordinate trade-off effect between ionic conductivity and alkaline stability of anion exchange membranes. The excellent performances make this series of hybrid membranes become good candidate for application as AEMs in fuel cells.     

In-situ molecular-level hybridization enabling high-sulfonation-degree sulfonated poly(ether ether ketone) membrane with excellent anti-swelling ability and proton conduction

Sulfonated poly(ether ether ketone) (SPEEK) membrane with high sulfonation degree (SD) is a promising substitute of Nafion as proton exchange membrane (PEM), due to the excellent proton conductivity and low cost. However, its widespread application is limited by the inferior structural stability. Here, we report the fabrication of high SD SPEEK membrane with outstanding structural stability through an in-situ molecular-level hybridization method. Concretely, the ionic nanophase of SPEEK membrane is filled with precursors, which are then in-situ converted into polymer quantum dots (PQDs) by a microwave-assisted polycondensation process. In this manner, the micro-phase separation structure of SPEEK membrane is well maintained. PQDs with abundant hydrophilic functional groups together with the inherent –SO₃H groups impart hybrid membrane highly enhanced proton conductivity of 138.2 mS cm⁻¹ at 80 °C, which is comparable to Nafion. This then offers a 116.3% enhancement in device output power. Meanwhile, PQDs act as cross-linkers via generated electrostatic interactions with SPEEK, affording hybrid membrane with SD of 94.1% an ultralow swelling ratio of 1.35% at 25 °C, about 35 times lower than control membrane. More importantly, the in-situ molecular-level hybridization method is versatile, which can also boost the performances of chitosan (CS)-based membranes.     

Branched poly(ether ether ketone) based anion exchange membrane for H2/O2 fuel cell

High-performance anion exchange membranes (AEMs) are in need for practical application of AEM fuel cells. Novel branched poly(ether ether ketone) (BPEEK) based AEMs were prepared by the copolymerization of phloroglucinol, methylhydroquinone and 4,4′-difluorobenzophenone and following functionalization. The effects of the branched polymer structures and functional groups on the membrane's properties were investigated. The swelling ratios of all the membranes were kept below 15% at room temperature and had good dimensional stability at elevated temperatures. The branching degree has almost no effect on the dimensional change, but plays a great role in tuning the nanophase separation structure. The cyclic ammonium functionalized membrane showed a lower conductivity but a much better stability than imidazolium one. The BPEEK-3-Pip-53 membrane with the branching degree of 3% and piperidine functionalization degree of 53% showed the best performances. The ionic conductivity was 43 mS cm⁻¹ at 60 °C. The ionic conductivity in 1 M KOH at 60 °C after 336 h was 75% of its initial value (25% loss of conductivity), and the IEC was 83% of its initial value (17% loss of IEC), suggesting good alkaline stability. The peak energy density (60 °C) of the single H₂/O₂ fuel cell with BPEEK-3-Pip-53 membrane reached 133 mW cm⁻² at 260 mA cm⁻².     

A novel strategy for constructing a highly conductive and swelling-resistant semi-flexible aromatic polymer based anion exchange membranes

A novel strategy was proposed to construct a bicontinuous hydrophilic/hydrophobic micro-phase separation structure which is crucial for high hydroxide conductivity and good dimensional stability anion exchange membranes (AEMs). A semi-flexible poly (aryl ether sulfone) containing a flexible aliphatic chain in the polymer backbone with imidazolium cationic group was synthesized by the polycondensation of bis(4-fluorophenyl) sulfone and the self-synthesized 4,4′-[butane-1,4-diylbis(oxy)] diphenol followed by a two-step functionalization. The corresponding membranes were prepared by solution casting. More continuous hydroxide conducting channels were formed in the semi-flexible polymer membranes compared with the rigid based ones as demonstrated by TEM. As a result, given the same swelling ratio, hydroxide conductivity of the semi-flexible polymer membrane was about 2-fold higher than the one of the rigid polymer based membrane (e.g., 45 vs. 22 mS cm^?1 with the same swelling ratio of 24% at 20 °C). The highest achieved conductivity for the semi-flexible polymer membranes at 60 °C was 93 mS cm^?1, which was much higher those of other random poly (aryl ether sulfone) based imidazolium AEMs (27–81 mS cm^?1). The single cell employing the semi-flexible polymer membrane exhibited a maximum power density of 125 mW cm^?2 which was also higher than those for other random poly (aryl ether sulfone) based imidazolium AEMs (16–105.2 mW cm^?2).     

An effective strategy to enhance the performance of the proton exchange membranes based on sulfonated poly(ether ether ketone)s

We report an effective and facile approach to enhance the dimensional and chemical stability of sulfonated poly(ether ether ketone) (SPEEK) type proton exchange membranes through simple polymer blending for fuel cell applications, using commercial available materials. The polymeric blends with sulfonated poly(aryl ether sulfone)s (SPAES) were simply fabricated by a three-component system, which contained SPEEK (10–50 wt%, 1.83 mmol/g), and SPAES-40 (1.72 mmol/g)/SPAES-50 (2.04 mmol/g) at 1:1 in weight. The SPAES-40 was selected for mechanical and dimensional stability reinforcing, while SPAES-50 for the good polymer compatibility. The obtained SPEEK/SPAES blend membranes showed depressed water uptake, better dimensional and oxidative stability, together with higher proton conductivity beyond 70 °C than the pristine SPEEK membrane. The apparent improvements in membrane properties were associated with the homogeneous dispersion of SPEEK and both SPAES copolymers inside the membranes as well as the rearrangements of the polymeric chains. The SPEEK content should be properly controlled in the range of 10–40% (B10 to B40). In a H₂/O₂ fuel cell test, B30 showed a maximum power density of 700 mW/cm², which was 1.6 times as high as that of B40 at 80 °C under 100% RH. The further cross-linking treatment produced more ductile and enduring blend membranes, indicating an appreciable prospective for fuel cell applications.     

Influence of mesoporous phosphotungstic acid on the physicochemical properties and performance of sulfonated poly ether ether ketone in proton exchange membrane fuel cell

This study demonstrates the successful development of hybrid mesoporous siliceous phosphotungstic acid (mPTA-Si) and sulfonated poly ether ether ketone (SPEEK) as a proton exchange membrane with a high performance in hydrogen proton exchange membrane fuel cells (PEMFC). SPEEK acts as a polymeric membrane matrix and mPTA-Si acts as the mechanical reinforcer and proton conducting enhancer. Interestingly, incorporating mPTA-Si did not affect the morphological aspect of SPEEK as dense membrane upon loading the amount of mPTA-Si up to 2.5 wt%. The water uptake reduced to 14% from 21.5% when mPTA-Si content increases from 0.5 to 2.5 wt% respectively. Meanwhile, the proton conductivity increased to 0.01 Scm^?1 with 1.0 wt% mPTA-Si and maximum power density of 180.87 mWcm^?2 which is 200% improvement as compared to pristine SPEEK membrane. The systematic study of hybrid SP-mPTA-Si membrane proved a substantial enhancement in the performance together with further improvement on physicochemical properties of parent SPEEK membrane desirable for the PEMFC application.     

Facile synthesis of poly (arylene ether ketone)s containing flexible sulfoalkyl groups with enhanced oxidative stability for DMFCs

After tethering sodium 2-mercaptoethanesulfonate (MTS) to the bromomethylated poly(arylene ether ketone) precursor, a novel clustered sulfonated poly(arylene ether ketone) containing flexible sulfoalkyl groups (MTSPAEK) was prepared and used as polymer electrolyte membrane for application in DMFCs. The chemical structure and the degree of grafting of MTSPAEK copolymers were identified by ¹H NMR spectra. The resulted MTSPAEK copolymers exhibited excellent thermal stability (T_d5% > 259 °C) and good mechanical properties (tensile strength at break > 52 MPa). Compared to conventional sulfonated aromatic hydrocarbon polymers, MTSPAEK membranes displayed enhanced oxidative stability in Fenton's reagent owing to the elimination of free radicals by the sulfide groups located on the polymer side chains. Especially, MTSPAEK-2.10 with the highest content of flexible sulfoalkyl groups exhibited a highest proton conductivity of 0.181 S cm⁻¹ at 80 °C. It could be attributed to the obvious hydrophilic/hydrophobic phase-separated structure within the membrane, which was confirmed by AFM images. Moreover, MTSPAEK-2.10 membrane performed a peak power density of 70 mW cm⁻² in DMFC when feeding with 2 M methanol at 80 °C, which was comparable to the performance of recast Nafion as reported. Therefore, the combination of good thermal stability and mechanical properties, good oxidative stability, and good methanol barrier performance of MTSPAEK membranes indicated that they have potential to be alternative materials for PEMs in DMFCs.     

Sulfonated poly(ether ether ketone) membranes with sulfonated graphene oxide fillers for direct methanol fuel cells

Sulfonated organosilane functionalized graphene oxides (SSi-GO) synthesized through the grafting of graphene oxide (GO) with 3-mercaptopropyl trimethoxysilane and subsequent oxidation have been used as a filler in sulfonated poly(ether ether ketone) (SPEEK) membranes. The incorporation of SSi-GOs greatly increases the ion-exchange capacity (IEC), water uptake, and proton conductivity of the membrane. With well-controlled contents of SSi-GOs, the composite membranes exhibit higher proton conductivity and lower methanol permeability than Nafion^® 112 and Nafion^® 115, making them particularly attractive as proton exchange membranes (PEMs) for direct methanol fuel cells (DMFC). The composite membrane with optimal SSi-GOs content exhibit over 38 and 17% higher power densities, respectively, than Nafion^® 112 and Nafion^® 115 membranes in DMFCs, offering the possibilities to reduce the DMFC membrane cost significantly while keeping high-performance.     

A facile approach to prepare self-cross-linkable sulfonated poly(ether ether ketone) membranes for direct methanol fuel cells

Sulfonated poly(ether ether ketone) containing hydroxyl groups (SPEEK-OH) has been prepared for use as a proton exchange membrane (PEM) by reducing the carbonyl groups on the main chain of the polymers. With the goal of reducing water uptake and methanol permeability, a facile thermal-cross-linking process is used to obtain the cross-linked membranes. The properties of the cross-linked membranes with different cross-linked density are measured and compared with the pristine membrane. Notably, SPEEK-4 with the highest cross-linked density shows a water uptake of 39% and a methanol permeability of 2.52 × 10⁻⁷ cm² s⁻¹, which are much lower than those of the pristine membrane (63.2% and 5.37 × 10⁻⁷ cm² s⁻¹, respectively). These results indicate that this simple approach is very effective to prepare cross-linked proton exchange membranes for reducing water uptake and methanol permeability.     

Sulfonated poly(ether ether ketone)/poly(ether sulfone) composite membranes as an alternative proton exchange membrane in microbial fuel cells

Custom-made proton exchange membranes (PEM) are synthesized by incorporating sulfonated poly(ether ether ketone) (SPEEK) in poly(ether sulfone) (PES) for electricity generation in microbial fuel cells (MFCs). The composite PES/SPEEK membranes at various composition of SPEEK are prepared by the phase inversion method. The membranes are characterized by measuring roughness, proton conductivity, oxygen diffusion, water crossover and electrochemical impedance. The conductivity of hydrophobic PES membrane increases when a small amount (3–5%) of hydrophilic SPEEK is added. The electrochemical impedance spectra shows that the conductivity and capacitance of PES/SPEEK composite membranes during MFC operation are reduced from 6.15 × 10⁻⁷ to 6.93 × 10⁻⁵ (3197 Ω–162 Ω) and from 3.00 × 10⁻⁷ to 1.56 × 10⁻³ F, respectively when 5% of SPEEK added into PES membrane. The PES/SPEEK 5% membrane has the highest performance compared to other membranes with a maximum power density of 170 mW m⁻² at the maximum current density of 340 mA m⁻². However, the interfacial reaction between the membrane and the cathode with Pt catalyst indicates moderate reaction efficiency compared to other membranes. The COD removal efficiency of MFCs with composite membrane PES/SPEEK 5% is nearly 26-fold and 2-fold higher than that of MFCs with Nafion 112 and Nafion 117 membranes respectively. The results suggest that the PES/SPEEK composite membrane is a promising alternative to the costly perfluorosulfonate membranes presently used as separators in MFC systems.     

HT-PEMs based on nitrogen-heterocycle decorated poly (arylene ether ketone) with enhanced proton conductivity and excellent stability

The proton transport can be enhanced by properly controlling the chemical structure of side chains. In this work, polyelectrolytes supported on poly (arylene ether ketone), decorated with four kinds of nitrogen-heterocycles, were prepared as alternative materials for high-temperature proton exchange membrane (HT-PEM) applications. Particularly, the “prominent basic” alongside backbone makes positive imidazole group more effective than other three to promote phosphoric acid doping, enhance proton conductivity and avoid phosphoric acid leakage. The obtained BrPAEK-MeIm1.6 membranes (1.6 imidazole/unit), with PA doping level of 19.2 in 1 h acid absorption process, exhibited the conductivity of 0.091 S cm^?1 at 170 °C. Under harsh experimental conditions, membrane with higher imidazole exhibited relatively higher phosphoric acid retention ability (27% enhancement). The stability of proton conductivity has also been demonstrated, which indicates that the PA/BrPAEK-MeIm1.6 come to an equilibrium state with 77.7% of initial conductivity after 5 h. Then, there is almost negligible conductivity loss within 30 h. These results provide a basic understanding of nitrogen-heterocyclic addition and PA absorption and open up avenues for further research in this area.