Solution‐blown SPEEK/POSS nanofiber–nafion hybrid composite membranes for direct methanol fuel cells

This study aims to develop novel hybrid composite membranes (NHMs) by impregnating Nafion solution into the porous sulfonated poly(ether ether ketone)/polyhedral oligomeric silsesquioxanes (SPEEK/POSS) nanofibers (NFs). The composite membrane was prepared by solution blowing of a mixture of SPEEK/POSS solution. The characteristics of the SPEEK/POSS NFs and the NHMs, including morphology, thermal stability, and performance of membrane as PEMs, were investigated. The performance of NHMs was compared with that of Nafion117 and SPEEK/Nafion composite membranes. Results showed that the introduction of POSS improved the proton conductivity, water swelling, and methanol permeability of membranes. A maximum proton conductivity of 0.163 S cm^?1 was obtained when the POSS content was 6 wt % at 80°C, which was higher than that of Nafion117 and SPEEK/Nafion. NHMs could be used as proton exchange membranes (PEMs) for fuel cell applications. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42843.     

Nafion‐115/aromatic poly(etherimide) with isopropylidene groups/imidazole membranes for polymer fuel cells

Proton exchange membrane fuel cells (PEMFCs) with Pt/C gas diffusion electrodes and graphite single‐serpentine monopolar plates were constructed based on an aromatic poly(etherimide) with isopropylidene groups (PI)/imidazole (Im) and a popular Nafion‐115 matrix. The electrochemical properties of PEMFCs were tested at 25 and 60°C. The maximum power density of 171 mW/cm² and the maximum current density of 484 mA/cm² were detected for Nafion‐115/PI membrane. For both constructed PEMFCs the efficiency at 0.6 V was found about 41%. Immersion of Nafion‐115 in PI or PI/Im increased the thermal stability and mechanical properties of membranes. Thermal, mechanical properties and morphology of membranes were characterized by TGA, and AFM techniques including force spectroscopy. Interactions between the components in composite membranes were established by FT‐IR. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42436.     

Studies on a novel anion‐exchange membrane based on chitosan and ionized organic compounds with multiwalled carbon nanotubes for alkaline fuel cells

In this work, a novel hydroxyl‐anion‐conducting membrane composed of chitosan (CTS), an ionized organic compound ([QAIM]OH), and hydroxylated multiwalled carbon nanotubes (MWCNTs‐OH) has been fabricated through a blending‐casting method assisted by a glutaraldehyde (GA) crosslinking process that can improve the mechanical properties of the membrane effectively. Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy revealed that [QAIM]OH and MWCNTs‐OH were successfully introduced into the CTS matrix. A chemical crosslinking reaction between CTS and GA could be confirmed by FTIR, X‐ray photoelectron spectroscopy, and contact angle tests. By tuning the mass fraction of [QAIM]OH and MWCNTs‐OH in the membrane, the maximum OH^? conductivity (5.66 × 10^?3 S cm^?1 at room temperature) could be achieved for the composition CTS:[QAIM]OH (1:0.75 in mass) blend doped with 3% MWCNTs‐OH. At a current density of 59.9 mA cm^?2, a membrane electrode assembly fabricated with the CTS/[QAIM]OH/ MWCNTs‐OH membrane (1:0.5/3%) achieved a power density of 31.6 mW cm^?2 in a H₂/O₂ system at room temperature. Under the condition of intermediate temperature (100–140 °C) without water, the conductivities of the membranes increased with increasing temperature and the amount of [QAIM]OH, which acted as an ionic liquid in the membrane, indicating that the ionic transport behaviors could still be occurring. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46323.     

Enhanced mechanical flexibility and performance of sodium alginate polymer electrolyte bio‐membrane for application in direct methanol fuel cell

A new membrane was synthesized containing pure alginate, crosslinking agent (CaCl₂), and plasticizer (glycerol). Characterization studies of the membrane were applied to determine the characteristics and morphology using field emission scanning electron microscope, EDX, FTIR, XRD, and atomic force microscopy analysis. The half‐cell performance test of the membrane was verified by several tests, including proton conductivity and methanol permeability. The best membrane had high proton conductivity (10.1 × 10^?3 S cm^?1) and very low methanol permeability (1.984 × 10^?7 cm² s^?1), which consequently resulted in very high selectivity (5.0907 × 10⁴ Ss cm^?3). Glycerol had a positive modification and good influence on the alginate characteristics. Furthermore, the poor mechanical properties of the alginate biopolymer were enhanced by calcium chloride and glycerol inside the polymer. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46666.     

Biocomposite proton‐exchange membrane electrolytes for direct methanol fuel cells

Poly(vinyl alcohol) (PVA)‐amino acid (AA) biocomposite membranes are prepared by blending PVA with AAs such as glycine, lysine (LY), and phenyl alanine followed by in situ crosslinking with citric acid (CA) and explored as a new class of biocomposite membrane electrolytes for direct methanol fuel cells (DMFCs). CA crosslinks with PVA through esterification offers adequate chemical, thermal, and morphological stability thereby produces methanol‐obstructing close‐packed polymeric network. These biocomposite membranes are characterized in terms of mechanical, thermal, sorption, and proton‐conducting properties. Hydrophilic nature of AA zwitterions significantly facilitates proton conduction and CA crosslinking mitigates methanol crossover through establishing appropriate balance between hydrophilic/hydrophobic domains. The rational design of membrane microstructure with proper arrangement of hydrophobic/hydrophilic domains is a key to enhance electrochemical selectivity of PVA‐AA/CA biocomposite membranes. Biocomposite membrane comprising LY exhibits nearly threefold higher electrochemical selectivity in relation to PVA/CA blend membrane. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43514.     

Quaternized poly(phenylene oxide) anion exchange membrane for alkaline direct methanol fuel cells in KOH‐free media

A series of anion exchange membrane (AEM) electrolytes with quaternary ammonium moiety are fabricated from poly (phenylene oxide) for its application in alkaline direct methanol fuel cells (ADMFCs). In the first step, poly(phenylene oxide) (PPO) is successfully chloromethylated by substituting chloromethyl groups in the aryl position of polymer. In the second step, the chloromethylated PPO (CPPO) is further homogeneously quaternized and ion‐exchanged to form an AEM. From the second step, series of AEMs are prepared by changing the mole ratio of amine in relation to CPPO. The presence of quaternary ammonium group in the membrane was confirmed by elemental analysis. The fabricated membranes are subjected to cell polarization studies in ADMFCs, wherein quaternized poly(2,6‐dimethyl‐1,4‐phenylene oxide) (CPPO:amine of 1:8) membrane exhibits higher peak power density of 3.5 mW cm^?2 when compared with the other ratios of CPPO:amine in the absence of KOH solution. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43693.     

Highly selective sulfonated poly(vinylidene fluoride‐co‐hexafluoropropylene)/poly(ether sulfone) blend proton exchange membranes for direct methanol fuel cells

Proton exchange membranes (PEMs) based on blends of poly(ether sulfone) (PES) and sulfonated poly(vinylidene fluoride‐co‐hexafluoropropylene) (sPVdF‐co‐HFP) were prepared successfully. Fabricated blend membranes showed favorable PEM characteristics such as reduced methanol permeability, high selectivity, and improved mechanical integrity. Additionally, these membranes afford comparable proton conductivity, good oxidative stability, moderate ion exchange capacity, and reasonable water uptake. To appraise PEM performance, blend membranes were characterized using techniques such as Fourier transform infrared spectroscopy, AC impedance spectroscopy; atomic force microscopy, and thermogravimetry. Addition of hydrophobic PES confines the swelling of the PEM and increases the ultimate tensile strength of the membrane. Proton conductivities of the blend membranes are about 10^?3 S cm^?1. Methanol permeability of 1.22 × 10^?7cm² s^?1 exhibited by the sPVdF‐co‐HFP/PES10 blend membrane is much lower than that of Nafion‐117. AFM studies divulged that the sPVdF‐co‐HFP/PES blend membranes have nodule like structure, which confirms the presence of hydrophilic domain. The observed results demonstrated that the sPVdF‐co‐HFP/PES blend membranes have promise for possible usage as a PEM in direct methanol fuel cells. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43907.     

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.     

Preparation and characterization of novel chitosan‐based mixed matrix membranes resistant in alkaline media

In this work, mixed matrix membranes (MMMs) based on chitosan (CS) and different fillers (room temperature ionic liquid [emim][OAc] (IL), metallic Sn powder, layered titanosilicate AM‐4 and layered stannosilicate UZAR‐S3) were prepared by solution casting. The room temperature electrical conductivity and electrochemical response in strong alkaline medium were measured by electrochemical impedance spectroscopy and cyclic voltammetry (CV). The ionic conductivity of pure CS membranes was enhanced, from 0.070 to 0.126 mS cm^?1, for the pristine CS and Sn/CS membranes, respectively, as a function of the hydrophilic nature of the membrane and the coordination state of Sn. This hydrophilic and charge nature was corroborated by water uptake measurements, where only the introduction of IL in the CS membrane led to a water uptake of 3.96 wt %, 20 or 30 times lower than the other membranes. Good thermal and chemical stability in alkaline media were observed by thermogravimetric analyses and X‐ray photoelectron spectroscopy analyses, respectively, and good interaction between CS and the fillers observed by X‐ray diffraction, scanning electron microscopy and CV. Thus, thin CS‐based MMMs (40–139 µm), resistant in high alkaline media, show higher conductivity than pure CS membranes, especially those fillers containing tin, and although the electrochemical performance is lower than commercially available anion‐exchange membranes they have potential in pervaporation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42240.     

Quaternized poly(2.6 dimethyl‐1.4 phenylene oxide)/polysulfone blend composite membrane doped with ZnO‐nanoparticles for alkaline fuel cells

A series of quaternized poly(2.6 dimethyl‐1.4 phenylene oxide)/polysulfone (QPPO/PSF) blend anion exchange membrane (AEM) were successfully fabricated and characterized for alkaline fuel cell application. Zinc oxide (ZnO) nanoparticles were introduced in the polymer matrix to enhance the intrinsic properties of the AEM. To confirm successful fabrication, Fourier‐transform infrared spectroscopy and nuclear magnetic resonance (¹H‐NMR) were used. The membrane properties were enhanced by the addition of ZnO nanoparticles. The addition of ZnO nanoparticles resulted to a higher ion exchange capacity (IEC) of 3.72 mmol g^?1, increase of ion conductivity (IC) up to 52.34 mS cm^?1 at 80 °C, enhancement of water uptake, and reduced methanol permeability. The QPPO/PSF/2% ZnO composite retained over 80% of its initial IC at room temperature and also retained over 50% of its initial IC at 80 °C when evaluated for alkaline stability. The maximum power output reached for the membrane electrode assembly constructed with QPPO/PSF/2%ZnO was 69 mW cm^?2 at room temperature, which is about three times more than the parent QPPO membrane. The above results indicate that QPPO/PSF/ZnO is a good candidate as an AEM for fuel cell application. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45959.     

Montmorillonite‐reinforced sulfonated poly(phthalazinone ether sulfone ketone) nanocomposite proton exchange membranes for direct methanol fuel cells

To produce a composite membrane with high conductivity and low permeability, SPPESK with a degree of sulfonation of 101% was carefully selected for the preparation of montmorillonite (MMT)‐reinforced SPPESK using solution intercalation. The fundamental characteristics such as water uptake, swelling ratio, proton conductivity, methanol permeability, and mechanical properties of the composite membranes were studied. Water uptake is improved when organic MMT (OMMT) loading increase. The composite membranes with CTAB‐MMT loading of 4–0.5% show 0.143–0.150 S cm^?1 proton conductivity at 80°C, which approaches the value of Nafion112. In addition, methanol permeability was decreased to 6.29 × 10^?8 cm² s^?1 by the addition of 6 wt % OMMT. As a result, the SPPESK‐MMT composite membrane is a good candidate for use in direct methanol fuel cells. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39852.     

Novel membranes based on poly(5‐(methacrylamido)tetrazole) and sulfonated polysulfone for proton exchange membrane fuel cells

Proton‐exchange membrane fuel cells (PEMFC)s are increasingly regarded as promising environmentally benign power sources. Heterocyclic molecules are commonly used in the proton conducting membranes as dopant or polymer side group due to their high proton transfer ability. In this study, 5‐(methacrylamido)tetrazole monomer, prepared by the reaction of methacryloyl chloride with 5‐aminotetrazole, was polymerized via conventional free radical mechanism to achieve poly(5‐(methacrylamido)tetrazole) homopolymer. Novel composite membranes, SPSU‐PMTetX, were successfully produced by incorporating sulfonated polysulfone (SPSU) into poly(5‐(methacrylamido)tetrazole) (PMTet). The sulfonation of polysulfone was performed with trimethylsilyl chlorosulfonate and high degree of sulfonation (140%) was obtained. The homopolymers and composite membranes have been characterized by NMR, FTIR, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). ¹H‐NMR and FTIR confirmed the sulfonation of PSU and the ionic interaction between sulfonic acid and poly(5‐(methacrylamido)tetrazole) units. TGA showed that the polymer electrolyte membranes are thermally stable up to ～190°C. Scanning electron microscopy analysis indicated the homogeneity of the membranes. This result was also supported by the appearance of a single T_g in the DSC curves of the blends. Water uptake and proton conductivity measurements were, as well, carried out. Methanol permeability measurements showed that the composite membranes have similar methanol permeability values with Nafion 112. The maximum proton conductivity of anhydrous SPSU‐PMTet0.5 at 150°C was determined as 2.2 × 10^?6 S cm^?1 while in humidified conditions at 20°C a value of 6 × 10^?3 S cm^?1 was found for SPSU‐PMTet2. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40107.     

Nanostructured membrane electrode assemblies from layer‐by‐layer composite/catalyst containing membranes and their fuel cell performances

In this study, two approaches are compared to develop nanostructured membrane electrode assemblies (MEA) using layer‐by‐layer (lbl) technique. The first is based on the direct deposition of polyallylamine hydrochloride (PAH) and sulfonated polyaniline (sPAni) on Nafion support to prepare lbl composite membrane. In the second approach, sPAni is coated on the support in the presence of platinum (Pt) salt, Nafion solution and Vulcan for obtaining catalyst containing membranes (CCMs). SEM and UV–vis analysis show that the multilayers are deposited on both sides of Nafion successfully. Although H₂/O₂ single cell performances of acid doped lbl composite membrane based MEA are found to be at the range of 126 and 160 mW cm^?2 depending on the number of deposited layers, the cell performance of MEA obtained from catalyst containing lbl self‐assembled thin membrane (PAH/sPAni‐H⁺)_10‐Pt is found to be 360 mW cm^?2 with a Pt utilization of 720 mW mgPt^?1. This performance is 82% higher as compared to original Nafion^®117 based MEA (198 mW cm^?2). From the cell performance evaluations for different structured MEAs, it is mainly found out that the use of lbl CCMs instead of composite membranes and fabrication of thinner electrolytes result in a higher H₂/O₂ cell activity due to significant reduction in ohmic resistivity. Also, it is observed that the use of sPAni slightly improves the cell performance due to an increased probability of the triple phase contact and it can lead to superior physicochemical properties such as conductivity and thermal stability. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40314.     

Basicity‐based screening of aniline derivative for composite proton exchange membranes

The aim of this study was to find a suitable aniline derivative to develop composite sulfonated poly(ether ether ketone) (SPEEK) membranes and detail evaluation of their physico‐ and electrochemical properties. The hypothesis was high basicity of the aniline derivatives could form good composite membranes with better physicochemical and electrochemical properties. To assess the basicity we measured the zeta potentials of the polymers and correlated them with ion‐exchange capacities, water uptakes, transport numbers, water‐diffusion coefficients, conductivities, and methanol permeabilities. The obtained values of zeta potentials at pH 7 were 6.52, ?14.66, ?25.17, and ?28 for SPEEK/polynaphthalene (PNAPH), SPEEK/polyanisidine (PANIS), SPEEK/polyaniline (PANI), and SPEEK/polyxylindine (PXYL), respectively supports the hypothesis and strongly suggests polyaniline derivative's basicity‐dependent properties. Of the four derivatives (PNAPH, PANIS, PANI, and PXYL), the SPEEK/PXYL composite membrane had the lowest methanol permeability of 1 × 10^?4 cm²/s and highest proton conductivity of 161 mS/cm. These values are far better than the neat SPEEK and SPEEK/PANI composite. The suitability of SPEEK/PXYL can be explained by the high basicity of the PXYL composite membrane, which leads to the formation of effective Debye spheres, meaning that the ionic complex can interact with surrounding hydronium ions and form hydrophilic channels resulting in high proton conductivity and low methanol permeability. These results suggest that SPEEK/PXYL is a highly suitable membrane for methanol fuel cells or other electrochemical applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43978.     

Sulfur/PAN/acetylene black composite prepared by a solution processing technique for lithium–sulfur batteries

A sulfur/poly(acrylonitrile)–PAN/acetylene black–AB composite, comprising sulfur and PAN encapsulated in the pores of AB was prepared by a solution‐based technique with dimethyl sulfoxide as the solvent. The composite was characterized by TGA, X‐ray diffraction, FTIR, Raman, SEM, TEM, and BET studies. The composite exhibited a high discharge capacity of 1330 mAh/g in the first cycle. The AB additive plays multiple roles in the composite, acting as a conducting matrix for electron transport and as a porous framework that adsorbs and retains electrolyte. The presence of PAN along with the porous carbon matrix in the composite provides the necessary resilience to absorb strains due to volume expansion during cycling. The observed improved performance of the composite is primarily attributed to the small size and homogeneous distribution of sulfur in the composite. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46598.     

Zinc ion conducting blended polymer electrolytes based on room temperature ionic liquid and ceramic filler

Zinc ion conducting nanocomposite gel polymer electrolytes (NCGPEs) comprising of poly(vinyl chloride) (PVC)/poly(ethyl methacrylate) (PEMA) blend, zinc triflate [Zn(OTf)₂] salt, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIMTFSI) ionic liquid (IL) and fumed silica (SiO₂) viz. [PVC/PEMA–Zn(OTf)₂–EMIMTFSI–SiO₂] exhibited the highest ionic conductivity value of 6.71 × 10⁻⁴ Scm⁻¹ at room temperature. The ion–filler–polymer interactions and probable conformational changes observed in the structure of the gel composites due to the entrapment of IL and dispersion of nano-sized SiO₂ were confirmed from X-ray diffraction (XRD) and Attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy. Scanning electron microscopic (SEM) images of NCGPEs demonstrated uniform surface with abundant interconnected micropores. The cationic transport number of NCGPE samples has been found to be appreciably enhanced up to a maximum of 0.69 thus demonstrating a considerable improvement in Zn²⁺ ion conductivity. The NCGPE film possesses an electrochemical stability window up to 5.07 V (vs. Zn/Zn²⁺) and ensures feasible zinc stripping/plating in the redox process. The addition of SiO₂ into the gel polymer electrolyte system has effectively reduced the glass-transition temperature (T_g) of the NCGPE films and also accomplished improved thermal stability up to approximately 180 °C which were ascertained from Differential scanning calorimetry (DSC) and Thermogravimetric (TG) results. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47654.     

Resin-silica composite nanoparticle grafted polyethylene membranes for lithium ion batteries

To avoid the peeling-off of ceramic nanoparticles (NPs) from polyolefin membranes usually occurred in commercially available ceramic NPs coated polyolefin separators for lithium batteries, we propose a simple one-pot in-situ reaction method to modify commercial polyethylene (PE) separators by surface grafting 3-Aminophenol/formaldehyde (AF)/silica (SiO₂) composite NPs. The AF/SiO₂ composite NPs form self-supporting connected pores on the modified layer of the separator surface, which ensures the transportation of Li⁺. Moreover, the PE@AF/SiO₂ separators has higher electrolyte wettability and compatibility than neat PE separators attributed to the plentiful polar functional groups in the AF/SiO₂ layer and AF/SiO₂ composite NPs, resulting in higher lithium ion transference number (= 0.62) and ionic conductivity (σ = 0.722 mS cm⁻¹). More importantly, the discharge capacity, capacity retention rate and coulombic efficiency (136.2 mA h g⁻¹, 87.9% and 99%, respectively) after 200 cycles of Li|NMC half batteries with PE@AF/SiO₂ separators, are all more excellent than that with the pure PE separator (125 mA h g⁻¹, 83.1% and 85%, respectively). Our results show that the PE@AF/SiO₂ separators obtained by this modification method have higher electrochemical stability in the lithium battery system.     

Improved specific capacity of sulfur/starch‐based activated carbon spheres composites by polyaniline‐based carbon encapsulation strategy

Lithium‐sulfur battery is one of the most promising electrochemical energy storage systems because of its high theoretical specific capacity and energy density. When carbon materials are used for immobilizing sulfur, the technical challenge is designing their framework to relieve the shuttle effect of polysulfides intermediates and the volume change of sulfur, and to improve the conductivity of sulfur. Herein, polyaniline‐based carbon (PANI‐C) coated corn starch‐based activated carbon spheres (ACS@PANI‐C) was prepared and used as hosts of sulfur, which can effectively combine the advantages of physical entrapment and chemical binding interactions of sulfur species. The results of electrochemical performance test indicate that S/ACS@PANI‐C composites exhibit much better electrochemical performance than S/ACS composites. Its reversible capacities at 320, 480, 800 and 1600 mA g^?1 are 687, 582, 504 and 393 mAh g^?1, respectively. The improved electrochemical performance can be attributed to the PANI‐C which can also act as a flexible cushion to accommodate volume changes of sulfur cathode as well as a barrier to trap soluble polysulfide intermediates during the charge–discharge process. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46544.     

Aliphatic SPI charge‐transfer complex hybrid films for high temperature polymer electrolyte membrane fuel cells

A new method to synthesize polymer electrolyte membranes based on charge‐transfer (CT) complexes for high temperature fuel cells is investigated. Aliphatic sulfonated polyimide (SPI) CT complex hybrid films are prepared. Aliphatic units are introduced into the SPI main chain to increase the elasticity compared with aromatic SPI films. Electron‐donating compounds are included to form a CT complex, resulting in improved control over mechanical strength, water uptake, and thermal stability. The resulting thermal properties of the SPI CT films are sufficient to operate at elevated temperature (up to 120 °C), and the proton conductivity is comparable to that of Nafion 115. These films are thus promising alternative membranes for high temperature polymer electrolyte fuel cell applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46087.     

Electrospinning preparation of a graphene oxide nanohybrid proton‐exchange membrane for fuel cells

Proton‐exchange membrane (PEM) is a core component of fuel cells that provides a channel for proton migration and transport. Prevailing PEMs fabricated using well‐established casting techniques have several limitations such as low proton conductivity, high fuel permeability, and poor stability. To overcome these shortcomings, this article introduces a graphene oxide (GO)‐based nanohybrid Nafion nanofiber membrane prepared using a facile electrospinning technique. On the one hand, electrospinning nanofibers provide efficient transport paths for protons, which tremendously enhance the proton conductivity. On the other hand, GO doping in PEM improves the self‐humidification, stabilities (mechanical, thermal, and chemical), and proton conductivity and reduces the fuel permeability. In this research, nanofiber membranes were obtained from Nafion solutions containing 0, 0.1, and 0.2 wt % GO via electrospinning. The morphology, structure, mechanical properties, proton conductivity, water uptake, and swelling properties of the membranes were studied. The results demonstrated that the comprehensive performance of PEM was significantly improved. The new findings may promote the wide application of PEM fuel cells. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46443.