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Enhancing Physicochemical Properties and Single Cell Performance of Sulfonated Poly(arylene ether) (SPAE) Membrane by Incorporation of Phosphotungstic Acid and Graphene Oxide: A Potential Electrolyte for Proton Exchange Membrane Fuel Cells.

ABSTRACT: The development of potential and novel proton exchange membranes (PEMs) is imperative for the further commercialization of PEM fuel cells (PEMFCs). In this work, phosphotungstic acid (PWA) and graphene oxide (GO) were integrated into sulfonated poly(arylene ether) (SPAE) through a solution casting approach to create a potential composite membrane for PEMFC applications. Thermal stability of membranes was observed using thermogravimetric analysis (TGA), and the SPAE/GO/PWA membranes exhibited high thermal stability compared to pristine SPAE membranes, owing to the interaction between SPAEK, GO, and PWA. By using a scanning electron microscope (SEM) and atomic force microscope (AFM), we observed that GO and PWA were evenly distributed throughout the SPAE matrix. The SPAE/GO/PWA composite membrane comprising 0.7 wt% GO and 36 wt% PWA exhibited a maximum proton conductivity of 186.3 mS cm^-1 at 90 °C under 100% relative humidity (RH). As a result, SPAE/GO/PWA composite membrane exhibited 193.3 mW cm^-2 of the maximum power density at 70 °C under 100% RH in PEMFCs.

SUBMITTER: Ryu SK

PROVIDER: S-EPMC8309513 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Sulfonated Poly(Arylene Ether Sulfone) and Perfluorosulfonic Acid Composite Membranes Containing Perfluoropolyether Grafted Graphene Oxide for Polymer Electrolyte Membrane Fuel Cell Applications.

Project description:Sulfonated poly(arylene ether sulfone) (SPAES) and perfluorosulfonic acid (PFSA) composite membranes were prepared using perfluoropolyether grafted graphene oxide (PFPE-GO) as a reinforcing filler for polymer electrolyte membrane fuel cell (PEMFC) applications. PFPE-GO was obtained by grafting poly(hexafluoropropylene oxide) having a carboxylic acid end group onto the surface of GO via ring opening reaction between the carboxylic acid group in poly(hexafluoropropylene oxide) and the epoxide groups in GO, using 4-dimethylaminopyridine as a base catalyst. Both SPAES and PFSA composite membranes containing PFPE-GO showed much improved mechanical strength and dimensional stability, compared to each linear SPAES and PFSA membrane, respectively. The enhanced mechanical strength and dimensional stability of composite membranes can be ascribed to the homogeneous dispersion of rigid conjugated carbon units in GO through the increased interfacial interactions between PFPE-GO and SPAES/PFSA matrices.

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Project description:Sulfonated poly(arylene perfluoroalkylene)s containing a sulfone-bonded ladder structure (SPAF-P-Lad) were synthesized by treating the precursor SPAF-P polymers with oleum as a novel proton exchange membrane for fuel cells. SPAF-P-Lad membranes had excellent solubility in polar organic solvents and high molecular weight (M n = 145.4-162.9 kDa, M w = 356.9-399.1 kDa) to provide bendable membranes with ion exchange capacity (IEC) ranging from 1.76 to 2.01 meq. g-1. SPAF-P-Lad membranes possessed higher proton conductivity than that of the precursor SPAF-P membranes because of the stronger water affinity. Compared with SPAF-P membranes (T g: 72-90 °C, Young's modulus: 0.08-0.42 GPa; yield stress: 5.7-15.1 MPa), SPAF-P-Lad membranes showed better mechanical stability to humidity and temperature and improved tensile properties (Young's modulus: 0.51-0.59 GPa; yield stress: 23.9-29.6 MPa). The selected membrane, SPAF-mP-Lad, exhibited improved fuel cell performance, in particular, under low humidity with air; the current density at 0.5 V was 0.56 A cm-2, while that for SPAF-pP was 0.46 A cm-2. The SPAF-mP-Lad membrane endured an open circuit voltage hold test for 1000 h with average decay of as small as 70 μV h-1. A series of post-analyses including current-voltage characteristics, molecular structure, molecular weight, and IEC suggested very minor degradation of the membrane under the accelerated testing conditions.

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Project description:We designed and synthesized a series of sulfonated poly(arylene ether sulfone) (SPES) with different hydrophilic or hydrophobic oligomer ratios using poly-condensation strategy. Afterward, we fabricated the corresponding membranes via a solution-casting approach. We verified the SPES membrane chemical structure using nuclear magnetic resonance (1H NMR) and confirmed the resulting oligomer ratio. Field-emission scanning electron microscope (FE-SEM) and atomic force microscope (AFM) results revealed that we effectively attained phase separation of the SPES membrane along with an increased hydrophilic oligomer ratio. Thermal stability, glass transition temperature (Tg) and membrane elongation increased with the ratio of hydrophilic oligomers. SPES membranes with higher hydrophilic oligomer ratios exhibited superior water uptake, ion-exchange capacity, contact angle and water sorption, while retaining reasonable swelling degree. The proton conductivity results showed that SPES containing higher amounts of hydrophilic oligomers provided a 74.7 mS cm-1 proton conductivity at 90 °C, which is better than other SPES membranes, but slightly lower than that of Nafion-117 membrane. When integrating SPES membranes with proton-exchange membrane fuel cells (PEMFCs) at 60 °C and 80% relative humidity (RH), the PEMFC power density exhibited a similar increment-pattern like proton conductivity pattern.

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Project description:As a traditional high-temperature proton exchange membrane (HT-PEM), phosphoric acid (PA)-doped polybenzimidazole (PBI) is often subject to severe mechanical strength deterioration owing to the "plasticizing effect" of a large amount of PA. In order to address this issue, we fabricated the HT-PEMs with a crosslinked network of poly (arylene ether ketone) to confine polybenzimidazole in semi-interpenetration network using self-synthesized amino-terminated PBI (PBI-4NH2) as a crosslinker. Compared with the pristine linear poly [2,2'-(p-oxdiphenylene)-5,5'-benzimidazole] (OPBI) membrane, the designed HT-PEMs (semi-IPN/xPBI), in the semi-IPN means that the membranes with a semi-interpenetration structure and x represent the combined weight percentage of PBI-4NH2 and OPBI. In addition, they also demonstrate an enhanced anti-oxidative stability and superior mechanical properties without the sacrifice of conductivity. The semi-IPN/70PBI exhibits a higher proton conductivity than OPBI at temperatures ranging from 80 to 180 °C. The HT-PEMFC with semi-IPN/70PBI exhibits excellent H2/O2 single cell performance with a power density of 660 mW cm-2 at 160 °C with flow rates of 250 and 500 mL min-1 for dry H2 and O2 at a backpressure of 0.03 MPa, which is 18% higher than that of OPBI (561 mW cm-2) under the same test conditions. The results indicate that the introduction of PBI containing crosslinked networks is a promising approach to improve the comprehensive performance of HT-PEMs.

| S-EPMC8912004 | biostudies-literature

Improving the Durability and Performance of Sulfonated Poly(arylene ether)s by Introducing 9,10-Dihydro-9-oxa-10-phosphaphenanthrene 10-oxide Structure for Fuel Cell Application.

Project description:Polymer electrolyte membranes in which the hydrophilic and hydrophobic domains phase separate exhibit improved properties and stability. Such a phase separation of hydrophilic and hydrophobic domains can be achieved by polymerizing a 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide-bisphenol A (DOPO-BPA) and 1,4-bis(4-fluorobenzoyl)benzene (1,4-FBB) monomer. In this work, sulfonated polymer membranes with various degrees of sulfonation (DS) were prepared and their physicochemical and electrochemical properties were studied. In addition, the effect of molecular structure on the durability of the copolymers was investigated. The sulfonated copolymers were characterized by Fourier-transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy. Then, sulfonated membranes were prepared using these copolymers by the solvent casting method, and their morphologies were investigated by atomic force microscopy. The effect of DS on the thermal, mechanical, and oxidative stabilities, water uptake behavior, and ion-exchange capacity of the membranes was determined. The results showed that compared with the commercially available Nafion 212 polymer electrolyte membrane, the electrolyte membrane based on DOPO-BPA and 1,4-FBB exhibited a lower water uptake and excellent dimensional stability despite having a relatively high ion-exchange capacity. The low water uptake is an important characteristic that ensures the stability of the polymer electrolyte membrane in fuel cell applications.

| S-EPMC8717375 | biostudies-literature

Sulfonated graphene oxide/Nafion composite membranes for high temperature and low humidity proton exchange membrane fuel cells.

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| S-EPMC9078422 | biostudies-literature

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