Silver nanoparticle-modified graphene oxide (Ag/GO) was reliably prepared by using sodium borohydride (NaBH4) in the presence of citric acid capping agent via a simple wet chemistry method. This rapidly formed Ag/GO composite exhibited good dispersity in a solution containing hydrophilic polyacrylonitrile (PAN). Subsequent electrospinning of this precursor solution resulted in the successful formation of nanofibers without any notable defects. The Ag/GO-incorporated PAN nanofibers showed thinner fiber strands (544 ± 82 nm) compared to those of GO-PAN (688 ± 177 nm) and bare-PAN (656 ± 59 nm). Subsequent thermal treatment of nanofibers resulted in the preparation of thin membranes to possess the desired pore property and outstanding wettability. The Ag/GO-PAN nanofiber membrane also showed 30% higher water flux value (390 LMH) than that of bare-PAN (300 LMH) for possible microfiltration (MF) application. In addition, the resulting Ag/GO-PAN nanofiber membrane exhibited antibacterial activity against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive). Furthermore, this composite membrane exhibited outstanding anti-fouling property compared to the GO-PAN nanofiber membrane in the wastewater treatment. Therefore, the simple modification strategy allows for the effective formation of Ag/GO composite as a filler that can be reliably incorporated into polymer nanofiber membranes to possess improved overall properties for wastewater treatment applications.
Alkaline water electrolysis (AWE) refers to a representative water electrolysis technology that applies electricity to synthesize hydrogen gas without the production of carbon dioxide. The ideal polymer electrolyte membranes for AWE should be capable of transporting hydroxide ions (OH−) quickly in harsh alkaline environments at increased temperatures. However, there has not yet been any desirable impedance measurement method for estimating hydroxide ions’ conduction behavior across the membranes, since their impedance spectra are significantly affected by connection modes between electrodes and membranes in the test cells and the impedance evaluation environments. Accordingly, the measurement method suitable for obtaining precise hydroxide ion conductivity values through the membranes should be determined. For this purpose, Zirfon®, a state-of-the-art AWE membrane, was adopted as the standard membrane sample to perform the impedance measurement. The impedance spectra were acquired using homemade test cells with different electrode configurations in alkaline environments, and the corresponding hydroxide ion conductivity values were determined based on the electrochemical spectra. Furthermore, a modified four-probe method was found as an optimal measurement method by comparing the conductivity obtained under alkaline conditions.
CeOx hybrid nanoparticles were synthesized and evaluated for use as radical scavengers, in place of commercially available Ce(NO3)3 and CeO2 nanoparticles, to avoid deterioration of the initial electrochemical performance and/or spontaneous aggregation/precipitation issues encountered in polymer electrolyte membranes. When CeOx hybrid nanoparticles were used for membrane formation, the resulting membranes exhibited improved proton conductivity (improvement level = 2–15% at 30–90 °C), and thereby electrochemical single cell performance, because the –OH groups on the hybrid nanoparticles acted as proton conductors. In spite of a small amount (i.e., 1.7 mg/cm3) of introduction, their antioxidant effect was sufficient enough to alleviate the radical-induced decomposition of perfluorinated sulfonic acid ionomer under a Fenton test condition and to extend the chemical durability of the resulting reinforced membranes under fuel cell operating conditions.
This study reports on an innovative press-loaded blister hybrid system equipped with gas-chromatography (PBS-GC) that is designed to evaluate the mechanical fatigue of two representative types of commercial Nafion membranes under relevant PEMFC operating conditions (e.g., simultaneously controlling temperature and humidity). The influences of various applied pressures (50 kPa, 100 kPa, etc.) and blistering gas types (hydrogen, oxygen, etc.) on the mechanical resistance loss are systematically investigated. The results evidently indicate that hydrogen gas is a more effective blistering gas for inducing dynamic mechanical losses of PEM. The changes in proton conductivity are also measured before and after hydrogen gas pressure-loaded blistering. After performing the mechanical aging test, a decrease in proton conductivity was confirmed, which was also interpreted using small angle X-ray scattering (SAXS) analysis. Finally, an accelerated dynamic mechanical aging test is performed using the homemade PBS-GC system, where the hydrogen permeability rate increases significantly when the membrane is pressure-loaded blistering for 10 min, suggesting notable mechanical fatigue of the PEM. In summary, this PBS-GC system developed in-house clearly demonstrates its capability of screening and characterizing various membrane candidates in a relatively short period of time (<1.5 h at 50 kPa versus 200 h).