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.

Exfoliated graphene oxide (GO) was reliably modified with a cetyltrimethylammonium chloride (CTAC) surfactant to greatly improve the dispersity of the GO in a polyacrylonitrile (PAN) polymer precursor solution. Subsequent electrospinning of the mixture readily resulted in the formation of GO–PAN composite nanofibers containing up to 30 wt % of GO as a filler without notable defects. The absence of common electrospinning problems associated with clogging and phase separation indicated the systematic and uniform integration of the GO within the PAN nanofibers beyond the typical limits. After thoroughly examining the formation and maximum loading efficiency of the modified GO in the PAN nanofibers, the resulting composite nanofibers were thermally treated to form membrane-type sheets. The wettability and pore properties of the composite membranes were notably improved with respect to the pristine PAN nanofiber membrane, possibly due to the reinforcing filler effect. In addition, the more GO loaded into the PAN nanofiber membranes, the higher the removal ability of the methylene blue (MB) and methyl red (MR) dyes in the aqueous system. The adsorption kinetics of a mixed dye solution were also monitored to understand how these MB and MR dyes interact differently with the composite nanofiber membranes. The simple surface modification of the fillers greatly facilitated the integration efficiency and improved the ability to control the overall physical properties of the nanofiber-based membranes, which highly impacted the removal performance of various dyes from water.

In this study, a series of novel modified graphene oxide (MGO)/polyacrylonitrile (PAN) hybrid nanofiber membranes were fabricated by electrospinning a PAN solution containing up to 1.0 wt.% MGO. The GO was initially prepared by a time-saving improved Hummer’s method. Subsequently, the formation of GO was confirmed by scanning electron microscopy (SEM), AFM, Fourier-transform infrared spectroscopy (FT–IR), and Raman spectroscopy. This study also prepared the modified GO with polydiallyldimethylammonium chloride (GP) by using a simple surface post-treatment method to improve its dispersion. Varying amounts of GP were incorporated into PAN nanofibers for the better properties of GP/PAN nanofibers, such as hydrophilicity, mechanical properties, and so on. The resulting GP/PAN hybrid nanofiber membranes were characterized by SEM, FTIR, contact angle, and thermal and mechanical properties. These results showed that the hydrophilic and mechanical properties of GP/PAN hybrid nanofiber membranes were dramatically improved, i.e., 50% improvement for hydrophilicity and 3–4 times higher strength for mechanical property, which indicated the possibility for water treatment application. In addition, the notably improved thermal stability results showed that the hybrid nanofiber membranes could also be a potential candidate for the secondary battery separator.

A highly improved strategy is established in order to systematically integrate excess exfoliated graphene oxide (GO) as fillers into polyacrylonitrile (PAN) nanofibers via electrospinning. Simple modification of GO surface allowed for their loading efficiency into the nanofibers to surpass the typical limits. Among many features, the hydrophilic and mechanical properties of these membranes were found to be significantly increased compared to the original PAN and bare GO-loaded membranes probably due to the effective reinforcing filler effect caused by the even distribution of the modified GO within the PAN nanofibers. Thus, the simple surface modification of fillers can facilitate the capability of controlling the loading efficiency into electrospun nanofibers which can highly impact the quality and performance of final composite membranes.

This work demonstrates the incorporation of gold nanoparticles (AuNPs) into crosslinker-free poly(N-isopropylacrylamide), PNIPAM, particles in situ and the examination of their structural and catalytic properties. The formation process of the AuNPs across the crosslinker-free PNIPAM particles are compared to that of crosslinked PNIPAM particles. Given the relatively larger free volume across the crosslinker-free polymer network, the AuNPs formed by the in situ reduction of gold ions are detectably larger and more polydisperse, but their overall integration efficiency is slightly inferior. The structural features and stability of these composite particles are also examined in basic and alcoholic solvent environments, where the crosslinker-free PNIPAM particles still offer comparable physicochemical properties to the crosslinked PNIPAM particles. Interestingly, the crosslinker-free composite particles as a colloidal catalyst display a higher reactivity toward the homocoupling of phenylboronic acid and reveal the importance of the polymer network density. As such, the capability to prepare composite particles in a controlled polymer network and reactive metal nanoparticles, as well as understanding the structure-dependent physicochemical properties, can allow for the development of highly practical catalytic systems.