Porous pure SnO₂ nanofibers (NFs) and La₂O₃ nanoparticles (NPs)-embedded porous SnO₂ NFs were successfully synthesized via electrospinning followed by calcination. These materials were systematically evaluated as gas-sensing elements in metal-oxide-semiconductor (MOS) sensors. The La₂O₃ NPs embedded in porous SnO₂ NFs demonstrated superior gas-sensing performance compared to pure SnO₂ NFs. Specifically, the incorporation of La₂O₃ resulted in a 12-fold enhancement in gas-sensing response towards ethanol, significantly improving both sensitivity and selectivity by tuning the carrier concentration and modifying oxygen deficiencies and chemisorbed oxygen levels. Thus, La₂O₃ NPs embedded in SnO₂ NFs present a promising strategy for the development of high-performance ethanol gas sensors.

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.

We describe a new strategy to prepare thermally- and electrochemically-stable polyimide (PI) nanofiber membranes by the hot-press treatment of polyamic acid (PAA) nanofiber sheets in situ and examine their performance as Li-ion battery separators. Typical thermal imidization of PAA to PI membranes using sequential high temperature treatments in an oven takes a long time, but our method readily completes this conversion process at a mild temperature in 30 min while generating a high probability of inter-nanofiber imidization. Along with the improved electrolyte uptake capability and uniform distribution of the pore size and porosity caused by the dense and compact arrangements, the hot-press-induced PI membrane exhibits relatively thin sheets and a much greater mechanical strength than the membrane prepared by the thermal treatment. Subsequently, these PI-based membranes are installed in Li-ion full coin cells as battery separators whose C-rate (charging and discharging) performances are comparable to a commercial polyethylene (PE) separator. In addition, the highly improved thermal stabilities of these PI separators over PE separators are observed during thermal shrinkage and hot-box tests. Overall, our strategy can allow for the manufacture of diverse PI-based membranes with minimal preparation time and cost that can be utilized in high power portable devices requiring thermal and electrochemical stability.

In this study, tin oxide (SnO₂)/polyaniline (PANI) composite nanowires (NWs) with varying amounts of PANI were synthesized for carbon dioxide (CO₂) gas sensing at room temperature (RT, 25 °C). SnO₂ NWs were fabricated via the vapor–liquid–solid (VLS) method, followed by coating with PANI. CO₂ sensing investigations revealed that the sensor with 186 μL PANI exhibited the highest response to CO₂ at RT. Additionally, the optimized sensor demonstrated excellent selectivity for CO₂, long-term stability, and reliable performance across different humidity levels. The enhanced sensing performance of the optimized sensor was attributed to the formation of SnO₂-PANI heterojunctions and the optimal PANI concentration. This study underscores the potential of SnO₂-PANI composites for CO₂ detection at RT.

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.