There has been increasing interest in the study and development of nanoparticle-embedded polymeric materials and their applications to special membranes. Nanoparticle-embedded polymeric materials have been observed to have a desirable compatibility with commonly used membrane matrices, a wide range of functionalities, and tunable physicochemical properties. The development of nanoparticle-embedded polymeric materials has shown great potential to overcome the longstanding challenges faced by the membrane separation industry. One major challenge that has been a bottleneck to the progress and use of membranes is the balance between the selectivity and the permeability of the membranes. Recent developments in the fabrication of nanoparticle-embedded polymeric materials have focused on how to further tune the properties of the nanoparticles and membranes to improve the performance of the membranes even further. Techniques for improving the performance of nanoparticle-embedded membranes by exploiting their surface characteristics and internal pore and channel structures to a significant degree have been incorporated into the fabrication processes. Several fabrication techniques are discussed in this paper and used to produce both mixed-matrix membranes and homogenous nanoparticle-embedded polymeric materials. The discussed fabrication techniques include interfacial polymerization, self-assembly, surface coating, and phase inversion. With the current interest shown in the field of nanoparticle-embedded polymeric materials, it is expected that better-performing membranes will be developed soon.

In this work, the solvothermal solidification method has been used to be prepared as a homogenous CuSn-organic nano-composite (CuSn-OC) to use as a catalyst for alkaline water electrolysis for cost-effective H₂ generation. FT-IR, XRD, and SEM techniques were used to characterize the CuSn-OC which confirmed the formation of CuSn-OC with a terephthalic acid linker as well as Cu-OC and Sn-OC. The electrochemical investigation of CuSn-OC onto a glassy carbon electrode (GCE) was evaluated using the cyclic voltammetry (CV) method in 0.1 M KOH at room temperature. The thermal stability was examined using TGA methods, and the Cu-OC recorded a 91.4% weight loss after 800 °C whereas the Sn-OC and CuSn-OC recorded 16.5 and 62.4%, respectively. The results of the electroactive surface area (ECSA) were 0.5, 0.42, and 0.33 m² g⁻¹ for the CuSn-OC, Cu-OC, and Sn-OC, respectively, and the onset potentials for HER were −420, −900, and −430 mV vs. the RHE for the Cu-OC, Sn-OC, and CuSn-OC, respectively. LSV was used to evaluate the electrode kinetics, and the Tafel slope for the bimetallic catalyst CuSn-OC was 190 mV dec⁻¹, which was less than for both the monometallic catalysts, Cu-OC and Sn-OC, while the overpotential was −0.7 vs. the RHE at a current density of −10 mA cm⁻².