The design and self-assembly of graphene oxide (GO)-based composite membranes have attracted enormous attention due to their wide application in nanomaterial and environmental fields. In this work, we have successfully developed a strategy to fabricate new composite membranes based on poly(vinyl alcohol)/poly(acrylic acid)/carboxyl-functionalized graphene oxide modified with silver nanoparticles (PVA/PAA/GO-COOH@AgNPs), which were prepared via thermal treatment and the electrospinning technique. Due to the strong π-π forces and strong electrostatic interactions of GO–COOH sheets, the prepared composite membranes and their lager surface areas were modified by scores of AgNPs, which demonstrated that a high-efficiency photocatalyst removed the organic dyes from the aqueous solutions. The prepared PVA/PAA/GO-COOH@AgNPs nanocomposite membranes showed a remarkable photocatalytic capacity in the catalytic degradation of the methylene blue dye solutions. Most importantly, the whole process was easy, mild, and eco-friendly. Additionally, the as-prepared membranes could be repeatedly used after the catalytic reaction.

The construction of heterojunctions provides a promising strategy to improve photocatalytic hydrogen evolution. However, how to fabricate a nanoscale TiO₂/g-C₃N₄ heterostructure and hinder the aggregation of bulk g-C₃N₄ using simple methods remains a challenge. In this work, we use a simple in situ construction method to design a heterojunction model based on molecular self-assembly, which uses a small molecule matrix for self-integration, including coordination donors (AgNO₃), inorganic titanium source (Ti(SO₄)₂) and g-C₃N₄ precursor (melamine). The self-assembled porous g-C₃N₄ nanotube can hamper carrier aggregation and it provides numerous catalytic active sites, mainly via the coordination of Ag⁺ ions. Meanwhile, the TiO₂ NPs are easily mineralized on the nanotube template in dispersive distribution to form a heterostructure via an N–Ti bond of protonation, which contributes to shortening the interfacial carrier transport, resulting in enhanced electron-hole pairs separation. Originating from all of the above synergistic effects, the obtained Ag/TiO₂/g-C₃N₄ heterogenous photocatalysts exhibit an enhanced H₂ evolution rate with excellent sustainability 20.6-fold-over pure g-C₃N₄. Our report provides a feasible and simple strategy to fabricate a nanoscale heterojunction incorporating g-C₃N₄, and has great potential in environmental protection and water splitting.

Dye wastewater is one of the most important problems to be faced and solved in wastewater treatment. However, the treatment cannot be single and simple adsorption due to the complexity of dye species. In this work, we prepared novel composite fiber adsorbent materials consisting of ε-polycaprolactone (PCL) and beta-cyclodextrin-based polymer (PCD) by electrospinning. The morphological and spectral characterization demonstrated the successful preparation of a series of composite fibers with different mass ratios. The obtained fiber materials have demonstrated remarkable selective adsorption for MB and 4-aminoazobenzene solutions. The addition of a PCD component in composite fibers enhanced the mechanical strength of membranes and changed the adsorption uptake due to the cavity molecular structure via host–guest interaction. The dye removal efficiency could reach 24.1 mg/g towards 4-aminoazobenzene. Due to the admirable stability and selectivity adsorption process, the present prepared beta-cyclodextrin-based composite fibers have demonstrated potential large-scale applications in dye uptake and wastewater treatment.

Polydopamine (PDA) nanoparticles can be used as an adsorbent with excellent adsorption capacity. However, nanosized adsorbents are prone to aggregation and thus are severely limited in the field of adsorption. In order to solve this problem, we utilized polydopamine in-situ oxidation self-polymerization on the surface of polycaprolactone (PCL)/polyethylene oxide (PEO) electrospun fiber after solvent vapor annealing (SVA) treatment, and successfully designed and prepared a PCL/PEO@PDA composite membrane. The SVA treatment regulated the microscopic morphology of smooth PCL/PEO electrospun fibers that exhibited a pleated microstructure, increasing the specific surface area, and providing abundant active sites for the anchoring of PDA nanoparticles. The PCL/PEO@PDA composite obtained by chemical modification of PDA demonstrated numerous active sites for the adsorption of methylene (MB) and methyl orange (MO). In addition, the PCL/PEO@PDA composites were reusable several times with good reutilization as adsorbents. Therefore, we have developed a highly efficient and non-agglomerated dye adsorbent that exhibits potential large-scale application in dye removal and wastewater purification.

Nano-sized palladium nanoparticles showed high catalytic activity with severe limitations in catalytic field due to the tendency to aggregate. A solid substrate with large specific surface area is an ideal carrier for palladium nanoparticles. In present work, polyethyleneimine/polycaprolactone/Pd nanoparticles (PEI/PCL@PdNPs) composite catalysts were successfully designed and prepared by electrospinning and reduction methods using PEI/PCL elexctrospun fiber as carrier. The added PEI component effectively regulated the microscopic morphology of the PEI/PCL fibers, following a large number of pit structures which increased the specific surface area of the electrospun fibers and provided active sites for loading of the palladium particles. The obtained PEI/PCL@PdNPs catalysts for reductions of 4-nitrophenol (4-NP) and 2-nitroaniline (2-NA) exhibited extremely efficient, stable, and reusable catalytic performance. It was worth mentioning that the reaction rate constant of catalytic reduction of 4-NP was as high as 0.16597 s⁻¹. Therefore, we have developed a highly efficient catalyst with potential applications in the field of catalysis and water treatment.

The effective synthesis and self-assembly of graphene oxide (GO) nanocomposites are of key importance for a broad range of nanomaterial applications. In this work, a one-step chemical strategy is presented to synthesize stable GO-polymer Langmuir composite films by interfacial thiol-ene photopolymerization at room temperature, without use of any crosslinking agents and stabilizing agents. It is discovered that photopolymerization reaction between thiol groups modified GO sheets and ene in polymer molecules is critically responsible for the formation of the composite Langmuir films. The film formed by Langmuir assembly of such GO-polymer composite films shows potential to improve the mechanical and chemical properties and promotes the design of various GO-based nanocomposites. Thus, the GO-polymer composite Langmuir films synthesized by interfacial thiol-ene photopolymerization with such a straightforward and clean manner, provide new alternatives for developing chemically modified GO-based hybrid self-assembled films and nanomaterials towards a range of soft matter and graphene applications.