▎ 摘　　要

We report an ultra-low loading of graphene oxide quantum dots (GQDs) into the polyamide (PA) layer of an outer-selective hollow fiber (OSHF) thin-film composite (TFC) membrane using the vacuum-assisted interfacial polymerization (VAIP) technique to improve the water permeability of OSHF TFC membranes without sacrificing membrane selectivity. Experimental results showed that GQD loading in the PA layer influenced membrane performance. The membrane with a GQD loading of 5 mg L-1 (TFN5) demonstrated an optimal water flux of 30.9 L m- 2 h-1 and a specific reverse solute flux (SRSF) of 0.12 g L-1. To investigate the effect of GQDs on the interfacial polymerization (IP) reaction and membrane performance, molecular dynamics (MD) simulation was employed at the water-hexane and water-PA interfaces. The simulation results showed that GQDs decreased the reaction rate during the IP process by reducing the diffusivities of m-phenylenediamine (MPD) and trimesoyl chloride (TMC). Additionally, GQDs reduced water permeability by acting as barriers to water molecules when present at a high concentration near the PA layer surface. At a very high loading, GQDs aggregated at the waterhexane interface and reduced the membrane selectivity by forming non-selective voids at the interface between the PA layer and GQDs. Together with the experimental findings, the MD simulation results delivered a good insight into the GQDs' effect on the TFC membrane's surface and transport properties at both macroscopic and microscopic levels.