▎ 摘　　要

In this study, custom-tailored graphene oxide quantum dots (GOQD) were synthesized as functional nanofillers to be embedded into the polyamide (PA) membrane for reverse osmosis (RO) via interfacial polymerization (IP). The heterostructured interface-functionalization of amine/sulfonic decoration on GOQD (N/S-d-GOQD) takes place via the tuning of the molecular design. The embedded N/S-d-GOQD inside the PA matrix contributes to facilitating water molecules quick transport due to the more accessible capturing sites with higher internal polarity, achieving a nearly 3-fold increase in water permeance when compared to the pristine thin-film composite (TFC) membrane. Covalent bonding between the terminal amine groups and the acyl chloride of trimesoyl chloride (TMC) enables the formation of an amplified selective layer, while the sulfonic part assists in maintaining a robust membrane surface negative charge, thus remarkably improving the membrane selectivity toward NaCl. As a result, the newly developed TFN membrane performed remarkably high water permeance up to 5.89 L m(-2) h(-1) bar(-1) without the compromising of its favorable salt (NaCl) rejection ratio of 97.1%, revealing a comparably high separation property when comparing to the state-of-the-art RO membranes, and surpassing the permeability-selectivity trade-off limits. Furthermore, we systematically investigated the GOQDs with different surface decorations but similar configurations (including 3 different nanofillers of pristine GOQD, amine decorated GOQD (N-d-GOQD), and N/S-d-GOQD) to unveil the underlying mechanisms of the swing effects of internal geometry and polarity of the embedded nanofillers on contributing to the uptake, and/or release of aqueous molecules within TFN membranes, providing a fundamental perspective to investigate the impact of embedded nanofillers on the formation of an IP layer and the overall transporting behavior of the RO process.