Polymeric thin film
composite (TFC) membranes have been proven promising for a wide range
of separation applications. However, their development is significantly
hindered by low permeance (below 8.0 L m–2 h–1 bar–1). Here, we report the fabrication
of new films with nanoparticle-assembled structure via interfacial
polymerization using quantum dots (QDs) as building blocks. The tailored
QDs with hydrophobic and hydrophilic regions permit cross-linking
into nanoparticle-assembled defect-free thin films. Significantly,
amphipathic QDs show good affinity to polar and nonpolar molecules,
facilitating their fast dissolution into film. Meanwhile, the nanopores
(∼1.4 nm) render fleet diffusion of molecules, which highly
promotes the transfer of molecules within the film. This synergetic
effect endows the resultant TFC membrane with high permeance, over
2 orders of magnitude higher than the conventional polyamide films.
The permeances for acetonitrile and n-hexane reach
46.9 and 50.8 L m–2 h–1 bar–1, respectively. We demonstrate that films fabricated
by hydrophilic and hydrophobic QDs exhibit different molecular transfer
mechanisms, and the corresponding model equations are established.
The film fabricated by amphipathic QDs shows a combination transfer
mechanism of the two models. Furthermore, those QD-based TFC membranes
display favorable structural and operational stability, holding promise
for industrial separation applications.