Developing advanced filtration membrane with high flux, good solute rejection and excellent antifouling performance is highly demanded. Hydrophilic graphene oxide (GO) nanosheets are attractive fillers for the preparation of composite membranes for water purification. However, strategies that can fully exploit the advantages and remedy the drawbacks of GO nanosheets are still needed. In this work, UiO-66 was specifically anchored to the GO layers as a porous modifier. The incorporated UiO-66 can effectively prevent the GO layers from stacking and introduce unique properties into the composite (UiO-66@GO). A series of novel composite membranes were prepared with the obtained UiO-66@GO composite and polyethersulfone (PES). As a result, the prepared composite membranes
Gas permeability and selectivity for CO2/N2 separation were improved simultaneously in mixed-matrix membranes formed by a nanoporous metal–organic framework with a task-specific ionic liquid in PIM-1.
Preserving the structural and functional integrity of interfaces and inhibiting deleterious chemical interactions are critical for realizing devices with sub-50 nm thin films and nanoscale units. Here, we demonstrate that ∼0.7-nm-thick self-assembled monolayers (SAMs) comprising mercapto-propyl-tri-methoxy-silane (MPTMS) molecules enhance adhesion and inhibit Cu diffusion at Cu/SiO2 structures used in device metallization. Cu/SAM/SiO2/Si(001) structures show three times higher interface debond energy compared to Cu/SiO2 interfaces due to a strong chemical interaction between Cu and S termini of the MPTMS SAMs. This interaction immobilizes Cu at the Cu/SAM interface and results in a factor-of-4 increase in Cu-diffusion-induced failure times compared with that for structures without SAMs.
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