Search

Inspired by biological membranes with charge-gated channels that allow the transport of water and ions but restrict the undesired substances, various regulated nanofiltration (NF) membranes containing charge-gated channels have been developed for water purification. However, most of these membranes are mono-charged (positively or negatively) that show high rejection only to the corresponding co-ions but low rejection to the counter-ions, which limits their wider applications. Herein, we report NF membranes with gas-tunable charge-gated channels and high rejection to different salts on demand. The membranes are prepared by assembling a CO 2 -responsive polymer, poly(N,N-dimethylaminoethyl methacrylate), on the surface of graphene oxide (GO). As a result of CO 2 -induced reversal of the charge sign, the membranes exhibit "self-regulation" of their surface charges. Upon bubbling CO 2 into water, the membranes are positively charged, which shows high rejection to MgCl 2. After bubbling Ar to remove CO 2 , the membranes gradually transform to negatively charged, and high rejection to Na 2 SO 4 is obtained. This study demonstrates the gas-tunable charge-gated ion transport behavior of the CO 2 -responsive NF membranes, and opens up new avenues for the design of on-demand NF membranes. New nanofiltration membranes exhibit on-demand switchable rejections toward cations and anions with the participation and departure of CO 2. Image 1 • New nanofiltration membrane was built with graphene oxide and CO 2 -responsive polymer. • The surface of nanopores can be reversibly switched between opposite charged state. • Charge sign can easily be reversed in a robust and contamination-free manner. • Ion transport behavior was dominated with the participation and departure of CO 2. [ABSTRACT FROM AUTHOR]

Processing two-dimensional (2D) covalent organic frameworks (COFs) into nanofilms has gained widespread attention in water treatment. However, the designed synthesis of COF-based membranes for ion separations still remains a huge challenge though the strategies to produce COF molecular separation membranes have been greatly developed. Herein, we report the construction of bi-layered COF nanofilms for efficient desalination through a simple yet effective secondary growth. The suggested strategy is capable of easily regulating the growth of another COF layer on the pre-synthesized first layer, thus producing crystalline and defect-free bi-layered COF nanofilms with distinct laminated structures. Most importantly, the offset channels are involved at the interface of two nanofilms obtained from the first and secondary growth, which leads to a constricted effective aperture that significantly enhances the ion separation performance. Specifically, the bi-layered COF nanofilms composited with macroporous supports exhibit high rejection rates (~95.8%) to Na 2 SO 4 , observably surpassing the desalination performance of single-layered COF nanofilms (rejection<10%). This work not only develops an ingenious way to fabricate COF-on-COF nanofilms with narrowed channels by tailoring the laminated structure of 2D COFs at the film interface, but also starts an avenue for the adoption of COF platforms for membrane separations with an improved precision. Image 1 • The secondary growth strategy is developed to build bi-layered COF nanofilms. • Nanofilm structures are controllable by adjusting the synthesis conditions. • Offset structures at the film interface enable a narrowed aperture down to ~0.71 nm. • The bi-layered COF nanofilms exhibit a greatly boosted desalination performance with a reasonable flux. [ABSTRACT FROM AUTHOR]