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Two‐dimensional (2D) graphitic carbon nitride (g‐C3N4) nanosheets show brilliant application potential in numerous fields. Herein, a membrane with artificial nanopores and self‐supporting spacers was fabricated by assembly of 2D g‐C3N4 nanosheets in a stack with elaborate structures. In water purification the g‐C3N4 membrane shows a better separation performance than commercial membranes. The g‐C3N4 membrane has a water permeance of 29 L m−2 h−1 bar−1 and a rejection rate of 87 % for 3 nm molecules with a membrane thickness of 160 nm. The artificial nanopores in the g‐C3N4 nanosheets and the spacers between the partially exfoliated g‐C3N4 nanosheets provide nanochannels for water transport while bigger molecules are retained. The self‐supported nanochannels in the g‐C3N4 membrane are very stable and rigid enough to resist environmental challenges, such as changes to pH and pressure conditions. Permeation experiments and molecular dynamics simulations indicate that a novel nanofluidics phenomenon takes place, whereby water transport through the g‐C3N4 nanosheet membrane occurs with ultralow friction. The findings provide new understanding of fluidics in nanochannels and illuminate a fabrication method by which rigid nanochannels may be obtained for applications in complex or harsh environments.  相似文献   
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Freestanding MOF films up to six‐inches across and replicating various surface (micro)patterns are prepared via a templated growth method. When grown on copper supports, these films have preferred orientation of the constituent crystallites, translating into markedly different wetting properties of the film's two surfaces (water‐pinning vs. water repellant). In addition, the films exhibit differential sorption of various organic solvents, can recover oil spills from seawater, and can also act as active layers of chemical sensors.  相似文献   
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Ohne Zusammenfassung
Determination of the urea content of the water of swimming pools
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C4 olefin separations present one of the great challenges in hydrocarbon purifications owing to their similar structures, thus a single separation mechanism often met with limited success. Herein we report a series of anion‐pillared interpenetrated copper coordination for which the cavity and functional site disposition can be varied in 0.2 Å scale increments by altering the anion pillars and organic linkers (GeFSIX‐2‐Cu‐i (ZU‐32), NbFSIX‐2‐Cu‐i (ZU‐52), GeFSIX‐14‐Cu‐i (ZU‐33)), which enable selective recognition of different C4 olefins. In these materials the rotation of the organic linkers is controlled to create a contracted flexible pore window that enables the size‐exclusion of specific C4 olefins, while still adsorbing significant amounts of 1,3‐butadiene (C4H6) or 1‐butene (n‐C4H8). Combining the molecular recognition and size‐sieving effect, these materials unexpectedly realized the sieving of C4H6/n‐C4H8, C4H6/iso‐C4H8, and n‐C4H8/iso‐C4H8 with high capacity.  相似文献   
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