Graphene Oxide Membranes with Strong Stability in Aqueous Solutions and Controllable Lamellar Spacing

Graphene oxide (GO) membranes become emerging efficient filters for molecular or ionic separation due to their well-defined two-dimensional nanochannels formed by closely spaced GO sheets and tunable physicochemical properties. The stability of GO membranes in aqueous solutions is a prerequisite for their applications. Here we show a novel and easy strategy for fabricating GO membranes with strong stability in aqueous solutions and controllable lamellar spacing by simply doping with partially reduced graphene oxide (prGO) sheets. With our prGO-doping strategy, the interlayer stabilizing force in GO membranes is enhanced due to the weakened repulsive hydration and enhanced π–π attraction between GO sheets; as a result, the fabricated GO membranes are featured with controllable lamellar spacing and extraordinary stability in water or even strong acid and base solutions as well as strong mechanical properties, which will expand the application scope of GO membranes and provide ever better performances in their applications with aqueous solution environments

Insights into the Effects of 2:1 “Sandwich-Type” Crown-Ether/Metal-Ion Complexes in Responsive Host–Guest Systems

In-depth investigations of the specific ion-responsive characteristics based on 2:1 “sandwich” structures and effects of crown ether cavity sizes on the metal-ion/crown-ether complexation are systematically performed with a series of PNIPAM-based responsive copolymers containing similar contents of crown ether units with different cavity dimensions (12-crown-4 (12C4), 15-crown-5 (15C5), 18-crown-6 (18C6)). The lower critical solution temperature (LCST) values of copolymers in deionized water shift to lower temperatures gradually when the crown ether contents increase or the ring sizes decrease from 18C6 to 12C4. With increasing the concentrations of alkali metal ions (Na⁺, K⁺, Cs⁺) or the contents of pendent crown ether groups, the copolymers with different crown ether cavity sizes exhibit higher selectivity and sensitivity to corresponding cations. Importantly, the ion sensitivities of the copolymers in response to corresponding alkali metal ions increase dramatically with an increase in the crown ether cavity size. Interestingly, a linear relationship between the crown ether cavity size and the diameter of corresponding cation for the formation of stable 2:1 “sandwich” complexes is found for the first time, from which the size of metal ions or other guests that able to form 2:1 “sandwich” complexes with crown ethers can be deduced. The results in this work are valuable and useful for further developments and practical applications of various crown-ether-based smart materials