Graphene-based materials can have well-defined nanometer pores and can exhibit low frictional water flow inside them, making their properties of interest for filtration and separation. We investigate permeation through micrometer-thick laminates prepared by means of vacuum filtration of graphene oxide suspensions. The laminates are vacuum-tight in the dry state but, if immersed in water, act as molecular sieves, blocking all solutes with hydrated radii larger than 4.5 angstroms. Smaller ions permeate through the membranes at rates thousands of times faster than what is expected for simple diffusion. We believe that this behavior is caused by a network of nanocapillaries that open up in the hydrated state and accept only species that fit in. The anomalously fast permeation is attributed to a capillary-like high pressure acting on ions inside graphene capillaries.

Graphene oxide membranes show exceptional molecular permeation properties, with a promise for many applications. However, their use in ion sieving and desalination technologies is limited by a permeation cutoff of 9 Å, which is larger than hydrated ion diameters for common salts. The cutoff is determined by the interlayer spacing d 13.5 Å, typical for graphene oxide laminates that swell in water. Achieving smaller d for the laminates immersed in water has proved to be a challenge. Here we describe how to control d by physical confinement and achieve accurate and tuneable ion sieving. Membranes with d from  9.8 Å to 6.4 Å are demonstrated, providing the sieve size smaller than typical ions' hydrated diameters. In this regime, ion permeation is found to be thermally activated with energy barriers of 10-100 kJ/mol depending on d. Importantly, permeation rates decrease exponentially with decreasing the sieve size but water transport is weakly affected (by a factor of <2). The latter is attributed to a low barrier for water molecules entry and large slip lengths inside graphene capillaries. Building on these findings, we demonstrate a simple scalable method to obtain graphene-based membranes with limited swelling, which exhibit 97% rejection for NaCl.Selectively permeable membranes with sub-nm pores attract strong interest due to analogies with biological membranes and potential applications in water filtration, molecular separation and desalination [1][2][3][4][5][6][7][8] . Nanopores with sizes comparable to, or smaller than, the diameter D of hydrated ions are predicted to show enhanced ion selectivity 7,9-12 because of dehydration required to pass through such atomic-scale sieves. Despite extensive research on ion dehydration effects 3,7,9-13 , experimental investigation of the ion sieving controlled by dehydration has been limited because of difficulties in fabricating uniform membranes with well-defined sub-nm pores. The realisation of membranes with dehydration-assisted selectivity would be a significant step forward. So far, research into novel membranes has mostly focused on improving the water flux rather than ion selectivity. On the other hand, modelling of practically relevant filtration processes shows that an increase in water permeation rates above the rates currently achieved (2-3 L/m 2 ×h×bar) would not contribute greatly to the overall efficiency of desalination 8,14,15 . Alternative approaches based on higher water-ion selectivity may open new possibilities for improving filtration technologies, as the performance of state-of-the-art membranes is currently limited by the solution-diffusion mechanism, in which water molecules dissolve in the membrane material and then diffuses across the membrane 8 . Recently, carbon nanomaterials including carbon nanotubes (CNT)

A simple and scalable method to fabricate graphene‐cellulose paper (GCP) membranes is reported; these membranes exhibit great advantages as freestanding and binder‐free electrodes for flexible supercapacitors. The GCP electrode consists of a unique three‐dimensional interwoven structure of graphene nanosheets and cellulose fibers and has excellent mechanical flexibility, good specific capacitance and power performance, and excellent cyclic stability. The electrical conductivity of the GCP membrane shows high stability with a decrease of only 6% after being bent 1000 times. This flexible GCP electrode has a high capacitance per geometric area of 81 mF cm−2, which is equivalent to a gravimetric capacitance of 120 F g−1 of graphene, and retains >99% capacitance over 5000 cycles. Several types of flexible GCP‐based polymer supercapacitors with various architectures are assembled to meet the power‐energy requirements of typical flexible or printable electronics. Under highly flexible conditions, the supercapacitors show a high capacitance per geometric area of 46 mF cm−2 for the complete devices. All the results demonstrate that polymer supercapacitors made using GCP membranes are versatile and may be used for flexible and portable micropower devices.

Graphene oxide (GO) membranes continue to attract intense interest due to their unique molecular sieving properties combined with fast permeation rates 1-9 . However, the membranes' use has been limited mostly to aqueous solutions because GO membranes appear to be impermeable to organic solvents 1 , a phenomenon not fully understood yet. Here, we report efficient and fast filtration of organic solutions through GO laminates containing smooth two-dimensional (

The classical strong metal–support interaction between TiO2 and IB metals was demonstrated.

Flexible barrier films preventing permeation of gases and moistures are important for many industries ranging from food to medical and from chemical to electronic. From this perspective, graphene has recently attracted particular interest because its defect-free monolayers are impermeable to all atoms and molecules. However, it has been proved to be challenging to develop large-area defectless graphene films suitable for industrial use. Here we report barrier properties of multilayer graphitic films made by gentle chemical reduction of graphene oxide laminates with hydroiodic and ascorbic acids. They are found to be highly impermeable to all gases, liquids and aggressive chemicals including, for example, hydrofluoric acid. The exceptional barrier properties are attributed to a high degree of graphitization of the laminates and little structural damage during reduction. This work indicates a close prospect of graphene-based flexible and inert barriers and protective coatings, which can be of interest for numerous applications.

Dry reforming of methane (DRM) is an attractive route to utilize CO2 as a chemical feedstock with which to convert CH4 into valuable syngas and simultaneously mitigate both greenhouse gases. Ni-based DRM catalysts are promising due to their high activity and low cost, but suffer from poor stability due to coke formation which has hindered their commercialization. Herein, we report that atomically dispersed Ni single atoms, stabilized by interaction with Ce-doped hydroxyapatite, are highly active and coke-resistant catalytic sites for DRM. Experimental and computational studies reveal that isolated Ni atoms are intrinsically coke-resistant due to their unique ability to only activate the first C-H bond in CH4, thus avoiding methane deep decomposition into carbon. This discovery offers new opportunities to develop large-scale DRM processes using earth abundant catalysts.

Atomically dispersed M-N-C (M refers to transition metals) materials represent the most promising catalyst alternatives to the precious metal Pt for the electrochemical reduction of oxygen (ORR), yet the genuine active sites in M-N-C remain elusive. Here, we develop a two-step approach to fabricate Cu-N-C single-atom catalysts with a uniform and well-defined Cu 2+ -N 4 structure that exhibits comparable activity and superior durability in comparison to Pt/C. By combining operando X-ray absorption spectroscopy with theoretical calculations, we unambiguously identify the dynamic evolution of Cu-N 4 to Cu-N 3 and further to HO-Cu-N 2 under ORR working conditions, which concurrently occurs with reduction of Cu 2+ to Cu + and is driven by the applied potential. The increase in the Cu + /Cu 2+ ratio with the reduced potential indicates that the low-coordinated Cu + -N 3 is the real active site, which is further supported by DFT calculations showing the lower free energy in each elemental step of the ORR on Cu + -N 3 than on Cu 2+ -N 4 . These findings provide a new understanding of the dynamic electrochemistry on M-N-C catalysts and may guide the design of more efficient low-cost catalysts.