2018
DOI: 10.1038/s41467-018-04904-3
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Single-layer graphene membranes by crack-free transfer for gas mixture separation

Abstract: The single-layer graphene film, when incorporated with molecular-sized pores, is predicted to be the ultimate membrane. However, the major bottlenecks have been the crack-free transfer of large-area graphene on a porous support, and the incorporation of molecular-sized nanopores. Herein, we report a nanoporous-carbon-assisted transfer technique, yielding a relatively large area (1 mm2), crack-free, suspended graphene film. Gas-sieving (H2/CH4 selectivity up to 25) is observed from the intrinsic defects generat… Show more

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Cited by 165 publications
(241 citation statements)
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“…Recently, we reported a nanoporous carbon film based reinforcement for crack-free transfer of graphene. 35 However, this approach requires a high-temperature pyrolysis step, which is not compatible with functional organic layers on graphene. Therefore, the PTMSP approach introduced here is uniquely appropriate as a mechanical support for organo-functionalized graphene membranes, such as the one in this work.…”
Section: The Microstructure Of Spong Membranesmentioning
confidence: 99%
See 1 more Smart Citation
“…Recently, we reported a nanoporous carbon film based reinforcement for crack-free transfer of graphene. 35 However, this approach requires a high-temperature pyrolysis step, which is not compatible with functional organic layers on graphene. Therefore, the PTMSP approach introduced here is uniquely appropriate as a mechanical support for organo-functionalized graphene membranes, such as the one in this work.…”
Section: The Microstructure Of Spong Membranesmentioning
confidence: 99%
“…34 Recently, we demonstrated the separation of gas molecules from single-layer graphene by the size-sieving mechanism, with a sieving-resolution of 1 Å (for example, H 2 from CH 4 ). 35 For postcombustion capture, one needs to separate CO 2 from N 2 , where the difference in the kinetic diameters is only 0.3 Å. A way forward to achieve this is to functionalize the graphene surface with CO 2 -philic groups, which can enhance the selective adsorption of CO 2 from the gas phase to the graphene nanopores.…”
mentioning
confidence: 99%
“…This problem can be resolved via exposing the graphene surface directly without removing the mechanical supporting film. Such methodology was developed by Agarwal's team 64 where they had grown a nanoporous carbon film (NPC) on top of graphene via coating a block copolymer followed by pyrolysis. Despite of its few intrinsic defects (5.4 × 10 10 cm −2 ), the CVD-grown mm-long graphene monolayer displayed an attractive high permeance (~4.1 × 10 −7 mol m −2 s −1 Pa −1 ) and selectivity (25) for H 2 against CH 4 .…”
Section: Monolayered Graphene Membranesmentioning
confidence: 99%
“…However, facile, cost‐effective processes to form nanoscale defects in the graphene lattice, specifically with a narrow size distribution and high density over large areas remain elusive. We emphasize that size selective separations with large‐area NATMs have so far been limited to using top‐down approaches for nanopore formation in graphene, i.e., lithography, ion bombardment followed by acid etch, oxygen plasma etching, ion bombardment followed by oxygen plasma etch, and oxide nanoparticle induced etching, among others . Top‐down approaches for nanopore formation generally add multiple processing steps, increasing process complexity for membrane fabrication and in some cases are not scalable …”
mentioning
confidence: 99%