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Single-layer graphene membranes by crack-free transfer for gas mixture separation

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...

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Detalles Bibliográficos
Autores principales: Huang, Shiqi, Dakhchoune, Mostapha, Luo, Wen, Oveisi, Emad, He, Guangwei, Rezaei, Mojtaba, Zhao, Jing, Alexander, Duncan T. L., Züttel, Andreas, Strano, Michael S., Agrawal, Kumar Varoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035196/
https://www.ncbi.nlm.nih.gov/pubmed/29980683
http://dx.doi.org/10.1038/s41467-018-04904-3
Descripción
Sumario: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 mm(2)), crack-free, suspended graphene film. Gas-sieving (H(2)/CH(4) selectivity up to 25) is observed from the intrinsic defects generated during the chemical-vapor deposition of graphene. Despite the ultralow porosity of 0.025%, an attractive H(2) permeance (up to 4.1 × 10(−7) mol m(−2) s(−1) Pa(−1)) is observed. Finally, we report ozone functionalization-based etching and pore-modification chemistry to etch hydrogen-selective pores, and to shrink the pore-size, improving H(2) permeance (up to 300%) and H(2)/CH(4) selectivity (up to 150%). Overall, the scalable transfer, etching, and functionalization methods developed herein are expected to bring nanoporous graphene membranes a step closer to reality.