Mesoporous monoliths of inverse bicontinuous cubic phases of block copolymer bilayers
Chiyoung Park,
Yunju La,
Tae Hyun An,
Hu Young Jeong,
Sebyung Kang,
Sang Hoon Joo,
Hyungju Ahn,
Tae Joo Shin and
Kyoung Taek Kim ()
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Chiyoung Park: Ulsan National Institute of Science and Technology (UNIST)
Yunju La: Ulsan National Institute of Science and Technology (UNIST)
Tae Hyun An: Ulsan National Institute of Science and Technology (UNIST)
Hu Young Jeong: UNIST Central Research Facilities, UNIST
Sebyung Kang: School of Life Sciences, UNIST
Sang Hoon Joo: Ulsan National Institute of Science and Technology (UNIST)
Hyungju Ahn: Pohang Accelerator Laboratory, POSTECH
Tae Joo Shin: Pohang Accelerator Laboratory, POSTECH
Kyoung Taek Kim: Ulsan National Institute of Science and Technology (UNIST)
Nature Communications, 2015, vol. 6, issue 1, 1-9
Abstract:
Abstract Solution self-assembly of block copolymers into inverse bicontinuous cubic mesophases is a promising new approach for creating porous polymer films and monoliths with highly organized bicontinuous mesoporous networks. Here we report the direct self-assembly of block copolymers with branched hydrophilic blocks into large monoliths consisting of the inverse bicontinuous cubic structures of the block copolymer bilayer. We suggest a facile and scalable method of solution self-assembly by diffusion of water to the block copolymer solution, which results in the unperturbed formation of mesoporous monoliths with large-pore (>25 nm diameter) networks weaved in crystalline lattices. The surface functional groups of the internal large-pore networks are freely accessible for large guest molecules such as protein complexes of which the molecular weight exceeded 100 kDa. The internal double-diamond (Pn3m) networks of large pores within the mesoporous monoliths could be replicated to self-supporting three-dimensional skeletal structures of crystalline titania and mesoporous silica.
Date: 2015
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7392
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DOI: 10.1038/ncomms7392
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