材料科学
膜
纳米纤维
聚合物
纳米技术
纳米材料
渗透
气体分离
化学工程
化学
复合材料
渗透
生物化学
工程类
作者
Haonan Li,Zeyu Sun,Zijia Yu,K.K.Y. Man,Chao Zhang,Zhi‐Kang Xu
标识
DOI:10.1038/s41467-025-63502-2
摘要
Abstract Mixed matrix membranes (MMMs) capable of breaking the permeability-selectivity trade-off suffer from the inefficient and disconnected bulky transport channels as well as inferior interfacial compatibility between nanomaterials and polymers. Herein, we propose an original photothermal-triggered in-situ gelation approach to elaborate an original class of MMMs, termed nanofiber-interwoven gel membranes (NIGMs) that feature tunable 3D-interconnected ultrafast transport channels and highly-selective CO 2 -philic gel for boosting CO 2 separation performance. The key design of NIGMs lies in leveraging dual functions of CNT-interwoven skeleton: (1) serving as a photothermal confined reactor that rapidly triggers in-situ gelation of highly-selective CO 2 -philic gel without phase separation-induced interfacial defects to construct defect-free and thickness-controllable NIGMs; (2) functioning as a 3D-interconnected continuous skeleton for providing ultrafast CO 2 transport channels. By orchestrating the distribution and configuration of interwoven nanofibers, the NIGMs possess a boosted CO 2 permeance of 211.0 GPU increased by 1558% over polymeric gel counterparts and an ultrahigh CO 2 /N 2 and CO 2 /CH 4 selectivity of up to 151 and 47 respectively. Our work offers a paradigm shift in developing advanced MMMs beyond gas separation.
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