纳米孔
纳米孔
膜
渗透力
材料科学
缩放比例
化学物理
多孔性
纳米技术
可扩展性
渗透
电压
离子
化学
计算机科学
正渗透
电气工程
工程类
复合材料
反渗透
数学
生物化学
有机化学
数据库
几何学
作者
Makusu Tsutsui,Wei‐Lun Hsu,Kazumichi Yokota,Iat Wai Leong,Hirofumi Daiguji,Tomoji Kawai
出处
期刊:Exploration
[Wiley]
日期:2024-01-08
卷期号:4 (2): 20220110-20220110
被引量:24
摘要
Artificial nanofluidic networks are emerging systems for blue energy conversion that leverages surface charge-derived permselectivity to induce voltage from diffusive ion transport under salinity difference. Here the pivotal significance of electrostatic inter-channel couplings in multi-nanopore membranes, which impose constraints on porosity and subsequently influence the generation of large osmotic power outputs, is illustrated. Constructive interference is observed between two 20 nm nanopores of 30 nm spacing that renders enhanced permselectivity to osmotic power output via the recovered electroneutrality. On contrary, the interference is revealed as destructive in two-dimensional arrays causing significant deteriorations of the ion selectivity even for the nanopores sparsely distributed at an order of magnitude larger spacing than the Dukhin length. Most importantly, a scaling law is provided for deducing the maximal membrane area and porosity to avoid the selectivity loss via the inter-pore electrostatic coupling. As the electric crosstalk is inevitable in any fluidic network, the present findings can be a useful guide to design nanoporous membranes for scalable osmotic power generations.
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