膜
叠氮
渗透力
共价有机骨架
化学工程
反向电渗析
材料科学
共价键
图层(电子)
功率密度
纳米技术
联氨(抗抑郁剂)
化学
色谱法
有机化学
正渗透
功率(物理)
电渗析
反渗透
生物化学
物理
量子力学
工程类
作者
Wen He,Jing Wang,Ziwen Dai,Xing Liu,Sha Liang,F. Xu,Zhen Hu,Zhao Yang,Pengrui Jin,Jiakuan Yang,Bart Van der Bruggen,Zhao Yang
出处
期刊:Small
[Wiley]
日期:2025-02-13
标识
DOI:10.1002/smll.202410140
摘要
Abstract Charged covalent organic framework (COF) membranes have gained wide interest as the key component in the reverse electrodialysis technique to harness salinity energy. However, maintaining rapid ion transport and high selectivity in a Ca 2+ ‐rich environment remains a formidable challenge. Herein, a highly cation‐conductive azine COF membrane is synthesized via a layer‐by‐layer chemical reaction between 2,4‐dihydroxy‐1,3,5‐diphenyltrialdehyde (DHTA) and hydrazine hydrate (HZ). The osmotic energy generator based on this membrane delivers a high power density of 17.8 W m −2 under 2.5 M/0.05 M CaCl 2 , outperforming the TFP‐HZ membrane (3.2 W m −2 ), commercial benchmark (5 W m −2 ), and other literature reported membranes owing to the simultaneous modulation of charges in angstrom scale channels and selective layer thickness. Moreover, this osmotic power density is comparable to that in a NaCl gradient (2.5 M/0.05 M, 16.9 W m −2 ), which is rare. These results indicate that the DHTA‐HZ membrane is highly suitable for application in hypersaline environments containing Ca 2+ , serving as an inspiration for the development of COF‐based nanofluidic membranes with high power output efficiency in a practical high‐salinity environment.
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