Ionic‐Nanotube Array Membrane Generating Ultrahigh Osmotic Energy Conversion

P Pengxiang Liu C Changhang Huang (School of Physics Beihang University Beijing 100191 P. R. China) Y Yurong Guo (State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China) Y Yi Zhai H Haoxian Wu (State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China) Q Qi Jiang (Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute) H Hewei Zhao W Wenhui Wang (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, Frontiers Center for Materiobiology and Dynamic Chemistry) X Xingkun Man (School of Physics Beihang University Beijing 100191 China) L Longcheng Gao (State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China) L Lei Jiang

Abstract

AbstractIon exchange membranes (IEMs) are critical components in osmotic energy conversion. However, traditional IEMs suffer from disordered nanochannels due to the lack of precise control over the content and distribution of ionic groups, resulting in an inherent trade‐off between ion selectivity and conductivity. One promising strategy is constructing high‐density ion channels with minimal ionic groups. Herein, high‐density ionic nanotube (INT) arrays are assembled from tiny carboxylic groups (≈0.22 meq·g−1), achieving efficient osmotic energy conversion. Using styrene‐ethylene/butylene‐styrene block copolymers, paired carboxyl groups and tetraphenylethylene (TPE) in the polyethylene/butylene block self‐assemble into a transmembrane cylindrical phase. Driven by the cross‐phase‐miscibility effect of TPE, carboxyl groups aggregate at the cylinder interface, forming INT array membranes with an exceptional density of ≈10¹¹ cm⁻2. The unique structure is directly observed and further validated by self‐consistent field theory. The INT array membranes exhibit 2 orders of magnitude higher current than the control membrane, and an ultrahigh power density of 39.5 W·m⁻2 under a 500‐fold salinity gradient, significantly outperforming the traditional IEMs. This INT design strategy not only provides a promising approach for osmotic energy harvesting but also opens new avenues for advanced membrane‐based separation processes.

Article Details

Volume / Issue Vol. 37, Issue 38
Published September 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

P

Pengxiang Liu

C

Changhang Huang

School of Physics Beihang University Beijing 100191 P. R. China

Y

Yurong Guo

State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China

Y

Yi Zhai

H

Haoxian Wu

State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China

Q

Qi Jiang

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute

H

Hewei Zhao

W

Wenhui Wang

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, Frontiers Center for Materiobiology and Dynamic Chemistry

X

Xingkun Man

School of Physics Beihang University Beijing 100191 China

L

Longcheng Gao

State Key Laboratory of Bioinspired Interfacial Materials Science Center for Bioinspired Science and Technology Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China

L

Lei Jiang