Ionic Transport and Robust Switching Properties of the Confined Self-Assembled Block Copolymer/Homopolymer in Asymmetric Nanochannels

The self-assembly of block copolymers in a confined space has been proven to be a facile and robust strategy for fabricating assembled structures with various potential applications. Herein, we employed a new pH-responsive polymer self-assembly method to regulate ion transport inside artificial nanochannels. The track-etched asymmetric nanochannels were functionalized with PS22k-b-P4VP(17k)/hPS(4k) blend polymers, and the ionic conductance and rectification properties of the proposed system were investigated. The pH-actuated changes in the surface charge and wettability resulted in the selective pH-gated ionic transport behavior. The designed system showed a good switching property to the pH stimulus and could recover during the repetitive experiments. The gating ability of the polymer-nanochannel system increased with increasing the weight of the homopolymer, and the proposed platform demonstrated robust stability and reusability. Numerical and the dissipative particle dynamics simulations were implemented to emulate the pH-dependent self-assembling behavior of diblock copolymers in a confined space, which were consistent with the experimental observations. As an example of the self-assembly of polymers in nanoconfinements, this work provides a facile and robust strategy for the regulation of ion transport in synthetic nanochannels. Meanwhile, this work can be further extended to design artificial smart nanogates for various applications such as mass delivery and energy harvesting.

Automated summary

This study utilizes a new pH-responsive polymer self-assembly method to regulate ion transport inside artificial nanochannels. The designed system shows good switching properties and gating ability, with the ability to recover during repetitive experiments. This work provides a novel and robust strategy for the regulation of ion transport in synthetic nanochannels.