亚2nm尺度下纳米多孔膜的动态调制门控过程

Cell Press Pub Date : 1900-01-01 DOI:10.2139/ssrn.3915014
Yahong Zhou, Junran Hao, Jiajia Zhou, J. Liao, Yan Wei, Xia‐Chao Chen, C. Ning, Xuliang Deng, Lei Jiang
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摘要

纳米通道的门控特性作为一种关键的纳米流体行为,在传感、物质传输和分离等方面有着广泛的应用。制备的纳米通道末端的“开”态和“闭”态随着环境的变化被广泛研究。但到目前为止,对动态门控过程的控制仍然是一个很大的挑战。在本文中,我们以亚2nm的速度调节聚吡咯(PPy)基纳米孔膜系统的动态电门控过程。纳米约束环境使聚合物链具有优异的电化学性能,聚合物膜以可控的速度膨胀或收缩,并伴有可逆的反离子吸收或排出。在这种开关过程中,聚合物的厚度变化了83%,形成了完全封闭的门控状态。此外,我们还通过原位AFM形貌直接观察了聚合物链在纳米尺度(约10 nm)上的连续变化。这种小的工作电压和超高应变范围,以及生物相容性材料,使这种设计在智能纳米机器人和可穿戴应用中具有前景。
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Dynamically Modulating Gating Process of Nanoporous Membrane at Sub-2 Nm Scale
Gating properties of nanochannels, as a key nanofluidic behavior, holds huge applications in sensing, mass transportation and separation. It has been widely studied the terminal “open” and “close” states in response to changes of environments, for prepared nanochannels. Yet to date, it remains great challenge to control the dynamic gating process. Here in this manuscript, we modulate the dynamically electric gating process in polypyrrole (PPy)-based nanoporous membranes system at sub-2 nm speed. The nano-confinement environment renders the polymer chain with excellent electrochemical property and the polymer film swells or contracts in a controlled speed accompanied by a reversible counter-ion uptake or expulsion. With this switching process, the thickness of the polymer changes by 83%, resulting a fully closed gating state. Besides, we directly observe the successive polymer chain variation at nanoscale (ca. 10 nm) by the AFM topography in situ . This small operation voltages and ultra-high strain scope, along with biocompatible materials, make this design promising for smart nanorobot and wearable applications.
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