Zhang-Rong Wu, , , Tao Feng, , , Ning Bao*, , and , Zeng-Qiang Wu*,
{"title":"可调离子输运的气泡导向泡沫纳米通道","authors":"Zhang-Rong Wu, , , Tao Feng, , , Ning Bao*, , and , Zeng-Qiang Wu*, ","doi":"10.1021/acs.jpclett.5c02401","DOIUrl":null,"url":null,"abstract":"<p >Biological nanochannels, as representative soft nanochannels, exhibit remarkably high efficiency, operating at energy levels only slightly above thermal noise. In contrast, solid-state nanochannels have garnered considerable attention across diverse fields due to their unique properties, including ionic current rectification, ionic Coulomb blockade, and ionic concentration polarization. However, their performance is strongly influenced by thermal noise, necessitating relatively high operating thresholds and, consequently, leading to substantial energy consumption. In this study, we report the fabrication of a bubble-regulated foam nanochannel on a nanocapillary platform and systematically investigate its ion-transport characteristics. Current–voltage (<i>I–V</i>) measurements reveal three distinct behaviors─rectification, linear, and voltage-activated─arising from variations in Tween 60 concentration and bubble volume. As the concentration of Tween 60 increases, a self-assembled monolayer (SAM) gradually forms on the surface of the foam nanochannel, leading to a reduction in the surface charge. This transition results in the progressive transformation of the <i>I–V</i> response from rectification to linear behavior. With further increases in Tween 60 concentration, a well-defined SAM layer develops at the gas–liquid interface, producing a confined nanochannel approximately 2 nm in diameter. Ion transport through this ultranarrow channel requires partial dehydration to overcome the energy barrier, likely driven by interactions between the hydrophilic SAM layer and solvated water molecules. The driving voltage is used to compensate for this ion dehydration, which results in voltage-activated transport behavior. The proposed mechanism was further validated using finite element method (FEM) simulations, which incorporate ionic hydration and size effects, offering quantitative insight into the observed phenomena. Overall, this work provides new mechanistic insights into the operation of soft nanofluidic systems and advances their potential for energy-efficient applications.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"16 39","pages":"10109–10116"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bubble-Guided Foam Nanochannels for Tunable Ionic Transport\",\"authors\":\"Zhang-Rong Wu, , , Tao Feng, , , Ning Bao*, , and , Zeng-Qiang Wu*, \",\"doi\":\"10.1021/acs.jpclett.5c02401\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Biological nanochannels, as representative soft nanochannels, exhibit remarkably high efficiency, operating at energy levels only slightly above thermal noise. In contrast, solid-state nanochannels have garnered considerable attention across diverse fields due to their unique properties, including ionic current rectification, ionic Coulomb blockade, and ionic concentration polarization. However, their performance is strongly influenced by thermal noise, necessitating relatively high operating thresholds and, consequently, leading to substantial energy consumption. In this study, we report the fabrication of a bubble-regulated foam nanochannel on a nanocapillary platform and systematically investigate its ion-transport characteristics. Current–voltage (<i>I–V</i>) measurements reveal three distinct behaviors─rectification, linear, and voltage-activated─arising from variations in Tween 60 concentration and bubble volume. As the concentration of Tween 60 increases, a self-assembled monolayer (SAM) gradually forms on the surface of the foam nanochannel, leading to a reduction in the surface charge. This transition results in the progressive transformation of the <i>I–V</i> response from rectification to linear behavior. With further increases in Tween 60 concentration, a well-defined SAM layer develops at the gas–liquid interface, producing a confined nanochannel approximately 2 nm in diameter. Ion transport through this ultranarrow channel requires partial dehydration to overcome the energy barrier, likely driven by interactions between the hydrophilic SAM layer and solvated water molecules. The driving voltage is used to compensate for this ion dehydration, which results in voltage-activated transport behavior. The proposed mechanism was further validated using finite element method (FEM) simulations, which incorporate ionic hydration and size effects, offering quantitative insight into the observed phenomena. Overall, this work provides new mechanistic insights into the operation of soft nanofluidic systems and advances their potential for energy-efficient applications.</p>\",\"PeriodicalId\":62,\"journal\":{\"name\":\"The Journal of Physical Chemistry Letters\",\"volume\":\"16 39\",\"pages\":\"10109–10116\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry Letters\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c02401\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c02401","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Bubble-Guided Foam Nanochannels for Tunable Ionic Transport
Biological nanochannels, as representative soft nanochannels, exhibit remarkably high efficiency, operating at energy levels only slightly above thermal noise. In contrast, solid-state nanochannels have garnered considerable attention across diverse fields due to their unique properties, including ionic current rectification, ionic Coulomb blockade, and ionic concentration polarization. However, their performance is strongly influenced by thermal noise, necessitating relatively high operating thresholds and, consequently, leading to substantial energy consumption. In this study, we report the fabrication of a bubble-regulated foam nanochannel on a nanocapillary platform and systematically investigate its ion-transport characteristics. Current–voltage (I–V) measurements reveal three distinct behaviors─rectification, linear, and voltage-activated─arising from variations in Tween 60 concentration and bubble volume. As the concentration of Tween 60 increases, a self-assembled monolayer (SAM) gradually forms on the surface of the foam nanochannel, leading to a reduction in the surface charge. This transition results in the progressive transformation of the I–V response from rectification to linear behavior. With further increases in Tween 60 concentration, a well-defined SAM layer develops at the gas–liquid interface, producing a confined nanochannel approximately 2 nm in diameter. Ion transport through this ultranarrow channel requires partial dehydration to overcome the energy barrier, likely driven by interactions between the hydrophilic SAM layer and solvated water molecules. The driving voltage is used to compensate for this ion dehydration, which results in voltage-activated transport behavior. The proposed mechanism was further validated using finite element method (FEM) simulations, which incorporate ionic hydration and size effects, offering quantitative insight into the observed phenomena. Overall, this work provides new mechanistic insights into the operation of soft nanofluidic systems and advances their potential for energy-efficient applications.
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.