@article{c7dcf63f310a46e2be6c3b95eebf19d3,
title = "Strong Electroosmotic Coupling Dominates Ion Conductance of 1.5 nm Diameter Carbon Nanotube Porins",
abstract = "Extreme confinement in nanometer-sized channels can alter fluid and ion transport in significant ways, leading to significant water flow enhancement and unusual ion correlation effects. These effects are especially pronounced in carbon nanotube porins (CNTPs) that combine strong confinement in the inner lumen of carbon nanotubes with the high slip flow enhancement due to smooth hydrophobic pore walls. We have studied ion transport and ion selectivity in 1.5 nm diameter CNTPs embedded in lipid membranes using a single nanopore measurement setup. Our data show that CNTPs are weakly cation selective at pH 7.5 and become nonselective at pH 3.0. Ion conductance of CNTPs exhibits an unusual 2/3 power law scaling with the ion concentration at both neutral and acidic pH values. Coupled Navier-Stokes and Poisson-Nernst-Planck simulations and atomistic molecular dynamics simulations reveal that this scaling originates from strong coupling between water and ion transport in these channels. These effects could result in development of a next generation of biomimetic membranes and carbon nanotube-based electroosmotic pumps.",
keywords = "carbon nanotube porins, electroosmosis, ion transport, nanofluidics, slip-flow coupling",
author = "Yao, {Yun Chiao} and Amir Taqieddin and Alibakhshi, {Mohammad A.} and Meni Wanunu and Aluru, {Narayana R.} and Aleksandr Noy",
note = "Funding Information: We thank Drs. R. Y. Henley and R. H. Tunuguntla for help with the measurement protocols used in this work. CNT synthesis and characterization were supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under award SCW0972. Ion conductance, ion selectivity studies and MD simulations were supported as part of the Center for Enhanced Nanofluidic Transport (CENT), an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under award no. DE-SC0019112. Nanopore conductance measurement platform fabrication was supported by the Division of Materials Research of the National Science Foundation under an award 1710211. Work at the Lawrence Livermore National Laboratory was performed under the auspices of the U.S. Department of Energy under contract DE-AC52-07NA27344. Work at the Molecular Foundry was supported by the Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under contract no. DE-AC02-05CH11231. A.T. and N.R.A acknowledge the use of Blue Waters which is provided by the University of Illinois and National Center for Supercomputing Applications supported by NSF awards OCI-0725070 and ACI-1238993 and the State of Illinois. Publisher Copyright: {\textcopyright} 2019 American Chemical Society.",
year = "2019",
doi = "10.1021/acsnano.9b05118",
language = "English (US)",
journal = "ACS Nano",
issn = "1936-0851",
publisher = "American Chemical Society",
}