Ionic transport through sub-10 nm diameter hydrophobic high-aspect ratio nanopores: experiment, theory and simulation

被引:81
作者
Balme, Sebastien [1 ]
Picaud, Fabien [2 ]
Manghi, Manoel [3 ]
Palmeri, John [4 ]
Bechelany, Mikhael [1 ]
Cabello-Aguilar, Simon [1 ]
Abou-Chaaya, Adib [1 ]
Miele, Philippe [1 ]
Balanzat, Emmanuel [5 ]
Janot, Jean Marc [1 ]
机构
[1] CNRS, Inst Europeen Membranes, ENSCM UM, UMR5635, F-34095 Montpellier 5, France
[2] Univ Franche Comte, Ctr Hosp Univ, Lab Nanomed Imagerie & Therapeut, F-25030 Besancon, France
[3] Univ Toulouse, CNRS UPS, Lab Phys Theor IRSAMC, UMR5152, F-31062 Toulouse, France
[4] Univ Montpellier, CNRS, L2C, UMR 5221, F-34059 Montpellier, France
[5] CEA, CNRS, ENSICAEN, Ctr Rech Ions Mat & Photon,UMR6252, F-14050 Caen 4, France
关键词
MOLECULAR-DYNAMICS; SURFACE; DNA; TRANSLOCATION; CHARGE; DISCRIMINATION; EXCLUSION; ENERGY; FORCE; WATER;
D O I
10.1038/srep10135
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fundamental understanding of ionic transport at the nanoscale is essential for developing biosensors based on nanopore technology and new generation high-performance nanofiltration membranes for separation and purification applications. We study here ionic transport through single putatively neutral hydrophobic nanopores with high aspect ratio (of length L = 6 mu m with diameters ranging from 1 to 10 nm) and with a well controlled cylindrical geometry. We develop a detailed hybrid mesoscopic theoretical approach for the electrolyte conductivity inside nanopores, which considers explicitly ion advection by electro-osmotic flow and possible flow slip at the pore surface. By fitting the experimental conductance data we show that for nanopore diameters greater than 4 nm a constant weak surface charge density of about 10(-2) C m(-2) needs to be incorporated in the model to account for conductance plateaus of a few pico-siemens at low salt concentrations. For tighter nanopores, our analysis leads to a higher surface charge density, which can be attributed to a modification of ion solvation structure close to the pore surface, as observed in the molecular dynamics simulations we performed.
引用
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页数:14
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