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Tuning electrokinetic flow, ionic conductance, and selectivity in a solid-state nanopore modified with a pH-responsive polyelectrolyte brush: A molecular theory approach

Sadeghi, M ; Sharif University of Technology | 2020

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  1. Type of Document: Article
  2. DOI: 10.1021/acs.jpcc.0c02904
  3. Publisher: American Chemical Society , 2020
  4. Abstract:
  5. We use an efficient molecular theory approach to study electrokinetic flow within a pH-responsive nanopore grafted with a polyelectrolyte (PE) brush. The flow rate, migration and convective conductance, electric potential and velocity fields, species distributions and the degree of ionization of the weak PE functional groups and nanopore selectivity are obtained and interpreted while considering pH-induced surface charges. The theory is generally based on writing the overall free energy of the system including the entropies arising from the conformations of flexible, excluded volume chains, the mixing of mobile species, electrostatic contribution, and the free energy due to the chemical acid−base equilibrium reactions. We demonstrate how, by controlling the bulk salt concentration, pH, surface grafting density, and PE drag coefficient, the flow inside the pore can be controlled. Generally, the flow rate gets enhanced upon decreasing pH, but the effect of salt concentration is more complex. As long as the pH is small (large), the flow rate decreases (increases) by increasing the salt concentration, while a nonmonotonic trend is evident at moderate pH values. We find that, when the PE drag coefficient is high (low), the flow rate decreases (increases) by increasing surface grafting density. For intermediate drag coefficients, the flow rate varies nonmonotonically with surface grafting density. It is observed that the convective ionic conductance obeys almost the same trend as the flow rate. It is also illustrated that the mean degree of ionization of the polymer chains and the migration ionic conductance enhance on increasing the background salt concentration, whereas the opposite is true for nanopore selectivity. However, when very low salt concentration is accompanied by a high pH value, there is a minimum in the nanopore selectivity. The present approach allows investigation of the application of PE-coated nanopores as smart nanovalves. © 2020 American Chemical Society
  6. Keywords:
  7. Drag ; Drag coefficient ; Electric potential ; Electrodynamics ; Flow rate ; Free energy ; Grafting (chemical) ; Ionization potential ; pH ; Polyelectrolytes ; Velocity ; Degree of ionization ; Electrokinetic flows ; Electrostatic contributions ; Low salt concentration ; Polyelectrolyte brushes ; Solid-state nanopore ; Species distributions ; Surface grafting density ; Nanopores
  8. Source: Journal of Physical Chemistry C ; Volume 124, Issue 34 , 2020 , Pages 18513-18531
  9. URL: https://pubs.acs.org/doi/10.1021/acs.jpcc.0c02904