Published October 11, 2019 | Version v1
Journal article

Direct observation of confinement-induced diffusophoresis

  • 1. Department of Physics, North Carolina State University, Raleigh, NC 27695, United States of America (United States)

Description

Nanofluidic devices have channel dimensions which come to within one order of magnitude of the Debye length of common aqueous solutions. Conventionally, external driving is used to create concentration polarization of ions and biomolecules in nanofluidic devices. Here we show that long-range ionic strength gradients intrinsic to all nanofluidic devices, even at equilibrium, also drive a drift of macromolecules. To demonstrate the effect, we confine long DNA to straight nanochannels of constant, rectangular cross-section (100 × 100 nm2) which are connected to large microfluidic reservoirs. The motion of DNA is observed in absence of any driving. We find that at low ionic strengths, molecules in nanochannels migrate toward the nano-micro interface, while they are undergoing purely diffusive motion in high salt. Using numerical models, we demonstrate that the motion is consistent with the ionic strength gradient at the micro-nano interface even at equilibrium, and that the dominant cause of the drift is diffusophoresis. (letter)

Availability note (English)

Available from http://dx.doi.org/10.1088/1361-6528/ab31f7

Additional details

Identifiers

Publishing Information

Journal Title
Nanotechnology (Print)
Journal Volume
30
Journal Issue
41
Journal Page Range
[5 p.]
ISSN
0957-4484

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
51054266
Subject category
S77: NANOSCIENCE AND NANOTECHNOLOGY;
Descriptors DEI
AQUEOUS SOLUTIONS; CONFINEMENT; DEBYE LENGTH; DNA; INTERFACES; MOLECULES; NANOFLUIDICS; POLARIZATION
Descriptors DEC
DIMENSIONS; DISPERSIONS; FLUID MECHANICS; HOMOGENEOUS MIXTURES; LENGTH; MECHANICS; MIXTURES; NUCLEIC ACIDS; ORGANIC COMPOUNDS; SOLUTIONS