Spontaneous Charging from Sliding Water Drops Determines the Interfacial Deposition of Charged Solutes

X Xiaoteng Zhou (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany) Y Yuwen Ji (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany) Z Zhongyuan Ni (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany) J Javier Garcia Lopez (Institute of Organic Chemistry and Macromolecular Chemistry Friedrich Schiller University Jena Lessingstraße 8 07743 Jena Germany) K Kalina Peneva (Institute of Organic Chemistry and Macromolecular Chemistry Friedrich Schiller University Jena Lessingstraße 8 07743 Jena Germany) S Shan Jiang N Nikolaus Knorr (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany) R Rüdiger Berger K Kaloian Koynov (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany) H Hans‐Jürgen Butt (Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany)

Abstract

AbstractIt has been discovered during the last decade that when water drops slide on hydrophobic surfaces, they spontaneously leave negative charges along the drop path. The drops become positively charged with a potential of 1 kV. This process, called slide electrification, influences drop motion and alters contact angles. Here, a third effect of slide electrification is demonstrated: the preferential deposition of dissolved solutes with positive charges. To illustrate this, water drops containing dissolved charged fluorophore ions are allowed to slide down a tilted hydrophobic surface, and their track is imaged. Two perylene derivatives are applied as fluorophores, one chromophore carrying positive charges, PDI+, and one carrying negative charges, PDI─. PDI+ is deposited at a concentration as low as 0.5 µm. In contrast, PDI─ is only deposited above 5 µm. Experiments using grounded drops or a hydrophobic coating on a conducting substrate indicate that the electric field generated from the negative surface charges behind the drop causes a preferential deposition of the dissolved ions near the interface. This hypothesis also agrees with Kelvin probe measurements. Complex biomolecules deposition e.g. DNA can be also affected by this. These findings contribute to a better understanding of mass transfer processes at interfaces.

Article Details

Volume / Issue Vol. 37, Issue 16
Published April 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

X

Xiaoteng Zhou

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany

Y

Yuwen Ji

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany

Z

Zhongyuan Ni

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany

J

Javier Garcia Lopez

Institute of Organic Chemistry and Macromolecular Chemistry Friedrich Schiller University Jena Lessingstraße 8 07743 Jena Germany

K

Kalina Peneva

Institute of Organic Chemistry and Macromolecular Chemistry Friedrich Schiller University Jena Lessingstraße 8 07743 Jena Germany

S

Shan Jiang

N

Nikolaus Knorr

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany

R

Rüdiger Berger

K

Kaloian Koynov

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany

H

Hans‐Jürgen Butt

Max Planck Institute for Polymer Research Ackermannweg 10 55128 Mainz Germany