Abstract
Dielectric interfaces are crucial to the behavior of charged membranes, from graphene to synthetic and biological lipid bilayers. Understanding electrolyte behavior near these interfaces remains a challenge, especially in the case of rough dielectric surfaces. A lack of analytical solutions consigns this problem to numerical treatments. We report an analytic method for determining electrostatic potentials near curved dielectric membranes in a two-dimensional periodic “slab” geometry using a periodic summation of Green’s functions. This method is amenable to simulating arbitrary groups of charges near surfaces with two-dimensional deformations. We concentrate on one-dimensional undulations. We show that increasing membrane undulation increases the asymmetry of interfacial charge distributions due to preferential ionic repulsion from troughs. In the limit of thick membranes, we recover results mimicking those for electrolytes near a single interface. Our work demonstrates that rough surfaces generate charge patterns in electrolytes of charged molecules or mixed-valence ions.
Original language | English (US) |
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Article number | 094704 |
Journal | Journal of Chemical Physics |
Volume | 160 |
Issue number | 9 |
DOIs | |
State | Published - Mar 7 2024 |
Funding
The authors acknowledge the support from the Department of Energy, Office of Basic Energy Sciences, under Contract No. DE-FG02-08ER46539. N.P. acknowledges the support from the Ryan Fellowship through the International Institute for Nanotechnology at Northwestern University and additionally the support of the Hierarchical Materials Cluster Program at Northwestern University. A.P.d.S. acknowledges the Department of Materials Science and Engineering at Northwestern University for appointing him Eschbach Visiting Professor. A.P.d.S. also acknowledges FAPERGS and CNPq. M.O.d.l.C. research was supported, in part, by Grant No. NSF PHY-1748958 to the Kavli Institute for Theoretical Physics (KITP).
ASJC Scopus subject areas
- General Physics and Astronomy
- Physical and Theoretical Chemistry