How accurate is the Poisson-Boltzmann theory for monovalent ions near highly charged interfaces?

ORAL

Abstract

Monovalent ion distributions next to highly charged interfaces were determined by synchrotron surface X-ray sensitive techniques. A lipid phosphate (dihexadecyl hydrogen-phosphate) was spread as a monolayer at the air-water interface, containing CsI at various concentrations. Using anomalous reflectivity off and at the $L_3$ Cs$^+$ resonance, we provide, for the first time, spatial counterion distributions (Cs$^+$) next to the negatively charged interface over a wide range of ionic concentrations. We argue that at low salt concentrations and for pure water the enhanced concentration of hydroniums H$_3 $O$^+$ at the interface leads to proton-transfer back to the phosphate group by a high contact-potential, whereas high salt concentrations lower the contact-potential resulting in proton- release and increased surface charge-density. The experimental ionic distributions are in excellent agreement with a renormalized-surface-charge Poisson-Boltzmann theory without fitting parameters or additional assumptions.

*The MUCAT sector at the APS and the use of the APS are supported by the U.S. DOE, Basic Energy Sciences through Ames Laboratory under Contracts No. W-7405-Eng-82, and No. W-31-109-Eng-38, respectively.

Authors

  • Wei Bu

    • Ames Laboratory, Iowa State Univerisity
  • Alex Travesset

    • Iowa State University
    • Ames Laboratory, Iowa State Univerisity
    • Iowa State University and Ames lab
  • David Vaknin

    • Ames Laboratory, Iowa State University
    • Iowa State University and Ames Lab
    • Ames Laboratory, Iowa State Univerisity