skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Connecting the Ion Separation Factor to the Sorption and Diffusion Selectivity of Ion Exchange Membranes
Award ID(s):
1752048
PAR ID:
10219595
Author(s) / Creator(s):
; ;
Date Published:
Journal Name:
Industrial & Engineering Chemistry Research
Volume:
59
Issue:
32
ISSN:
0888-5885
Page Range / eLocation ID:
14189 to 14206
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Organic ionic plastic crystals (OIPCs) are emerging as promising electrolyte materials for solid-state batteries. However, despite the fast ionic diffusion, OIPCs exhibit relatively low DC conductivity in solid phases caused by strong ion-ion correlations that suppress charge transport. To understand the origin of this suppression, we performed a study of ion dynamics in the OIPC 1-Ethyl-1-methylpyrrolidinium bis (trifluoromethyl sulfonyl) imide [P12][TFSI] utilizing dielectric spectroscopy, light scattering, and Nuclear Magnetic Resonance diffusometry. Comparison of the results obtained in this study with the published earlier results on an OIPC with a completely different structure (Diethyl(methyl)(isobutyl)phosphonium Hexafluorophosphate [P1,2,2,4][PF6]) revealed strong similarities in ion dynamics in both systems. Unlike DC conductivity, which may drop more than ten times between melted and solid phases, diffusion of anions and cations remains high and does not show strong changes at phase transition. The conductivity spectra in the broad frequency range demonstrate unusual shapes in solid phases with an additional step separating fast local ion motions from suppressed long-range charge diffusion controlling DC conductivity. We suggested that in solid phases, anions and cations can jump only between the specific ion sites defined by the crystalline structure. These constraints lead to strong cation-cation and anion-anion correlations strongly suppressing long-range charge transport. 
    more » « less
  2. We consider the classical Euler-Poisson system for electrons and ions, interacting through an electrostatic field. The mass ratio of an electron and an ion is small and we establish an asymptotic expansion of solutions, where the main term is obtained from a solution to a self-consistent equation involving only the ion variables. Moreover, on R^3, the validity of such an expansion is established even with \ill-prepared" Cauchy data, by including an additional initial layer correction. 
    more » « less
  3. We consider the classical Euler-Poisson system for electrons and ions, interacting through an electrostatic field. The mass ratio of an electron and an ion $$ m_e/M_i\ll 1$$ is small and we establish an asymptotic expansion of solutions, where the main term is obtained from a solution to a self-consistent equation involving only the ion variables. Moreover, on $$ \mathbb{R}^3$$, the validity of such an expansion is established even with ``ill-prepared'' Cauchy data, by including an additional initial layer correction. 
    more » « less