Influence of Electrospun Poly(vinylidene difluoride) Nanofiber Matrix on the Ion Dynamics of a Protic Organic Ionic Plastic Crystal

2018 ◽  
Vol 122 (26) ◽  
pp. 14546-14553 ◽  
Author(s):  
Jun Rao ◽  
R. Vijayaraghavan ◽  
Xiaoen Wang ◽  
Yundong Zhou ◽  
Patrick C. Howlett ◽  
...  
2016 ◽  
Vol 4 (25) ◽  
pp. 9873-9880 ◽  
Author(s):  
Xiaoen Wang ◽  
Haijin Zhu ◽  
George W. Greene ◽  
Jiaye Li ◽  
Nahid Iranipour ◽  
...  

Organic ionic plastic crystal (OIPC) modified poly(vinylidene difluoride) (PVDF) composite fiber membrane with enhanced ion dynamics and almost pure β-PVDF are demonstrated.


2021 ◽  
Vol 2 (5) ◽  
pp. 1683-1694
Author(s):  
Frederick Nti ◽  
George W. Greene ◽  
Haijin Zhu ◽  
Patrick C. Howlett ◽  
Maria Forsyth ◽  
...  

Ion dynamics enhancements derived from anion–polymer interactions are proposed in organic ionic plastic crystal–poly(vinylidene fluoride)composite electrolytes.


2017 ◽  
Vol 5 (47) ◽  
pp. 24909-24919 ◽  
Author(s):  
N. Iranipour ◽  
D. J. Gunzelmann ◽  
A. J. Seeber ◽  
J. Vongsvivut ◽  
A. F. Hollenkamp ◽  
...  

Microstructural features significantly affecting lithium ion dynamics and conduction within the crystalline structure of pyrrolidinium based organic ionic plastic crystals.


2003 ◽  
Vol 50 (15-17) ◽  
pp. 2615-2643 ◽  
Author(s):  
Yusheng Dou ◽  
Ben R. Torralva ◽  
Roland E. Allen

2018 ◽  
Author(s):  
Nicola Molinari ◽  
Jonathan P. Mailoa ◽  
Boris Kozinsky

<div> <div> <div> <p>The model and analysis methods developed in this work are generally applicable to any polymer electrolyte/cation-anion combination, but we focus on the currently most prominent polymer electrolyte material system: poly(ethylene) oxide/Li- bis(trifluoromethane) sulfonamide (PEO + LiTFSI). The obtained results are surprising and challenge the conventional understanding of ionic transport in polymer electrolytes: the investigation of a technologically relevant salt concentration range (1 - 4 M) revealed the central role of the anion in coordinating and hindering Li ion movement. Our results provide insights into correlated ion dynamics, at the same time enabling rational design of better PEO-based electrolytes. In particular, we report the following novel observations. 1. Strong binding of the Li cation with the polymer competes with significant correlation of the cation with the salt anion. 2. The appearance of cation-anion clusters, especially at high concentration. 3. The asymmetry in the composition (and therefore charge) of such clusters; specifically, we find the tendency for clusters to have a higher number of anions than cations.</p> </div> </div> </div>


2018 ◽  
Author(s):  
Nicola Molinari ◽  
Jonathan P. Mailoa ◽  
Boris Kozinsky

<div> <div> <div> <p>The model and analysis methods developed in this work are generally applicable to any polymer electrolyte/cation-anion combination, but we focus on the currently most prominent polymer electrolyte material system: poly(ethylene) oxide/Li- bis(trifluoromethane) sulfonamide (PEO + LiTFSI). The obtained results are surprising and challenge the conventional understanding of ionic transport in polymer electrolytes: the investigation of a technologically relevant salt concentration range (1 - 4 M) revealed the central role of the anion in coordinating and hindering Li ion movement. Our results provide insights into correlated ion dynamics, at the same time enabling rational design of better PEO-based electrolytes. In particular, we report the following novel observations. 1. Strong binding of the Li cation with the polymer competes with significant correlation of the cation with the salt anion. 2. The appearance of cation-anion clusters, especially at high concentration. 3. The asymmetry in the composition (and therefore charge) of such clusters; specifically, we find the tendency for clusters to have a higher number of anions than cations.</p> </div> </div> </div>


2020 ◽  
Vol 65 (12) ◽  
pp. 1905-1911
Author(s):  
R. S. Ablizen ◽  
M. A. Monastyrskiy ◽  
M. G. Skoblin ◽  
A. V. Pento ◽  
A. B. Bukharina ◽  
...  
Keyword(s):  

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