scholarly journals Investigation of Solvent Type and Salt Addition in High Transference Number Nonaqueous Polyelectrolyte Solutions for Lithium Ion Batteries

2018 ◽  
Vol 51 (21) ◽  
pp. 8761-8771 ◽  
Author(s):  
Kyle M. Diederichsen ◽  
Kara D. Fong ◽  
Rickey C. Terrell ◽  
Kristin A. Persson ◽  
Bryan D. McCloskey
2019 ◽  
Vol 5 (7) ◽  
pp. 1250-1260 ◽  
Author(s):  
Kara D. Fong ◽  
Julian Self ◽  
Kyle M. Diederichsen ◽  
Brandon M. Wood ◽  
Bryan D. McCloskey ◽  
...  

2019 ◽  
Vol 572 ◽  
pp. 382-389 ◽  
Author(s):  
Chih-Hao Tsao ◽  
Hou-Ming Su ◽  
Hsiang-Ting Huang ◽  
Ping-Lin Kuo ◽  
Hsisheng Teng

2017 ◽  
Vol 2 (11) ◽  
pp. 2563-2575 ◽  
Author(s):  
Kyle M. Diederichsen ◽  
Eric J. McShane ◽  
Bryan D. McCloskey

2021 ◽  
Author(s):  
Xinru Li ◽  
Pengcheng Xu ◽  
Yue Tian ◽  
Alexis Fortini ◽  
Seungho Choi ◽  
...  

Abstract Lithium-ion batteries for electric vehicles (EV) are subject to fast charging, dynamic acceleration, and regenerative braking. However, the polarization arises from these high-rate operations and tends to deteriorate the battery performance and therefore the driving range and lifespan of EVs. Using metal organic frameworks (MOF) as electrolyte modulators (MEM), we report herein a facile strategy for effective mitigation of polarization, where the MEM can confine anions and enrich electrolyte, affording boosted lithium-ion transference number (up to 0.76) and high ionic conductivity (up to 9 mS cm−1). In addition, such MEM could implant itself into electrolyte interface, conferring the interface with low-resistance and ability to suppress concentration polarization. As a result, commercial cells with MEM deliver remarkably enhanced power output, energy efficiency, and lifespan during high rate (2C, > 3000 cycles) as well as dynamic stress tests (tripled cycle life) that mimic realistic operation of EV. This work introduces a readily implementable approach towards optimizing ion transport in electrolyte and developing polarization immune battery for power-intensive applications.


2020 ◽  
Author(s):  
Kara D. Fong ◽  
Julian Self ◽  
Bryan D. McCloskey ◽  
Kristin Persson

Electrolytes featuring negatively-charged polymers such as nonaqueous polyelectrolyte solutions and polymerized ionic liquids are currently under investigation as potential high cation transference number (t<sub>+</sub>) electrolytes for lithium ion batteries. Herein, we use coarse-grained molecular dynamics simulations to characterize the Onsager transport coefficients of polyelectrolyte solutions as a function of chain length and concentration. For all systems studied, we find that the rigorously computed transference number is substantially lower than that approximated by the ideal solution (Nernst-Einstein) equations typically used to characterize these systems due to the presence of strong anion-anion and cation-anion correlations. None of the polyelectrolyte solutions achieve t<sub>+</sub> greater than that of the conventional binary salt electrolyte, with some solutions having negative t<sub>+</sub>. This work demonstrates that the Nernst-Einstein assumption does not provide a physically meaningful estimate of the transference number in these solutions and calls into question the expectation of polyelectrolytes to exhibit high cation transference number.


2020 ◽  
Author(s):  
Kara D. Fong ◽  
Julian Self ◽  
Bryan D. McCloskey ◽  
Kristin Persson

Electrolytes featuring negatively-charged polymers such as nonaqueous polyelectrolyte solutions and polymerized ionic liquids are currently under investigation as potential high cation transference number (t<sub>+</sub>) electrolytes for lithium ion batteries. Herein, we use coarse-grained molecular dynamics simulations to characterize the Onsager transport coefficients of polyelectrolyte solutions as a function of chain length and concentration. For all systems studied, we find that the rigorously computed transference number is substantially lower than that approximated by the ideal solution (Nernst-Einstein) equations typically used to characterize these systems due to the presence of strong anion-anion and cation-anion correlations. None of the polyelectrolyte solutions achieve t<sub>+</sub> greater than that of the conventional binary salt electrolyte, with some solutions having negative t<sub>+</sub>. This work demonstrates that the Nernst-Einstein assumption does not provide a physically meaningful estimate of the transference number in these solutions and calls into question the expectation of polyelectrolytes to exhibit high cation transference number.


2020 ◽  
Vol 5 (1) ◽  
pp. 91-96 ◽  
Author(s):  
Kyle M. Diederichsen ◽  
Bryan D. McCloskey

In this work, crown ethers are shown to significantly improve the conductivity of nonaqueous polyelectrolyte solutions, enabling their use in a battery.


2020 ◽  
Vol 7 (5) ◽  
pp. 1187-1192
Author(s):  
Xin Wang ◽  
Longqing Peng ◽  
Haiming Hua ◽  
Yizheng Liu ◽  
Peng Zhang ◽  
...  

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