The Electrolyte Additive Effects on Commercialized Ni-Rich LiNixCoyMnzO2 (x + y + z = 1) Based Lithium-Ion Pouch Batteries at High Temperature

Author(s):  
Chengyun Wang ◽  
Qianqian Hu ◽  
Junnan Hao ◽  
Xijun Xu ◽  
Liuzhang Ouyang ◽  
...  
MRS Advances ◽  
2019 ◽  
Vol 4 (49) ◽  
pp. 2641-2649
Author(s):  
Jonathan Boltersdorf ◽  
Jin Yan ◽  
Samuel A. Delp ◽  
Ben Cao ◽  
Jianping P. Zheng ◽  
...  

ABSTRACTLithium-ion capacitors (LICs) and Hybrid LICs (H-LICs) were assembled as three-layered pouch cells in an asymmetric configuration employing Faradaic pre-lithiated hard carbon anodes and non-Faradaic ion adsorption-desorption activated carbon (AC) cathodes for LICs and lithium iron phosphate (LiFePO4-LFP)/AC composite cathodes for H-LICs. The room temperature rate performance was evaluated after the initial LIC and H-LIC cell formation as a function of the electrolyte additives. The capacity retention was measured after charging at high temperature conditions, while the design factor explored was electrolyte additive formulation, with a focus on their stability. The high temperature potential holds simulate electrochemical energy materials under extreme environments and act to accelerate the failure mechanisms associated with cell degradation to determine robust electrolyte/additive combinations.


2020 ◽  
Vol 8 (37) ◽  
pp. 19573-19587 ◽  
Author(s):  
Felix Aupperle ◽  
Gebrekidan Gebresilassie Eshetu ◽  
Kevin W. Eberman ◽  
Ang Xioa ◽  
Jean-Sebastien Bridel ◽  
...  

The dosage of (2-cyanoethyl)triethoxysilane (TEOSCN) is investigated as the electrode/electrolyte interface modulating electrolyte additive to improve the performance of LiN0.6Mn0.2Co0.2O2/silicon–graphite batteries at a high temperature (45 °C).


2020 ◽  
Vol 56 (60) ◽  
pp. 8420-8423
Author(s):  
Kaijia Duan ◽  
Jingrong Ning ◽  
Lai Zhou ◽  
Wenjia Xu ◽  
Chuanqi Feng ◽  
...  

1-(2-Cyanoethyl)pyrrole electrolyte additive via a capturing strategy enables high-performance of lithium-ion batteries at high temperature.


2015 ◽  
Vol 294 ◽  
pp. 248-253 ◽  
Author(s):  
Agnese Birrozzi ◽  
Fabio Maroni ◽  
Rinaldo Raccichini ◽  
Roberto Tossici ◽  
Roberto Marassi ◽  
...  

2021 ◽  
pp. 2003756
Author(s):  
Sven Klein ◽  
Patrick Harte ◽  
Jonas Henschel ◽  
Peer Bärmann ◽  
Kristina Borzutzki ◽  
...  

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 330
Author(s):  
Sangryun Kim ◽  
Kazuaki Kisu ◽  
Shin-ichi Orimo

We report the stabilization of the high-temperature (high-T) phase of lithium carba-closo-decaborate, Li(CB9H10), via the formation of solid solutions in a Li(CB9H10)-Li2(B12H12) quasi-binary system. Li(CB9H10)-based solid solutions in which [CB9H10]− is replaced by [B12H12]2− were obtained at compositions with low x values in the (1−x)Li(CB9H10)−xLi2(B12H12) system. An increase in the extent of [B12H12]2− substitution promoted stabilization of the high-T phase of Li(CB9H10), resulting in an increase in the lithium-ion conductivity. Superionic conductivities of over 10−3 S cm−1 were achieved for the compounds with 0.2 ≤ x ≤ 0.4. In addition, a comparison of the Li(CB9H10)−Li2(B12H12) system and the Li(CB9H10)−Li(CB11H12) system suggests that the valence of the complex anions plays an important role in the ionic conduction. In battery tests, an all-solid-state Li–TiS2 cell employing 0.6Li(CB9H10)−0.4Li2(B12H12) (x = 0.4) as a solid electrolyte presented reversible battery reactions during repeated discharge–charge cycles. The current study offers an insight into strategies to develop complex hydride solid electrolytes.


2007 ◽  
Vol 174 (2) ◽  
pp. 628-631 ◽  
Author(s):  
C. Korepp ◽  
W. Kern ◽  
E.A. Lanzer ◽  
P.R. Raimann ◽  
J.O. Besenhard ◽  
...  

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