Effect of additives in PEO/PAA/PMAA composite solid polymer electrolytes on the ionic conductivity and Li ion battery performance

2009 ◽  
Vol 39 (9) ◽  
pp. 1573-1578 ◽  
Author(s):  
Sang Yong An ◽  
Il Chen Jeong ◽  
Mi-Sook Won ◽  
Euh Duck Jeong ◽  
Yoon-Bo Shim
Keyword(s):  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Li Ion Battery ◽  
Effect Of Additives ◽  
Li Ion ◽  
Composite Solid

scholarly journals Contribution Succinonitrile additive for Performa LiTFSi Solid Polymer Electrolytes for Li-Ion Battery

2020 ◽  
Vol 20 (2) ◽  
Author(s):  
Qolby Sabrina ◽  
Titik Lestariningsih ◽  
Christin Rina Ratri ◽  
Achmad Subhan
Keyword(s):  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Room Temperature ◽  
Lithium Salt ◽  
Ionic Conduction ◽  
Lithium Ion ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Half Cell ◽  
Li Ion

Solid polymer electrolyte (SPE) appropriate to solve packaging leakage and expansion volume in lithium-ion battery systems. Evaluation of electrochemical performance of SPE consisted of mixture lithium salt, solid plasticizer, and polymer precursor with different ratio. Impedance spectroscopy was used to investigate ionic conduction and dielectric response lithium bis(trifluoromethane)sulfony imide (LiTFSI) salt, and additive succinonitrile (SCN) plasticizer. The result showing enhanced high ionic conductivity. In half-cell configurations, wide electrochemical stability window of the SPE has been tested. Have stability window at room temperature, indicating great potential of SPE for application in lithium ion batteries. Additive SCN contribute to forming pores that make it easier for the li ion to move from the anode to the cathode and vice versa for better perform SPE. Pore of SPE has been charaterization with FE-SEM. Additive 5% w.t SCN shows the best ionic conductivity with 4.2 volt wide stability window and pretty much invisible pores.

Reactivity-Guided Formulation of Composite Solid Polymer Electrolytes for Superior Sodium Metal Batteries

2021 ◽  
Author(s):  
Edward Matios ◽  
Huan Wang ◽  
Yiwen Zhang ◽  
Jianmin Luo ◽  
Chuanlong Wang ◽  
...  
Keyword(s):  
Solid State ◽  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Dendrite Growth ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Safety Concerns ◽  
Sodium Metal ◽  
Solid State Electrolytes ◽  
Composite Solid

Solid-state electrolytes (SSEs) can effectively address the dendrite growth and safety concerns associated with current battery technologies, but their implementation is still plagued by low ionic conductivity and high interfacial...

Solid Polymer Electrolytes from Crosslinked PEG and Dilithium N,N'-Bis(trifluoromethanesulfonyl)perfluoroalkane-1,ω-disulfonamide and Lithium Bis(trifluoromethanesulfonyl)imide Salts

2008 ◽  
Vol 73 (12) ◽  
pp. 1777-1798 ◽  
Author(s):  
Olt E. Geiculescu ◽  
Rama V. Rajagopal ◽  
Emilia C. Mladin ◽  
Stephen E. Creager ◽  
Darryl D. Desmarteau
Keyword(s):  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Minimum Energy ◽  
Ionic Conductivities ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Segmental Motion ◽  
Concentrated Electrolytes ◽  
Two Factors ◽  
Poly Ethylene

The present work consists of a series of studies with regard to the structure and charge transport in solid polymer electrolytes (SPE) prepared using various new bis(trifluoromethanesulfonyl)imide (TFSI)-based dianionic dilithium salts in crosslinked low-molecular-weight poly(ethylene glycol). Some of the thermal properties (glass transition temperature, differential molar heat capacity) and ionic conductivities were determined for both diluted (EO/Li = 30:1) and concentrated (EO/Li = 10:1) SPEs. Trends in ionic conductivity of the new SPEs with respect to anion structure revealed that while for the dilute electrolytes ionic conductivity is generally rising with increased length of the perfluoroalkylene linking group in the dianions, for the concentrated electrolytes the trend is reversed with respect to dianion length. This behavior could be the result of a combination of two factors: on one hand a decrease in dianion basicity that results in diminished ion pairing and an enhancement in the number of charge carriers with increasing fluorine anion content, thereby increasing ionic conductivity while on the other hand the increasing anion size and concentration produce an increase in the friction/entanglements of the polymeric segments which lowers even more the reduced segmental motion of the crosslinked polymer and decrease the dianion contribution to the overall ionic conductivity. DFT modeling of the same TFSI-based dianionic dilithium salts reveals that the reason for the trend observed is due to the variation in ion dissociation enthalpy, derived from minimum-energy structures, with respect to perfluoroalkylene chain length.

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