scholarly journals In Situ Preparation of Crosslinked Polymer Electrolytes for Lithium Ion Batteries: A Comparison of Monomer Systems

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1707
Author(s):  
Eike T. Röchow ◽  
Matthias Coeler ◽  
Doris Pospiech ◽  
Oliver Kobsch ◽  
Elizaveta Mechtaeva ◽  
...  

Solid polymer electrolytes for bipolar lithium ion batteries requiring electrochemical stability of 4.5 V vs. Li/Li+ are presented. Thus, imidazolium-containing poly(ionic liquid) (PIL) networks were prepared by crosslinking UV-photopolymerization in an in situ approach (i.e., to allow preparation directly on the electrodes used). The crosslinks in the network improve the mechanical stability of the samples, as indicated by the free-standing nature of the materials and temperature-dependent rheology measurements. The averaged mesh size calculated from rheologoical measurements varied between 1.66 nm with 10 mol% crosslinker and 4.35 nm without crosslinker. The chemical structure of the ionic liquid (IL) monomers in the network was varied to achieve the highest possible ionic conductivity. The systematic variation in three series with a number of new IL monomers offers a direct comparison of samples obtained under comparable conditions. The ionic conductivity of generation II and III PIL networks was improved by three orders of magnitude, to the range of 7.1 × 10−6 S·cm−1 at 20 °C and 2.3 × 10−4 S·cm−1 at 80 °C, compared to known poly(vinylimidazolium·TFSI) materials (generation I). The transition from linear homopolymers to networks reduces the ionic conductivity by about one order of magnitude, but allows free-standing films instead of sticky materials. The PIL networks have a much higher voltage stability than PEO with the same amount and type of conducting salt, lithium bis(trifluoromethane sulfonyl)imide (LiTFSI). GII-PIL networks are electrochemically stable up to a potential of 4.7 V vs. Li/Li+, which is crucial for a potential application as a solid electrolyte. Cycling (cyclovoltammetry and lithium plating-stripping) experiments revealed that it is possible to conduct lithium ions through the GII-polymer networks at low currents. We concluded that the synthesized PIL networks represent suitable candidates for solid-state electrolytes in lithium ion batteries or solid-state batteries.

RSC Advances ◽  
2015 ◽  
Vol 5 (54) ◽  
pp. 43581-43588 ◽  
Author(s):  
Juan Wang ◽  
Xiaohui He ◽  
Hongyu Zhu ◽  
Defu Chen

Solid polymer electrolytes with high ionic conductivity have been prepared based on an imidazolium-functionalized norbornene ionic liquid block copolymer.


Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1237 ◽  
Author(s):  
Yu Jiang ◽  
Xuemin Yan ◽  
Zhaofei Ma ◽  
Ping Mei ◽  
Wei Xiao ◽  
...  

Solid polymer electrolytes (SPEs) have attracted considerable attention due to the rapid development of the need for more safety and powerful lithium ion batteries. The prime requirements of solid polymer electrolytes are high ion conductivity, low glass transition temperature, excellent solubility to the conductive lithium salt, and good interface stability against Li anode, which makes PEO and its derivatives potential candidate polymer matrixes. This review mainly encompasses on the synthetic development of PEO-based SPEs (PSPEs), and the potential application of the resulting PSPEs for high performance, all-solid-state lithium ion batteries.


ChemSusChem ◽  
2015 ◽  
Vol 8 (24) ◽  
pp. 4133-4138 ◽  
Author(s):  
Jimin Shim ◽  
Ki Yoon Bae ◽  
Hee Joong Kim ◽  
Jin Hong Lee ◽  
Dong-Gyun Kim ◽  
...  

Author(s):  
Adi Vinegrad ◽  
Heftsi Ragones ◽  
Nishani Jayakodi ◽  
Gilat Ardel ◽  
Meital Goor ◽  
...  

Abstract In the current research, we developed and printed by fused-filament fabrication polylactide-polyethylene-oxide blended membranes. The influence of relative content of polymers on the ease of extrusion and printing processes was studied. Ionic liquid N-butyl-N-methylpyrrolidinium bis(trifluoromethane-sulfonyl)imide (Pyr14TFSI) with dissolved LiTFSI salt was infused into the membranes to produce free-standing films of quasi-solid polymer electrolytes. The printed membranes were characterized by ESEM, DSC, XPS, NMR and EIS methods. Neat-printed PLA membrane exhibited poor wetting and low uptake of ionic liquid. However, the XPS tests of 3D-printed PLA-PEO membrane infused with LiTFSI solvated ionic liquid show evidence of the interaction between lithium cations with both, PEO and PLA. The measurements of diffusion coefficients by PGSE-NMR suggest that the Li+ ions are coordinated by the PEO segments in the polymer blend. Increase of the PEO content at the expense of PLA polymer, leads to more than one order of magnitude improvement of bulk conductivity, approaching 0.2mS/cm at 60℃.


2019 ◽  
Vol 23 (10) ◽  
pp. 2785-2792 ◽  
Author(s):  
Dingsheng Shao ◽  
Xianyou Wang ◽  
Xiaolong Li ◽  
Kaili Luo ◽  
Li Yang ◽  
...  

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Yingjian Zhao ◽  
Yong Wang

AbstractPolyethylene oxide (PEO)-based solid polymer electrolytes (SPEs) have important significance for the development of next-generation rechargeable lithium-ion batteries. However, strong coordination between lithium ions and PEO chains results the ion conductivity usually lower than the expectation. In this study, sub-micron montmorillonite is incorporated into the PEO frames as Lewis base center which enables the lithium ions to escape the restraint of PEO chains. After involving montmorillonite (MMT) into the SPEs, the ionic conductivity of SPEs is 4.7 mS cm− 1 at 70 °C which shows a comparable value with that of liquid electrolyte. As coupling with LiFePO4 material, the battery delivers a high discharge capacity of 150.3 mAh g− 1 and an excellent rate performance with a capacity of 111.8 mAh g− 1 at 0.16 C and maintains 58.2 mAh g− 1 at 0.8 C. This study suggests that the customized incorporation of Lewis base materials could offer a promising solution for achieving high-performance PEO-based solid-state electrolyte.


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