Ionic plastic crystal-polymeric ionic liquid solid-state electrolytes with high ionic conductivity for lithium ion batteries

2019 ◽  
Vol 236 ◽  
pp. 554-557 ◽  
Author(s):  
Kaihua Yang ◽  
Zhu Liao ◽  
Zhengxi Zhang ◽  
Li Yang ◽  
Shin-ichi Hirano
Nanoscale ◽  
2021 ◽  
Author(s):  
Mengmeng Gao ◽  
Xiaolei Wu ◽  
Shuhong Yi ◽  
Shuwei Sun ◽  
Caiyan Yu ◽  
...  

Upgrading liquid electrolytes with all-solid-state electrolytes (ASEs) or quasi-solid-state electrolytes (QSEs) for solid-state batteries (SBs) have emerged not only to address the intrinsic disadvantages of traditional liquid lithium ion batteries,...


2016 ◽  
Vol 307 ◽  
pp. 678-683 ◽  
Author(s):  
Xiaowei Li ◽  
Zhengxi Zhang ◽  
Sijian Li ◽  
Li Yang ◽  
Shin-ichi Hirano

2020 ◽  
Vol 8 (2) ◽  
pp. 706-713 ◽  
Author(s):  
Jiaying Bi ◽  
Daobin Mu ◽  
Borong Wu ◽  
Jiale Fu ◽  
Hao Yang ◽  
...  

An LLTO/PAN/SNE hybrid solid electrolyte membrane with high ionic conductivity and excellent compatibility with both LiFePO4 cathode and metallic lithium anode.


2020 ◽  
Vol 38 (5) ◽  
pp. 506-513 ◽  
Author(s):  
Deng-Zhou Zhang ◽  
Yong-yuan Ren ◽  
Yin Hu ◽  
Liang Li ◽  
Feng Yan

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.


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