TY - JOUR
T1 - Immobilized cation functional gel polymer electrolytes with high lithium transference number for lithium ion batteries
AU - Tsao, Chih Hao
AU - Su, Hou Ming
AU - Huang, Hsiang Ting
AU - Kuo, Ping Lin
AU - Teng, Hsisheng
N1 - Funding Information:
The authors would like to thank the Ministry of Science and Technology , Taipei, Taiwan within the project “Developing key technologies for the synthesis of high-ionic conductivity solid-state electrolytes assembled in lithium ion batteries” for their generous financial support of this research.
Funding Information:
The authors would like to thank the Ministry of Science and Technology, Taipei, Taiwan within the project “Developing key technologies for the synthesis of high-ionic conductivity solid-state electrolytes assembled in lithium ion batteries” for their generous financial support of this research.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/2/15
Y1 - 2019/2/15
N2 - The ionic liquid (IL) incorporated hybrid membranes were synthesized via sol-gel process to simultaneously act as a separator and functionalized gel polymer electrolytes (GPEs). These IL functionalized hybrid GPEs provide an adequate ionic conductivity of 6.0 mS cm−1 at 30 °C and good electrochemical stability up to 5.0 V. Moreover, the differential scanning calorimetry (DSC) results demonstrated that the IL group hardened the polymer chain without liquid electrolytes. However, the glass transition temperature (Tg) dramatically decreased when liquid electrolytes were incorporated, which means the polymer has good affinity for carbonate electrolytes and good ionic transport ability. Further, the immobilized cationic group anchored in the polymer matrix can be seen as a Lewis acid; thus, it interacts with the PF6- anion and enhances the lithium transference number from 0.28 to 0.57. In addition, compared to the GEP without the IL group (SiEO), the GPE with high IL group (ImEO51) shows relatively superior battery performance. For the Li/GPE/LiFePO4 battery application, cell capacities of both SiEO and ImEO51 were close to 150 mAh g−1 at 0.1 C. However, at high current density of 5 C, the capacities of ImEO51 can reach 90 mAh g−1, significantly higher than that without the IL group (35 mAh g−1). Therefore, the aforementioned properties of the IL functional GPEs can be a potential alternative polymer electrolyte for high-performance rechargeable lithium ion batteries.
AB - The ionic liquid (IL) incorporated hybrid membranes were synthesized via sol-gel process to simultaneously act as a separator and functionalized gel polymer electrolytes (GPEs). These IL functionalized hybrid GPEs provide an adequate ionic conductivity of 6.0 mS cm−1 at 30 °C and good electrochemical stability up to 5.0 V. Moreover, the differential scanning calorimetry (DSC) results demonstrated that the IL group hardened the polymer chain without liquid electrolytes. However, the glass transition temperature (Tg) dramatically decreased when liquid electrolytes were incorporated, which means the polymer has good affinity for carbonate electrolytes and good ionic transport ability. Further, the immobilized cationic group anchored in the polymer matrix can be seen as a Lewis acid; thus, it interacts with the PF6- anion and enhances the lithium transference number from 0.28 to 0.57. In addition, compared to the GEP without the IL group (SiEO), the GPE with high IL group (ImEO51) shows relatively superior battery performance. For the Li/GPE/LiFePO4 battery application, cell capacities of both SiEO and ImEO51 were close to 150 mAh g−1 at 0.1 C. However, at high current density of 5 C, the capacities of ImEO51 can reach 90 mAh g−1, significantly higher than that without the IL group (35 mAh g−1). Therefore, the aforementioned properties of the IL functional GPEs can be a potential alternative polymer electrolyte for high-performance rechargeable lithium ion batteries.
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U2 - 10.1016/j.memsci.2018.11.033
DO - 10.1016/j.memsci.2018.11.033
M3 - Article
AN - SCOPUS:85056891532
VL - 572
SP - 382
EP - 389
JO - Journal of Membrane Science
JF - Journal of Membrane Science
SN - 0376-7388
ER -
