Journal
ACS APPLIED ENERGY MATERIALS
Volume 4, Issue 4, Pages 3633-3643Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c00040
Keywords
lithium-ion battery; polybenzimidazole; gel polymer electrolyte; gamma-LiAlO2; energy storage
Funding
- National Science Foundation of China [52063025]
- Foundation of Qinghai Science and Technology Department [2020-HZ-808, 2017-ZJ-794]
- National Natural Science Foundation of China [21764011]
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The study developed a novel GPE, PHOP-LAO, with improved ionic conductivity and thermal stability due to the addition of gamma-LiAlO2. This new GPE shows potential for achieving ultra-stable and safe LIBs in the future, with outstanding cycling performance and power capability retention rates.
Poly(vinylidene fluoride) (PVDF) gel polymer electrolytes (GPEs) show great potential for application in lithium-ion batteries (LIBs) due to their outstanding characteristics. However, the inferior thermal stability and low ionic conductivity limit their practical application. Herein, gamma-LiAlO2 was synthesized and applied in a polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP)-polybenzimidazole containing an ether bond (OPBI)-polyoxyethylene (PEO) (PHOP-LAO) GPE for improving its thermal stability and ionic conductivity properties. The ionic conductivity of PHOP-LAO is 4.83 mS cm(-1), which increased by 210% compared with that of the PHOP sample. It is worth noting that the thermal shrinkage of the PHOP-LAO membrane is greatly reduced (less than 1% at 230 degrees C for 1 h). PHOP-LAO shows outstanding thermal stability, which is beneficial for the safety of LIBs. When the PHOP-LAO GPE was applied to LIBs with Li1.04Ni1/3Co1/3Mn1/3O2 as a cathode, the LIBs exhibit remarkable and stable cycling performance with a discharge capacity retention rate of 85% after 500 cycles at a 2 C rate and maintain a power capability retention rate of up to 77% of the initial capability at the high rate of 10 C (50 degrees C). PHOP-LAO thus shows great potential for achieving ultra-stable and safe LIBs in the future.
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