2016
DOI: 10.1016/j.nanoen.2016.02.008
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Novel gel polymer electrolyte for high-performance lithium–sulfur batteries

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Cited by 406 publications
(254 citation statements)
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“…The variation of current with time in the polarization process shows that the current reaches a steady value of 61.6 μA from the initial state of 68.2 μA before polarization. Therefore, the t Li+ can be readily calculated according to the Bruce–Vincent equation and the value is 0.51 for the CPE in the current experiment, while the value for the liquid electrolyte is only 0.35, and for PVDF‐HFP based GPE without LATP nanoparticles, the value is 0.36 (Figure S2). The remarkable improvement of t Li+ for the CPE can be attributed to the addition of LATP nanoparticles.…”
Section: Resultsmentioning
confidence: 84%
“…The variation of current with time in the polarization process shows that the current reaches a steady value of 61.6 μA from the initial state of 68.2 μA before polarization. Therefore, the t Li+ can be readily calculated according to the Bruce–Vincent equation and the value is 0.51 for the CPE in the current experiment, while the value for the liquid electrolyte is only 0.35, and for PVDF‐HFP based GPE without LATP nanoparticles, the value is 0.36 (Figure S2). The remarkable improvement of t Li+ for the CPE can be attributed to the addition of LATP nanoparticles.…”
Section: Resultsmentioning
confidence: 84%
“…The gel polymer electrolytes have also been studied in flexible Li–S batteries. Kang and co‐workers studied pentaerythritol tetraacrylate‐based gel polymer electrolyte . The prepared electrolyte showed low interfacial resistance and high ionic conductivity of 1.13 × 10 −2 S cm −1 .…”
Section: Strategy For Future Practical Applicationmentioning
confidence: 99%
“…However, a critical issue facing the Li anode is the infinite volume change that can breach the in‐situ formed passivation layer over repeated Li stripping/plating cycles as shown in Figure a ,. In consequence, Li 2 S can be continuously deposited onto the Li anode surface over cycling, leading to the irreversible capacity loss and considerably lowered Li + conductivity ,,. In this regard, it occurs to us that to form an ex‐situ porous layer impregnated with Li 2 S might be more effective with two‐fold effects, including (i) low‐order Li 2 S prefilled inside the porous separator will partially sacrifice to chemically interact with polysulfides and physically block the migration of polysulfides towards Li anode; (ii) the loss of Li 2 S in the separator can be replenished by polysulfide disproportion to achieve a stabilized separator/cathode interface.…”
Section: Introductionmentioning
confidence: 99%