The time-resolved attenuated total reflectance-Fourier transform infrared(ATR-FTIR) spectroscopy is employed to investigate the transport mechanism of gel electrolytes by monitoring the diffusion behavior of propylene carbonate-lithium bis(trifluoromethylsulfonyl)imide(PC-LiTFSI) solution through poly(vinylidene fluoride-co-hexafluoropropylene)(P(VDF-HFP)) films. Fickian behavior has been observed for both TFSI-and PC. Higher temperature leads to faster diffusion of TFSI~-and PC, which could be related to the increased free volume in P(VDF-HFP)matrix and rapid molecular movements upon heating. Various molecular interactions among LiTFSI, PC and P(VDF-HFP) have been recognized.During the diffusion process, PC molecules, in the form of small clusters, can firstly diffuse through the P(VDF-HFP) film and interact with P(VDFHFP) by dipole-dipole interaction, acting as the plasticizer. Then, Li~+ diffuses into P(VDF-HFP) with the help of ion-dipole interactions between Li~+and C=O of PC. Meanwhile, TFSI-diffuses through the polymer matrix in solvation states. In addition, slight ion-dipole interactions between Li~+and P(VDF-HFP) have been observed as well. Results in this work contribute to a better understanding of transport process in gel polymer electrolytes for lithium-ion batteries and support the development of improved gel polymer electrolytes by rationally regulating molecular interactions. 相似文献
A random copolymer of ethylene oxide with CO2, namely, poly(ethylene carbonate/ethylene oxide) (P(EC/EO)), has been synthesized as a novel candidate for polymer electrolytes. Electrolyte composed of P(EC/EO) and lithium bis(fluorosulfonyl)imide has an ionic conductivity of 0.48 mS cm−1 and a Li transference number (t +) of 0.66 at 60 °C. To study ion‐conductive behavior of P(EC/EO)‐based electrolytes, the Fourier transform infrared (FT‐IR) technique is used to analyze the interactions between Li+ and functional groups of the copolymer. The carbonate groups may interact preferentially with Li+ rather than the ether groups in P(EC/EO). This study suggests that copolymerization of carbonate and flexible ether units can realize both high conductivity and t + for polymer electrolytes. High‐performance P(EC/EO) electrolyte is expected to be a candidate material for use in all‐solid‐state batteries.
Nafion, the most widely used polymer for electrolyte membranes (PEMs) in fuel cells, consists of a fluorocarbon backbone and acidic groups that, upon hydration, swell to form percolated channels through which water and ions diffuse. Although the effects of the channel structures and the acidic groups on water/ion transport have been studied before, the surface chemistry or the spatially heterogeneous diffusivity across water channels has never been shown to directly influence water/ion transport. By the use of molecular spin probes that are selectively partitioned into heterogeneous regions of the PEM and Overhauser dynamic nuclear polarization relaxometry, this study reveals that both water and proton diffusivity are significantly faster near the fluorocarbon and the acidic groups lining the water channels than within the water channels. The concept that surface chemistry at the (sub)nanometer scale dictates water and proton diffusivity invokes a new design principle for PEMs. 相似文献
In the present work, nanofibrous composite polymer electrolytes consist of polyethylene oxide (PEO), ethylene carbonate (EC), propylene carbonate (PC), lithium perchlorate (LiClO4), and titanium dioxide (TiO2) were designed using response surface method (RSM) and synthesized via an electrospinning process. Morphological properties of the as‐prepared electrolytes were studied using SEM. FTIR spectroscopy was conducted to investigate the interaction between the components of the composites. The highest room temperature ionic conductivity of 0.085 mS.cm?1 was obtained with incorporation of 0.175 wt. % TiO2 filler into the plasticized nanofibrous electrolyte by EC. Moreover, the optimum structure was compared with a film polymeric electrolyte prepared using a film casting method. Despite more amorphous structure of the film electrolyte, the nanofibrous electrolyte showed superior ion conductivity possibly due to the highly porous structure of the nanofibrous membranes. Furthermore, the mechanical properties illustrated slight deterioration with incorporation of the TiO2 nanoparticles into the electrospun electrolytes. This investigation indicated the great potential of the electrospun structures as all‐solid‐state polymeric electrolytes applicable in lithium ion batteries. 相似文献
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