Studies on thin films of PVC-PMMA blend polymer electrolytes

2013 ◽  
Vol 33 (7) ◽  
pp. 633-638 ◽  
Author(s):  
Mohammad Saleem Khan ◽  
Rahmat Gul ◽  
Mian Sayed Wahid

Abstract Thin films of poly (vinyl chloride) (PVC)/poly (methyl methacrylate) (PMMA) blend polymers complexed with different concentrations of LiClO4 salt, containing ethylene carbonate (EC) as the plasticizer, were fabricated by the solution cast procedure. Ionic conductivity, thermal stability and X-ray diffraction (XRD) studies were undertaken. AC impedance measurements were done in the temperature range of 20–70°C. The highest ionic conductivity at room temperature was found to be 2.23×10-5 S cm-1 for the sample containing 15 wt% of LiClO4 salt. The XRD technique was used to investigate the structure and complex formation of solid polymer electrolytes. There was a decrease in degree of crystallinity. The amorphous nature of complexed solid polymer blend electrolyte films increased, due to the addition of LiClO4 salt. Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) revealed the effect of salt on the thermal stability of the polymer electrolytes. It was found that these polymer electrolyte systems show stability up to about 280°C. It was also found that, with increased LiClO4 salt content in complexed polymer electrolyte systems, the degradation temperature decreased.

2020 ◽  
pp. 152808372097062
Author(s):  
Muhammad Yameen Solangi ◽  
Umair Aftab ◽  
Muhammad Ishaque ◽  
Aqeel Bhutto ◽  
Ayman Nafady ◽  
...  

Solid polymer electrolytes (SPEs) are the best choice to replace liquid electrolytes in supercapacitors, fuel cells, solar cells and batteries. The main challenge in this filed is the ionic conductivity and thermal stability of SPEs which is still not up to mark, therefore more investigations are needed to address these issues. In this study, PVA/salt based SPEs was fabricated using both solution cast and electro-spinning methods to probe the effect of different salts such as (NaCl, KCl and KI) and their concentrations on the ionic conductivity. Scanning electron microscopy (SEM) x and Fourier Transform Infra-Red (FTIR) have been employed to study the morphology as well as the different functional groups of SPEs, respectively. It was noted that small addition of NaCl, KCl and KI salts in SPEs dramatically increased the ionic conductivity to 5.95×10−6, 5.31×10−6 and 4.83×10−6 S/cm, respectively. Importantly, the SPEs obtained with NaCl via electro-spinning have higher ionic conductivity (5.95×10−6 S/cm) than their casted SPEs (1.87×10−6 S/cm). Thermal stability was also studied at two different temperatures i.e. 80 °C and 100 °C. The weight loss percentage of electrospun SPEs have zero percent weight loss than the solution based SPEs. The combined results clearly indicated that the nature of salt, concentration and fabrication process play a vital role in the ionic conductivity. Also, the NaCl salt with low molecular weight at low concentrations shows an enhanced ionic conductivity.


2015 ◽  
Vol 6 (7) ◽  
pp. 1052-1055 ◽  
Author(s):  
Suting Yan ◽  
Jianda Xie ◽  
Qingshi Wu ◽  
Shiming Zhou ◽  
Anqi Qu ◽  
...  

A solid polymer electrolyte fabricated using ion containing microgels manifests high ionic conductivity for potential use in lithium batteries.


Processes ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 2090
Author(s):  
Parisa Bashiri ◽  
T. Prasada Rao ◽  
Gholam-Abbas Nazri ◽  
Ratna Naik ◽  
Vaman M. Naik

Ionic conductivity of the polyethylene oxide-LiClO4 (PEOnLiClO4) solid polymer electrolyte (SPE) films with an EO:Li ratio (n) of 10, 12, 15, as well as the hybrid composite solid polymer electrolyte (CSPE) films of PEOnLiClO4 containing 50 wt% of cubic-Li7La3Zr2O12 (LLZO) sub-micron sized particles, have been studied by varying Li-salt content in the films. The complex AC dielectric permittivity and conductivity data obtained from electrical impedance measurements were fitted using a generalized power-law, including the effects of electrode polarization applied at low AC frequencies to obtain various relaxation times. In addition to increased mechanical and thermal robustness, the CSPE films show higher values of ionic conductivity, >10−4 S/cm at room temperature compared to those of SPE films with n = 12 and 15. On the contrary, the ionic conductivity of CSPE with n = 10 decreases by a factor of three compared to the corresponding SPE film due to increased polymer structural reorientation and Li-ion pairing effects. The Vogel–Tammann–Fulcher behavior of the temperature-dependent conductivity data indicates a close correlation between the ionic conductivity and polymer segmental relaxation. The PEO12LiClO4-LLZO film shows the lowest activation energy of ~0.05 eV.


2021 ◽  
Author(s):  
Chandni Devi ◽  
Jnaneswari Gellanki ◽  
Håkan Pettersson ◽  
Sandeep Kumar

Abstract Solid-state sodium ion batteries are frequently referred to as the most promising technology for future energy storage applications. However, developing a solid electrolyte with high ionic conductivity and a wide electrochemical stability window, remains a major challenge. Although solid-polymer electrolytes have attracted great interest due to their low cost, low density and very good processability, they generally have significantly lower ionic conductivity and poor mechanical strength. Here, we report on the development of a low-cost solid polymer electrolyte comprised of poly(ethylene oxide), poly(vinylpyrrolidone) and sodium hexafluorophosphate, mixed with indium arsenide nanowires. We show that the addition of 1.0 percent by weight of nanowires increases the sodium ion conductivity in the polymer to 1.50 × 10-4 Scm−1 at 40° C. This is the highest reported conductivity for any solid polymer electrolyte to date. In order to explain this remarkable characteristic, we propose a new transport model where sodium ions hop between close-spaced defect sites present on the surface of the nanowires, forming an effective complex conductive percolation network. Our work represents a significant advance in the development of novel solid polymer electrolytes with embedded ultrafast 1D percolation networks for next generations of low-cost, high-performance batteries with excellent energy storage capabilities.


Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 452 ◽  
Author(s):  
Jorge Olmedo-Martínez ◽  
Leire Meabe ◽  
Andere Basterretxea ◽  
David Mecerreyes ◽  
Alejandro Müller

Poly(ethylene oxide) (PEO) is the most widely used polymer in the field of solid polymer electrolytes for batteries. It is well known that the crystallinity of polymer electrolytes strongly affects the ionic conductivity and its electrochemical performance. Nowadays, alternatives to PEO are actively researched in the battery community, showing higher ionic conductivity, electrochemical window, or working temperature range. In this work, we investigated polymer electrolytes based on aliphatic polyethers with a number of methylene units ranging from 2 to 12. Thus, the effect of the lithium bis(trifluoromethanesulfone) imide (LiTFSI) concentration on the crystallization behavior of the new aliphatic polyethers and their ionic conductivity was investigated. In all the cases, the degree of crystallinity and the overall crystallization rate of the polymers decreased drastically with 30 wt % LiTFSI addition. The salt acted as a low molecular diluent to the polyethers according to the expectation of the Flory–Huggins theory for polymer–diluent mixtures. By fitting our results to this theory, the value of the interaction energy density (B) between the polyether and the LiTFSI was calculated, and we show that the value of B must be small to obtain high ionic conductivity electrolytes.


Energies ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 2559 ◽  
Author(s):  
Ye Lim ◽  
Hyun-Ah Jung ◽  
Haejin Hwang

To improve the ionic conductivity and thermal stability of a polyethylene oxide (PEO)-ethylene carbonate (EC)-LiClO4-based solid polymer electrolyte for lithium-ion batteries, polymethyl methacrylate (PMMA) and silica aerogel were incorporated into the PEO matrix. The effects of the PEO:PMMA molar ratio and the amount of silica aerogel on the structure of the PEO-PMMA-LiClO4 solid polymer electrolyte were studied by X-ray diffraction, Fourier-transform infrared spectroscopy and alternating current (AC) impedance measurements. The solid polymer electrolyte with PEO:PMMA = 8:1 and 8 wt% silica aerogel exhibited the highest lithium-ion conductivity (1.35 × 10−4 S∙cm−1 at 30 °C) and good mechanical stability. The enhanced amorphous character and high degree of dissociation of the LiClO4 salt were responsible for the high lithium-ion conductivity observed. Silica aerogels with a high specific surface area and mesoporosity could thus play an important role in the development of solid polymer electrolytes with improved structure and stability.


RSC Advances ◽  
2017 ◽  
Vol 7 (33) ◽  
pp. 20373-20383 ◽  
Author(s):  
Ta-Ming Liu ◽  
Diganta Saikia ◽  
Sze-Yuan Ho ◽  
Ming-Chou Chen ◽  
Hsien-Ming Kao

The blended hybrid solid polymer electrolyte possessed a high ionic conductivity value of 1.2 × 10−4 S cm−1 at 30 °C.


2008 ◽  
Vol 73 (12) ◽  
pp. 1777-1798 ◽  
Author(s):  
Olt E. Geiculescu ◽  
Rama V. Rajagopal ◽  
Emilia C. Mladin ◽  
Stephen E. Creager ◽  
Darryl D. Desmarteau

The present work consists of a series of studies with regard to the structure and charge transport in solid polymer electrolytes (SPE) prepared using various new bis(trifluoromethanesulfonyl)imide (TFSI)-based dianionic dilithium salts in crosslinked low-molecular-weight poly(ethylene glycol). Some of the thermal properties (glass transition temperature, differential molar heat capacity) and ionic conductivities were determined for both diluted (EO/Li = 30:1) and concentrated (EO/Li = 10:1) SPEs. Trends in ionic conductivity of the new SPEs with respect to anion structure revealed that while for the dilute electrolytes ionic conductivity is generally rising with increased length of the perfluoroalkylene linking group in the dianions, for the concentrated electrolytes the trend is reversed with respect to dianion length. This behavior could be the result of a combination of two factors: on one hand a decrease in dianion basicity that results in diminished ion pairing and an enhancement in the number of charge carriers with increasing fluorine anion content, thereby increasing ionic conductivity while on the other hand the increasing anion size and concentration produce an increase in the friction/entanglements of the polymeric segments which lowers even more the reduced segmental motion of the crosslinked polymer and decrease the dianion contribution to the overall ionic conductivity. DFT modeling of the same TFSI-based dianionic dilithium salts reveals that the reason for the trend observed is due to the variation in ion dissociation enthalpy, derived from minimum-energy structures, with respect to perfluoroalkylene chain length.


2012 ◽  
Vol 585 ◽  
pp. 185-189 ◽  
Author(s):  
Rajni Sharma ◽  
Anjan Sil ◽  
Subrata Ray

In the present work, the effect of Li salt i.e. LiClO4 contained in composite plasticizer (PC+DEC) with three different concentrations on ionic transport and other electrochemical properties of PMMA based gel polymer electrolytes synthesized has been investigated. The electrolytes have been synthesized by solution casting technique by varying the wt (%) of salt and plasticizer. The formation of polymer-salt complexes and their structural characterization have been carried out by FTIR spectroscopic and XRD analyses. The room temperature ionic conductivity of the electrolyte composition 0.6PMMA-0.125(PC+DEC)-0.15LiClO4 (wt %) has been found to be maximum whose magnitude is 0.40×10-5 S/cm as determined by ac impedance analysis. The temperature dependent ionic conductivity of electrolyte sample0.6PMMA-0.125(PC+DEC)-0.15LiClO4 has further been investigated. Thermal analyses of electrolyte samples of all three compositions have also been done.


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