scholarly journals Compatible Solid Polymer Electrolyte Based on Methyl Cellulose for Energy Storage Application: Structural, Electrical, and Electrochemical Properties

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2257 ◽  
Author(s):  
Shujahadeen B. Aziz ◽  
Iver Brevik ◽  
Muhamad H. Hamsan ◽  
M. A. Brza ◽  
Muaffaq M. Nofal ◽  
...  

Compatible green polymer electrolytes based on methyl cellulose (MC) were prepared for energy storage electrochemical double-layer capacitor (EDLC) application. X-ray diffraction (XRD) was conducted for structural investigation. The reduction in the intensity of crystalline peaks of MC upon the addition of sodium iodide (NaI) salt discloses the growth of the amorphous area in solid polymer electrolytes (SPEs). Impedance plots show that the uppermost conducting electrolyte had a smaller bulk resistance. The highest attained direct current DC conductivity was 3.01 × 10−3 S/cm for the sample integrated with 50 wt.% of NaI. The dielectric analysis suggests that samples in this study showed non-Debye behavior. The electron transference number was found to be lower than the ion transference number, thus it can be concluded that ions are the primary charge carriers in the MC–NaI system. The addition of a relatively high concentration of salt into the MC matrix changed the ion transfer number from 0.75 to 0.93. From linear sweep voltammetry (LSV), the green polymer electrolyte in this work was actually stable up to 1.7 V. The consequence of the cyclic voltammetry (CV) plot suggests that the nature of charge storage at the electrode–electrolyte interfaces is a non-Faradaic process and specific capacitance is subjective by scan rates. The relatively high capacitance of 94.7 F/g at a sweep rate of 10 mV/s was achieved for EDLC assembly containing a MC–NaI system.

2014 ◽  
Vol 895 ◽  
pp. 130-133 ◽  
Author(s):  
W.F. Ng ◽  
Mui Nyuk Chai ◽  
M.I.N. Isa

Novel solid polymer electrolytes containing carboxy methylcellulose (CMC) are prepared based on the vary concentration (0 - 45 wt. %) of citric acid (CA) via solution casting technique. The ion conductivity is studied by electrical impedance spectroscopy and the ionic mobility, μ and the diffusion coefficient, D is investigated by transference number measurement. The highest ionic conductivity at room temperature (303K) is 4.38 x 10-7 S cm-1 for 40 wt. % CA. The values of μ+ and D+ were higher than μ- and D- respectively, implying that the CMC-CA solid polymer electrolytes are proton conductor.


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.


2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Vincent St-Onge ◽  
Mengyang Cui ◽  
Sylviane Rochon ◽  
Jean-Christophe Daigle ◽  
Jerome P. Claverie

AbstractThe discovery that polyethylene oxide promotes ionic conductivity led to the development of solid polymer electrolytes. However, their conductivity is severely reduced by crystallinity. Here, statistical copolymerization is used to design macromolecular architectures where crystallinity is disrupted by a minimal amount of non-ethylene oxide comonomer units. Using the Flory exclusion model, we demonstrate that polymers containing 18 mol% comonomer and 18 wt% LiTFSI are devoid of crystallinity. A 10 mol% comonomer content is sufficient to reach a conductivity of 0.3 × 10−4 S cm−1 at 25 °C. The Li+ transference number is 0.6, indicating that the comonomer units not only limit the crystallinity but also weaken the strength of the Li+ coordination to the polymer. The resulting solid polymer electrolyte is effective in an all-solid LFP|Li-metal battery operating at 25 °C, demonstrating that statistical copolymerization is an efficient tool for polymer electrolyte design.


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.


2021 ◽  
Vol 12 (5) ◽  
pp. 6114-6123

Solid polymer electrolytes (SPEs) based carboxymethyl cellulose (CMC) with lithium perchlorate (LiClO4) were prepared via solution drop-cast technique. The CMC host is complexed by different concentrations of LiClO4 salt. SPEs were characterized by Electrochemical Impedance Spectroscopy (EIS) and Linear Sweep Voltammetry (LSV) in coin cells with lithium metal electrodes. EIS performed unique results based on various ionic conductivity values and dielectric properties. The higher ionic conductivity (1.32 × 10-5 S/cm) was obtained by SPEs 2 following by short-range ionic transport results based on dielectric properties depending on frequency. SPEs with LiClO4 addition are electrochemically stable over 2 V in lithium battery coin cells from LSV results.


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