scholarly journals Synthesis of Porous Proton Ion Conducting Solid Polymer Blend Electrolytes Based on PVA: CS Polymers: Structural, Morphological and Electrochemical Properties

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4890 ◽  
Author(s):  
Muaffaq M. Nofal ◽  
Shujahadeen B. Aziz ◽  
Jihad M. Hadi ◽  
Rebar T. Abdulwahid ◽  
Elham M. A. Dannoun ◽  
...  

In this study, porous cationic hydrogen (H+) conducting polymer blend electrolytes with an amorphous structure were prepared using a casting technique. Poly(vinyl alcohol) (PVA), chitosan (CS), and NH4SCN were used as raw materials. The peak broadening and drop in intensity of the X-ray diffraction (XRD) pattern of the electrolyte systems established the growth of the amorphous phase. The porous structure is associated with the amorphous nature, which was visualized through the field-emission scanning electron microscope (FESEM) images. The enhancement of DC ionic conductivity with increasing salt content was observed up to 40 wt.% of the added salt. The dielectric and electric modulus results were helpful in understanding the ionic conductivity behavior. The transfer number measurement (TNM) technique was used to determine the ion (tion) and electron (telec) transference numbers. The high electrochemical stability up to 2.25 V was recorded using the linear sweep voltammetry (LSV) technique.

2019 ◽  
Vol 20 (13) ◽  
pp. 3369 ◽  
Author(s):  
Shujahadeen B. Aziz ◽  
Muhamad H. Hamsan ◽  
Mohd F. Z. Kadir ◽  
Wrya O. Karim ◽  
Ranjdar M. Abdullah

Solid polymer blend electrolyte membranes (SPBEM) composed of chitosan and dextran with the incorporation of various amounts of lithium perchlorate (LiClO4) were synthesized. The complexation of the polymer blend electrolytes with the salt was examined using FTIR spectroscopy and X-ray diffraction (XRD). The morphology of the SPBEs was also investigated using field emission scanning electron microscopy (FESEM). The ion transport behavior of the membrane films was measured using impedance spectroscopy. The membrane with highest LiClO4 content was found to exhibit the highest conductivity of 5.16 × 10−3 S/cm. Ionic (ti) and electronic (te) transference numbers for the highest conducting electrolyte were found to be 0.98 and 0.02, respectively. Electrochemical stability was estimated from linear sweep voltammetry and found to be up to ~2.3V for the Li+ ion conducting electrolyte. The only existence of electrical double charging at the surface of electrodes was evidenced from the absence of peaks in cyclic voltammetry (CV) plot. The discharge slope was observed to be almost linear, confirming the capacitive behavior of the EDLC. The performance of synthesized EDLC was studied using CV and charge–discharge techniques. The highest specific capacitance was achieved to be 8.7 F·g−1 at 20th cycle. The efficiency (η) was observed to be at 92.8% and remained constant at 92.0% up to 100 cycles. The EDLC was considered to have a reasonable electrode-electrolyte contact, in which η exceeds 90.0%. It was determined that equivalent series resistance (Resr) is quite low and varies from 150 to 180 Ω over the 100 cycles. Energy density (Ed) was found to be 1.21 Wh·kg−1 at the 1st cycle and then remained stable at 0.86 Wh·kg−1 up to 100 cycles. The interesting observation is that the value of Pd increases back to 685 W·kg−1 up to 80 cycles.


e-Polymers ◽  
2014 ◽  
Vol 14 (2) ◽  
pp. 115-120 ◽  
Author(s):  
N. Ataollahi ◽  
A. Ahmad ◽  
T.K. Lee ◽  
A.R. Abdullah ◽  
M.Y.A. Rahman

AbstractThe ionic conductivity of ammonium-based solid polymer films of poly(vinylidene fluoride) (PVDF) blended with MG49, a graft of natural rubber and poly(methyl methacrylate), with various compositions of ammonium triflate NH4CF3SO3, was investigated. As a result, 30 wt.% of NH4CF3SO3-doped polymer electrolyte exhibits the highest ionic conductivity at 6.32×10-4 S/cm at room temperature. The conductivity enhancement can be attributed to the increase in the number of NH4+ as charge carriers. The significance of the blend is the increase of one order in ionic conductivity as compared with pure PVDF electrolyte. The temperature dependence of conductivity of the electrolyte does not obey the Arrhenius law. However, the conductivity increases with temperature and it reached 1.56×10-3 S/cm at 363 K. X-ray diffraction reveals a decrease in crystallinity of the electrolyte upon the addition of NH4CF3SO3 salt. This result is supported by scanning electron microscopy. Linear sweep voltammetry demonstrates that the anodic stability of the electrolyte is up to 4 V. Therefore, the electrolyte shows good compatibility with high-voltage electrode. Hence, this electrolyte system can be a prospective candidate as lithium-ion conducting electrolyte for lithium batteries.


2015 ◽  
Vol 1107 ◽  
pp. 158-162
Author(s):  
Siti Fadzilah Ayub ◽  
R. Zakaria ◽  
K. Nazir ◽  
A.F. Aziz ◽  
Muhd Zu Azhan Yahya ◽  
...  

In this work, solid polymer electrolyte compose of blended 30% poly (methyl methacrylate) grafted natural rubber (MG30)-poly (ethyl methacrylate) (PEMA) polymer blend doped with Lithium trimethasulfonate (LiCF3SO3) films were prepared by solution casting technique. . FTIR analysis showed that the interactions between lithium ions and oxygen atoms occur at the carbonyl functional group C=O where there is shifting in wavenumber from 1728 cm-1 of pure blend to lower wavenumber of blended MG30-PEMA on the MMA structure in both MG30 and PEMA. DSC analysis showed miscibility of polymer blend. From Electrochemical Impedance Spectrocopy analysis, ionic conductivity increase with the increasing of salt concentration. Maximum conductivity at room temperature is 9.20 x 10-6 Scm-1 was obtained when 30 wt% of LiCF3SO3 was added into the system. Ionic conductivity temperature dependence plots found obeys the Arrhenius rule.


2013 ◽  
Vol 33 (4) ◽  
pp. 315-322 ◽  
Author(s):  
Muthuvinayagam Muthiah ◽  
Gopinathan Chellasamy ◽  
Rajeswari Natarajan ◽  
Selvasekarapandian Subramanian ◽  
Sanjeeviraja Chinnappa

Abstract Conducting polymer electrolyte films were prepared based on poly (vinylidene fluoride) (PVdF) and poly (vinyl alcohol) (PVA) by using a solution casting technique. The optimized PVdF-PVA polymer blend ratio was doped with different concentrations of NH4NO3 and polymer blend electrolytes were prepared. The increase in amorphous nature of the polymer electrolytes was confirmed by X-ray diffraction (XRD) analysis and optical microscopic studies. The complex formation between the polymers and the salt was confirmed by Fourier transform infrared spectroscopy (FTIR) analysis. The ac impedance studies were performed to evaluate the ionic conductivity of the polymer electrolyte membranes in the range 303–333 K and the highest ionic conductivity was found to be 2.91×10-4 S/cm at ambient temperature for PVdF-PVA-NH4NO3 (80:20:25 MWt%) polymer electrolyte, with activation energy Ea=0.7 eV. The dielectric behavior of the electrolytes was also studied.


Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3508 ◽  
Author(s):  
Shujahadeen B. Aziz ◽  
Rebar T. Abdulwahid ◽  
Muhamad H. Hamsan ◽  
Mohamad A. Brza ◽  
Ranjdar M. Abdullah ◽  
...  

In this report, a facile solution casting technique was used to fabricate polymer blend electrolytes of chitosan (CS):poly (ethylene oxide) (PEO):NH4SCN with high electrochemical stability (2.43V). Fourier transform infrared (FTIR) spectroscopy was used to investigate the polymer electrolyte formation. For the electrochemical property analysis, cyclic voltammetry (CV), linear sweep voltammetry (LSV), and electrochemical impedance spectroscopy (EIS) techniques were carried out. Referring to the FTIR spectra, a complex formation between the added salt and CS:PEO was deduced by considering the decreasing and shifting of FTIR bands intensity in terms of functional groups. The CS:PEO:NH4SCN electrolyte was found to be electrochemically stable as the applied voltage linearly swept up to 2.43V. The cyclic voltammogram has presented a wide potential window without showing any sign of redox peaks on the electrode surface. The proved mechanisms of charge storage in these fabricated systems were found to be double layer charging. The EIS analysis showed the existence of bulk resistance, wherein the semicircle diameter decreased with increasing salt concentration. The calculated maximum DC conductivity value was observed to be 2.11 × 10−4 S/cm for CS:PEO incorporated with 40 wt% of NH4SCN salt. The charged species in CS:PEO:NH4SCN electrolytes were considered to be predominantly ionic in nature. This was verified from transference number analysis (TNM), in which ion and electron transference numbers were found to be tion = 0.954 and tel = 0.045, respectively. The results obtained for both ion transference number and DC conductivity implied the possibility of fabricating electrolytes for electrochemical double layer capacitor (EDLC) device application. The specific capacitance of the fabricated EDLC was obtained from the area under the curve of the CV plot.


Membranes ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 151 ◽  
Author(s):  
Jihad M. Hadi ◽  
Shujahadeen B. Aziz ◽  
Muaffaq M. Nofal ◽  
Sarkawt A. Hussein ◽  
Muhamad H. Hafiz ◽  
...  

In the present work, chitosan (CS) as a natural biopolymer was used to prepare nanocomposite polymer electrolytes (NCPEs) in order to reduce plastic waste pollution. The plasticized CS-based NCSPE has been prepared via the solution casting technique. The electrical properties of the films were investigated using AC conductivity, dielectric properties, electric modulus, and electrical impedance spectroscopy (EIS). The obtained results from the dielectric properties and electric modulus study confirm the non-Debye behavior of ion dynamics. The effect of glycerol plasticizer on ionic conductivity of the CS:AgNO3:Al2O3 system was investigated via AC conductivity and impedance studies. The conductivity of the samples was explained based on electrical equivalent circuits and Bode plots. The electrochemical properties such as transfer number measurement (TNM), linear sweep voltammetry (LSV), and cyclic voltammetry (CV) were carried out to inspect the sample suitability for electrochemical double-layer capacitor (EDLC) application. The highest conductivity was 3.7 × 10−4 S cm−1 with the electrochemical stability window up to 2.1 V at room temperature. Through the TNM study, the ionic conductivity of plasticized CS-based NCSPE was confirmed, and ion transport (tion) of the highest conducting sample was found to be 0.985. The activated carbon electrode with the highest conducting sample was employed in the EDLC device fabrication. Accordingly, it can be said that the highest conducting sample had capable performance to be applied in electrochemical device application.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2531 ◽  
Author(s):  
Elham M.A. Dannoun ◽  
Shujahadeen B. Aziz ◽  
Mohamad A. Brza ◽  
Muaffaq M. Nofal ◽  
Ahmad S.F.M. Asnawi ◽  
...  

In this work, plasticized magnesium ion-conducting polymer blend electrolytes based on chitosan:methylcellulose (CS:MC) were prepared using a solution cast technique. Magnesium acetate [Mg(CH3COO)2] was used as a source of the ions. Nickel metal-complex [Ni(II)-complex)] was employed to expand the amorphous phase. For the ions dissociation enhancement, glycerol plasticizer was also engaged. Incorporating 42 wt% of the glycerol into the electrolyte system has been shown to improve the conductivity to 1.02 × 10−4 S cm−1. X-ray diffraction (XRD) analysis showed that the electrolyte with the highest conductivity has a minimum crystallinity degree. The ionic transference number was estimated to be more than the electronic transference number. It is concluded that in CS:MC:Mg(CH3COO)2:Ni(II)-complex:glycerol, ions are the primary charge carriers. Results from linear sweep voltammetry (LSV) showed electrochemical stability to be 2.48 V. An electric double-layer capacitor (EDLC) based on activated carbon electrode and a prepared solid polymer electrolyte was constructed. The EDLC cell was then analyzed by cyclic voltammetry (CV) and galvanostatic charge–discharge methods. The CV test disclosed rectangular shapes with slight distortion, and there was no appearance of any redox currents on both anodic and cathodic parts, signifying a typical behavior of EDLC. The EDLC cell indicated a good cyclability of about (95%) for throughout of 200 cycles with a specific capacitance of 47.4 F/g.


2021 ◽  
pp. 096739112110473
Author(s):  
Jayanthi S ◽  
Kalapriya K

A new series of nanocomposite polymer electrolytes (NCPEs) was prepared using poly(vinylidene fluoride–co–hexafluoro propylene) P(VdF-HFP) as polymer, magnesium triflate (MgTr) as salt and nano-sized barium titanate (BaTiO3) (<100 nm) as nanofiller via traditional solution casting technique. Decrease in crystalline nature of the samples due to the incorporation of nano BaTiO3 was revealed through X-ray diffraction (XRD) analysis. From AC impedance spectroscopy, maximum conductivity of 4.11 × 10−4 Scm−1 was attained for the addition of 6 wt% of nano BaTiO3 to the P(VdF-HFP)/MgTr matrix. Dielectric studies were found to be in accordance with the ionic conductivity studies. For the most highly conducting sample, a greater number of mountain valley pattern was observed from Atomic Force Microscopy (AFM) analysis. Thermal stability of the sample, P(VdF-HFP)/MgTr/BaTiO3 (6 wt%) (which possessed maximum ionic conductivity) was observed through TG/differential thermal analysis studies. All these results suggested that these materials are favorable and find application in practical electrochemical devices.


2017 ◽  
Vol 17 ◽  
pp. 202-216
Author(s):  
R. Premila ◽  
S. Rajendran ◽  
K. Kesavan

The polymer blend electrolytes composed of poly (ethyl methacrylate)(PEMA) and Poly (vinyl acetate)(PVAc) as host polymer and lithium perchlorate (LiClO4) as a salt are synthesized by solvent casting technique. The polymer membranes with different wt% of PEMA and PVAc are subjected to AC impedance analysis for the investigation of ionic conductivity. The maximum ionic conductivity of 3.541 X 10- 5Scm- 1 at 303K is reported for PEMA/PVAC (70/30wt%) –LiClO4 (8wt%) polymer blend electrolyte system.The complexation has been confirmed by XRD and FTIR techniques. The glass transition temperature (Tg) of the blend polymer electrolytes has been obtained from DSC measurements. The SEM micrographs show the surface morphology of the prepared samples. The electrochemical stability of the sample exhibiting high conductivity has been carried out using linear sweep voltammetry (LSV) and cyclic voltammetry (CV) measurements. The potential window has been found to be-2.5 to +2.5 V. The lithium transference number evaluated using chronoamperometry technique results in a value of 0.90. The dielectric behavior of the solid polymer blend electrolytes has been analyzed as a function of frequency and temperature. The dc conductivity values obtained from the conductance spectra match the ac impedance results. The photoluminescence spectra that contain information about the local free volume of the prepared samples justify the conductivity results. The two and three dimensional images of the maximum ionic conducting sample exhibit numerous micropores.


Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1896 ◽  
Author(s):  
Mohamad A. Brza ◽  
Shujahadeen B. Aziz ◽  
Hazleen Anuar ◽  
Elham M. A. Dannoun ◽  
Fathilah Ali ◽  
...  

In the present work, a novel polymer composite electrolytes (PCEs) based on poly(vinyl alcohol) (PVA): ammonium thiocyanate (NH4SCN): Cd(II)-complex plasticized with glycerol (Gly) are prepared by solution cast technique. The film structure was examined by XRD and FTIR routes. The utmost ambient temperature DC ionic conductivity (σDC) of 2.01 × 10−3 S cm−1 is achieved. The film morphology was studied by field emission scanning electron microscopy (FESEM). The trend of σDC is further confirmed with investigation of dielectric properties. Transference numbers of ions (tion) and electrons (tel) are specified to be 0.96 and 0.04, respectively. Linear sweep voltammetry (LSV) displayed that the PCE potential window is 2.1 V. The desired mixture of activated carbon (AC) and carbon black was used to fabricate the electrodes of the EDLC. Cyclic voltammetry (CV) was carried out by sandwiching the PCEs between two carbon-based electrodes, and it revealed an almost rectangular shape. The EDLC exhibited specific capacitance, energy density, and equivalent series resistance with average of 160.07F/g, 18.01Wh/kg, and 51.05Ω, respectively, within 450 cycles. The EDLC demonstrated the initial power density as 4.065 × 103 W/Kg.


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