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This article investigates the influence of NaPF6 salt content (0–30 wt.% in a varying interval of 5 wt.%) on the structural, electrical, and biodegradable properties of HEC/NaPF6 solid biopolymer electrolyte (SBE) films. The interaction of salt with the HEC polymer matrix is confirmed by FTIR and SEM studies. The elemental composition and mapping confirm the appearance of NaPF6 moieties in the HEC polymer matrix. XRD deconvolution reveals that HEC samples with 20 wt.% (H4) and 10 wt.% of salt (H2) have a significantly lower crystallinity index than pure HEC polymer. The H2 and H4 samples show the highest room temperature conductivity values (1.62 × 10−5 and 1.13 × 10−5 S cm−1, respectively) among all other prepared samples since carrier concentration influences the ionic conductivity and shares a similar order of conductivity. Thus, the H2 and H4 samples are employed as electrolyte separators in the sodium ion battery, and the results suggest that the H2‐based electrolyte system is more significant. Battery matrices like open circuit voltage (V), current density (μA cm−2), power density (mW kg−1), energy density (Wh kg−1) and discharge capacity (μA h−1) were calculated and found to be 2.48, 5.49, 44.60, 1.69, and 71.05, respectively for H2 electrolyte based cell. Wagner polarization reveals that H2 and H4 constitute the predominant charge carriers (ions) with total ion transference numbers of ⁓0.98 and ⁓0.99, respectively. To evaluate sample degradability, H2 and H4 samples were subjected to 20 and 5‐day biodegradation processes, during which the polymers completely (100%) broke down. [ABSTRACT FROM AUTHOR]

In this study, different weight percentages of Mg(NO3)2 were added to a polymer blend composed of chitosan (CS) and methylcellulose (MC). The solution casting method was adopted to prepare the polymer electrolyte films. As the host matrix, the polymer blend consists of 70 wt.% of CS and 30 wt.% of MC. The interactions between the blend and the Mg(NO3)2 salt were revealed by FTIR analysis. The deconvolution of XRD peaks followed by the calculation of crystallinity indicates that the electrolyte samples were amorphous. The bulk resistance decreased with increasing salt content, according to the results of electrical impedance spectroscopy (EIS), and this was caused by the influence of carrier concentration. The sample containing 30 wt.% of Mg(NO3)2 was determined to have a maximum value of DC conductivity of 2.12 × 10–5 Scm−1 at room temperature by EIS analysis. The highest conducting film's potential stability was found to be 3.65 V. It was found that the ion transference number was 0.86. The performance of the magnesium ion battery was then evaluated after it was built using the highest conducting polymer electrolyte. Considering this, the current work proposes an eco-friendly, practical, and affordable electrolyte appropriate for making electrochemical devices. [ABSTRACT FROM AUTHOR]

Solid polymer blend electrolyte (SPE) films of Polyethylene oxide(PEO)/Carboxymethyl cellulose (NaCMC) doped with Sodium iodide (NaI), were prepared by solution cast method and their structural, optical and electrical properties were investigated using X-Ray diffraction, Fourier transform infrared spectroscopy, UV–Vis spectrophotometer and Electrical impedance analyser respectively. X-Ray diffraction spectra indicate that, deformation occurred in the structure of the blend followed by doping with NaI salt. The variation in intensity and shifting of characteristic bands in FTIR spectra provides the evidence for formation of complex due to the interaction occurred in the blend with the dopant. Optical energy band gap decreases in the blend samples upon doping and is confirmed by UV–Vis spectrophotometer analysis. Increase of dielectric constant and loss upon doping, exhibits usual behaviour of the polymer electrolytes. An increase in AC conductivity is observed upon doping and maximum conductivity of 9.41 × 10−3 Scm−1 is obtained for 10/90 sample doped with 0.03% Sodium iodide and DC conductivity for the same sample at room temperature is 1.05 × 10–2 Scm−1. In addition, I-T studies confirm the conductivity exhibited by the sample as due to ions and I-V studies show electrochemical stability in the range of good working potential. From the results obtained, it can be inferred that, the prepared sample can be used as polymer electrolytes in the manufacturing of energy storage devices. [ABSTRACT FROM AUTHOR]

In this present work, we have synthesized silver nanoparticles (AgNPs) using the chemical reduction method and systematically studied the effect of AgNPs of different loading into polyvinyl alcohol/sodium bromide (PVA/NaBr) polymer electrolytes. X‐ray diffraction and Fourier transform infrared spectroscopy confirmed the variation in the crystallinity and complexation with AgNPs loading, respectively. AgNPs are uniformly distributed in the polymer matrix as depicted in FESEM. According to transport property studies, it is observed that carrier concentration has a strong influence on ionic conductivity. Additionally, I‐t studies showed that most charge carriers are ions and not electrons. The sample PVA/NaBr with AgNPs, prepared from 6 mM AgNO3 solution (PNAg6) with ionic conductivity 1.22 × 10−4 S cm−1 (one order increase with respect to undoped sample) and highest electrochemical stability window (ESW) of 2.86 V, can be chosen as a suitable candidate for energy storage device applications. [ABSTRACT FROM AUTHOR]

The effects of Mg (NO 3) 2. 6H 2 O salt on an eco-friendly biopolymer blend matrix comprising hydroxypropyl methylcellulose (HPMC) and poly (vinyl alcohol) (PVA) is presented in this work which is prepared using the solution casting method. Structural, chemical composition (functional moieties), morphological, and thermal features were investigated by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FE-SEM), Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). FTIR spectrum and XRD pattern confirmed that the magnesium nitrate salt was dissolved, and complexation was observed through a coordination bond and a hydrogen bond with -OH and -CH groups in the host polymer blend. The glass transition temperature (T g) values of HPMC:PVA composites are greater than those of the pure blend, demonstrating transient cross-linking. For P0, P2, and P3 samples, the pore diameter and % porosity is calculated, and the morphology of the P4 sample is non-porous and shows ionic conductivity of P4 = 3.25 × 10−4 S/cm at 27 °C. Based on the Nyquist plot fitting and FTIR deconvolution methods, it is used to determine the transport characteristics and noticed that the carrier concentration affects the ionic conductivity. The highest conducting electrolyte has been integrated into a primary battery to demonstrate its potential use in energy storage systems. [ABSTRACT FROM AUTHOR]