Ionic transport properties of protonic conducting solid biopolymer electrolytes based on enhanced carboxymethyl cellulose - NH<Subscript>4</Subscript>Br with glycerol

The present work investigates the ionic conductivity as well as its transport properties of carboxymethyl cellulose–NH₄Br plasticized with various weight percentage of glycerol for solid biopolymer electrolytes (SBEs) prepared by solution-casting technique. It was shown from the FTIR analysis that the complexation transpires at C=O and C–O^? from COO^? of CMC upon the addition of glycerol into the SBEs system. The highest room temperature ionic conductivity of ~10^?3 S cm^?1 was achieved at 6 wt.% of glycerol owing to the broadening in the amorphous state as demonstrated in the XRD analysis. The conductivity-temperature plots were found to be in good agreement with the conventional Arrhenius relationship. It was further shown that the conducting element is mainly due to the protonation of H⁺ where ionic mobility and diffusion coefficient was found to contribute towards the enhancement in the ionic conductivity of SBEs system.     

Biopolymeric electrolyte based on glycerolized methyl cellulose with NH<Subscript>4</Subscript>Br as proton source and potential application in EDLC

In the present work, biopolymer electrolyte films based on MC doped with NH₄Br salt and plasticized with glycerol were prepared by solution casting method. Fourier transform infrared (FTIR) spectroscopy analysis confirms the interaction between MC, NH₄Br, and glycerol. X-ray diffraction (XRD) explains that the enhancement of conductivity is affected by the degree of crystallinity. This result is verified by field emission scanning electron microscopy (FESEM). For unplasticized system, sample containing 25 wt% of NH₄Br possesses the highest ionic conductivity of (1.89 ± 0.05) × 10^?4 S cm^?1. The addition of 30 wt% glycerol increases the conductivity value up to (1.67 ± 0.04) × 10^?3 S cm^?1. The conduction mechanism was best presented by the correlated barrier hopping (CBH) model. The linear sweep voltammetry (LSV) and cyclic voltammetry (CV) result confirms the suitability of the highest conducting electrolyte to be employed in the fabrication of electrochemical double layer capacitor (EDLC).     

The effect of LiCF<Subscript>3</Subscript>SO<Subscript>3</Subscript> on the complexation with potato starch-chitosan blend polymer electrolytes

This work examines the effect of lithium trifluoromethanesulfonate (LiCF₃SO₃) and glycerol on the conductivity and dielectric properties of potato starch-chitosan blend-based electrolytes. The electrolytes are prepared via solution cast technique. From X-ray diffraction (XRD) analysis, the blend of 50 wt.% starch and 50 wt.% chitosan is found to be the most amorphous blend. Fourier transform infrared (FTIR) spectroscopy studies show the interaction between the electrolyte materials. The room temperature conductivity of pure starch-chitosan film is found to be (2.85 ± 1.31) × 10^?10 S cm^?1. The incorporation of 45 wt.% LiCF₃SO₃ increases the conductivity to (7.65 ± 2.27) × 10^?5 S cm^?1. Further conductivity enhancement up to (1.32 ± 0.35) × 10^?3 S cm^?1 has been observed on addition of 30 wt.% glycerol. This trend in conductivity is verified by XRD and dielectric analysis. The temperature dependence of conductivity of all electrolytes are Arrhenian.     

Green electrolytes based on dextran-chitosan blend and the effect of NH<Subscript>4</Subscript>SCN as proton provider on the electrical response studies

Dextran-chitosan blend added with ammonium thiocyanate (NH₄SCN)-based solid polymer electrolytes are prepared by solution cast method. The interaction between the components of the electrolyte is verified by Fourier transform infrared (FTIR) analysis. The blend of 40 wt% dextran-60 wt% chitosan is found to be the most amorphous ratio. The room temperature conductivity of undoped 40 wt% dextran-60 wt% chitosan blend film is identified to be (3.84?±?0.97)?×?10^?10 S cm^?1. The inclusion of 40 wt.% NH₄SCN to the polymer blend has optimized the room temperature conductivity up (1.28?±?0.43)?×?10^?4 S cm^?1. Result from X-ray diffraction (XRD) and differential scanning calorimetry (DSC) analysis shows that the electrolyte with the highest conductivity value has the lowest degree of crystallinity (χ _c) and the glass transition temperature (T _g), respectively. Temperature-dependence of conductivity follows Arrhenius theory. From transport analysis, the conductivity is noticed to be influenced by the mobility (μ) and number density (n) of ions. Conductivity trend is further verified by field emission scanning electron microscopy (FESEM) and dielectric results.     

Poly (ethylene oxide) (PEO)-based,sodium ion-conducting‚ solid polymer electrolyte films,dispersed with Al<Subscript>2</Subscript>O<Subscript>3</Subscript> filler,for applications in sodium ion cells

The studies on solid polymer electrolyte (SPE) films with high ionic conductivity suitable for the realization of all solid-state Na-ion cells? form the focal theme of the work presented in this paper. The SPE films are obtained by the solution casting technique using the blend solution of poly (ethylene oxide) (PEO) with ethylene carbonate (EC) and propylene carbonate (PC) and complexed with sodium nitrate. Structural and thermal studies of SPE films are done by XRD, FTIR spectroscopy, and TGA techniques. Surface morphology of the films is studied using the FESEM. The ionic conductivity of SPE films is determined from the electrochemical impedance spectroscopy studies. For the SPE film with 16 wt% of NaNO₃ used for reacting with the polymer blend of PEO with EC and PC, the ionic conductivity obtained is around 1.08 × 10^?5 S cm^?1. Addition of the Al₂O₃ as the filler material is found to enhance the ionic conductivity of the SPE films. The studies on the Al₂O₃ modified SPE film show an ionic conductivity of 1.86 × 10^–4 S cm^?1, which is one order higher than that of the SPE films without the filler content. For the SPE film dispersed with 8 wt% of Al₂O₃, the total ion transport number observed is around 0.9895, which is quite impressive from the perspective of the applications in electrochemical energy storage devices. From the cyclic voltammetry studies, a wide electrochemical stability window up to 4 V is observed, which further emphasizes the commendable electrochemical behavior of these SPE films.     

NH<Subscript>4</Subscript>NO<Subscript>3</Subscript> as charge carrier contributor in glycerolized potato starch-methyl cellulose blend-based polymer electrolyte and the application in electrochemical double-layer capacitor

Potato starch (PS)-methyl cellulose (MC) blend solid biopolymer electrolytes infused with ammonium nitrate (NH₄NO₃) and glycerol as plasticizer are made via the solution cast technique. Fourier transform infrared (FTIR) spectroscopy indicates that NH₄NO₃ has interacted with the polymer blend host. The addition of 40 wt% glycerol in the highest conducting plasticizer free electrolyte has improved the conductivity to the order of ～10^?3 S cm^?1. The thermal stability of the electrolytes is identified by thermogravimetric analysis (TGA). Result from X-ray diffraction (XRD) analysis shows that the electrolyte with maximum conductivity value has the lowest degree of crystallinity. Differential scanning calorimetry (DSC) analysis reveals that the highest conducting plasticized electrolyte possesses the lowest glass transition temperature (T _g) of ?27.5 °C. Conductivity trend is further verified by dielectric analysis. Transference numbers of ion (t _ion) and electron (t _e) for the highest conducting electrolyte are identified to be 0.98 and 0.02, respectively, confirming that ions are the dominant charge carriers. Linear sweep voltammetry (LSV) evaluates that the potential window for the electrolyte is 1.88 V. The internal resistance of the electrochemical double-layer capacitor (EDLC) is between 29 and 64 Ω. From the charged-discharged measurement, the value of C _s is 31 F g^?1. The EDLC is stable over 1000 cycles.     

Poly(ethylene oxide)-lithium difluoro(oxalato)borate new solid polymer electrolytes: ion–polymer interaction,structural, thermal,and ionic conductivity studies

Solid polymer electrolytes based on high molecular weight poly(ethylene oxide) (PEO) complexed with lithium difluoro(oxalato)borate (LiDFOB) salt in various EO:Li molar ratios from 30:1 to 8:1 were prepared by using solution casting technique. Ion–polymer interaction, structural, thermal, and ionic conductivity studies have been reported by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), polarized optical microscopy (POM), differential scanning calorimeter (DSC), and impedance analysis. FTIR spectral studies suggested that the interaction of Li⁺ cations with the ether oxygen of PEO, where a triple peak broad band centered at 1105 cm^?1, corresponds to C–O–C stretching and extreme deformation occurs. XRD, POM, and DSC indicated that the inclusion of LiDFOB salt could reduce the crystallinity of PEO. The melting temperature of PEO shifted to lower temperature side by the addition of LiDFOB. The glass transition temperature obtained for the system 10:1 was ?38.2 °C. An increase in the ionic conductivity from 3.95?×?10^?9 to 3.18?×?10^?5 S/cm at room temperature (23 °C) was obtained through the addition of LiDFOB to a high molecular weight PEO. In addition, the ionic conductivity of the polymer electrolyte films followed an Arrhenius relation, and the activation energy decreased with increasing LiDFOB concentration.     

Structural, conductivity, and dielectric characterization of PEO–PEG blend composite polymer electrolyte dispersed with TiO2 nanoparticles

A solid polymer electrolyte (SPE) composites consisting blend of poly(ethylene oxide) (PEO) and poly(ethylene glycol) (PEG) as the polymer host with LiCF₃SO₃ as a Li⁺ cation salt and TiO₂ nanoparticle which acts as a filler were prepared using solution-casting technique. The SPE films were characterized by X-ray diffraction and Fourier transform infrared analysis to ensure complexation of the polymer composites. Frequency-dependent impedance spectroscopy observation was used to determine ionic conductivity and dielectric parameters. Ionic conductivity was found to vary with increasing salt and filler particle concentrations in the polymer blend complexes. The optimum ambient temperature conductivity achieved was 2.66?×?10^?4?S?cm^?1 for PEO (65 %), PEG (15 %), LiCF₃SO₃ (15 %), ethylene carbonate (5 %), and TiO₂ (3 %) using weight percentage. The dielectric relaxation time obtained from a loss tangent plot is fairly consistent with the conductivity studies. Both Arrhenius and VTF behaviors of all the composites confirm that the conductivity mechanism of the solid polymer electrolyte is thermally activated.     

The effect of NH<Subscript>4</Subscript>NO<Subscript>3</Subscript> towards the conductivity enhancement and electrical behavior in methyl cellulose-starch blend based ionic conductors

Solid polymer electrolytes based on methyl cellulose (MC)-potato starch (PS) blend doped with ammonium nitrate (NH₄NO₃) are prepared by solution cast technique. The interaction between the electrolyte’s materials is proven by Fourier transform infrared (FTIR) analysis. The thermal stability of the electrolytes is obtained from thermogravimetric analysis (TGA). The room temperature conductivity of undoped 60 wt.% MC-40 wt.% PS blend film is identified to be (1.04 ± 0.19) × 10^?11 S cm^?1. The addition of 30 wt.% NH₄NO₃ to the polymer blend has optimized the room temperature conductivity to (4.37 ± 0.16) × 10^?5 S cm^?1. Conductivity trend is verified by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and dielectric analysis. Temperature-dependence of conductivity obeys Arrhenius rule. Conductivity is found to be influenced by the number density (n) and mobility (μ) of ions. From transference number measurements (TNM), ions are found to be the dominant charge carriers.     

Incorporation of NH<Subscript>4</Subscript>NO<Subscript>3</Subscript> into MC-PVA blend-based polymer to prepare proton-conducting polymer electrolyte films

Proton-conducting solid polymer blend electrolytes based on methylcellulose-polyvinyl alcohol:ammonium nitrate (MC-PVA:NH₄NO₃) were prepared by the solution cast technique. The structural and electrical properties of the samples were examined by X-ray diffraction (XRD), Fourier transform infrared (FTIR), and electrical impedance (EI) spectroscopy. The shifting and change in the intensity of FTIR bands of the electrolyte samples confirm the complex formation between the MC-PVA polymer blend and the NH₄NO₃ added salt. The observed broadening in the XRD pattern of the doped samples reveals the increase of the amorphous fraction of polymer electrolyte samples. The increase in electrical conductivity of polymer electrolyte samples with increasing salt concentration attributed to the formation of charge-transfer complexes, and to increase in the amorphous domains. A maximum ionic conductivity of about 7.39 × 10^?5 S cm^?1 was achieved at room temperature for the sample incorporating 20 wt% of NH₄NO₃. The DC conductivity of the present polymer system exhibits Arrhenius-type dependence with temperature. The decrease in the values of activation energies with increasing salt concentration indicates the ease mobility of ions. The decrease in dielectric constant with increasing frequency was observed at all temperatures. Optical properties such as absorption edge, optical band gap, and tail of localized state were estimated for polymer blend and their electrolyte films. It was found that the optical band gap values shifted towards lower photon energy from 6.06 to 4.75 eV by altering the NH₄NO₃ salt content.     

A novel application for oil palm empty fruit bunch: extraction and modification of cellulose for solid polymer electrolyte

Biopolymer-based materials from renewable sources are the core target of the researchers in modern time. Following this motivation, we have developed solid polymer electrolytes (SPEs) from empty fruit branch (EFB) of oil palm. The cellulose was extracted from EFB and modified to carboxymethyl cellulose (CMC) by its reaction with monochloroacetic acid in a strongly alkaline medium. The samples were characterized by FTIR, ¹³C NMR, and XRD to confirm the presence of different functional groups, new connectivity, and crystalline/amorphous nature of the materials, respectively. The CMC-based SPEs were fabricated by blending it with different quantities of lithium iodide (LiI) as dopant. The existence of polymer-salt interactions was revealed by FTIR analysis. The maximum ionic conductivity of 5.58?×?10^?3 S cm^?1 was observed on sample containing 65 wt% LiI with the lowest activation energy of 0.249 eV.     

Evaluation of NaFeTiO<Subscript>4</Subscript> as an electrode for energy storage application

We report a polycrystalline NaFeTiO₄ prepared via conventional solid-state reaction route. X-ray diffraction (XRD) results and Rietveld refinement confirmed single-phase NaFeTiO₄ having an orthorhombic unit cell with lattice parameters a = 9.17051 Å, b = 2.96310 Å, and c = 10.73676 Å and Pnma space group (No. 62). Energy dispersive spectrum (EDS) yielded sample stoichiometry that agrees well with its molecular formula. The surface morphology indicated a cylindrical rod-like microstructure comprising well-defined grains having variable dimension, i.e., diameter ~?250 to 350 nm and length ~?1 to 5 μm. Vibrational spectroscopy (FTIR/Raman) results indicated presence of FeO₆ and TiO₆ octahedra in good agreement with crystallographic study. Brunner-Emmet-Teller (BET) surface area measurement yielded a specific surface area as high as ~?4.28 m² g^?1. Electrical impedance spectrum indicated presence of grains separated by well-defined grain boundaries in agreement with microstructural analysis. Electrical conductivity of the material was estimated to be ~?6.05 × 10^?6 S cm^?1. The structural model obtained using XRD and vibrational spectrum results suggest layered tunnel/cage structure of cage dimension ~?4.65 Å, along [010] direction in the xz plane, which is larger than the size of Na⁺ ion (0.98 Å). So, easier Na⁺ migration feasibility exists in NaFeTiO₄ crystal lattice making it a good candidate for electrode applications.     

Structure,thermal behavior,and dielectric properties of new cesium hydrogen sulfate arsenate: Cs<Subscript>2</Subscript>(HSO<Subscript>4</Subscript>)(H<Subscript>2</Subscript>AsO<Subscript>4</Subscript>)

Synthesis and structural characterization by single-crystal X-ray diffraction method, thermal behavior, and electrical proprieties are given for a new compound with a superprotonic phase transition Cs₂(HSO₄)(H₂AsO₄). The title compound crystallizes in the monoclinic system with the P2₁/n space group. The structure contains zigzag chains of hydrogen-bonded anion tetrahedra that extend in the [010] direction. Each tetrahedron is additionally linked to a tetrahedron neighboring chain to give a planar structure with hydrogen-bonded sheets lying parallel to (10ī). The existence of O–H and (S/As)–O bonds in the structure at room temperature has been confirmed by IR and Raman spectroscopy in the frequency ranges 4000–400 cm^?1and 1200–50 cm^?1, respectively. Differential scanning calorimetry analysis of the superprotonic transition in Cs₂(HSO₄)(H₂AsO₄) showed that the transformation to high temperature phase occurs at 417 K by one-step process. Thermal decomposition of the product takes place at much higher temperatures, with an onset of approximately 534 K. The superprotonic transition was also studied by impedance and modulus spectroscopy techniques. The conductivity in the high temperature phase at 423 K is 1.58 × 10^?4 Ω^?1 cm^?1, and the activation energy for the proton transport is 0.28 eV. The conductivity relaxation parameters associated with the high disorder protonic conduction have been examined from analysis of the M”/M”_max spectrum measured in a wide temperature range. Transport properties of this material appear to be due to the proton hopping mechanism.     

Thermal properties and ionic conductivity of Li<Subscript>1,3</Subscript>Ti<Subscript>1,7</Subscript>Al<Subscript>0,3</Subscript>(PO<Subscript>4</Subscript>)<Subscript>3</Subscript> solid electrolytes sintered by field-assisted sintering

Li_1,3Ti_0,7Al_0,3(PO₄)₃ (LATP) powder was obtained by a conventional melt-quenching method and consolidated by field-assisted sintering technology (FAST) at different temperatures. Using this technique, the samples could be sintered to relative densities in the range of 93 to 99 % depending on the sintering conditions. Ionic and thermal conductivity were measured and the results are discussed under consideration of XRD and SEM analyses. Thermal conductivity values of 2 W/mK and ionic conductivities of 4?×?10^?4 Scm^?1 at room temperature were obtained using relatively large particles and a sintering temperature of 1000 °C at an applied uniaxial pressure of 50 MPa.     

Conductivity studies of plasticized proton conducting PVA–PVIM blend doped with NH4BF4

The proton conducting solid-state polymer electrolyte comprising blend of poly(vinyl alcohol) (PVA) and poly(N-vinylimidazole) (PVIM), ammonium tetrafluoroborate (NH₄BF₄) as salt, and polyethylene glycol (PEG) (molecular weight 300 and 600) as plasticizer is prepared at various compositions by solution cast technique. The prepared films are characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry, X-ray diffraction, and scanning electron microscopy analysis. The conductivity–temperature plots are found to follow an Arrhenius nature. The conductivity of solid polymer electrolytes is found to depend on salt and plasticizer content and also on the dielectric constant value and molecular weight of the plasticizer. Maximum ionic conductivity values of 2.20?×?10^?4 and 1.28?×?10^?4?S?cm^?1 at 30 °C are obtained for the system (PVA–PVIM)?+?20 wt.% NH₄BF₄?+?150 wt.% PEG300 and (PVA–PVIM)?+?20 wt.% NH₄BF₄?+?150 wt.% PEG300, respectively. The blended polymer, complexed with salt and plasticizer, is shown to be a predominantly ionic conductor. The proton transport in the system may be expected to follow Grotthuss-type mechanism.     

Studies on structural and electrical properties of Mg<Subscript>0. 5+y</Subscript> (Zr<Subscript>2-y</Subscript>Fe<Subscript>y</Subscript>) <Subscript>2</Subscript> (PO<Subscript>4</Subscript>) <Subscript>3</Subscript> ceramic electrolytes

The sample of Mg_{0. 5+y} (Zr_1-y Fe_y) ₂ (PO₄) ₃ (0.0 ≤y ≤0.5) was synthesized using the sol-gel method. The structures of the samples were investigated using X-ray diffraction and Fourier transform infrared spectroscopy measurement. XRD studies showed that samples had a monoclinic structure which was iso-structured with the parent compound, Mg_0.5Zr (PO₄) ₃. The complex impedance spectroscopy was carried out in the frequency range 1–6 MHz and temperature range 303 to 773 K to study the electrical properties of the electrolytes. The substitutions of Fe³⁺ with Zr⁴⁺ in the Mg_0.5Zr (PO₄) ₃ structure was introduced as an extrainterstitial Mg²⁺ ion in the modified structured. The compound of Mg_0.5+y (Zr_1-y Fe_y)₂(PO₄)₃ with y?=?0.4 gives a maximum conductivity value of 1.25?×?10^?5 S cm^?1 at room temperature and 7.18?×?10^?5 S cm^?1 at 773 K. Charge carrier concentration, mobile ion concentration, and ion hopping rate are calculated by fitting the conductance spectra to power law variation, σ _ac (ω)?=?σ _o ? +?Aω ^α . The charge carrier concentration and mobile ion concentration increases with increase of Fe³⁺ inclusion. This implies the increase in conductivity of the compounds was due to extra interstitial Mg²⁺ ions.     

LiClO4-doped plasticized chitosan and poly(ethylene glycol) blend as biodegradable polymer electrolyte for supercapacitors

Biodegradable polymer electrolyte comprising the blend of chitosan (CS) and poly(ethylene glycol) (PEG) plasticized with ethylene carbonate and propylene carbonate, as host polymer, and lithium perchlorate (LiClO₄), as a dopant, was prepared by solution casting technique. The ionic conductivity has been calculated using the bulk impedance obtained through impedance spectroscopy. The variation of conductivity and dielectric properties has been investigated as a function of polymer blend ratio, plasticizer content and LiClO₄ concentration at temperature range of 298–343 K. The DSC thermograms show two broad peaks for CS/PEG blend and increased with increase in the LiClO₄ content. The maximum conductivity has been found to be 1.1?×?10^?4 S cm^?1 at room temperature for 70:30 (CS/PEG) concentration. The electric modulus of the electrolyte film exhibits a long tail feature indicative of good capacitance. The activation energy of all samples was calculated using the Arrhenius plot, and it has been found to be 0.12 to 0.38 eV. A carbon–carbon supercapacitor has been fabricated using this electrolyte, and its electrochemical characteristics and performance have been studied. The supercapacitor showed a fairly good specific capacitance of 47 F?g^?1.     

Low-temperature sintering effects on NASICON-structured LiSn<Subscript>2</Subscript>P<Subscript>3</Subscript>O<Subscript>12</Subscript> solid electrolytes prepared via citric acid-assisted sol-gel method

LiSn₂P₃O₁₂ with sodium (Na) super ionic conductor (NASICON)-type rhombohedral structure was successfully obtained at low sintering temperature, 600 °C via citric acid-assisted sol-gel method. However, when the sintering temperature increased to 650 °C, triclinic structure coexisted with the rhombohedral structure as confirmed by X-ray diffraction analysis. Conductivity–temperature dependence of all samples were studied using impedance spectroscopy in the temperature range 30 to 500 °C, and bulk, grain boundary and total conductivity increased as the temperature increased. The highest bulk conductivity found was 3.64?×?10^?5 S/cm at 500 °C for LiSn₂P₃O₁₂ sample sintered at 650 °C, and the lowest bulk activation energy at low temperature was 0.008 eV, showing that sintering temperature affect the conductivity value. The voltage stability window for LiSn₂P₃O₁₂ sample sintered at 600 °C at ambient temperature was up to 4.4 V. These results indicated the suitability of the LiSn₂P₃O₁₂ to be exploiting further for potential applications as solid electrolytes in electrochemical devices.     

The development of Li<Superscript>+</Superscript> conducting polymer electrolyte based on potato starch/graphene oxide blend

Solid polymer electrolytes based on potato starch (PS) and graphene oxide (GO) have been developed in this study. Blending GO with PS has improved the ionic conductivity and mechanical properties of the electrolytes. In this work, series of polymer blend consisting of PS and GO as co-host polymer were prepared using solution cast method. The most amorphous PS-GO blend was obtained using 80 wt% of PS and 20 wt% of GO as recorded by X-ray diffraction (XRD). Incorporation of 40 wt% lithium trifluoromethanesulfonate (LiCF₃SO₃) into the PS-GO blend increases the conductivity to (1.48 ± 0.35) × 10^?5 S cm^?1. Further enhancement of conductivity was made using 1-butyl-3-methylimidazolium chloride ([Bmim][Cl]). The highest conductivity at room temperature is obtained for the electrolyte containing 30 wt% of [Bmim][Cl] with conductivity value of (4.8?0 ± 0.69) × 10^?4 S cm^?1. Analysis of the Fourier transform infrared spectroscopy (FTIR) spectra confirmed the interaction between LiCF₃SO₃, [Bmim][Cl], and PS-GO blend. The variation of the dielectric constant and modulus studies versus frequency indicates that system of PS-GO-LiCF₃SO₃-[Bmim][Cl] obeys non-Debye behavior.     

Incorporation of NH4Br in PVA-chitosan blend-based polymer electrolyte and its effect on the conductivity and other electrical properties

Polymer electrolyte system based on poly(vinyl alcohol) (PVA)-chitosan blend doped with ammonium bromide (NH₄Br) has been prepared by solution cast method. Fourier transform infrared (FTIR) spectroscopy analysis confirms the complexation between salt and polymer host. The highest ionic conductivity obtained at room temperature is (7.68?±?1.24)?×?10^?4 S cm^?1 for the sample comprising of 30 wt% NH₄Br. X-ray diffraction (XRD) patterns reveal that PVA-chitosan with 30 wt% NH₄Br exhibits the most amorphous structure. Thermogravimetric analysis (TGA) reveals that the electrolytes are stable until ～260 °C. The conductivity variation can also be explained by field emission scanning electron microscopy (FESEM) study. Dielectric properties of the electrolytes follow non-Debye behavior. The conduction mechanism of the highest conducting electrolyte can be represented by the correlated barrier hopping (CBH) model. From linear sweep voltammetry (LSV) result, the highest conducting electrolyte is electrochemically stable at 1.57 V.