scholarly journals Dielectric properties and conductivity of PVdF-co-HFP/LiClO4 polymer electrolytes

2018 ◽  
Vol 96 (7) ◽  
pp. 786-791 ◽  
Author(s):  
Kemal Ulutaş ◽  
Ugur Yahsi ◽  
Hüseyin Deligöz ◽  
Cumali Tav ◽  
Serpil Yılmaztürk ◽  
...  
Keyword(s):  
Dielectric Constant ◽  
Dielectric Properties ◽  
Dielectric Loss ◽  
Polymer Electrolytes ◽  
Room Temperature ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Maximum Conductivity

In this study, it was aimed to prepare a series of PVdF-co-HFP based electrolytes with different LiClO4 loadings and to investigate their chemical and electrical properties in detail. For this purpose, PVdF-co-HFP based electrolytes with different LiClO4 loadings (1–20 weight %) were prepared using solution casting method. X-ray diffraction (XRD), differential scanning calorimetry, and thermogravimetric (TGA) –differential thermal and dielectric spectroscopy analysis of PVdF-co-HFP/LiClO4 were performed to characterize their structural, thermal, and dielectric properties, respectively. XRD results showed that the diffraction peaks of PVdF-co-HFP/LiClO4 electrolytes broadened and decreased with LiClO4. TGA patterns exhibited that PVdF-co-HFP/LiClO4 electrolytes with 20 wt % of LiClO4 had the lowest thermal stability and it degraded above 473 K, which is highly applicable for solid polymer electrolytes. Dielectric constant, dielectric loss, and conductivities were calculated by measuring capacitance and dielectric loss factor of PVdF-co-HFP/LiClO4 in the range from 10 mHz to 20 MHz frequencies at room temperature. In consequence, conductivities of PVdF-co-HFP/LiClO4 increased significantly with frequency for low loading of LiClO4 while they only slightly changed with higher LiClO4 addition. On the other hand, dielectric constant values of PVdF-co-HFP/LiClO4 films decreased with frequency whereas they rose with LiClO4 addition. The dielectric studies showed an increase in dielectric constant and dielectric loss with decreasing frequency. This result was attributed to high contribution of charge accumulation at the electrode–electrolyte interface. The electrolyte showed the maximum conductivity of 8 × 10−2 S/cm at room temperature.

Conductivity and Dielectric Analysis of Cellulose Based Solid Polymer Electrolytes Doped with Ammonium Carbonate (NH4CO3)

2015 ◽  
Vol 719-720 ◽  
pp. 67-72 ◽  
Author(s):  
M.I.H. Sohaimy ◽  
Mohd Ikmar Nizam Isa
Keyword(s):  
Dielectric Constant ◽  
Polymer Electrolytes ◽  
Room Temperature ◽  
Ammonium Carbonate ◽  
Dielectric Behavior ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Dielectric Analysis ◽  
Solution Cast ◽  
Cast Technique

The present work investigated the effect of carboxy methylcellulose (CMC) solid polymer electrolytes doped with ammonium carbonate (AC) prepared from solution cast technique. The CMC-AC solid polymer electrolytes system has been analyzed using EIS to understand its conductivity and dielectric behavior at temperature range of 303 K to 363 K. The highest conductivity achieved at room temperature (303K) is 7.71 x 10-6S cm-1doped with 7wt.% of AC and all samples follows Arrhenius behaviour. The dielectric constant (εr) value was found to be dependent of ionic dopant.

scholarly journals Electrical Conduction Mechanism in Solid Polymer Electrolytes: New Concepts to Arrhenius Equation

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Shujahadeen B. Aziz ◽  
Zul Hazrin Z. Abidin
Keyword(s):  
Dielectric Constant ◽  
Polymer Electrolytes ◽  
Conduction Mechanism ◽  
Dc Conductivity ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Arrhenius Behavior ◽  
Different Temperatures ◽  
Solution Cast ◽  
The Fourier Transform

Solid polymer electrolytes based on chitosan NaCF3SO3 have been prepared by the solution cast technique. X-ray diffraction shows that the crystalline phase of the pure chitosan membrane has been partially disrupted. The fourier transform infrared (FTIR) results reveal the complexation between the chitosan polymer and the sodium triflate (NaTf) salt. The dielectric constant and DC conductivity follow the same trend with NaTf salt concentration. The increase in dielectric constant at different temperatures indicates an increase in DC conductivity. The ion conduction mechanism follows the Arrhenius behavior. The dependence of DC conductivity on both temperature and dielectric constant (σdc(T,ε′)=σ0e−Ea/KBT) is also demonstrated.

scholarly journals Contribution Succinonitrile additive for Performa LiTFSi Solid Polymer Electrolytes for Li-Ion Battery

2020 ◽  
Vol 20 (2) ◽  
Author(s):  
Qolby Sabrina ◽  
Titik Lestariningsih ◽  
Christin Rina Ratri ◽  
Achmad Subhan
Keyword(s):  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Room Temperature ◽  
Lithium Salt ◽  
Ionic Conduction ◽  
Lithium Ion ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Half Cell ◽  
Li Ion

Solid polymer electrolyte (SPE) appropriate to solve packaging leakage and expansion volume in lithium-ion battery systems. Evaluation of electrochemical performance of SPE consisted of mixture lithium salt, solid plasticizer, and polymer precursor with different ratio. Impedance spectroscopy was used to investigate ionic conduction and dielectric response lithium bis(trifluoromethane)sulfony imide (LiTFSI) salt, and additive succinonitrile (SCN) plasticizer. The result showing enhanced high ionic conductivity. In half-cell configurations, wide electrochemical stability window of the SPE has been tested. Have stability window at room temperature, indicating great potential of SPE for application in lithium ion batteries. Additive SCN contribute to forming pores that make it easier for the li ion to move from the anode to the cathode and vice versa for better perform SPE. Pore of SPE has been charaterization with FE-SEM. Additive 5% w.t SCN shows the best ionic conductivity with 4.2 volt wide stability window and pretty much invisible pores.

scholarly journals Salt Concentration Effect on Electrical and Dielectric Properties of Solid Polymer Electrolytes based Carboxymethyl Cellulose for Lithium-ion Batteries

2021 ◽  
Vol 12 (5) ◽  
pp. 6114-6123
Keyword(s):  
Dielectric Properties ◽  
Ionic Conductivity ◽  
Polymer Electrolytes ◽  
Carboxymethyl Cellulose ◽  
Electrochemical Impedance ◽  
Lithium Ion ◽  
Lithium Perchlorate ◽  
Linear Sweep Voltammetry ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer

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.

scholarly journals Effect of TeO2 addition on the dielectric properties of CaCu3Ti4O12 ceramics derived from the oxalate precursor route

2013 ◽  
Vol 03 (04) ◽  
pp. 1350028 ◽  
Author(s):  
P. Thomas ◽  
K. B. R. Varma
Keyword(s):  
Dielectric Properties ◽  
Dielectric Loss ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Oxalate Precursor ◽  
X Ray ◽  
Practical Applications ◽  
Low Dielectric ◽  
Precursor Route ◽  
Tan Δ

CaCu 3 Ti 4 O 12 (CCTO) ceramics which has perovskite structure gained considerable attention due to its giant permittivity. But it has high tan δ (0.1 at 1 kHz) at room temperature, which needs to be minimized to the level of practical applications. Hence, TeO 2 which is a good glass former has been deliberately added to CCTO nanoceramic (derived from the oxalate precursor route) to explore the possibility of reducing the dielectric loss while maintaining the high permittivity. The structural, morphological and dielectric properties of the pure CCTO and TeO 2 added ceramics were studied using X-ray diffraction, Scanning Electron Microscope along with Energy Dispersive X-ray Analysis (EDX), spectroscopy and Impedance analyzer. For the 2.0 wt.% TeO 2 added ceramics, there is a remarkable difference in the microstructural features as compared to that of pure CCTO ceramics. This sample exhibited permittivity values as high as 7387 at 10 KHz and low dielectric loss value of 0.037 at 10 kHz, which can be exploited for the high frequency capacitors application.

Thermal transport, thermomechanical, and dielectric properties of chalcogenide Se98–xAg2Inx (x = 0, 2, 4, 6) system

2014 ◽  
Vol 92 (7/8) ◽  
pp. 648-653
Author(s):  
C. Dohare ◽  
N. Mehta
Keyword(s):  
Dielectric Constant ◽  
Electron Microscope ◽  
Dielectric Loss ◽  
Thermal Transport ◽  
Microstructural Analysis ◽  
Thermomechanical Properties ◽  
X Ray Diffraction ◽  
Glassy System ◽  
Scanning Calorimetry ◽  
Transmission Electron

The present work reports a detailed study of some physical properties of some novel glasses of Se98–xAg2Inx (x = 0, 2, 4, 6) system. Measurements of thermal transport properties (i.e., thermal conductivity, κ, and thermal diffusivity, χe) have been carried out using the transient plane source technique. Specific heat measurements have been done by differential scanning calorimetry. Thermomechanical properties (i.e., Vickers hardness, Hv, and modulus of elasticity, E) have been evaluated by the indenter test. The minimal energy for formation of microvoids, Eh, and microvoids volume, Vh, of the previously mentioned glassy system are discussed in terms of microhardness, Hv. Temperature and frequency dependence of dielectric constant, ε1, and dielectric loss, ε2, for the same system were measured in the frequency (50 Hz – 1000 kHz) and temperature (303–338 K) range. The experimental results illustrate that the values of dielectric constant, ε1, and dielectric loss, ε2, are decreased with frequency and increased with temperature. The maximum barrier height, Wb, is calculated using the dielectric measurements according to the Guintini equation. The morphology and microstructural analysis of as-prepared alloys are confirmed by X-ray diffraction, scanning electron microscope, and transmission electron microscope.

DIELECTRIC PROPERTIES OF CHEMICALLY SYNTHESIZED PbTiO3 NANOCRYSTALS SUITABLE FOR HIGH FREQUENCY DEVICES

2010 ◽  
Vol 24 (23) ◽  
pp. 4547-4554
Author(s):  
K. C. VERMA ◽  
M. SINGH ◽  
N. THAKUR ◽  
N. S. NEGI
Keyword(s):  
Dielectric Constant ◽  
Dielectric Properties ◽  
Room Temperature ◽  
Pt Nanoparticles ◽  
X Ray Diffraction ◽  
Chemical Route ◽  
Xrd Pattern ◽  
High Frequency Devices ◽  
Room Temperature Dielectric Constant ◽  
Transmission Scanning Electron Microscopy

PbTiO 3 (PT) nanoparticles have been prepared by chemical route using polyvinyl alcohol (PVA) as an efficient surfactant. The effect of PVA to reduce the particle's sizes of PT has been observed. X-ray diffraction (XRD) pattern shows that the PT nanoparticles are tetragonal with distortion ratio, c/a ~1.061. The average particle's size calculated from XRD and transmission/scanning electron microscopy is ~24 nm for PT powder sintered at 700°C. The nanostructured grains were also observed in PT pellet sintered at 1000°C. The dielectric properties of PT pellet have been measured from room temperature to 200°C and in the frequency range of 0.075 to 10 MHz. The values of room temperature dielectric constant and tanδ are 117 and 0.05 respectively, measured at 0.5 MHz. It is found that the dielectric constant of PT nanoparticles can be controlled up to higher frequency region of 5 MHz.

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