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1.
Solid polymer electrolytes (SPE) based on poly-(vinyl alcohol) (PVA)0.7 and sodium iodide (NaI)0.3 complexed with sulfuric acid (SA) at different concentrations were prepared using solution casting technique. The structural
properties of these electrolyte films were examined by X-ray diffraction (XRD) studies. The XRD data revealed that sulfuric
acid disrupt the semi-crystalline nature of (PVA)0.7(NaI)0.3 and convert it into an amorphous phase. The proton conductivity and impedance of the electrolyte were studied with changing
sulfuric acid concentration from 0 to 5.1 mol/liter (M). The highest conductivity of (PVA)0.7(NaI)0.3 matrix at room temperature was 10−5 S cm−1 and this increased to 10−3 S cm−1 with doping by 5.1 M sulfuric acid. The electrical conductivity (σ) and dielectric permittivity (ε′) of the solid polymer electrolyte in frequency range (500 Hz–1 MHz) and temperature range (300–400) K were carried out.
The electrolyte with the highest electrical conductivity was used in the fabrication of a sodium battery with the configuration
Na/SPE/MnO2. The fabricated cells give open circuit voltage of 3.34 V and have an internal resistance of 4.5 kΩ. 相似文献
2.
A sodium ion conducting composite polymer electrolyte (CPE) prepared by solution-caste technique by dispersion of an electrochemically
inert ceramic filler (SnO2) in the PEO–salt complex matrix is reported. The effect of filler concentration on morphological, electrical, electrochemical,
and mechanical stability of the CPE films has been investigated and analyzed. Composite nature of the films has been confirmed
from X-ray diffraction and scanning electron microscopy patterns. Room temperature d.c. conductivity observed as a function
of filler concentration indicates an enhancement (maximum) at 1–2 wt% filler concentration followed by another maximum at
∼10 wt% SnO2. This two-maxima feature of electrical conductivity as a function of filler concentration remains unaltered in the CPE films
even at 100 °C (i.e., after crystalline melting), suggesting an active role of the filler particles in governing electrical
transport. Substantial enhancement in the voltage stability and mechanical properties of the CPE films has been noticed on
filler dispersion. The composite polymer films have been observed to be predominantly ionic in nature with t
ion ∼ 0.99 for 1–2 wt% SnO2. However, this value gets lowered on increasing addition of SnO2 with t
ion ∼ 0.90 for 25 wt% SnO2. A calculation of ionic and electronic conductivity for 25 wt% of SnO2 film works out to be ∼2.34 × 10−6 and 2.6 × 10−7 S/cm, respectively. 相似文献
3.
The ionic conductivity of PVC–ENR–LiClO4 (PVC, polyvinyl chloride; ENR, epoxidized natural rubber) as a function of LiClO4 concentration, ENR concentration, temperature, and radiation dose of electron beam cross-linking has been studied. The electrolyte
samples were prepared by solution casting technique. Their ionic conductivities were measured using the impedance spectroscopy
technique. It was observed that the relationship between the concentration of salt, as well as temperature, and conductivity
were linear. The electrolyte conductivity increases with ENR concentration. This relationship was discussed using the number
of charge carrier theory. The conductivity–temperature behaviour of the electrolyte is Arrhenian. The conductivity also varies
with the radiation dose of the electron beam cross-linking. The highest room temperature conductivity of the electrolyte of
8.5 × 10−7 S/cm was obtained at 30% by weight of LiClO4. The activation energy, E
a and pre-exponential factor, σ
o, are 1.4 × 10−2 eV and 1.5 × 10−11 S/cm, respectively. 相似文献
4.
The [N(CH3)4][N(C2H5)4]ZnCl4 compound has been synthesized by a solution-based chemical method. The X-ray diffraction study at room temperature revealed
an orthorhombic system with P21212 space group. The complex impedance has been investigated in the temperature and frequency ranges 420–520 K and 200 Hz–5 MHz,
respectively. The grain interior and grain boundary contribution to the electrical response in the material have been identified.
Dielectric data were analyzed using the complex electrical modulus M
* for the sample at various temperature. The modulus plots can be characterized by full width at half height or in terms of
a non-exponential decay function ϕ(t) = exp[(−t/τ)
β
]. The detailed conductivity study indicated that the electrical conduction in the material is a thermally activated process.
The variation of the AC conductivity with frequency at different temperatures obeys the Almond and West universal law. 相似文献
5.
The ZnO filler has been introduced into a solid polymeric electrolyte of polyvinyl chloride (PVC)–ZnO–LiClO4, replacing costly organic filler for conductivity improvement. Ionic conductivity of PVC–ZnO–LiClO4 as a function of ZnO concentration and temperature has been studied. The electrolyte samples were prepared by solution casting
technique. The ionic conductivity was measured using impedance spectroscopy technique. It was observed that the conductivity
of the electrolyte varies with ZnO concentration and temperature. The temperature dependence on the conductivity of electrolyte
was modelled by Arrhenius and Vogel–Tammann–Fulcher equations, respectively. The temperature dependence on the conductivity
does not fit in both models. The highest room temperature conductivity of the electrolyte of 3.7 × 10−7 Scm−1 was obtained at 20% by weight of ZnO and that without ZnO filler was found to be 8.8 × 10−10 Scm−1. The conductivity has been improved by 420 times when the ZnO filler was introduced into the PVC–LiClO4 electrolyte system. It was also found that the glass transition temperature of the electrolyte PVC–ZnO–LiClO4 is about the same as PVC–LiClO4. The increase in conductivity of the electrolyte with the ZnO filler was explained in terms of its surface morphology. 相似文献
6.
Composite materials used for electrode and electrolyte materials have been intensely studied in view of their advantages such
as higher conductivity and better operational performance compared to their single-phase counterparts. The present work aims
at studying the electrical and structural characteristics of a new composite electrolyte namely, (PbI2)
x
− (Ag2O–Cr2O3)100−x
where x = 5, 10, 15, 20, and 25 mol%, respectively, prepared by the melt quenching technique. The room temperature X-ray diffraction
spectra revealed certain crystalline phases in the samples. AC conductivity analysis for all the prepared samples was carried
out over the frequency range 1 MHz–20 Hz and in the temperature window 297–468 K. The room temperature conductivity values
were calculated to be in the order of 10−5–10−3 Scm−1. An Arrhenius dependence of temperature with conductivity was observed, and the activation energies calculated were found
to be in the range 0.27–0.31 eV. Furthermore, the total ionic transport number (t
i) values obtained for all these indicated the ionic nature of this system.
Paper presented at the Third International Conference on Ionic Devices (ICID 2006), Chennai, Tamilnadu, India, Dec. 7–9, 2006. 相似文献
7.
M.?Cristina?Gon?alves Verónica?de?Zea Bermudez M.?M.?Silva M.?J.?Smith Enrique?Morales Rute?A.?Sá Ferreira Luís?D.?Carlos 《Ionics》2010,16(3):193-201
Variable chain length di-urethane cross-linked poly(oxyethylene) (POE)/siloxane hybrid networks were prepared by application
of a sol-gel strategy. These materials, designated as di-urethanesils (represented as d-Ut(Y′), where Y′ indicates the average
molecular weight of the polymer segment), were doped with lithium triflate (LiCF3SO3). The two host hybrid matrices used, d-Ut(300) and d-Ut(600), incorporate POE chains with approximately 6 and 13 (OCH2CH2) repeat units, respectively. All the samples studied, with compositions ∞ > n ≥ 1 (where n is the molar ratio of (OCH2CH2) repeat units per Li+), are entirely amorphous. The di-urethanesils are thermally stable up to at least 200 °C. At room temperature the conductivity
maxima of the d-Ut(300)- and d-Ut(600)-based di-urethanesil families are located at n = 1 (approximately 2.0 × 10−6 and 7.4 × 10−5 Scm−1, respectively). At about 100 °C, both these samples also exhibit the highest conductivity of the two electrolyte systems
(approximately 1.6 × 10−4 and 1.0 × 10−3 Scm−1, respectively). The d-Ut(600)-based xerogel with n = 1 displays excellent redox stability. 相似文献
8.
A nanoparticle TiO2 solid-state photoelectrochemical cell utilizing as a solid electrolyte of poly(acrylonitrile)–propylene–carbonate–lithium
perchlorate (PAN–PC–LiClO4) has been fabricated. The performance of the device has been tested in the dark and under illumination of 100-mW cm−2 light. A nanoparticle TiO2 film was deposited onto indium tin oxide-covered glass substrate by controlled hydrolysis technique assisted with spin-coating
technique. The average grain size for the TiO2 film is 76 nm. LiClO4 salt was used as a redox couple. The room temperature conductivity of the electrolyte is 4.2 × 10−4 S cm−1. A graphite electrode was prepared onto a glass slide by electron beam evaporation technique. The device shows the rectification
property in the dark and shows the photovoltaic effect under illumination. The best J
sc and V
oc of the device were 2.82 μA cm−2 and V
oc of 0.58 V, respectively, obtained at the conductivity of 4.2 × 10−4 S cm−1 and intensity of 100 mW cm−2. The J
sc was improved by about three times by introducing nanoparticle TiO2 and by using a solid electrolyte of PAN–PC–LiClO4 replacing PVC–PC–LiClO4 in the device. The current transport mechanism of the cell is also presented in this paper. 相似文献
9.
Solvent-free films of poly (ethylene oxide)–silver triflate (PEO–AgCF3SO3)/MgO-based nanocomposite polymer electrolytes (PEO)50AgCF3SO3–x wt.% MgO (x = 1, 3, 5, 7, and 10) obtained using solution casting technique were found to exhibit an appreciably good complexation of
MgO nanofiller within the polymer electrolyte system and non-Debye type of relaxation as revealed by Fourier transform infrared
and complex impedance analyses. Optimized filler (5 wt.% MgO) when incorporated into the polymer electrolyte resulted in a
maximum electrical conductivity of 2 × 10−6 S cm−1 in conjunction with a silver ionic transference number (t
Ag+) of 0.23 at room temperature (298 K). Detailed structural, thermal, and surface morphological investigation indicated a slight
reduction in the degree of crystallinity owing to the addition of MgO nanofiller. 相似文献
10.
Here we report the synthesis, chemical stability, and electrical conductivity of Ti-doped perovskite-type BaCe0.8-x
Ti
x
Y0.2O3-δ
(x = 0.05, 0.1, 0.2, and 0.3; BCTY). Samples were synthesized by conventional solid state (ceramic) reaction from corresponding
metal salts and oxides at elevated temperature of 1,300–1,500 °C in air. The powder X-ray diffraction confirmed the formation
of a simple cubic perovskite-type structure with a lattice constant of a = 4.374(1), 4.377(1), and 4.332(1) ? for x = 0.05, 0.1, and 0.2 members of BCTY, respectively. Like BaCe0.8Y0.2O3-δ
(BCY), Ti substituted BCTY was found to be chemically not stable in 100% CO2 and form BaCO3 at elevated temperature. The bulk electrical conductivity of BCTY decreased with increasing Ti content and the x = 0.05 member exhibited the highest conductivity of 2.3 × 10−3 S cm−1 at 650 °C in air, while a slight increase in the conductivity, especially at low temperatures (below 600 °C), was observed
in humidified atmospheres. 相似文献
11.
H. Kim A. Cepler C. Cetina D. Knies M. S. Osofsky R. C. Y. Auyeung A. Piqué 《Applied Physics A: Materials Science & Processing》2008,93(3):593-598
Present p-type ZnO films tend to exhibit high resistivity and low carrier concentration, and they revert to their natural n-type state
within days after deposition. One approach to grow higher quality p-type ZnO is by codoping the ZnO during growth. This article describes recent results from the growth and characterization
of Zr–N codoped p-type ZnO thin films by pulsed laser deposition (PLD) on (0001) sapphire substrates. For this work, both N-doped and Zr–N
codoped p-type ZnO films were grown for comparison purposes at substrate temperatures ranging between 400 to 700 °C and N2O background pressures between 10−5 to 10−2 Torr. The carrier type and conduction were found to be very sensitive to substrate temperature and N2O deposition pressure. P-type conduction was observed for films grown at pressures between 10−3 to 10−2 Torr. The Zr–N codoped ZnO films grown at 550 °C in 1×10−3 Torr of N2O show p-type conduction behavior with a very low resistivity of 0.89 Ω-cm, a carrier concentration of 5.0×1018 cm−3, and a Hall mobility of 1.4 cm2 V−1 s−1. The structure, morphology and optical properties were also evaluated for both N-doped and Zr–N codoped ZnO films. 相似文献
12.
In the present study, a kind of solid polymer electrolyte (SPE) based on poly(vinylidene difluoride-co-hexafluoropropylene)/poly(methyl methacrylate) blends was prepared by a casting method to solve the safety problem of lithium
secondary batteries. Owing to being plasticized with a room temperature ionic liquid, N-butyl-N′-methyl-imidiazolium hexafluorophosphate, the obtained SPE shows a thermal decomposition temperature over 300°C and an ionic
conductivity close to 10−3 S cm−1. The SPE-3 sample, in which the weight of two polymers is equivalent, possesses an ionic conductivity of 0.45 × 10−3 S cm−1 at 25°C and presents an electrochemical window of 4.43 V. The ionic conductivity of the SPE-3 is as high as 1.73 × 10−3 S cm−1 at 75°C approaching to that of liquid electrolyte. The electrochemical performances of the Li/LiFePO4 cells confirmed its feasibility in lithium secondary batteries. 相似文献
13.
It is found that silver nanoparticles (AgNPs) can further enhance the fluorescence intensity of curcumin (CU) - cetyltrimethylammonium
bromide (CTAB) – nucleic acids and improve its anti-photobleaching activity. Under optimum conditions, the enhanced fluorescence
intensity is proportion to the concentration of nucleic acids in the range of 2.0 × 10−8–1.0 × 10−6 g mL−1 for fish sperm DNA (fsDNA), 2.0 × 10−8–1.0 × 10−6 g mL−1 for calf thymus DNA (ctDNA), 1.0 × 10−8–1.0 × 10−6 g mL−1 for yeast RNA (yRNA), and their detection limits (S/N = 3) are 8.0 ng mL−1, 10.5 ng mL−1 and 5.8 ng mL−1, respectively. This method is used for determining the concentration of DNA in actual sample with satisfactory results. The
interaction mechanism is also studied. 相似文献
14.
The crystallization and glass transition kinetics using differential scanning calorimetry (DSC) in 50AgI–33.33Ag2O–16.67[(V2O5)1−x
–(MoO3)
x
] superionic glassy system is discussed. Thermal stability of glass, studied using various criteria, does not vary significantly
with glass former variation. However, the activation energies for structural relaxation (E
s) at glass transition temperature and crystallization (E
c) obtained using Moynihan and Kissinger, Matusita-Sakka formulations found to exhibit interesting trends with MoO3 substitution in the glass matrix. It is noticed that the electrical conductivity (σ)–temperature (T) cycles obtained at a typical heating rate of 1 °C/min do exhibit significant thermal events. The conductivity after first
heating cycle at room temperature is found to be increasing with MoO3 content and maximum for x = 0.3 (~10−3 Ω−1 cm−1 at 30 °C) which is comparable to that of the host 50AgI–33.33Ag2O–16.67V2O5 glassy system. The parameters obtained from σ–T plots and DSC scans do complement each other in a particular range of composition. 相似文献
15.
K. P. Andryushin A. A. Pavelko I. A. Verbenko O. N. Razumovskaya L. A. Shilkina V. A. Aleshin L. A. Reznichenko 《Bulletin of the Russian Academy of Sciences: Physics》2011,75(8):1082-1084
Ceramic samples of bismuth ferrite and solid solutions of Bi1 − x
A
x
FeO3 type (where A = Lu, Yb, Tm, Er, Ho, Dy, Tb, Gb, Eu, Sm, Nd, Pr, La; 0.05 ≤ x ≤ 0.20; Δx = 0.05) were prepared. Spectra of the real part of electrical conductivity were studied within the range 10−4–10−6 Hz. The dependence of the samples’ thermal stability and electrical conductivity on the size of the substituting ions was
established. 相似文献
16.
The Ac electrical conductivity and the dielectric relaxation properties of the [(C3H7)4N]2Cd2Cl6 polycrystalline sample have been investigated by means of impedance spectroscopy measurements over a wide range of frequencies
and temperatures, 209 Hz–5 MHz and 361–418 K, respectively. The purpose is to make a difference between the electrical and
dielectric properties of the polycrystalline sample and single crystal. Besides, a detailed analysis of the impedance spectrum
suggests that the electrical properties of the material are strongly temperature-dependent. Plots of (Z" versus Z') are well
fitted to an equivalent circuit model consisting of a series combination of grains and grains boundary elements. Moreover,
the temperature dependence of the electrical conductivity in the different phases follows the Arrhenius law and the frequency
dependence of σ (ω) follows the Jonscher’s universal dynamic law. Furthermore, the modulus plots can be characterized by full
width at half height or in terms of a nonexperiential decay function φ(t) = exp(t/t)β. Finally, the imaginary part of the permittivity constant is analyzed with the Cole–Cole formalism. 相似文献
17.
Kamlesh Pandey Mrigank Mauli Dwivedi Mridula Tripathi Markandey Singh S. L. Agrawal 《Ionics》2008,14(6):515-523
Development and characterisation of polyethylene oxide (PEO)-based nanocomposite polymer electrolytes comprising of (PEO-SiO2): NH4SCN is reported. For synthesis of the said electrolyte, polyethylene oxide has been taken as polymer host and NH4SCN as an ionic charge supplier. Sol–gel-derived silica powder of nano dimension has been used as ceramic filler for development
of nanocomposite electrolytes. The maximum conductivity of electrolyte ∼2.0 × 10−6 S/cm is observed for samples containing 30 wt.% silica. The temperature dependence of conductivity seems to follow an Arrhenius-type,
thermally activated process over a limited temperature range. 相似文献
18.
Conductivity studies of plasticized anhydrous PEO-KOH alkaline solid polymer electrolyte 总被引:1,自引:0,他引:1
Polyethylene oxide (PEO)–potassium hydroxide (KOH)-based alkaline solid polymer electrolyte films have been prepared by using
methanol as solvent. The highest room temperature ionic conductivity of (2.1 ± 0.5) × 10−8 S cm−1 was achieved for the composition of 70 wt% PEO:30 wt% KOH. The addition of plasticizer, ethylene carbonate, propylene carbonate,
or polyethylene glycol to the highest conductivity of PEO–KOH system helps to increase the ambient ionic conductivity to the
order of 10−6–10−4 S cm−1. The log σ vs 1/T plot of PEO–KOH showed a small conductivity decrease at 50–60 °C range. The small decrease and the hysteresis that occur
during the heating–cooling cycle was overcome by the presence of the plasticizer. X-ray diffraction observation supports the
conductivity results. 相似文献
19.
Dillip K. Pradhan B. K. Samantaray R. N. P. Choudhary N. K. Karan Reji Thomas R. S. Katiyar 《Ionics》2011,17(2):127-134
The solid polymer electrolyte films based on polyethylene oxide, NaClO4 with dodecyl amine modified montmorillonite as filler, and polyethylene glycol as plasticizer were prepared by a tape casting
method. The effect of plasticization on structural, microstructural, and electrical properties of the materials has been investigated.
A systematic change in the structural and microstructural properties of plasticized polymer nanocomposite electrolytes (PPNCEs)
on addition of plasticizer was observed in our X-ray diffraction pattern and scanning electron microscopy micrographs. Complex
impedance analysis technique was used to calculate the electrical properties of the nanocomposites. Addition of plasticizer
has resulted in the lowering of the glass transition temperature, effective dissociation of the salt, and enhancement in the
electrical conductivity. The maximum value of conductivity obtained was ∼4.4 × 10−6 S cm−1 (on addition of ∼20% plasticizer), which is an order of magnitude higher than that of pure polymer nanocomposite electrolyte
films (2.82 × 10−7 S cm−1). The enhancement in conductivity on plasticization was well correlated with the change in other physical properties. 相似文献
20.
Plasticized polymer electrolytes composed of poly(methyl methacrylate) (PMMA) as the host polymer and lithium bis(trifluoromethanesulfonyl)imide
LiN(CF3SO2)2 as a salt were prepared by solution casting technique at different ratios. The ionic conductivity varied slightly and exhibited
a maximum value of 3.65 × 10−5 S cm−1 at 85% PMMA and 15% LiN(CF3SO2)2. The complexation effect of salt was investigated using FTIR. It showed some simple overlapping and shift in peaks between
PMMA and LiN(CF3SO2)2 salt in the polymer electrolyte. Ethylene carbonate (EC) and propylene carbonate (PC) were added to the PMMA–LiN(CF3SO2)2 polymer electrolyte as plasticizer to enhance the conductivity. The highest conductivities obtained were 1.28 × 10−4 S cm−1 and 2.00 × 10−4 S cm−1 for EC and PC mixture system, respectively. In addition, to improve the handling of films, 1% to 5% fumed silica was added
to the PMMA–LiN(CF3SO2)2–EC–PC solid polymer electrolyte which showed a maximum value at 6.11 × 10−5 S cm−1 for 2% SiO2. 相似文献