scholarly journals Investigation of Piezoelectricity and Resistivity of Surface Modified Barium Titanate Nanocomposites

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2123 ◽  
Author(s):  
Udhay Sundar ◽  
Zichen Lao ◽  
Kimberly Cook-Chennault
Keyword(s):  
Barium Titanate ◽  
Particle Surface ◽  
Dielectric Films ◽  
Filler Concentration ◽  
Ceramic Filler ◽  
Energy Storage Devices ◽  
Storage Devices ◽  
Interfacial Layers ◽  
Piezoelectric Strain ◽  
Surface Modified

Polymer-ceramic nanocomposite piezoelectric and dielectric films are of interest because of their possible application to advanced embedded energy storage devices for printed wired electrical boards. The incompatibility of the two constituent materials; hydrophilic ceramic filler, and hydrophobic epoxy limit the filler concentration, and thus, their piezoelectric properties. This work aims to understand the role of surfactant concentration in establishing meaningful interfacial layers between the epoxy and ceramic filler particles by observing particle surface morphology, piezoelectric strain coefficients, and resistivity spectra. A comprehensive study of nanocomposites, comprising non-treated and surface treated barium titanate (BTO), embedded within an epoxy matrix, was performed. The surface treatments were performed with two types of coupling agents: Ethanol and 3-glycidyloxypropyltrimethoxysilan. The observations of particle agglomeration, piezoelectric strain coefficients, and resistivity were compared, where the most ideal properties were found for concentrations of 0.02 and 0.025. This work demonstrates that the interfacial core-shell processing layer concentration influences the macroscopic properties of nanocomposites, and the opportunities for tuning interfacial layers for desirable characteristics of specific applications.

scholarly journals Enhanced Dielectric Permittivity of Optimized Surface Modified of Barium Titanate Nanocomposites

Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 827 ◽  
Author(s):  
Udhay Sundar ◽  
Zichen Lao ◽  
Kimberly Cook-Chennault
Keyword(s):  
Barium Titanate ◽  
Dielectric Permittivity ◽  
Particle Surface ◽  
Ceramic Particle ◽  
Dielectric Films ◽  
Filler Concentration ◽  
Energy Storage Devices ◽  
Electrostatic And Steric Stabilization ◽  
Ceramic Fillers ◽  
Surface Modified

High permittivity polymer-ceramic nanocomposite dielectric films take advantage of the ease of flexibility in processing of polymers and the functionality of electroactive ceramic fillers. Hence, films like these may be applied to embedded energy storage devices for printed circuit electrical boards. However, the incompatibility of the hydrophilic ceramic filler and hydrophobic epoxy limit the filler concentration and therefore, dielectric permittivity of these materials. Traditionally, surfactants and core-shell processing of ceramic fillers are used to achieve electrostatic and steric stabilization for adequate ceramic particle distribution but, questions regarding these processes still remain. The purpose of this work is to understand the role of surfactant concentration ceramic particle surface morphology, and composite dielectric permittivity and conductivity. A comprehensive study of barium titanate-based epoxy nanocomposites was performed. Ethanol and 3-glycidyloxypropyltrimethoxysilan surface treatments were performed, where the best reduction in particle agglomeration, highest value of permittivity and the lowest value of loss were observed. The results demonstrate that optimization of coupling agent may lead to superior permittivity values and diminished losses that are ~2–3 times that of composites with non-optimized and traditional surfactant treatments.

Effect of substrate on the performance of flexible energy storage devices based on surface modified C60 – β Ni(OH)2 nanocomposite

2021 ◽  
Vol 13 ◽  
Author(s):  
Soorya Sasi ◽  
Sunish K. Sugunan ◽  
Radhakrishnan Nair P. ◽  
Suresh Mathew
Keyword(s):  
Electrical Conductivity ◽  
Energy Storage ◽  
Specific Capacitance ◽  
Current Collector ◽  
Energy Storage Devices ◽  
Storage Devices ◽  
Binder Free ◽  
Surface Modified ◽  
Inorganic Composite ◽  
Charge Discharge

Aim: Aim of this study is to find the effect of the current collector in the performance of flexible energy storage devices based on surface modified organic-inorganic composite. Objective: As a part of our pursuit to develop flexible supercapacitive electrodes, we recently reported the fabrication of an electrode from an organic-inorganic composite slurry of surface functionalized fullerene and nickel hydroxide coated onto a copper sheet substrate using simple doctor blade method. We reported that the electrodes deliver specific energy and specific power of 661.5 Wh/kg and 8.8 KW/kg, respectively, and a specific capacitance of 675 Fg−1, which showed excellent cycling stabilities. In an effort to search for various combinatorial combinations of the composite and the substrate, in lieu of copper, in the present study, we incorporate nickel sheet as the current collector. Methods: The structure and composition of the binder-free, flexible super capacitive electrodes were characterized using XRD, TEM, FTIR, XPS, BET, Raman Spectroscopy, and their electrochemical properties were characterized using cyclic voltammetry, galvanostatic charge-discharge measurements, chronoamperommetry and impedance spectroscopy. Result: The as-prepared films stuck readily onto the substrate without the need of any binder material, exhibited remarkable flexibility, and were proven to be crack-free when subjected to repeated bending and twisting. The developed flexible super capacitive electrodes deliver a specific capacitance of 296 F g−1, maximum energy density of 82.2 Wh kg−1, and a maximum power density of 1056 W kg−1. The device retains 91.2 % of its capacitance when subjected to 1000 charge-discharge cycles. Conclusion: Our observations indicate that copper is the better choice as the current collector, which can be ascribed to the better electrical conductivity of copper compared to nickel. We conclude that the poor electrical conductivity of nickel sheet compared to copper substrate make the bottleneck for the performance of electrodes made using nickel substrate. To recapitulate, judicious choice of a current collector with high electrical conductivity along with a suitable surface modification strategy to form a composite in an amorphous form that forms smooth slurry are vital to the fabrication of binder-free, flexible supercapacitive devices.

scholarly journals Preparation of Barium Titanate from Barite Ore of Andhra Pradesh

2019 ◽  
Vol 8 (4) ◽  
pp. 1524-1526
Keyword(s):  
Dielectric Constant ◽  
Energy Storage ◽  
Barium Titanate ◽  
Andhra Pradesh ◽  
High Dielectric Constant ◽  
Low Loss ◽  
Energy Storage Devices ◽  
Storage Devices ◽  
Multilayer Capacitors ◽  
High Dielectric

Barium titanate (BaTiO3 ) is an attractive material in the field of electro ceramics and microelectronics due to its better characteristics. It is having high dielectric constant and low loss characteristics and hence barium titanate is an excellent choice for many applications, such as capacitors, multilayer capacitors (MLCs) and energy storage devices. In the present study an attempt is made to prepare barium titanate from ore using reduction ,leaching ,precipitation and calcinations techniques. The material is giving higher dielectric constant compared to the synthetically prepared materials.

An aqueous hybrid electrolyte for low-temperature zinc-based energy storage devices

2020 ◽  
Vol 13 (10) ◽  
pp. 3527-3535 ◽  
Author(s):  
Nana Chang ◽  
Tianyu Li ◽  
Rui Li ◽  
Shengnan Wang ◽  
Yanbin Yin ◽  
...  
Keyword(s):  
Energy Storage ◽  
Low Temperature ◽  
Energy Storage Devices ◽  
Storage Devices

A frigostable aqueous hybrid electrolyte enabled by the solvation interaction of Zn2+–EG is proposed for low-temperature zinc-based energy storage devices.

NMR studies of alkali intercalted carbon nanotubes

2003 ◽  
Vol 772 ◽  
Author(s):  
M. Schmid ◽  
C. Goze-Bac ◽  
M. Mehring ◽  
S. Roth ◽  
P. Bernier
Keyword(s):  
Carbon Nanotubes ◽  
Lattice Relaxation ◽  
Spin Lattice Relaxation ◽  
Energy Storage Devices ◽  
Nmr Studies ◽  
Storage Devices ◽  
Spin Lattice ◽  
Relaxation Measurements ◽  
Resonance Spin ◽  
Walled Carbon Nanotubes

AbstractLithium intercalted carbon nanotubes have attracted considerable interest as perspective components for energy storage devices. We performed 13C Nuclear Magnetic Resonance spin lattice relaxation measurements in a temperature range from 4 K up to 300 on alkali intercalated Single Walled Carbon Nanotubes in order to investigate the modifications of the electronic properties. The density of states at the Fermi level were determined for pristine, lithium and cesium intercalated carbon nanotubes and are discussed in terms of intercalation and charge transfer effects.

How Certain Are the Reported Ionic Conductivities of Thiophosphate-Based Solid Electrolytes? an Interlaboratory Study

2020 ◽  
Author(s):  
Saneyuki Ohno ◽  
Tim Bernges ◽  
Johannes Buchheim ◽  
Marc Duchardt ◽  
Anna-Katharina Hatz ◽  
...  
Keyword(s):  
Standard Deviation ◽  
Ionic Conductivity ◽  
Relative Standard Deviation ◽  
Solid Electrolytes ◽  
Ionic Conductivities ◽  
Ionic Conductors ◽  
Energy Storage Devices ◽  
Activation Barriers ◽  
Storage Devices ◽  
Relative Standard

<p>Owing to highly conductive solid ionic conductors, all-solid-state batteries attract significant attention as promising next-generation energy storage devices. A lot of research is invested in the search and optimization of solid electrolytes with higher ionic conductivity. However, a systematic study of an <i>interlaboratory reproducibility</i> of measured ionic conductivities and activation energies is missing, making the comparison of absolute values in literature challenging. In this study, we perform an uncertainty evaluation via a Round Robin approach using different Li-argyrodites exhibiting orders of magnitude different ionic conductivities as reference materials. Identical samples are distributed to different research laboratories and the conductivities and activation barriers are measured by impedance spectroscopy. The results show large ranges of up to 4.5 mScm<sup>-1</sup> in the measured total ionic conductivity (1.3 – 5.8 mScm<sup>-1</sup> for the highest conducting sample, relative standard deviation 35 – 50% across all samples) and up to 128 meV for the activation barriers (198 – 326 meV, relative standard deviation 5 – 15%, across all samples), presenting the necessity of a more rigorous methodology including further collaborations within the community and multiplicate measurements.</p>

Ultrathin Carbon Nanosheets for Highly-efficient Capacitive K-ion and Zn-ion Storage

2020 ◽  
Author(s):  
Yamin Zhang ◽  
Zhongpu Wang ◽  
Deping Li ◽  
Qing Sun ◽  
Kangrong Lai ◽  
...  
Keyword(s):  
Energy Storage ◽  
Porous Carbon ◽  
Metal Ion ◽  
Rate Capability ◽  
Energy Storage Devices ◽  
Capacity Retention ◽  
Carbon Nanosheets ◽  
Storage Devices ◽  
High Efficient ◽  
Ion Storage

<p></p><p>Porous carbon has attracted extensive attentions as the electrode material for various energy storage devices considering its advantages like high theoretical capacitance/capacity, high conductivity, low cost and earth abundant inherence. However, there still exists some disadvantages limiting its further applications, such as the tedious fabrication process, limited metal-ion transport kinetics and undesired structure deformation at harsh electrochemical conditions. Herein, we report a facile strategy, with calcium gluconate firstly reported as the carbon source, to fabricate ultrathin porous carbon nanosheets. <a>The as-prepared Ca-900 electrode delivers excellent K-ion storage performance including high reversible capacity (430.7 mAh g<sup>-1</sup>), superior rate capability (154.8 mAh g<sup>-1</sup> at an ultrahigh current density of 5.0 A g<sup>-1</sup>) and ultra-stable long-term cycling stability (a high capacity retention ratio of ~81.2% after 4000 cycles at 1.0 A g<sup>-1</sup>). </a>Similarly, when being applied in Zn-ion capacitors, the Ca-900 electrode also exhibits an ultra-stable cycling performance with ~90.9% capacity retention after 4000 cycles at 1.0 A g<sup>-1</sup>, illuminating the applicable potentials. Moreover, the origin of the fast and smooth metal-ion storage is also revealed by carefully designed consecutive CV measurements. Overall, considering the facile preparation strategy, unique structure, application flexibility and in-depth mechanism investigations, this work will deepen the fundamental understandings and boost the commercialization of high-efficient energy storage devices like potassium-ion/sodium-ion batteries, zinc-ion batteries/capacitors and aluminum-ion batteries.</p><br><p></p>

Further Evidence for Energy Landscape Flattening in the Superionic Argyrodites Li6+xP1−xMxS5I (M = Si, Ge, Sn)

2019 ◽  
Author(s):  
Saneyuki Ohno ◽  
Bianca Helm ◽  
Till Fuchs ◽  
Georg Dewald ◽  
Marvin Kraft ◽  
...  
Keyword(s):  
Solid State ◽  
Activation Barrier ◽  
Energy Landscape ◽  
General Mechanism ◽  
Ionic Conductors ◽  
Energy Storage Devices ◽  
Ion Conductor ◽  
Storage Devices ◽  
Open Questions ◽  
Sudden Decrease

<p>All-solid-state batteries are promising candidates for next-generation energy storage devices. Although the list of candidate materials for solid electrolytes has grown in the past decade, there are still many open questions concerning the mechanisms behind ionic migration in materials. In particular, the lithium thiophosphate family of materials has shown very promising properties for solid-state battery applications. Recently, the Ge-substituted Li<sub>6</sub>PS<sub>5</sub>I argyrodite was shown to be a very fast Li-ion conductor, despite the poor ionic conductivity of the unsubstituted Li<sub>6</sub>PS<sub>5</sub>I. Therein, the conductivity was enhanced by over three orders of magnitude due to the emergence of I<sup>−</sup>/S<sup>2−</sup>exchange, <i>i.e.</i>site-disorder, which led to a sudden decrease of the activation barrier with a concurrent flattening of the energy landscapes. Inspired by this work, two series of elemental substitutions in Li<sub>6+<i>x</i></sub>P<sub>1−<i>x</i></sub><i>M<sub>x</sub></i>S<sub>5</sub>I (<i>M</i>= Si and Sn) were investigated in this study and compared to the Ge-analogue. A sharp reduction in the activation energy was observed at the same <i>M</i><sup>4+</sup>/P<sup>5+</sup>composition as previously found in the Ge-analogue, suggesting a more general mechanism at play. Furthermore, structural analyses with X-ray and neutron diffraction indicate that similar changes in the Li-sublattice occur despite a significant variation in the size of the substituents, suggesting that in the argyrodites, the lithium substructure is most likely influenced by the occurring Li<sup>+</sup>– Li<sup>+</sup>interactions. This work provides further evidence that the energy landscape of ionic conductors can be tailored by inducing local disorder.</p>

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