scholarly journals Development of Ti/Ni Nanolayered Structures to Be a New Candidate for Energy Storage Applications

2020 ◽  
Vol 10 (19) ◽  
pp. 6935
Author(s):  
Osama Saber ◽  
Sajid Ali Ansari ◽  
Adil Alshoaibi
Keyword(s):  
Energy Storage ◽  
Double Layer ◽  
Layer Structure ◽  
Morphological Characteristics ◽  
Building Blocks ◽  
Interplanar Distance ◽  
Energy Storage Devices ◽  
Supercapacitor Electrode ◽  
Double Layer Structure ◽  
Energy Storage Applications

Development of electrochemical supercapacitor electrode is the best way to improve the performance and conductivity of the alone materials and support energy storage devices. In this work, cyanate anions have used as building blocks to build series of nanolayered materials based on Ti/Ni layered double hydroxides (LDHs). The structural and morphological characteristics of the prepared Ti/Ni LDHs were examined using different techniques. The electrochemical supercapacitive behavior of the prepared LDHs was observed in the three-assembly electrochemical cell. These results showed that the optimized ratio of the nickel and titanium plays an important role to enhance the electrochemical performance of the LDHs. The optimized Ti/Ni LDHs, which has the highest content of titanium, showed the highest specific capacitance (675 F/g) value. In this trend, this LDH also retain a high percentage of the cyclic retention after long cyclic charging-discharging process. The enhanced performance could be due to the double layer structure, enough interplanar distance between the layer, and large number of exposed active site within the double layer structure of the LDHs. Finally, although there are no reports for the electrochemical supercapacitive performance of Ti/Ni LDHs in the literature, it is interesting to produce a new candidate for energy storage applications.

scholarly journals Surface polarization effects in confined polyelectrolyte solutions

2020 ◽  
Vol 117 (33) ◽  
pp. 19677-19684 ◽  
Author(s):  
Debarshee Bagchi ◽  
Trung Dac Nguyen ◽  
Monica Olvera de la Cruz
Keyword(s):  
Energy Storage ◽  
Double Layer ◽  
Layer Structure ◽  
Differential Capacitance ◽  
Dielectric Constants ◽  
Electrostatic Energy ◽  
Coulombic Interaction ◽  
Polarization Effects ◽  
Double Layer Structure ◽  
Polyelectrolyte Solutions

Understanding nanoscale interactions at the interface between two media with different dielectric constants is crucial for controlling many environmental and biological processes, and for improving the efficiency of energy storage devices. In this contributed paper, we show that polarization effects due to such dielectric mismatch remarkably influence the double-layer structure of a polyelectrolyte solution confined between two charged surfaces. Surprisingly, the electrostatic potential across the adsorbed polyelectrolyte double layer at the confining surface is found to decrease with increasing surface charge density, indicative of a negative differential capacitance. Furthermore, in the presence of polarization effects, the electrostatic energy stored in the double-layer structure is enhanced with an increase in the charge amplification, which is the absorption of ions on a like-charged surface. We also find that all of the important double-layer properties, such as charge amplification, energy storage, and differential capacitance, strongly depend on the polyelectrolyte backbone flexibility and the solvent quality. These interesting behaviors are attributed to the interplay between the conformational entropy of the confined polyelectrolytes, the Coulombic interaction between the charged species, and the repulsion from the surfaces with lower dielectric constant.

scholarly journals Comparison of Quantitative Morphology of Layered and Arbitrary Patterns: Contrary to Visual Perception, Binary Arbitrary Patterns Are Layered from a Structural Point of View

2021 ◽  
Vol 11 (14) ◽  
pp. 6300
Author(s):  
Igor Smolyar ◽  
Daniel Smolyar
Keyword(s):  
Boolean Function ◽  
Layer Structure ◽  
Central Element ◽  
Morphological Characteristics ◽  
Building Blocks ◽  
Point Of View ◽  
Living Systems ◽  
Seismic Profiles ◽  
Contour Maps ◽  
Anisotropic Layers

Patterns found among both living systems, such as fish scales, bones, and tree rings, and non-living systems, such as terrestrial and extraterrestrial dunes, microstructures of alloys, and geological seismic profiles, are comprised of anisotropic layers of different thicknesses and lengths. These layered patterns form a record of internal and external factors that regulate pattern formation in their various systems, making it potentially possible to recognize events in the formation history of these systems. In our previous work, we developed an empirical model (EM) of anisotropic layered patterns using an N-partite graph, denoted as G(N), and a Boolean function to formalize the layer structure. The concept of isotropic and anisotropic layers was presented and described in terms of the G(N) and Boolean function. The central element of the present work is the justification that arbitrary binary patterns are made up of such layers. It has been shown that within the frame of the proposed model, it is the isotropic and anisotropic layers themselves that are the building blocks of binary layered and arbitrary patterns; pixels play no role. This is why the EM can be used to describe the morphological characteristics of such patterns. We present the parameters disorder of layer structure, disorder of layer size, and pattern complexity to describe the degree of deviation of the structure and size of an arbitrary anisotropic pattern being studied from the structure and size of a layered isotropic analog. Experiments with arbitrary patterns, such as regular geometric figures, convex and concave polygons, contour maps, the shape of island coastlines, river meanders, historic texts, and artistic drawings are presented to illustrate the spectrum of problems that it may be possible to solve by applying the EM. The differences and similarities between the proposed and existing morphological characteristics of patterns has been discussed, as well as the pros and cons of the suggested method.

scholarly journals Research on molecular energy storage

2021 ◽  
Vol 1 (3) ◽  
pp. 49-56
Author(s):  
S.M. Zuyev ◽  
◽  
R.A. Maleyev ◽  
YU.M. Shmatkov ◽  
M.YU. Khandzhalov ◽  
...  
Keyword(s):  
Comparative Analysis ◽  
Energy Storage ◽  
Lithium Ion Battery ◽  
Double Layer ◽  
Lithium Ion ◽  
Storage Device ◽  
Energy Storage Device ◽  
Energy Storage Devices ◽  
Storage Devices ◽  
Advantages And Disadvantages

This article provides a comparative analysis of various energy storage devices. A detailed review and analysis of molecular energy storage units is carried out, their main characteristics and parame-ters, as well as their application areas, are determined. The main types of molecular energy storage are determined: electric double layer capacitors, pseudo capacitors, hybrid capacitors. Comparison of the characteristics of various batteries is given. The parameters of various energy storage devices are presented. The analysis of molecular energy storage devices and accumulators is carried out. Ttheir advantages and disadvantages are revealed. It has been shown that molecular energy storage or double layer electrochemical capacitors are ideal energy storage systems due to their high specific energy, fast charging and long life compared to conventional capacitors. The article presents oscillograms of a lithium-ion battery with a voltage of 10.8 V at a pulsed load current of 2A of a laptop with and without a molecular energy storage device, as well as oscil-lograms of a laptop with DVD lithium-ion battery with a voltage of 10.8 V with a parallel shutdown of a molecular energy storage device with a capacity of 7 F and without it. The comparative analysis shows that when the molecular energy storage unit with a 7 F capacity is switched on and off, transient processes are significantly improved and there are no supply voltage dips. The dependenc-es of the operating time of a 3.6 V 600 mAh lithium-ion battery at a load of 2 A for powering mo-bile cellular devices with and without a molecular energy storage are given. It is shown that when the molecular energy storage device is switched on, the battery operation time increases by almost 20%.

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