Optimization of switching charge and recoverable energy density mediated by structural transformation in Sr-substituted BaNiO3 perovskites.

Because of their distinctive characteristics, ferroelectric perovskites are considered among the most potent and auspicious candidates for energy storage and pulsed power devices. But their energy storage properties and switching capabilities need to be further enhanced which can be done by substitutions of appropriate cations. Hence, a series of lead-free Ba1-xSrxNiO3 (x = 0.00, 0.33, 0.67, and 1.00) ceramics was fabricated using a sol-gel auto combustion technique. Rietveld's refinement of X-ray diffraction plots verified the complete development of the required hexagonal perovskite structure. Scanning electron microscopy images revealed a gradual increase in average grain sizes and agglomeration with the increase in Sr-content. Moreover, the existence of all the constituent elements exactly in proportion to their stoichiometric ratios was verified by energy dispersive X-ray spectroscopy. The characteristic parameters of ferroelectric materials such as ferroelectric response, electrical conductivity, and switching charge density were also determined. The P-E loops indicated that with the increase in Sr-content, the coercive field, remanent polarization, and maximum polarization all decreased gradually, but the recoverable energy density (Wrec) increased as the loops became slimmer. The maximum value of Wrec was found in the Ba0.33Sr0.67NiO3 sample. Moreover, SrNiO3 exhibited minimum energy loss with the highest efficiency of ∼47.21%. The existence of a current barrier in all the samples was proved from the low leakage current values (∼10-7 A). In addition, the pure SrNiO3 showed a low electrical conductivity and minimum value of switching charge density. All these findings make SrNiO3 a promising candidate for fast switching and energy storage applications.

Investigation and optimization of In-Vitro behaviour of Perovskite barium titanate as a scaffold and protective coatings.

The piezoelectric effect is widely known to have a significant physiological function in bone development, remodeling, and fracture repair. As a well-known piezoelectric material, barium titanate is particularly appealing as a scaffold layer to improve bone tissue engineering applications. Currently, the chemical bath deposition method is used to prepare green synthesized barium titanate coatings to improve mechanical and biological characteristics. Molarity of the solutions, an essential parameter in chemical synthesis, is changed at room temperature (0.1-1.2 Molar) to prepare coatings. The XRD spectra for as deposited coatings indicate amorphous behavior, while polycrystalline nature of coatings is observed after annealing (300 °C). Coatings prepared with solutions of relatively low molarities, i.e. from 0.1 to 0.8 M, exhibit mixed tetragonal - cubic phases. However, the tetragonal phase of Perovskite barium titanate is observed using solution molarities of 1.0 M and 1.2 M. Relatively high value of transmission, i.e. ∼80%, is observed for the coatings prepared with high molarities. Band gap of annealed coatings varies between 3.47 and 3.70 eV. For 1.2 M sample, the maximum spontaneous polarization (Ps) is 0.327x10-3 (µC/cm2) and the residual polarization (Pr) is 0.072x10-3 (µC/cm2). For 1.2M solution, a high hardness value (1510 HV) is recorded, with a fracture toughness of 28.80 MPam-1/2. Low values of weight loss, after dipping the coatings in simulated body fluid, is observed. The antibacterial activity of BaTiO3 is tested against E. coli and Bacillus subtilis. Drug encapsulation capability is also tested for different time intervals. As a result, CBD-based coatings are a promising nominee for use as scaffold and protective coatings.

Enhancing QoS of Telecom Networks through Server Load Management in Software-Defined Networking (SDN).

In the modern era, with the emergence of the Internet of Things (IoT), big data applications, cloud computing, and the ever-increasing demand for high-speed internet with the aid of upgraded telecom network resources, users now require virtualization of the network for smart handling of modern-day challenges to obtain better services (in terms of security, reliability, scalability, etc.). These requirements can be fulfilled by using software-defined networking (SDN). This research article emphasizes one of the major aspects of the practical implementation of SDN to enhance the QoS of a virtual network through the load management of network servers. In an SDN-based network, several servers are available to fulfill users' hypertext transfer protocol (HTTP) requests to ensure dynamic routing under the influence of the SDN controller. However, if the number of requests is directed to a specific server, the controller is bound to follow the user-programmed instructions, and the load on that server is increased, which results in (a) an increase in end-to-end user delay, (b) a decrease in the data transfer rate, and (c) a decrease in the available bandwidth of the targeted server. All of the above-mentioned factors will result in the degradation of network QoS. With the implementation of the proposed algorithm, dynamic active sensing server load management (DASLM), on the SDN controller, the load on the server is shared based on QoS control parameters (throughput, response time, round trip time, etc.). The overall delay is reduced, and the bandwidth utilization along with throughput is also increased.

Elucidating an efficient super-capacitive response of a Sr2Ni2O5/rGO composite as an electrode material in supercapacitors.

Mixed transition metal oxides have emerged as efficient electrode materials because of their significant cycling stability, and superior capacitance values, resulting in remarkable electrochemical outputs. In this regard, Sr2Ni2O5/rGO composites were synthesized using a facile solvothermal method to achieve efficient electrochemical pursuits. X-ray diffraction confirmed the formation of finely crystallized samples with the phase evolution from orthorhombic to hexagonal. Morphological studies using field emission scanning electron microscopy depicted the desired porosity in samples with well-defined shapes and sizes of homogeneously distributed grains. Elemental analysis verified the pictorial depiction of sample compositions in terms of their stoichiometric ratios. The composite sample with composition Sr2Ni2O5@15%rGO exhibited superior electrochemical performance compared to other samples, depicting the highest specific capacitance of 148.09 F g-1 at a lower scan rate of 0.005 V s-1 observed via cyclic voltammetry. In addition, the cyclability performance of Sr2Ni2O5@15%rGO exhibits 68.5% capacitive retention after 10 000 cycles. The energy density as determined using a two-electrode system remained 4.375 W h kg-1 for the first cycle which reduced to 1.875 W h kg-1 for the 10 000th cycle, with a maximum power density of 1.25 W kg-1. The Nyquist plot represented less barrier to charge transfer. The electrode with particular composition Sr2Ni2O5@15%rGO emerged as significant, exhibiting a superior surface capacitive charge storage, that makes it a potential candidate as an electrode material.

Gateway toward efficient and miniaturized A 2 B 2O7-type fluorite structure-based energy storage devices.

Defect fluorite structure with A 2 B 2O7 composition exhibits an intense potential for utilization in modern smart electrical devices. Efficient energy storage with low loss factors like leakage current makes them a prominent candidate for energy storage applications. Here we report a series of the form Nd2-2x La2x Ce2O7 with x = 0.0, 0.2, 0.4, 0.6, 0.8, and 1.0, synthesized via a sol-gel auto-combustion route. The fluorite structure of Nd2Ce2O7 is slightly expanded with the incorporation of La without any phase transformation. A gradual replacement of Nd with La causes a decrease in grain size, which increases the surface energy and thus leads to grain agglomeration. The formation of exact composition without any impurity element is confirmed by energy-dispersive X-ray spectra. The polarization versus electric field loops, energy storage efficiency, leakage current, switching charge density, and normalized capacitance, which are considered key features of any ferroelectric material, are comprehensively examined. The highest energy storage efficiency, low leakage current, small switching charge density, and large value of normalized capacitance are observed for pure Nd2Ce2O7. This reveals the enormous potential of the fluorite family for efficient energy storage devices. The temperature-dependent magnetic analysis exhibited very low transition temperatures throughout the series.

Highly Tunable Beyond-Room-Temperature Intrinsic Ferromagnetism in Cr-Doped Topological Crystalline Insulator SnTe Crystals.

The combination of topological phase and intrinsic beyond-room-temperature ferromagnetism is expected to realize the quantum anomalous Hall effect at a high temperature. However, no beyond-room-temperature intrinsic ferromagnetism has been reported in either topological insulator or topological crystalline insulator (TCI) so far. Here, we report Cr-doping in TCI-phase SnTe crystals which possess highly tunable beyond-room-temperature intrinsic ferromagnetism including Tc, magnetic moment, and coercivity by varying Cr contents and crystal thickness. With the increase of the Cr content, the Tc increases by 159 K from 221 to 380 K and the saturation magnetic moments increase by ∼23.6 times from 0.018 to 0.421 µB/f.u. This intrinsic beyond-room-temperature ferromagnetism is fully demonstrated by the anomalous Hall effect and magneto-optical Kerr effect in a single CrxSn1-xTe nanosheet. Moreover, the room-temperature tunneling magnetoresistance effect has been realized by using a CrxSn1-xTe flake, a Fe thin film, and a commercially compatible ultrathin AlOx tunneling barrier. This work indicates a great potential of CrxSn1-xTe crystals in room-temperature magnetoelectronic and spintronic devices.

Ethylene glycol assisted three-dimensional floral evolution of BiFeO3-based nanostructures with effective magneto-electric response.

Controlled growth of nanostructures plays a vital role in tuning the physical and chemical properties of functional materials for advanced energy and memory storage devices. Herein, we synthesized hierarchical micro-sized flowers, built by the self-assembly of highly crystalline, two-dimensional nanoplates of Co- and Ni-doped BiFeO3, using a simple ethylene glycol-mediated solvothermal method. Pure BiFeO3 attained scattered one-dimensional nanorods-type morphology having diameter nearly 60 nm. Co-doping of Co and Ni at Fe-site in BiFeO3 does not destabilize the morphology; rather it generates three-dimensional floral patterns of self-assembled nanoplates. Unsaturated polarization loops obtained for BiFeO3 confirmed the leakage behaviour of these rhombohedrally distorted cubic perovskites. These loops were then used to determine the energy density of the BiFeO3 perovskites. Enhanced ferromagnetic behaviour with high coercivity and remanence was observed for these nanoplates. A detailed discussion about the origin of ferromagnetic behaviour based on Goodenough-Kanamori's rule is also a part of this paper. Impedance spectroscopy revealed a true Warburg capacitive behaviour of the synthesized nanoplates. High magneto-electric (ME) coefficient of 27 mV cm-1 Oe-1 at a bias field of -0.2 Oe was observed which confirmed the existence of ME coupling in these nanoplates.

Dilute magnetic ions mediated magneto-dielectric, optical and ferroelectric response of MgAl2O4 spinels.

Magnesium aluminate (MgAl2O4) commonly termed as spinel has been a subject of intense research due to its excellent thermal, optical and dielectric characteristics. These properties in such compounds can efficiently be tuned by introducing small contents of different transition metals. In this work, dilute contents of transition metals (Mn, Fe, Co, and Ni) are incorporated in MgAl2O4 to produce the dilute magnetic compositions of these aluminates. Crystallographic information reveals the formation of spinel cubic crystal structure with Fd-3m space group. Magnetic measurements demonstrate a clear magnetization response to an external magnetic field establishing dilute magnetic behavior of these spinels. The increase in ferroelectric characteristics with the incorporation of transition elements suggests that these materials are quite suitable for energy storage devices. A sharp variation in dielectric constant and magneto-dielectric coupling with the response to the external magnetic field, further exposes them as an excellent candidate for magneto-dielectric applications.

Dielectric Properties of Graphene/Titania/Polyvinylidene Fluoride (G/TiO2/PVDF) Nanocomposites.

Flexible electronics have gained eminent importance in recent years due to their high mechanical strength and resistance to environmental conditions, along with their effective energy storage and energy generating abilities. In this work, graphene/ceramic/polymer based flexible dielectric nanocomposites have been prepared and their dielectric properties were characterized. The composite was formulated by combining graphene with rutile and anatase titania, and polyvinylidene fluoride in different weight ratios to achieve optimized dielectric properties and flexibility. After preparation, composites were characterized for their morphologies, structures, functional groups, thermal stability and dielectric characterizations by using scanning electron microscopy, X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, thermal gravimetric analysis and impedance spectroscopy. Dielectric results showed that prepared flexible composite exhibited dielectric constant of 70.4 with minor leakage current (tanδ) i.e., 0.39 at 100 Hz. These results were further confirmed by calculating alternating current (AC) conductivity and electric modulus which ensured that prepared material is efficient dielectric material which may be employed in electronic industry for development of next generation flexible energy storage devices.

Electrochemical performance of Li+ insertion/extraction in Ni-substituted ZnCo2O4 as an emerging highly efficient anode material.

With the industrial revolution in electronics, the demand for lithium-ion batteries, particularly those designed for electric vehicles and energy storage systems, has accelerated in recent years. This continuously increasing demand requires high-performance electrode materials, as commonly used graphite anodes show limited lithium intercalation. In this context, Ni-substituted ZnCo2O4 nanostructures, thanks to their high storage capacity, have potential for use as an anode material in lithium-ion batteries. Structural analysis concludes that the prepared materials show improved crystallinity with increasing Ni at the Zn-site in ZnCo2O4. The intermediate composition, Zn0.5Ni0.5Co2O4, of this series exhibits a specific capacity of 65 mA h g-1 at an elevated current rate of 10 A g-1. The lithium insertion/extraction mechanism is investigated via cyclic voltammetry, showing two redox peaks from ZnCo2O4 and a single redox peak from NiCo2O4. Additionally, the lithium diffusion coefficient in the prepared electrodes is computed to be 2.22 × 10-12 cm2 s-1 for the intermediate composition, as obtained using cyclic voltammetry. Electrochemical impedance spectroscopy is used to observe the charge transport mechanism and the charge transfer resistance values of all the samples, which are calculated to be in the range of 235 to 306 Ω.

Fluoride ion assisted growth of hierarchical flowerlike nanostructures of Co/Ni ferrites and their magnetoresistive response.

One-dimensional nanorod arrays exhibiting hierarchical flowerlike morphologies, of Co and Ni based ferrites were synthesized by hydrothermal treatment and using ammonium fluoride (NH4F) as a mineralizing agent. The effects of NH4F concentration and synthesis temperature were probed to control the morphology of these nanorods that were formed as a result of crystal nucleation. It was observed that a higher concentration of NH4F leads to several other nucleation sites above these nanorods while controlled concentration of precursors and NH4F results in the synthesis of floral patterns. The specific geometries of these nanorods leads to a shape anisotropy effect resulting in increased magnetic coercive fields. To study the effect of magnetic field on the resistance and current density, impedance spectroscopy and I-V-R characteristics, respectively, were performed. Nanorods show enhanced values for resistance with the increase in magnetic field confirming the effect of magnetoresistive coupling while a decrease in current densities with increasing magnetic field highlights the potential of these structures for magnetoresistive applications.

Advancing Dielectric and Ferroelectric Properties of Piezoelectric Polymers by Combining Graphene and Ferroelectric Ceramic Additives for Energy Storage Applications.

To address the limitations of piezoelectric polymers which have a low dielectric constant andto improve their dielectric and ferroelectric efficiency for energy storage applications, we designed and characterized a new hybrid composite that contains polyvinylidene fluoride as a dielectric polymer matrix combined with graphene platelets as a conductive and barium titanite as ceramic ferroelectric fillers. Different graphene/barium titanate/polyvinylidene fluoride nanocomposite films were synthesized by changing the concentration of graphene and barium titanate to explore the impact of each component and their potential synergetic effect on dielectric and ferroelectric properties of the composite. Results showed that with an increase in the barium titanate fraction, dielectric efficiency ofthe nanocomposite was improved. Among all synthesized nanocomposite films, graphene/barium titanate/polyvinylidene fluoride nanocomposite in the weight ratio of 0.15:0.5:1 exhibited thehighest dielectric constant of 199 at 40 Hz, i.e., 15 fold greater than that of neat polyvinylidene fluoride film at the same frequency, and possessed a low loss tangent of 0.6. However, AC conductivity and ferroelectric properties of graphene/barium titanate/polyvinylidene fluoride nanocomposite films were enhanced with an increase in the graphene weight fraction. Graphene/barium titanate/polyvinylidene fluoride nanocomposite films with a weight ratio of 0.2:0.1:1 possessed a high AC conductivity of 1.2 × 10-4 S/m at 40 Hz. While remanent polarization, coercive field, and loop area of the same sample were 0.9 µC/cm², 9.78 kV/cm, and 24.5 µC/cm²·V, respectively. Our results showed that a combination of graphene and ferroelectric ceramic additives are an excellent approach to significantly advance the performance of dielectric and ferroelectric properties of piezoelectric polymers for broad applications including energy storage.

Synthesis and Characterization of BaTiO3/Polypyrrole Composites with Exceptional Dielectric Behaviour.

Higher concentrations of ceramic fillers induce brittleness in the ceramic/polymer hybrids which restrict their applications to limited fields especially when such hybrids are prepared for their use as dielectrics. We have synthesized and characterized different BaTiO3-polypyrrole (PPy) composites by changing the concentration of BaTiO3 from 1% by weight of PPy taken to 5 wt % to explore its effect on the dielectric parameters of the final product and found that the BaTiO3-polypyrrole composite with weight ratio of 0.05:1 exhibited highest dielectric constant, lowest dielectric loss and thermally most stable. All the composites were prepared using in-situ polymerization of pyrrole in an aqueous dispersion of low content of BaTiO3 in the presence of small amount of Hydrochloric acid. These composites were characterized for their microstructure and crystallinity by X-ray diffractometer (XRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM) while thermal stability by thermo gravimetric (TGA) analysis. An impedance analyser (LCR meter) was utilized to investigate the dielectric parameters. FT-IR data confirmed the presence of the two phases and their interaction, inferred from the shifting of normal PPy peaks. The data obtained from XRD confirmed the presence of crystallites of 2.8 to 5 nm with dominant crystallinity of the filler, TGA analysis (25 to 600 °C) confirmed the higher thermal stability induced on successive addition of the filler into the prepared composites as compared to that of pure PPy in a wide temperature range which is unusual for such a low % age addition of the filler. The SEM analysis together with XRD results reveal that the successive introduction of BaTiO3 particles produced crystallites of 2 to 5 nm size which bonded together and changed the hemispherical shaped larger grains of the matrix to regular shaped smaller grains. The dielectric constant of the composites was enhanced with filler contents from 178 to 522 at 1 MHz for 1 wt % and 5 wt % BaTiO3 respectively. It was concluded that the introduction of BaTiO3 into the polymer matrix with this new procedure has greatly affected the polymerization process, thermal stability, morphology and dielectric properties of the host matrix and has resulted in a novel series of the composites which may have broad applications.