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Due to their distinctive security characteristics, all-solid-state batteries are seen as a potential technology for the upcoming era of energy storage. The flexibility of nanomaterials shows enormous potential for the advancement of all-solid-state batteries' exceptional power and energy storage capacities. These batteries might be applied in many areas such as large-scale energy storage for power grids, as well as in the creation of foldable and flexible electronics, and portable gadgets. The most difficult aspect of creating a comprehensive nanoscale all-solid-state battery assembly is the task of decreasing the particle size of the solid electrolyte while maintaining its excellent ionic conductivity. Materials possessing nanoscale structural features and a substantial electrochemically active surface area have the potential to significantly enhance power characteristics and the cycle life. This might bring about substantial changes to existing energy storage models. The primary objective of this research is to summarize the latest advancements in utilizing nanomaterials for energy harvesting in various all-solid-state battery assemblies. This study examines the most complex solid–solid interfaces of all-solid-state batteries, as well as feasible methods for implementing nanomaterials in such interfaces. Currently, there is significant attention on the necessity to develop electrode–solid electrolyte interfaces that exhibit nanoscale particle articulation and other characteristics related to the behavior of lithium ions. [ABSTRACT FROM AUTHOR]

Prussian blue and Prussian blue analogues have attracted increasing attention as versatile framework materials with a wide range of applications in catalysis, energy conversion and storage, and biomedical and environmental fields. In terms of energy storage and conversion, Prussian blue-based materials have emerged as suitable candidates of growing interest for the fabrication of batteries and supercapacitors. Their outstanding electrochemical features such as fast charge–discharge rates, high capacity and prolonged cycling life make them favorable for energy storage application. Furthermore, Prussian blue and its analogues as rechargeable battery anodes can advance significantly by the precise control of their structure, morphology, and composition at the nanoscale. Their tunable structural and electronic properties enable the detection of many types of analytes with high sensitivity and specificity, and thus, they are ideal materials for the development of sensors for environmental detection, disease trend monitoring, and industrial safety. Additionally, Prussian blue-based catalysts display excellent photocatalytic performance for the degradation of pollutants and generation of hydrogen. Specifically, their excellent light capturing and charge separation capabilities make them stand out in photocatalytic processes, providing a sustainable option for environmental remediation and renewable energy production. Besides, Prussian blue coatings have been studied particularly for corrosion protection, forming stable and protective layers on metal surfaces, which extend the lifespan of infrastructural materials in harsh environments. Prussian blue and its analogues are highly valuable materials in healthcare fields such as imaging, drug delivery and theranostics because they are biocompatible and their further functionalization is possible. Overall, this review demonstrates that Prussian blue and related framework materials are versatile and capable of addressing many technical challenges in various fields ranging from power generation to healthcare and environmental management. [ABSTRACT FROM AUTHOR]

This paper proposed a control method for output and circulating currents of modular multilevel converter (MMC). The output and circulating current are controlled with the help of arm currents, which contain DC, fundamental frequency, and double frequency components. The arm current is transformed into a stationary reference frame (SRF) to isolate the DC and AC components. The AC component is controlled with a conventional proportional resonant (PR) controller, while the DC component is controlled by a proportional controller. The effective control of the upper arm and lower arm ultimately controls the output current so that it delivers the required power to the grid and circulating current in such a way that the second harmonic component is completely vanished leaving behind only the DC component. Comparative results of leg-level control based on PR controller are included in the paper to show the effectiveness of the proposed control scheme. A three-phase, five-level MMC is developed in MATLAB/Simulink to verify the effectiveness of the proposed control method.

Over the past few decades, the application of new novel materials in energy storage system has seen excellent development. We report a novel MnCo2O4/NiO nanostructure prepared by a simplistic chemical bath deposition method and employed it as a binder free electrode in the supercapacitor. The synergistic attraction from a high density of active sites, better transportation of ion diffusion and super-most electrical transportation, which deliver boost electrochemical activities. X-ray diffraction, field-emission scanning electron microscopy, and X-ray photoelectron spectroscopy have been used to investigate the crystallinity, morphology, and elemental composition of the as-synthesized precursors, respectively. Cyclic voltammetry, galvanostatic charge/discharge, and electron impedance spectroscopy have been employed to investigate the electrochemical properties. The unique nanoparticle structures delivered additional well-organized pathways for the swift mobility of electrons and ions. The as-prepared binder-free MnCo2O4/NiO nanocomposite electrode has a high specific capacity of 453.3 C g−1 at 1 Ag−1, and an excellent cycling reliability of 91.89 percent even after 4000 cycles, which are significantly higher than bare MnCo2O4 and NiO electrodes. Finally, these results disclose that the as-fabricated MnCo2O4/NiO electrode could be a favored-like electrode material holds substantial potential and supreme option for efficient supercapacitor and their energy storage-related applications.

The composites of NiCo2O4 with unique structures were substantially investigated as promising electrodes. In this study, the unique structured nanosheets anchored on nickel foam (Ni foam) were prepared under the hydrothermal technique of NiCo2O4 and subsequent preparation of Co(OH)2. The Co(OH)2@NiCo2O4 nanosheet composite has demonstrated higher specific capacitances owing to its excellent specific surface region, enhanced rate properties, and outstanding electrical conductivities. Moreover, the electrochemical properties were analyzed in a three-electrode configuration to study the sample material. The as-designed Co(OH)2@NiCo2O4 nanosheet achieves higher specific capacitances of 1308 F·g−1 at 0.5 A·g−1 and notable long cycles with 92.83% capacity retention over 6000 cycles. The Co(OH)2@NiCo2O4 nanosheet electrode exhibits a long life span and high capacitances compared with the NiCo2O4 and Co(OH)2 electrodes, respectively. These outstanding electrochemical properties are mainly because of their porous construction and the synergistic effects between NiCo2O4 and Co(OH)2. Such unique Co(OH)2@NiCo2O4 nanosheets not only display promising applications in renewable storage but also reiterate to scientists of the unlimited potential of high-performance materials. [ABSTRACT FROM AUTHOR]

NiCo2O4 nanoleaf arrays (NCO NLAs) and NiCo2O4/NiCO2O4 nanofile arrays (NCO/NCO NFAs) material was fabricated on flexible nickel foam (NF) using a facile hydrothermal approach. The electrochemical performance, including the specific capacitance, charge/discharge cycles, and lifecycle of the material after the hydrothermal treatment, was assessed. The morphological and structural behaviors of the NF@NCO NLAs and NF@NCO/NCO NFAs electrodes were analyzed using a range of analysis techniques. The as-obtained nanocomposite of the NF@NCO/NCO NFAs material delivered outstanding electrochemical performance, including an ultrahigh specific capacitance (Cs) of 2312 F g−1 at a current density of 2 mA cm−2, along with excellent cycling stability (98.7% capacitance retention after 5000 cycles at 5 mA cm−2). These values were higher than those of NF@NCO NLAs (Cs of 1950 F g−1 and 96.3% retention). The enhanced specific capacitance was attributed to the large electrochemical surface area, which allows for higher electrical conductivity and rapid transport between the electrons and ions as well as a much lower charge-transfer resistance and superior rate capability. These results clearly show that a combination of two types of binary metal oxides could be favorable for improving electrochemical performance and is expected to play a major role in the future development of nanofile-like composites (NF@NCO/NCO NFAs) for supercapacitor applications.

Hierarchical NiMoO4/NiMoO4 nanoflowers were fabricated on highly conductive flexible nickel foam (NF) substrates using a facile hydrothermal method to achieve rapid charge-discharge ability, high energy density, long cycling lifespan, and higher flexibility for high-performance supercapacitor electrode materials. The synthesized composite electrode material, NF/NiMoO4/NiMoO4 with a nanoball-like NF/NiMoO4 structure on a NiMoO4 surface over a NF substrate, formed a three-dimensional interconnected porous network for high-performance electrodes. The novel NF/NiMoO4/NiMoO4 nanoflowers not only enhanced the large surface area and increased the electrochemical activity, but also provided an enhanced rapid ion diffusion path and reduced the charge transfer resistance of the entire electrode effectively. The NF/NiMoO4/NiMoO4 composite exhibited significantly improved supercapacitor performance in terms of a sustained cycling life, high specific capacitance, rapid charge-discharge capability, high energy density, and good rate capability. Electrochemical analysis of the NF/NiMoO4/NiMoO4 nanoflowers fabricated on the NF substrate revealed ultra-high electrochemical performance with a high specific capacitance of 2121 F g−1 at 12 mA g−1 in a 3 M KOH electrolyte and 98.7% capacitance retention after 3000 cycles at 14 mA g−1. This performance was superior to the NF/NiMoO4 nanoball electrode (1672 F g−1 at 12 mA g−1 and capacitance retention 93.4% cycles). Most importantly, the SC (NF/NiMoO4/NiMoO4) device displayed a maximum energy density of 47.13 W h kg−1, which was significantly higher than that of NF/NiMoO4 (37.1 W h kg−1). Overall, the NF/NiMoO4/NiMoO4 composite is a suitable material for supercapacitor applications.

MgCo2O4 nanomaterial is thought to be a promising candidate for renewable energy storage and conversions. Nevertheless, the poor stability performances and small specific areas of transition-metal oxides remain a challenge for supercapacitor (SC) device applications. In this study, sheet-like Ni(OH)2@MgCo2O4 composites were hierarchically developed on nickel foam (NF) using the facile hydrothermal process with calcination technology, under carbonization reactions. The combination of the carbon–amorphous layer and porous Ni(OH)2 nanoparticles was anticipated to enhance the stability performances and energy kinetics. The Ni(OH)2@MgCo2O4 nanosheet composite achieved a superior specific capacitance of 1287 F g−1 at a current value of 1 A g−1, which is higher than that of pure Ni(OH)2 nanoparticles and MgCo2O4 nanoflake samples. At a current density of 5 A g−1, the Ni(OH)2@MgCo2O4 nanosheet composite delivered an outstanding cycling stability of 85.6%, which it retained over 3500 long cycles with an excellent rate of capacity of 74.5% at 20 A g−1. These outcomes indicate that such a Ni(OH)2@MgCo2O4 nanosheet composite is a good contender as a novel battery-type electrode material for high-performance SCs. [ABSTRACT FROM AUTHOR]

In this study, we designed mixed metal oxides with doping compound nano-constructions as efficient electrode materials for supercapacitors (SCs). We successfully prepared the Fe-dopant with NiCoOx grown on nickel foam (Fe-dopant@NiCoOx@NF) through a simple hydrothermal route with annealing procedures. This method provides an easy route for the preparation of high activity SCs for energy storage. Obtained results revealed that the Fe dopant has successfully assisted NiCoOx lattices. The electrochemical properties were investigated in a three-electrode configuration. As a composite electrode for SC characteristics, the Fe-dopant@NiCoOx@NF exhibits notable electrochemical performances with very high specific capacitances of 1965 F g−1 at the current density of 0.5 A g−1, and even higher at 1296 F g−1 and 30 A g−1, respectively, which indicate eminent and greater potential for SCs. Moreover, the Fe-dopant@NiCoOx@NF nanoneedle composite obtains outstanding cycling performances of 95.9% retention over 4500 long cycles. The improved SC activities of Fe-dopant@NiCoOx@NF nanoneedles might be ascribed to the synergistic reactions of the ternary mixed metals, Fe-dopant, and the ordered nanosheets grown on NF. Thus, the Fe-dopant@NiCoOx@NF nanoneedle composite with unique properties could lead to promising SC performance. [ABSTRACT FROM AUTHOR]

Battery-type electrode materials have attracted much attention as efficient and unique types of materials for hybrid battery supercapacitors due to their multiple redox states and excellent electrical conductivity. Designing composites with high chemical and electrochemical stabilities is beneficial for improving the energy storage capability of battery-type electrode materials. We report on an interfacial engineering strategy to improve the energy storage performance of a Co(OH)2-based battery-type material by constructing polypyrrole-assisted and Ag-doped (Ag-doped@Co(OH)2@polypyrrole) nanosheets (NSs) on a Ni foam using a hydrothermal process that provides richer electroactive sites, efficient charge transportation, and an excellent mechanical stability. Physical characterization results revealed that the subsequent decoration of Ag nanoparticles on Co(OH)2 nanoparticles offered an efficient electrical conductivity as well as a reduced interface adsorption energy of OH- in Co(OH)2 nanoparticles as compared to Co(OH)2@polypyrrole-assisted nanoparticles without Ag particles. The heterogeneous interface of the Ag-doped@Co(OH)2@polypyrrole composite exhibited a high specific capacity of 291.2 mAh g−1 at a current density of 2 A g−1, and showed a good cycling stability after 5000 cycles at 5 A g−1. The specific capacity of the doped electrode was enhanced approximately two-fold compared to that of the pure electrode. Thus, the fabricated Ag-doped@Co(OH)2@polypyrrole nanostructured electrodes can be a potential candidate for fabricating low-cost and high-performance energy storage supercapacitor devices. [ABSTRACT FROM AUTHOR]