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Zinc oxide (ZnO) and materials based on it are often used to create battery-type supercapacitor electrodes and are considered as promising materials for hybrid asymmetric supercapacitors. However, when creating such electrodes, it is necessary to take into account the instability and degradation of zinc oxide in aggressive environments with a non-neutral pH. To the best of our knowledge, studies of the changes in the properties of ZnO-containing electrodes in alkaline electrolytes have not been carried out. In this work, changes in the structure and properties of these electrodes under alkaline treatment were investigated using the example of ZnO-containing composites, which are often used for the manufacturing of supercapacitor electrodes. Supercapacitor electrodes made of two materials containing ZnO were studied: (i) a heterogeneous ZnO-Co3O4 system, and (ii) a hexagonal h-Zn-Co-O solid solution. A comparison was made between the structure and properties of these materials before and after in situ electrochemical oxidation in the process of measuring cyclic voltammetry and galvanostatic charge/discharge. It has been shown that the structure of both nanoparticles of the heterogeneous ZnO-Co3O4 system and the h-Zn-Co-O solid solution changes due to the dissolution of ZnO in the alkaline electrolyte 3.5 M KOH, with the short-term alkaline treatment producing cobalt and zinc hydroxides, and long-term exposure leading to electrochemical cyclic oxidation–reduction, forming cobalt oxide Co3O4. Since the resulting cobalt oxide nanoparticles are immobilized in the electrode structure, a considerable specific capacity of 446 F g−1 or 74.4 mA h g−1 is achieved at a mass loading of 0.0105 g. The fabricated hybrid capacitor showed a good electrochemical performance, with a series resistance of 0.2 Ohm and a capacitance retention of 87% after 10,000 cycles. [ABSTRACT FROM AUTHOR]

Swift developments in electronic devices and future transportation/energy production directions have forced researchers to develop new and contemporary devices with higher power capacities, extended cycle lives, and superior energy densities. Supercapacitors are promising devices with excellent power densities and exceptionally long cycle lives. However, commercially available supercapacitors, which commonly use high-surface-area carbon-based electrodes and organic solutions as electrolytes, suffer from inferior energy densities due to the limited accessibility of surface area and constrained operating potential window of electrolytes. To address the issue of inferior energy densities, new high-capacity electrode materials and new/state-of-the-art electrolytes, such as ionic liquids, gel polymers, or even solid-state electrolytes, have been developed and evaluated vigorously in recent years. In this brief review, different types of supercapacitors, according to their charge storage mechanisms, have been discussed in detail. Since carbon-based active materials are the key focus of this review, synthesis parameters, such as carbonisation, activation, and functionalisation, which can impact a material's physiochemical characteristics, ultimately affecting the performance of supercapacitors, are also discussed. Finally, the synthesis and applications of different carbon-based materials, i.e., carbon nanotubes, graphene, and activated carbon, have been reviewed, followed by conclusions and outlook. [ABSTRACT FROM AUTHOR]

Summary: Extensive use of carbon‐based materials has revolutionised the number of modern scientific areas such as transportation, electronic, material chemistry and electrochemical energy storage, mainly due to their outstanding characteristics such as excellent conductivity, mechanical strength, ease of availability and cost‐effectiveness. However, it is difficult to fine‐tune the physiochemical characteristics of naturally occurring carbonaceous materials according to desired applications. High purity carbon aerogels with control over porous structure prepared using synthetic chemistry techniques such as polymerisation can be a potential substitute carbon material due to their outstanding characteristics including superior conductivity, high level of porosity and chemical inertness. Designing tailored polymeric carbon materials according to their anticipated uses is advantageous and can be achieved by altering various synthesis parameters at the initial stages of preparation. This not only helps in fine tuning porous structure of carbon aerogels but can also assist in producing composite materials by introducing materials on the surface or within the bulk of produced carbons. [ABSTRACT FROM AUTHOR]