The electrodes of lithium-ion batteries (LIBs) are multicomponent systems and their electrochemical properties are influenced by each component, therefore the composition of electrodes should be properly balanced. At the beginning of lithium-ion battery research, most attention was paid to the nature, size, and morphology peculiarities of inorganic active components as the main components which determine the functional properties of electrode materials. Over the past decade, considerable attention has been paid to development of new binders, as the binders have shown great effect on the electrochemical performance of electrodes in LIBs. The study of new conductive binders, in particular water-based binders with enhanced electronic and ionic conductivity, has become a trend in the development of new electrode materials, especially the conversion/alloying-type anodes. This mini-review provides a summary on the progress of current research of the effects of binders on the electrochemical properties of intercalation electrodes, with particular attention to the mechanisms of binder effects. The comparative analysis of effects of three different binders (PEDOT:PSS/CMC, CMC, and PVDF) for a number of oxide-based and phosphate-based positive and negative electrodes for lithium-ion batteries was performed based on literature and our own published research data. It reveals that the combined PEDOT:PSS/CMC binder can be considered as a versatile component of lithium-ion battery electrode materials (for both positive and negative electrodes), effective in the wide range of electrode potentials.
Aqueous zinc-ion batteries (AZIBs) are being intensively developed as potential alternative electrochemical power sources, due to their advantages such as low cost, high safety, abundance of natural zinc resources and appropriate energy density. Among currently investigated prospective cathode materials for AZIBs, vanadium oxide-based composites with intrinsically conducting polymers have shown many advantages, such as high capacity, high power density and long battery life. This review gives a focused view of the design for the boosting of zinc ion storage performance using intrinsically conducting polymers in vanadium oxide-based composites and the mechanism of intercalation processes. The main challenges in interfacial engineering of vanadium oxide-conducting polymers composite structures and the prospects for further development of such cathode materials are summarized and discussed. The review would give rise to a broad interest focusing on the advantageous strategy of the development of vanadium oxide composite cathodes with intrinsically conducting polymers (polyaniline, polypyrrole, poly(3,4-ethylenedioxythiophene)) for AZIBs with improved energy density, high-rate capability and stability.
Aqueous zinc-ion batteries (AZIBs) and, in particular, Zn//MnO2 rechargeable batteries have attracted great attention due to the abundant natural resources of zinc and manganese, low cost, environmental friendliness, and high operating voltage. Among the various ways to improve the electrochemical performance of MnO2-based cathodes, the development of MnO2 cathodes doped with metal ions or composites of MnO2 with conducting polymers has shown such advantages as increasing the specific capacity and cycling stability. This mini-review focuses on the strategies to improve the electrochemical performance of manganese-based cathodes of AZIBs.