The limited resources and uneven distribution of lithium stimulate strong motivation to develop new rechargeable batteries that use alternative charge carriers. Potassium-ion batteries (PIBs) are at the top of the list of alternatives because of the abundant raw materials and relatively high energy density, fast ion transport kinetics in the electrolyte, and low cost. However, several challenges still hinder the development of PIBs, such as low reversible capacity, poor rate performance, and inferior cycling stability. Research on the cathode is currently focused on developing materials with high energy density and cycling stability, mainly including layered transition metal oxides, polyanion compounds, organic compounds, etc. Anodes based on intercalation reactions, conversion reactions, and alloying with potassium are currently under development, and promising results have been published. This review comprehensively summarizes the research effort to date on the electrode material optimization (e.g., crystals, morphology, reaction mechanisms, and interface control), the synthesis methods, and the full cell fabrication for PIBs to enhance the electrochemical potassium storage and provide a platform for further development in this battery system.

Since the beginning of the ‘graphene era’ post-2004, there has been significant interest in developing a high purity, high yield, and scalable fabrication route toward graphene materials for both primary research purposes and industrial production. One suitable approach to graphene production lies in the realm of electrochemical exfoliation, in which a potential difference is applied between a graphite anode/cathode in the presence of an electrolyte-containing medium. Herein we review various works on the electrochemical fabrication of graphene materials specifically through the use of electrochemical intercalation and exfoliation of a graphite source electrode, focusing on the quality and purity of products formed. We categorise the most significant works in terms of anodic and cathodic control, highlighting the merits of the respective approaches, as well as indicating the challenges associated with both procedures.

Graphene‐based textiles show promise for next‐generation wearable electronic applications due to their advantages over metal‐based technologies. However, current reduced graphene oxide (rGO)‐based electronic textiles (e‐textiles) suffer from poor electrical conductivity and higher power consumption. Here, highly conductive, ultraflexible, and machine washable graphene‐based wearable e‐textiles are reported. A simple and scalable pad−dry−cure method with subsequent roller compression and a fine encapsulation of graphene flakes is used. The graphene‐based wearable e‐textiles thus produced provide lowest sheet resistance (≈11.9 Ω sq⁻¹) ever reported on graphene e‐textiles, and highly conductive even after 10 home laundry washing cycles. Moreover, it exhibits extremely high flexibility, bendability, and compressibility as it shows repeatable response in both forward and backward directions before and after home laundry washing cycles. The scalability and multifunctional applications of such highly conductive graphene‐based wearable e‐textiles are demonstrated as ultraflexible supercapacitor and skin‐mounted strain sensors.

Multiwalled carbon nanotube (MWNT)/cellulose composite nanofibers have been prepared by electrospinning a MWNT/cellulose acetate blend solution followed by deacetylation. These composite nanofibers were then used as precursors for carbon nanofibers (CNFs). The effect of nanotubes on the stabilization of the precursor and microstructure of the resultant CNFs were investigated using thermogravimetric analysis, transmission electron microscopy and Raman spectroscopy. It is demonstrated that the incorporated MWNTs reduce the activation energy of the oxidative stabilization of cellulose nanofibers from ∼230 to ∼180 kJ mol^–1. They also increase the crystallite size, structural order, and electrical conductivity of the activated CNFs (ACNFs). The surface area of the ACNFs increased upon addition of nanotubes which protrude from the fiber leading to a rougher surface. The ACNFs were used as the electrodes of a supercapacitor. The electrochemical capacitance of the ACNF derived from pure cellulose nanofibers is demonstrated to be 105 F g^–1 at a current density of 10 A g^–1, which increases to 145 F g^–1 upon the addition of 6% of MWNTs.