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Carbon materials/MXenes composite materials have gained widespread attention in the field of supercapacitors due to their excellent electrochemical performance. Carbon materials are considered ideal electrode materials for supercapacitors due to their high specific surface area, good conductivity, and outstanding electrochemical stability. MXenes, as a novel two-dimensional material, exhibit prominent conductivity, mechanical properties, and ionic conductivity, thereby showing great potential for applications in energy storage devices. The combination of carbon materials and MXenes is expected to fully leverage the advantages of both, optimizing electrode conductivity, enhancing the energy density and power density, and improving the charge–discharge performance. This article reviews the key research progress of carbon/MXenes composite materials in supercapacitors in recent years, including their synthesis methods, structural tuning, and improvements in their electrochemical performance. Finally, the article looks forward to future research directions and proposes potential strategies to enhance the overall performance of the composite materials and achieve large-scale applications. By addressing the existing challenges, carbon/MXenes composite materials are anticipated to achieve higher energy and power outputs for the supercapacitor field in the future, providing strong support for the development of new energy storage technologies such as electric vehicles and wearable devices. [ABSTRACT FROM AUTHOR]

Potassium is a harmful impurity in the rhenium sinter, which adversely affects its mechanical properties by significantly reducing the density of sintered rhenium. Cationic resin is a promising material for potassium removal. In this study, the strong acid cationic exchange resin C160H was pretreated with an HNO 3 solution to enhance its performance in potassium removal. The pretreated C160H resin was characterized using BET, SEM and point of zero charge (PZC) measurements to understand its physicochemical properties. It was verified that the lower PZC value of C160H than that of pristine C160 resin resulted in increased potassium adsorption efficiency. Moreover, the pretreated C160H resin exhibited a maximum potassium adsorption efficiency of 99.28% for 2.00 g L -1 KReO 4 at 25 °C and pH 7.0 for 6 h, with a solid-to-liquid ratio of 1 : 20. The cation sequence affecting potassium adsorption efficiency was found to be Na + < Ca 2+ < Fe 3+ < NH 4 + . Isothermal adsorption thermodynamics showed that potassium adsorption by C160H resin followed a heterogeneous and exothermic process. The pseudo-second-order kinetics model best fitted the data, suggesting that potassium adsorption was primarily chemical in nature. DFT calculations confirmed that the adsorption mechanism was based on ion exchange between H + and K + , with electrostatic interactions serving as the primary driving force for adsorption. The C160H resin demonstrated outstanding regeneration performance, maintaining an adsorption efficiency above 99% after ten cycles. These findings could contribute to improve the potassium adsorption capacity of the resin, thereby reducing both resin dosage and cost in the purification of perrhenate salts., Competing Interests: The authors declare that they have no conflicts of interest., (This journal is © The Royal Society of Chemistry.)