Co-MnO2 Nanorods for High-Performance Sodium/Potassium-Ion Batteries and Highly Conductive Gel-Type Supercapacitors

Manganese dioxide (MnO2) is considered as a strong candidate in the field of new-generation electronic equipment. Herein, Co-MnO2 has excellent electrochemical properties in tests as the cathode electrode of sodium-ion batteries and potassium-ion batteries. The rate performance remains at 50.2 mAh g(-1) at 200 mA g(-1) for sodium-ion batteries. X-ray diffraction (XRD) is utilized to evaluate the crystal structure transition from Co-0.2-MnO2 to NaMnO2 with discharge to 1 V, proving that Co-doping does indeed facilitate the acceleration of ion transport and support layer spacing to stabilize the structure of MnO2. Subsequently, highly conductive (0.0848 S cm(-1)) gel-type supercapacitors are prepared by combining Co-0.2-MnO2, potassium hydroxide (KOH), and poly(vinyl alcohol) (PVA) together. Co-0.2-MnO2 provides capacitive behavior and strengthens the hydrogen bonds between molecules. KOH acts as an ion crosslinker to enhance hydrogen bond and as electrolyte to transport ions. 5 wt% Co-0.2-MnO2@KOH/PVA has superb mechanical endurance, appreciable electrical conductivity, and ideal capacitive behavior. The quasi-solid-state supercapacitor demonstrates stabilized longevity (86.5% at 0.2 mA cm(-3) after 500 cycles), which can greatly promote the integration of flexible energy storage fabric devices.

Automated summary

Co-MnO2 shows excellent electrochemical properties as the cathode electrode of sodium-ion and potassium-ion batteries, with Co-doping facilitating ion transport acceleration and stabilizing the crystal structure of MnO2. A gel-type supercapacitor combining Co-0.2-MnO2, KOH, and PVA demonstrates high conductivity, mechanical endurance, and ideal capacitive behavior, with stable longevity after 500 cycles, promoting the integration of flexible energy storage fabric devices.