2 research outputs found

    Carbon Quantum Dots-Derived Carbon Nanosphere Coating on Ti<sub>3</sub>C<sub>2</sub> MXene as a Superior Anode for High-Performance Potassium-Ion Batteries

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    Potassium-ion batteries (PIBs) are receiving increasing attention at present because of their cheap and lithium-like charge/discharge processes. Nevertheless, the large potassium-ion radius leads to poor potassium intercalation/depotassium kinetics and unstable structure, hindering their development. Here, we synthesized a novel carbon quantum dot-derived carbon nanosphere-encapsulated Ti3C2 MXene (CNS@Ti3C2) composite by polymer pyrolysis, while carbon nanospheres were derived from carbon quantum dots. The composites can suppress the layer stacking of Ti3C2 and prevent oxidation, thereby stabilizing the layered structure of Ti3C2 MXene and improving the cycle life. Besides, carbon nanospheres can increase the specific surface area and active sites, and then more potassium ions can enter the electrode material and boost the reversible capacity. Further, carbon nanospheres are embedded between the Ti3C2 layers, which can increase the interlayer spacing, and the potassium ions are more easily inserted and extracted, thereby improving the potassium storage power and rate performance. The CNS@Ti3C2 composite possesses an excellent synergy, resulting in a high reversible capacity of 229 mAh g–1 at 100 mA g–1 after 200 repeated cycles and a long cycle life of 205 mAh g–1 at 500 mA g–1 after 1000 repeated cycles with high coulombic efficiency (above 99%). This work offers a novel strategy to utilize carbon with MXene in energy storage

    In Situ Oxygen-Doped Porous Carbon Nanoribbons with Expanded Interlayer Distance for Enhanced Potassium Ion Storage

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    Carbon materials have been widely concerned and studied for potassium-ion batteries because of abundant resources and low prices. But, the large radius of potassium ions (1.38 Å) restricts its smooth intercalation and deintercalation into the carbon layer, resulting in poor cycling stability and rate performance. Herein, in situ oxygen-doped porous carbon nanoribbons (OPCNBs) have been fabricated by freeze-drying and pyrolysis of the polymer with enlarged interlayer spacing for the first time. Due to the porosity and the enlarged interlayer spacing (0.413 nm) of OPCNB, the potassium ions can be rapidly intercalated into the carbon layer and smoothly extracted and some of the potassium ions are adsorbed on the surface active site stemming from the oxygen-doped group. Further, ex situ TEM showed that the enlarged interlayer spacing was well preserved during repeated cycling. Therefore, OPCNB exhibits excellent long cycle stability (180.5 mAh g–1 at 500 mA g–1 after 1000 cycles) and outstanding rate capability (170 mAh g–1 at 1 A g–1) as a new generation electrode material with development potential for potassium ions
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