Abstract
Potassium-ion batteries (PIBs) hold great potential as an alternative to lithium-ion batteries due to the abundant reserves of potassium and similar redox potentials of K+/K and Li+/Li. Unfortunately, PIBs with carbonaceous electrodes present sluggish kinetics, resulting in unsatisfactory cycling stability and poor rate capability. Herein, we demonstrate that the synergistic effects of the enlarged interlayer spacing and enhanced capacitive behavior induced by the co-doping of nitrogen and sulfur atoms into a carbon structure (NSC) can improve its potassium storage capability. Based on the capacitive contribution calculations, electrochemical impedance spectroscopy, the galvanostatic intermittent titration technique, and density functional theory results, the NSC electrode is found to exhibit favorable electronic conductivity, enhanced capacitive adsorption behavior, and fast K+ ion diffusion kinetics. Additionally, a series of ex-situ characterizations demonstrate that NSC exhibits superior structural stability during the (de)potassiation process. As a result, NSC displays a high reversible capacity of 302.8 mAh g−1 at 0.1 A g−1 and a stable capacity of 105.2 mAh g−1 even at 2 A g−1 after 600 cycles. This work may offer new insight into the effects of the heteroatom doping of carbon materials on their potassium storage properties and facilitate their application in PIBs.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
