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Nitrogen and sulfur co-doped graphene nanoribbons with well-ordered stepped edges for high-performance potassium-ion battery anodes

Authors
Back, SeoinYu, Seung-HoPiao, YuanzheChoi, JuhyungJin, AihuaJung, Hyun DongKo, DongjinUm, Ji HyunChoi, YoonKim, So Hee
Issue Date
6월-2022
Publisher
ELSEVIER
Citation
ENERGY STORAGE MATERIALS, v.48, pp.325 - 334
Indexed
SCIE
SCOPUS
Journal Title
ENERGY STORAGE MATERIALS
Volume
48
Start Page
325
End Page
334
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/141814
DOI
10.1016/j.ensm.2022.03.041
ISSN
2405-8297
Abstract
Graphitic carbon materials, particularly few-layered graphene, exhibit great potentials as potassium-ion battery (PIBs) anodes. However, bulk graphene-based ma-terials have the disordered structure owing to randomly stacked graphene layers, which causes the high migration barrier during K+ intercalation/deintercalation reactions and thus the surface-dominated capacitive response. Here, we present a novel nanoarchitecture of nitrogen and sulfur co-doped graphene nanoribbons with well-ordered stepped edges (NS-sGNR) via the electrochemical unzipping of multiwalled carbon nanotubes (MWCNTs) and the subsequent N/S co-doping process for high-performance PIB anodes. As an anode material for PIBs, the prepared sample exhibits high initial capacity (329.1 mAh g(-1) at 50 mA g(-1)), superior rate capability (211.7 mAh g(-1) at high current density, 2000 mA g(-1)), outstanding reversibility of K-staging, and stable long-term cyclability. Theoretical calculations were conducted to demonstrate that sGNRs with NS co-doping (NS-sGNR) exhibit much improved K+ intercalation properties, such as the K+ adsorption energy, charge transfer, and migration barriers, compared with the parallel-edged GNRs. Particularly, the migration barrier (the rate-determining step) can be substantially reduced at the stepped edges during K+ intercalation.
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