Mechanochemical constructing quasi-pyridinic nitrogen/sulfur co-doped γ-graphyne for promoting lithium storage

Elemental engineering has been employed to adjust molecular framework and electronic configuration of γ-graphyne for rapid lithium storage. Here, we construct a quasi-pyridinic nitrogen/sulfur co-doped γ-graphyne (N/S-GY) via a mechanochemical strategy and reveal its lithium storage behavior by quan...

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Veröffentlicht in:Diamond and related materials 2024-06, Vol.146, p.111216, Article 111216
Hauptverfasser: Hao, Zixiang, Chen, Yang, Wang, Linrui, Lu, Yuxuan, He, Chengli, Wang, Mingyan, Cui, Xiaoli
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Sprache:eng
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Zusammenfassung:Elemental engineering has been employed to adjust molecular framework and electronic configuration of γ-graphyne for rapid lithium storage. Here, we construct a quasi-pyridinic nitrogen/sulfur co-doped γ-graphyne (N/S-GY) via a mechanochemical strategy and reveal its lithium storage behavior by quantitative kinetics analysis and theoretical calculations. The internal pyridinic-N atoms create rhombic channels for Li+ passing through, while sulfur dopants anchored with alkynyl groups induce electron cloud rearrangement to facilitate intralayer Li+ diffuse between C12-triangular channels and interlayer transfer through open rhombic channels. As a result, the as-prepared N/S-GY exhibits a high reversible capacity of 1003 mAh g−1 at 50 mA g−1 after 150 cycles, with Li+ diffusion coefficient up to 2.6 × 10−12 cm2 s−1, both of which are larger than that of N-doped γ-graphyne. This work highlights synergistic effect of sulfur and nitrogen co-doping in alkynyl carbon and inspires bottom-up heteroatom modification in framework design. [Display omitted] •Sulfur and nitrogen co-doped γ-graphyne has been prepared through a mechanochemical route.•The N/S-GY anode displays high lithium-ion capacity with 1003 mAh g−1 at 50 mA g−1 after 150 cycles.•The N/S-GY anode exhibits lithium diffusion efficiency with 2.6 × 10−12 cm2 s−1.
ISSN:0925-9635
1879-0062
DOI:10.1016/j.diamond.2024.111216