Advanced nanoarchitectural superstructure hybridized with covalent organic nanosheets and 2H-MoS2 to boost the performance of sodium-ion batteries

Push–pull structured covalent organic nanosheets (CONs) are promising anode materials for sodium-ion batteries (SIBs) owing to their flexible π-conjugated frameworks and tunable porosity. In contrast, MoS 2 anodes have a high capacity but suffer from capacity degradation owing to their low intrinsic conductivity and volume expansion. To address these limitations, we developed a composite of 2H-MoS 2 nanosheets and multi-layered hollow CON spheres (CON/MoS 2 -HS). This composite was fabricated via the solvothermal synthesis of 2H-MoS 2 using CONs stacked on polystyrene beads as a template. CON/MoS 2 -HS exhibited improved electrical and ionic conductivities and reversible capacity, while its robust structural integration limited the changes in volume and mechanical stress during cycling, resulting in excellent long-term cycling stability. In contrast, reduced graphene oxide (rGO)/MoS 2 -HS was characterized by weaker interactions between rGO and 2H-MoS 2 , meaning that MoS 2 aggregation and volume expansion could not be prevented, thus compromising cycle stability and capacity. The CON/MoS 2 -HS electrode delivered a high reversible capacity of 671.8 mA h g −1 (~97% of the theoretical capacity) after 600 cycles at 100 mA g −1 and retained a capacity of 203.1 mA h g −1 after 5000 cycles at 5000 mA g −1 . The rate performance and long-term cycling stability of the CON/MoS 2 -HS electrode outperformed those of conventional MoS 2 -based anodes, demonstrating the strong synergistic relationship between the multilayered CON architecture and 2H-MoS 2 nanosheets. In this work, high-performance hybrid anodes were developed by integrating push-pull structured covalent organic nanosheets (CONs) with 2H-MoS 2 nanosheets. The CON/MoS 2 nano junction and hollow sphere structure provided a large contact area and shortened the ion/charge transport distance, significantly improving the Na + ion storage properties. • A hybrid anode (CON/MoS 2 -HS) was developed with covalent organic nanosheets and MoS 2 nanosheets. • The CONs framework provides rapid electron transport pathways, enhancing Na + storage kinetics. • The CON/MoS 2 -HS anode exhibits a high reversible capacity of 671.8 mA h g −1 . • The CON/MoS 2 -HS anode exhibits ~97% of the theoretical capacity and long-term cycle stability. • The hollow spherical nanoarchitecture facilitates rapid ion diffusion and buffers volume changes.

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Publication Details

Journal
Chemical Engineering Journal
Published
2025-06-16
DOI
https://doi.org/10.1016/j.cej.2025.164931
Citations
7
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
5.11

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article

Advanced nanoarchitectural superstructure hybridized with covalent organic nanosheets and 2H-MoS2 to boost the performance of sodium-ion batteries

Jin Kuen Park, Minseop Lee, Seung‐Min Paek, Nakyeong Lee et al.
7 citations
Chemical Engineering Journal
Advancements in Battery Materials
5.11
article

Advanced nanoarchitectural superstructure hybridized with covalent organic nanosheets and 2H-MoS2 to boost the performance of sodium-ion batteries

Jin Kuen Park, Minseop Lee, Seung‐Min Paek, Nakyeong Lee, Jimin Kim
article en
7 citations

Abstract

Push–pull structured covalent organic nanosheets (CONs) are promising anode materials for sodium-ion batteries (SIBs) owing to their flexible π-conjugated frameworks and tunable porosity. In contrast, MoS 2 anodes have a high capacity but suffer from capacity degradation owing to their low intrinsic conductivity and volume expansion. To address these limitations, we developed a composite of 2H-MoS 2 nanosheets and multi-layered hollow CON spheres (CON/MoS 2 -HS). This composite was fabricated via the solvothermal synthesis of 2H-MoS 2 using CONs stacked on polystyrene beads as a template. CON/MoS 2 -HS exhibited improved electrical and ionic conductivities and reversible capacity, while its robust structural integration limited the changes in volume and mechanical stress during cycling, resulting in excellent long-term cycling stability. In contrast, reduced graphene oxide (rGO)/MoS 2 -HS was characterized by weaker interactions between rGO and 2H-MoS 2 , meaning that MoS 2 aggregation and volume expansion could not be prevented, thus compromising cycle stability and capacity. The CON/MoS 2 -HS electrode delivered a high reversible capacity of 671.8 mA h g −1 (~97% of the theoretical capacity) after 600 cycles at 100 mA g −1 and retained a capacity of 203.1 mA h g −1 after 5000 cycles at 5000 mA g −1 . The rate performance and long-term cycling stability of the CON/MoS 2 -HS electrode outperformed those of conventional MoS 2 -based anodes, demonstrating the strong synergistic relationship between the multilayered CON architecture and 2H-MoS 2 nanosheets. In this work, high-performance hybrid anodes were developed by integrating push-pull structured covalent organic nanosheets (CONs) with 2H-MoS 2 nanosheets. The CON/MoS 2 nano junction and hollow sphere structure provided a large contact area and shortened the ion/charge transport distance, significantly improving the Na + ion storage properties. • A hybrid anode (CON/MoS 2 -HS) was developed with covalent organic nanosheets and MoS 2 nanosheets. • The CONs framework provides rapid electron transport pathways, enhancing Na + storage kinetics. • The CON/MoS 2 -HS anode exhibits a high reversible capacity of 671.8 mA h g −1 . • The CON/MoS 2 -HS anode exhibits ~97% of the theoretical capacity and long-term cycle stability. • The hollow spherical nanoarchitecture facilitates rapid ion diffusion and buffers volume changes.

Chemical Engineering JournalVol. 519
Kyungpook National University (KR), Hankuk University of Foreign Studies (KR)
Hankuk University of Foreign Studies, Ministry of Science, ICT and Future Planning, National Research Foundation of Korea
Industry, innovation and infrastructure
Openalex Percentile: Top 4%
Advancements in Battery Materials
5.11
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