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Synthesis of a monolayer fullerene network

Author

Listed:
  • Lingxiang Hou

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Xueping Cui

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

  • Bo Guan

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

  • Shaozhi Wang

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Ruian Li

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

  • Yunqi Liu

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

  • Daoben Zhu

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

  • Jian Zheng

    (Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences)

Abstract

Two-dimensional (2D) carbon materials, such as graphene, have attracted particular attention owing to the exceptional carrier transport characteristics that arise from the unique π-electron system in their conjugated carbon network structure1–4. To complement zero-bandgap graphene, material scientists have devoted considerable effort to identifying 2D carbon materials5–8. However, it is a challenge to prepare large-sized single-crystal 2D carbon materials with moderate bandgaps5,9. Here we prepare a single-crystal 2D carbon material, namely monolayer quasi-hexagonal-phase fullerene (C60), with a large size via an interlayer bonding cleavage strategy. In this monolayer polymeric C60, cluster cages of C60 are covalently bonded with each other in a plane, forming a regular topology that is distinct from that in conventional 2D materials. Monolayer polymeric C60 exhibits high crystallinity and good thermodynamic stability, and the electronic band structure measurement reveals a transport bandgap of about 1.6 electronvolts. Furthermore, an asymmetric lattice structure endows monolayer polymeric C60 with notable in-plane anisotropic properties, including anisotropic phonon modes and conductivity. This 2D carbon material with a moderate bandgap and unique topological structure offers an interesting platform for potential application in 2D electronic devices.

Suggested Citation

  • Lingxiang Hou & Xueping Cui & Bo Guan & Shaozhi Wang & Ruian Li & Yunqi Liu & Daoben Zhu & Jian Zheng, 2022. "Synthesis of a monolayer fullerene network," Nature, Nature, vol. 606(7914), pages 507-510, June.
  • Handle: RePEc:nat:nature:v:606:y:2022:i:7914:d:10.1038_s41586-022-04771-5
    DOI: 10.1038/s41586-022-04771-5
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    Cited by:

    1. Lidan Guo & Xianrong Gu & Shunhua Hu & Wenchao Sun & Rui Zhang & Yang Qin & Ke Meng & Xiangqian Lu & Yayun Liu & Jiaxing Wang & Peijie Ma & Cheng Zhang & Ankang Guo & Tingting Yang & Xueli Yang & Guor, 2024. "Strain-restricted transfer of ferromagnetic electrodes for constructing reproducibly superior-quality spintronic devices," Nature Communications, Nature, vol. 15(1), pages 1-10, December.

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