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:
- Lingxin Luo & Lingxiang Hou & Xueping Cui & Pengxin Zhan & Ping He & Chuying Dai & Ruian Li & Jichen Dong & Ye Zou & Guoming Liu & Yanpeng Liu & Jian Zheng, 2024.
"Self-condensation-assisted chemical vapour deposition growth of atomically two-dimensional MOF single-crystals,"
Nature Communications, Nature, vol. 15(1), pages 1-8, December.
- 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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