化学
石墨烯
聚合
Diels-Alder反应
桤木
高分子化学
有机化学
聚合物
计算化学
密度泛函理论
生态学
催化作用
生物
作者
Fang Li,Xingyu Tang,Yunfan Fei,Jie Zhang,Jie Liu,Puyi Lang,Guangwei Che,Zihan Zhao,Yuqing Zheng,Yuan Fang,Chen Li,Dexiang Gao,Xiao Yi Dong,Takanori Hattori,Jun Abe,Ho‐kwang Mao,Haiyan Zheng,Kuo Li
摘要
Graphane shares the same two-dimensional honeycomb structure of graphene, but its saturated carbon skeleton gives rise to a bandgap and therefore provides more possibilities for the development of novel carbon-based semiconductors. However, the hydrogenation of graphene usually leads to disordered and incompletely hydrogenated graphane, and the precise synthesis of graphane with a specific configuration is still very challenging. Here, we synthesized a crystalline graphane nanoribbon (GANR) via pressure-induced polymerization of 2,2′-bipyrazine (BPZ). By performing Rietveld refinement of in situ neutron diffraction data, nuclear magnetic resonance spectroscopy, infrared spectra, and theoretical calculation, we found that BPZ experienced Diels–Alder polymerization between the π···π stacked aromatic rings and formed extended boat-GANR structures with exceptional long-range order. The unreacted −C═N– groups bridge the two ends of the boat and are ready for further functionalization. The GANR has a bandgap of 2.25 eV, with booming photoelectric response ( I ON / I OFF = 18.8). Our work highlights that high-pressure topochemical polymerization is a promising method for the precise synthesis of graphane with specific structure and desired properties.
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