Wang Yan, Wang Zishu, Qiu Zijie, Zhang Xiaoxi, Chen Jianing, Li Juan, Narita Akimitsu, Müllen Klaus, Palma Carlos-Andres
School of Physics, Beijing Institute of Technology, 100081 Beijing, People's Republic of China.
Institute of Physics, Chinese Academy of Sciences, 100190 Beijing, People's Republic of China.
ACS Nano. 2023 Oct 10;17(19):18832-18842. doi: 10.1021/acsnano.3c03538. Epub 2023 Sep 20.
The fabrication of atomically precise nanographanes is a largely unexplored frontier in carbon-sp nanomaterials, enabling potential applications in phononics, photonics and electronics. One strategy is the hydrogenation of prototypical nanographene monolayers and multilayers under vacuum conditions. Here, we study the interaction of atomic hydrogen, generated by a hydrogen source and hydrogen plasma, with hexa--hexabenzocoronene on gold using integrated time-of-flight mass spectrometry, scanning tunneling microscopy and Raman spectroscopy. Density functional tight-binding molecular dynamics is employed to rationalize the conversion to sp carbon atoms. The resulting hydrogenation of hexa--hexabenzocoronene molecules is demonstrated computationally and experimentally, and the potential for atomically precise hexa--hexabenzocoronene-derived nanodiamond fabrication is proposed.
原子精确的纳米石墨烯的制备在碳-sp纳米材料领域是一个很大程度上未被探索的前沿领域,有望在声子学、光子学和电子学中得到应用。一种策略是在真空条件下对典型的纳米石墨烯单层和多层进行氢化。在此,我们使用集成飞行时间质谱、扫描隧道显微镜和拉曼光谱研究了由氢源和氢等离子体产生的原子氢与金表面的六-六苯并蔻的相互作用。采用密度泛函紧束缚分子动力学来解释向sp碳原子的转化。通过计算和实验证明了六-六苯并蔻分子的氢化反应,并提出了原子精确的六-六苯并蔻衍生纳米金刚石制备的可能性。