自旋电子学
扫描隧道显微镜
之字形的
化学物理
石墨烯
密度泛函理论
分子
材料科学
光谱学
共轭体系
计算机科学
自旋(空气动力学)
Atom(片上系统)
纳米技术
分子物理学
凝聚态物理
化学
计算化学
物理
铁磁性
聚合物
几何学
复合材料
有机化学
嵌入式系统
数学
热力学
量子力学
作者
Jie Su,Mykola Telychko,Pan Hu,Gennevieve Macam,Pingo Mutombo,Hejian Zhang,Yang Bao,Fang Cheng,Zhi-Quan Huang,Zhizhan Qiu,Sherman J. R. Tan,Hsin Lin,Pavel Jelı́nek,Feng‐Chuan Chuang,Jishan Wu,Jiong Lu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2019-07-05
卷期号:5 (7)
被引量:174
标识
DOI:10.1126/sciadv.aav7717
摘要
The zigzag-edged triangular graphene molecules (ZTGMs) have been predicted to host ferromagnetically coupled edge states with the net spin scaling with the molecular size, which affords large spin tunability crucial for next-generation molecular spintronics. However, the scalable synthesis of large ZTGMs and the direct observation of their edge states have been long-standing challenges because of the molecules' high chemical instability. Here, we report the bottom-up synthesis of π-extended [5]triangulene with atomic precision via surface-assisted cyclodehydrogenation of a rationally designed molecular precursor on metallic surfaces. Atomic force microscopy measurements unambiguously resolve its ZTGM-like skeleton consisting of 15 fused benzene rings, while scanning tunneling spectroscopy measurements reveal edge-localized electronic states. Bolstered by density functional theory calculations, our results show that [5]triangulenes synthesized on Au(111) retain the open-shell π-conjugated character with magnetic ground states.
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