On-Surface Synthesis of Triaza[5]triangulene through Cyclodehydrogenation and its Magnetism

被引:4
|
作者
Li, Donglin [1 ]
Silveira, Orlando J. [2 ]
Matsuda, Takuma [3 ]
Hayashi, Hironobu [1 ]
Maeda, Hiromitsu [3 ]
Foster, Adam S. [2 ,4 ]
Kawai, Shigeki [1 ,5 ]
机构
[1] Natl Inst Mat Sci, Ctr Basic Res Mat, Tsukuba 3050047, Japan
[2] Aalto Univ, Dept Appl Phys, Box 11100, Espoo 00076, Finland
[3] Ritsumeikan Univ, Coll Life Sci, Dept Appl Chem, Kusatsu 5258577, Japan
[4] Kanazawa Univ, Nano Life Sci Inst WPI NanoLSI, Kanazawa 9201192, Japan
[5] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba 3058571, Japan
基金
日本学术振兴会; 芬兰科学院;
关键词
on-surface synthesis; triangulene; graphitic nitrogen; scanning tunneling microscopy/spectroscopy; density functional theory; GRAPHENE NANORIBBONS;
D O I
10.1002/anie.202411893
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triangulenes as neutral radicals are becoming promising candidates for future applications such as spintronics and quantum technologies. To extend the potential of the advanced materials, it is of importance to control their electronic and magnetic properties by multiple graphitic nitrogen doping. Here, we synthesize triaza[5]triangulene on Au(111) by cyclodehydrogenation, and its derivatives by cleaving C-N bonds. Bond-resolved scanning tunneling microscopy and scanning tunneling spectroscopy provided detailed structural information and evidence for open-shell singlet ground state. The antiferromagnetic arrangement of the spins in positively doped triaza[5]triangulene was further confirmed by density function theory calculations. The key aspect of triangulenes with multiple graphitic nitrogen is the extra pz electrons composing the pi orbitals, favoring charge transfer to the substrate and changing their low-energy excitations. Our findings pave the way for the exploration of exotic low-dimensional quantum phases of matter in heteroatom doped organic systems.
引用
收藏
页数:6
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