Designer topological flat bands in one-dimensional armchair graphene antidot lattices

被引:2
|
作者
Wang, Jianing [1 ,2 ]
Chen, Weiwei [3 ]
Wang, Zhengya [1 ,2 ]
Meng, Jie [1 ,2 ]
Yin, Ruoting [1 ,2 ]
Chen, Miaogen [3 ]
Tan, Shijing [1 ,2 ,4 ]
Ma, Chuanxu [1 ,2 ,4 ]
Li, Qunxiang [1 ,2 ,4 ]
Wang, Bing [1 ,2 ,4 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Synerget Innovat Ctr Quantum Informat & Quantum Ph, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, New Cornerstone Sci Lab, Hefei 230026, Anhui, Peoples R China
[3] China Jiliang Univ, Coll Sci, Key Lab Intelligent Mfg Qual Big Data Tracing & An, Hangzhou 310018, Peoples R China
[4] Univ Sci & Technol China, Hefei Natl Lab, Hefei 230088, Peoples R China
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; SURFACE SYNTHESIS; NANORIBBONS; STATES;
D O I
10.1103/PhysRevB.110.115138
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report a viable strategy to realize topological flat bands in one-dimensional armchair graphene antidot lattices. The quantum destructive interference effect leads to largely quenched intra-antidot hopping with nearly zero values, creating flat bands with a nontrivial topology, as unveiled by an effective Su-Schrieffer-Heeger model under extreme conditions. As a proof of concept, we demonstrate our approach in the on-surface synthesized porous seven-carbon-wide armchair graphene nanoribbons with periodic divacancy-type antidots, and showcase the robust flatness of the designer topological flat bands with a high tunability through strain and structural engineering which are investigated by combining tight-binding and density functional theory calculations with scanning probe microscopy measurements. We show that such available one-dimensional graphene nanoribbons can provide a rich platform for exploiting novel physics at the confluence of strong correlation and topology, opening up new avenues for research in the field of topological materials and their potential applications in quantum devices.
引用
收藏
页数:8
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