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Tunable Optical Excitations in Twisted Bilayer Graphene Form Strongly Bound Excitons
被引:56
|作者:
Patel, Hiral
[1
]
Havener, Robin W.
[2
,3
]
Brown, Lola
[2
,3
]
Liang, Yufeng
[4
]
Yang, Li
[4
]
Park, Jiwoong
[2
,3
]
Graham, Matt W.
[1
]
机构:
[1] Oregon State Univ, Dept Phys, Corvallis, OR 97331 USA
[2] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14850 USA
[3] Kavli Inst Cornell Nanoscale Sci, Ithaca, NY 14853 USA
[4] Washington Univ, Dept Phys, St Louis, MO 63130 USA
关键词:
Graphene;
ultrafast microscopy;
ghost Fano resonance;
excitons;
TRANSIENT ABSORPTION;
CONDUCTIVITY;
ULTRAFAST;
D O I:
10.1021/acs.nanolett.5b02035
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
When two sheets of graphene stack in a twisted bilayer graphene (tBLG) configuration, the resulting constrained overlap between interplanar 2p orbitals produce angle-tunable electronic absorption resonances. By applying a novel combination of multiphoton transient absorption (TA) microscopy and TEM, we resolve the electronic structure and ensuing relaxation by probing resonant excitations of single tBLG domains. Strikingly, we find that the transient electronic population in resonantly excited tBLG domains is enhanced many fold, forming a major electronic relaxation bottleneck. Two-photon TA microscopy shows this bottleneck effect originates from a strongly bound, dark exciton state lying similar to 0.37 eV below the 1-photon absorption resonance. This stable coexistence of strongly bound excitons alongside free-electron continuum states has not been previously observed in a metallic, 2D material.
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页码:5932 / 5937
页数:6
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