Disentangling Many-Body Effects in the Coherent Optical Response of 2D Semiconductors

被引:32
|
作者
Trovatello, Chiara [1 ,2 ]
Katsch, Florian [3 ]
Li, Qiuyang [4 ]
Zhu, Xiaoyang [4 ]
Knorr, Andreas [3 ]
Cerullo, Giulio [1 ]
Dal Conte, Stefano [1 ]
机构
[1] Politecn Milan, Dipartimento Fis, I-20133 Milan, Italy
[2] Columbia Univ, Dept Mech Engn, New York, NY 10027 USA
[3] Tech Univ Berlin, Inst Theoret Phys Nichtlineare Opt & Quantenelekt, D-10623 Berlin, Germany
[4] Columbia Univ, Dept Chem, New York, NY 10027 USA
基金
美国国家科学基金会; 欧盟地平线“2020”;
关键词
Transition metal dichancogenides; pump-probe; exciton dynamics; Kramers-Kronig analysis; many-body effects; coherent optical response; PHOTOINDUCED BANDGAP RENORMALIZATION; WS2;
D O I
10.1021/acs.nanolett.2c01309
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In single-layer (1L) transition metal dichalcogenides, the reduced Coulomb screening results in strongly bound excitons which dominate the linear and the nonlinear optical response. Despite the large number of studies, a clear understanding on how many-body and Coulomb correlation effects affect the excitonic resonances on a femtosecond time scale is still lacking. Here, we use ultrashort laser pulses to measure the transient optical response of 1L-WS2. In order to disentangle many-body effects, we perform exciton line-shape analysis, and we study its temporal dynamics as a function of the excitation photon energy and fluence. We find that resonant photoexcitation produces a blue shift of the A exciton, while for above resonance photoexcitation the transient response at the optical bandgap is largely determined by a reduction of the exciton oscillator strength. Microscopic calculations based on excitonic Heisenberg equations of motion quantitatively reproduce the nonlinear absorption of the material and its dependence on excitation conditions.
引用
收藏
页码:5322 / 5329
页数:8
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