Interlayer exciton dynamics in a dichalcogenide monolayer heterostructure

Interlayer exciton dynamics in a dichalcogenide monolayer heterostructure
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DOI:
10.1088/2053-1583/aa7352
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发表时间:
2017-06-01
期刊:
影响因子:
5.5
通讯作者:
Korn, Tobias
Korn, Tobias
中科院分区:
材料科学2区
文献类型:
--
作者:
Nagler, Philipp;Plechinger, Gerd;Korn, Tobias

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在由不同的过渡金属二硫属化物单层组成的异质结构中,可以发生交错的能带对准,导致光学产生的电子-空穴对快速电荷分离成相对的单层。这些空间上分离的电子-空穴对是库仑耦合的并且形成层间激子。在这里,我们研究了这些层间激子的异质结构组成的MoSe 2和WSe 2单层使用光致发光光谱。我们观察到一个非平凡的层间激子的线宽和峰值能量的温度依赖性,包括一个异常强大的初始红移的过渡与温度,以及显着的蓝移的发射能量随着激发功率的增加。通过结合这些观察与时间分辨的光致发光测量,我们能够解释所观察到的行为作为层间激子扩散和偶极,排斥激子-激子相互作用的组合。
In heterostructures consisting of different transition-metal dichalcogenide monolayers, a staggered band alignment can occur, leading to rapid charge separation of optically generated electron-hole pairs into opposite monolayers. These spatially separated electron-hole pairs are Coulomb-coupled and form interlayer excitons. Here, we study these interlayer excitons in a heterostructure consisting of MoSe2 and WSe2 monolayers using photoluminescence spectroscopy. We observe a non-trivial temperature dependence of the linewidth and the peak energy of the interlayer exciton, including an unusually strong initial redshift of the transition with temperature, as well as a pronounced blueshift of the emission energy with increasing excitation power. By combining these observations with time-resolved photoluminescence measurements, we are able to explain the observed behavior as a combination of interlayer exciton diffusion and dipolar, repulsive exciton-exciton interaction.