Liu Ben, Si Jinhai, Yan Lihe, Shen Yanan, Hou Xun
Opt Express. 2024 May 20;32(11):19458-19466. doi: 10.1364/OE.521726.
Two-dimensional molybdenum disulfide (MoS) has been proven to be a candidate in photodetectors, and MoS/lead sulfide (PbS) quantum dots (QDs) heterostructure has been used to expand the optical response wavelength of MoS. Time-resolved pump-probe transient absorption measurements are performed to clarify the carrier transfer dynamics in the MoS/PbS heterostructure. By comparing the carrier dynamics in MoS and MoS/PbS under different pump wavelengths, we found that the excited electrons in PbS QDs can transfer rapidly (<100 fs) to MoS, inducing its optical response in the near-infrared region, although the pump light energy is lower than the bandgap of MoS. Besides, interfacial excitons can be formed in the heterostructure, prolonging the lifetime of the excited carriers, which could be beneficial for the extraction of the carriers in devices.
二维二硫化钼(MoS)已被证明是光电探测器的候选材料,并且二硫化钼/硫化铅(PbS)量子点(QD)异质结构已被用于扩展MoS的光响应波长。进行了时间分辨泵浦-探测瞬态吸收测量,以阐明MoS/PbS异质结构中的载流子转移动力学。通过比较不同泵浦波长下MoS和MoS/PbS中的载流子动力学,我们发现,尽管泵浦光能量低于MoS的带隙,但PbS量子点中的激发电子可以迅速(<100飞秒)转移到MoS,从而在近红外区域诱导其光响应。此外,异质结构中可以形成界面激子,延长激发载流子的寿命,这可能有利于器件中载流子的提取。