声子
材料科学
激子
超短脉冲
超快激光光谱学
光电子学
二硫化钼
凝聚态物理
分子物理学
光学
物理
激光器
冶金
作者
Houk Jang,Krishna P. Dhakal,Kyung‐Il Joo,Won Seok Yun,Sachin M. Shinde,Xiang Chen,Soon Moon Jeong,Suk Woo Lee,Zonghoon Lee,Jae-Dong Lee,Jong‐Hyun Ahn,Hyunmin Kim
标识
DOI:10.1002/adma.201705190
摘要
Abstract Understanding the collaborative behaviors of the excitons and phonons that result from light–matter interactions is important for interpreting and optimizing the underlying fundamental physics at work in devices made from atomically thin materials. In this study, the generation of exciton‐coupled phonon vibration from molybdenum disulfide (MoS 2 ) nanosheets in a pre‐excitonic resonance condition is reported. A strong rise‐to‐decay profile for the transient second‐harmonic generation (TSHG) of the probe pulse is achieved by applying substantial (20%) beam polarization normal to the nanosheet plane, and tuning the wavelength of the pump beam to the absorption of the A‐exciton. The time‐dependent TSHG signals clearly exhibit acoustic phonon generation at vibration modes below 10 cm −1 (close to the Γ point) after the photoinduced energy is transferred from exciton to phonon in a nonradiative fashion. Interestingly, by observing the TSHG signal oscillation period from MoS 2 samples of varying thicknesses, the speed of the supersonic waves generated in the out‐of‐plane direction (Mach 8.6) is generated. Additionally, TSHG microscopy reveals critical information about the phase and amplitude of the acoustic phonons from different edge chiralities (armchair and zigzag) of the MoS 2 monolayers. This suggests that the technique could be used more broadly to study ultrafast physics and chemistry in low‐dimensional materials and their hybrids with ultrahigh fidelity.
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