光激发
异质结
激子
放松(心理学)
超快激光光谱学
超短脉冲
材料科学
电子转移
电荷(物理)
单层
电子
凝聚态物理
化学物理
光电子学
光谱学
化学
纳米技术
激发态
原子物理学
光学
物理
光化学
量子力学
社会心理学
激光器
心理学
作者
C. T. Sun,He-Qin Zhou,Tianyu Sheng,Shuangshuang Li,Haiming Zhu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-12-28
标识
DOI:10.1021/acsnano.3c09681
摘要
While 2D transition metal dichalcogenides (TMDs) feature interesting layer-tunable multivalley band structures, their preeminent role in determining the photoexcitation charge transfer dynamics in 2D heterostructures (HSs) is yet to be unraveled, as previous charge transfer studies on TMD HSs have been mostly focused on monolayers with a direct bandgap at the K valley. By ultrafast transient absorption spectroscopy and deliberately designed few-layer WSe2/WS2 HSs, we have observed an ultrafast interlayer electron transfer from photoexcited few-layer WSe2 to WS2, prior to intralayer relaxation to lower lying dark valleys. More interestingly, we have identified an unconventional ∼0.5 ps electron back-transfer process after the initial interlayer electron transfer in HSs with WSe2 layers ≥ 3, regenerating indirect intralayer excitons. The result reveals an ielectron and valley relaxation pathway mediated by interlayer charge transfer in 2D HSs, faster than intralayer relaxation. It also sheds light on the origin of generally observed robust ultrafast interlayer charge transfer in TMD HSs and provides guidance toward optoelectronic and valleytronic devices using few-layer TMDs.
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