堆积
异质结
电荷(物理)
超短脉冲
材料科学
双层
联轴节(管道)
化学物理
密度泛函理论
光电子学
凝聚态物理
纳米技术
膜
化学
光学
计算化学
物理
核磁共振
激光器
生物化学
量子力学
冶金
作者
Jin Zhang,Hao Hong,Chao Lian,Wei Ma,Xiaozhi Xu,Xu Zhou,Huixia Fu,Kaihui Liu,Sheng Meng
标识
DOI:10.1002/advs.201700086
摘要
Light-induced interlayer ultrafast charge transfer in 2D heterostructures provides a new platform for optoelectronic and photovoltaic applications. The charge separation process is generally hypothesized to be dependent on the interlayer stackings and interactions, however, the quantitative characteristic and detailed mechanism remain elusive. Here, a systematical study on the interlayer charge transfer in model MoS2/WS2 bilayer system with variable stacking configurations by time-dependent density functional theory methods is demonstrated. The results show that the slight change of interlayer geometry can significantly modulate the charge transfer time from 100 fs to 1 ps scale. Detailed analysis further reveals that the transfer rate in MoS2/WS2 bilayers is governed by the electronic coupling between specific interlayer states, rather than the interlayer distances, and follows a universal dependence on the state-coupling strength. The results establish the interlayer stacking as an effective freedom to control ultrafast charge transfer dynamics in 2D heterostructures and facilitate their future applications in optoelectronics and light harvesting.
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