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准二维钙钛矿/MoS单层异质结构中的载流子转移

Carrier transfer in quasi-2D perovskite/MoS monolayer heterostructure.

作者信息

Qin Chaochao, Wang Wenjing, Song Jian, Jiao Zhaoyong, Ma Shuhong, Zheng Shuwen, Zhang Jicai, Jia Guangrui, Jiang Yuhai, Zhou Zhongpo

机构信息

Henan Key Laboratory of Infrared Materials & Spectrum Measures and Applications, and School of Physics, Henan Normal University, Xinxiang 453007, China.

School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.

出版信息

Nanophotonics. 2023 Nov 28;12(24):4495-4505. doi: 10.1515/nanoph-2023-0570. eCollection 2023 Dec.

Abstract

Two-dimensional layered semiconductors have attracted intense interest in recent years. The van der Waals coupling between the layers tolerates stacking various materials and establishing heterostructures with new characteristics for a wide range of optoelectronic applications. The interlayer exciton dynamics at the interface within the heterostructure are vitally important for the performance of the photodetector and photovoltaic device. Here, a heterostructure comprising two-dimensional organic-inorganic Ruddlesden-Popper perovskites and transition metal dichalcogenide monolayer was fabricated and its ultrafast charge separation processes were systematically studied by using femtosecond time-resolved transient absorption spectroscopy. Significant hole and electron transfer processes in the ps and fs magnitude at the interface of the heterostructure were observed by tuning pump wavelengths of the pump-probe geometries. The results emphasize the realization of the exciton devices based on semiconductor heterostructures of two-dimensional perovskite and transition metal dichalcogenide.

摘要

近年来,二维层状半导体引起了广泛关注。层间的范德华耦合允许堆叠各种材料,并建立具有新特性的异质结构,以用于广泛的光电子应用。异质结构界面处的层间激子动力学对于光电探测器和光伏器件的性能至关重要。在此,制备了一种由二维有机-无机Ruddlesden-Popper钙钛矿和过渡金属二硫属化物单层组成的异质结构,并利用飞秒时间分辨瞬态吸收光谱系统地研究了其超快电荷分离过程。通过调整泵浦-探测几何结构的泵浦波长,在异质结构界面处观察到了皮秒和飞秒量级的显著空穴和电子转移过程。这些结果强调了基于二维钙钛矿和过渡金属二硫属化物半导体异质结构的激子器件的实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f904/11501760/f64f465665f2/j_nanoph-2023-0570_fig_001.jpg

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