1.Advanced Membranes and Porous Materials Center (AMPM), Division of Physical Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia
2.Key Laboratory of Material Physics, Ministry of Education, School of Physics, Zhengzhou University, Zhengzhou, China
3.Department of Applied Physics, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China
4.KAUST Solar Center (KSC), King Abdullah University of Science (KAUST), Thuwal, Saudi Arabia
5.KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia
Omar F. Mohammed (omar.abdelsaboor@kaust.edu.sa)
收稿日期:2024-08-06,
修回日期:2024-12-29,
录用日期:2025-01-13,
网络出版日期:2025-03-18,
纸质出版日期:2025-05-31
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Real-space imaging of photo-generated surface carrier transport in 2D perovskites[J]. LSA, 2025,14(5):1290-1299.
Wang, L. J. et al. Real-space imaging of photo-generated surface carrier transport in 2D perovskites. Light: Science & Applications, 14, 1290-1299 (2025).
Real-space imaging of photo-generated surface carrier transport in 2D perovskites[J]. LSA, 2025,14(5):1290-1299. DOI: 10.1038/s41377-025-01758-5.
Wang, L. J. et al. Real-space imaging of photo-generated surface carrier transport in 2D perovskites. Light: Science & Applications, 14, 1290-1299 (2025). DOI: 10.1038/s41377-025-01758-5.
In layered two-dimensional (2D) perovskites
the inorganic perovskite layers sandwiched between cation spacers create quantum well (QW) structures
showing large exciton binding energies that hinder the efficient dissociation of excitons into free carriers. This leads to poor carrier transport properties and low-performance light-conversion-based devices
and the direct understanding of the underlying physics
particularly concerning surface states
remains extremely difficult
if not impossible
due to the challenges in real-time accessibility. Here
we utilized four-dimensional scanning ultrafast electron microscopy (4D-SUEM)
a highly sensitive technique for mapping surface carrier diffusion that diverges from those in the bulk and substantially affects material properties. We directly visualize photo-generated carrier transport over both spatial and temporal dimensions on the top surface of 2D perovskites with varying inorganic perovskite layer thicknesses (
n
= 1
2
and 3). The results reveal the photo-induced surface carrier diffusion rates of ~30 cm
2
·s
-1
for
n
= 1
~180 cm
2
·s
-1
for
n
= 2
and ~470 cm
2
·s
-1
for
n
= 3
which are over 20 times larger than bulk. This is because charge carrier transmission channels have much wider distributions on the top surface compared to the bulk
as supported by the Density Functional Theory (DFT) calculations. Finally
our findings represent the demonstration to directly correlate the discrepancies between surface and bulk carrier diffusion behaviors
their relationship with exciton binding energy
and the number of layers in 2D perovskites
providing valuable insights into enhancing the performance of 2D perovskite-based optoelectronic devices through interface engineering.
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