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Ambipolar Charge Carrier Transport Properties at the S-Benzyl-l-cysteine-Induced 2D/3D Halide Perovskite Interface

Authors
Kim, TaewonPark, Byoungnam
Issue Date
Jan-2024
Publisher
American Chemical Society
Citation
Chemistry of Materials, v.36, no.2, pp 675 - 681
Pages
7
Journal Title
Chemistry of Materials
Volume
36
Number
2
Start Page
675
End Page
681
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/32635
DOI
10.1021/acs.chemmater.3c02061
ISSN
0897-4756
1520-5002
Abstract
We fabricated a 2D/3D perovskite film by adding a molecular spacer, S-benzyl-l-cysteine (SBLC), during MAPbI3 perovskite film formation and investigated the effect of SBLC on the electronic conduction with a field-effect transistor. The addition of SBLC resulted in a larger grain size on the top surface and activated the electronic conduction modulated by the gate electric field. The field-effect modulation is attributed to the presence of the 2D perovskite surface layer induced by the SBLC molecular spacer on the 3D MAPbI3 perovskite bulk, resulting from the passivation of interfacial localized states and suppression of ion migration within the MAPbI3 perovskite film. Illumination with green light activated hole transport, resulting in ambipolar transport in the SBLC-induced MAPbI3 perovskite 2D/3D film, explaining that the SBLC treatment reduced the hole trap density of states. Illumination with green light maximized the effect of the surface 2D layer of the 2D/3D MAPbI3 perovskite film on the field effect-induced charge transport, enabling ambipolar electronic transport with the 2D/3D configuration due to suppression of the ionic behavior on the surface. This study highlights the electronic and structural effects of the organic molecular spacer on the electrical properties of the 3D bulk layer, hinting that defect-induced electronic and structural instability in the 3D bulk can be overcome by the passivation of the 3D bulk surface by the formation of the 2D/3D perovskite interface. © 2024 American Chemical Society.
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