4.8 Article

Property Modulation of Two-Dimensional Lead-Free Perovskite Thin Films by Aromatic Polymer Additives for Performance Enhancement of Field-Effect Transistors

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 20, Pages 24272-24284

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c03041

Keywords

(PEA)(2)SnI4; 2D layered structure; aromatic polymer additives; interactions; field-effect transistors

Funding

  1. National Natural Science Foundation of China [61674012, 62075009, 61775011, 61875009]

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In this study, the properties of phenethylammonium tin iodide perovskite thin films were modulated by introducing aromatic polymer additives, leading to improved morphology, crystallization, and inhibition of Sn2+ oxidation. The performance of the field-effect transistors based on the polymer-assisted thin films differed significantly, with one showing improved on-off current ratio and reduced leakage current, while the other exhibited relatively poor overall performance. The use of PVP and PVPD additives also enhanced the chemical stability of the perovskite and operational stabilities of the corresponding transistors.
The inevitable oxidation of Sn2+ and p-type self-doping has plagued the development of two-dimensional (2D) Sn-based perovskite field effect transistors. In this work, we demonstrate the modulation of the properties of phenethylammonium tin iodide ((PEA)(2)SnI4) perovskite thin films by introducing the aromatic polymer additives of poly(4-vinylphenol) (PVP) and poly(vinyl pyrrolidone) (PVPD) during the crystallization processes, keeping the 2D layered structure of (PEA)(2)SnI4 unchanged. The proposed formation mechanisms of the polymer-assisted (PEA)(2)SnI4:PVP and (PEA)(2)SnI4:PVPD films disclose that the interactions between the polymers and (PEA)(2)SnI4, such as hydrogen bonds, p-p interactions, and coordination bonds, lead to the improvement of the morphology and crystallization as well as the inhibition of Sn2+ oxidation of the films. However, the field-effect transistors based on the two polymer-assisted (PEA)(2)SnI4 thin films constructed on the dielectric of poly(vinyl alcohol) (PVA) modified by crosslinking PVP (CL-PVP) exhibit quite a different performance. Compared with the (PEA)(2)SnI4 transistor, without sacrificing the hole mobility, the on-off current ratio of the (PEA)(2)SnI4:PVP device increases by one order of magnitude, and the subthreshold slope declines slightly due to the reduced leakage current, which results from the reduction of p-type self-doping of the perovskite film and the improved quality of the perovskite/dielectric interface because of the strong pi-pi interactions between the benzene rings in CL-PVP and (PEA)(2)SnI4:PVP. In contrast, the (PEA)(2)SnI4:PVPD transistor exhibits relatively poor overall performance because of the N-vinylpyrrolidone of PVPD. More importantly, employing PVP and PVPD as additives can effectively enhance the chemical stability of (PEA)(2)SnI4 as well as the operational stabilities of the corresponding transistors. Our work provides an effective strategy for selecting chemical additives to improve 2D perovskite properties and suppress the oxidation of Sn-based perovskites, and paves a way toward the future applications of Sn-based perovskite optoelectronic devices with high performance and stability.

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