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Understanding of Defect Passivation Effect on Wide Band Gap p-i-n Perovskite Solar Cell
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Title
Understanding of Defect Passivation Effect on Wide Band Gap p-i-n Perovskite Solar Cell
Issued Date
2024-06
Citation
Enkhbayar, Enkhjargal. (2024-06). Understanding of Defect Passivation Effect on Wide Band Gap p-i-n Perovskite Solar Cell. ACS Applied Materials & Interfaces, 16(27), 35084–35094. doi: 10.1021/acsami.4c05838
Type
Article
Author Keywords
defect passivationperovskite solar cellwide band gap perovskitep-i-n structure2D/3D heterojunction
Keywords
METAL HALIDE PEROVSKITESEFFICIENTENERGYFILMSLIMITSTABILITYORIGINSLEAD
ISSN
1944-8244
Abstract
The wide band gap perovskite solar cells (PSCs) have attracted considerable attention for their great potential as top cells in high efficiency tandem cell application. However, the photovoltaic performance and stability of PSCs are constrained by nonradiative recombination, primarily stemming from defects within the bulk and at the interface of charge transport layer/perovskite and phase segregation. In this study, we systematically investigated the effects of 2-thiopheneethylammonium chloride (TEACl) on a wide band gap (∼1.67 eV) Cs0.15FA0.65MA0.20Pb(I0.8Br0.2)3 (CsFAMA) perovskite solar cell. TEACl was employed as a passivation layer between the perovskite and electron transport layer (ETL). With TEACl treatment, charged defects responsible for sub-band absorption and electrostatic potential fluctuation were effectively suppressed by the passivation of bulk defects. The incorporation of TEACl, which led to the formation of a TEA2PbX4/Perovskite (2D/3D) heterojunction, facilitated better band alignment and effective passivation of interface defects at the ETL/CsFAMA. Owing to these beneficial effects, the TEACl passivated PSC achieved a photo conversion efficiency (PCE) of 19.70% and retained ∼85% of initial PCE over ∼1900 h, surpassing the performance of the untreated PSC, which exhibited a PCE of 16.69% and retained only ∼37% of its initial PCE. © 2024 American Chemical Society.
URI
http://hdl.handle.net/20.500.11750/57165
DOI
10.1021/acsami.4c05838
Publisher
American Chemical Society
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