Flexible perovskite solar cells (F-PSCs) are appealing for their flexibility and high power-to-weight ratios. However, the fragile grain boundaries (GBs) in perovskite films can lead to stress and strain cracks under bending conditions, limiting the performance and stability of F-PSCs. Herein, we show that the perovskite film can facilely achieve in situ bifacial capping via introducing 4-(methoxy)benzylamine hydrobromide (MeOBABr) as the precursor additive. The spontaneously formed MeOBABr capping layers flatten the grain boundary grooves (GBGs), enable the release of the mechanical stress at the GBs during bending, rendering enhanced film robustness. They also contribute to the reduction of the residual strain and the passivation of the surface defects of the perovskite film. Besides, the molecular polarity of MeOBABr can result in surface band bending of the perovskite that favors the interfacial charge extraction. The corresponding inverted F-PSCs based on nickel oxide (NiO)/poly(triaryl amine) (PTAA) hole transport bilayer reach a 23.7% power conversion efficiency (PCE) (22.9% certified) under AM 1.5 G illumination and a 42.46% PCE under 1000 lux indoor light illumination. Meanwhile, a robust bending durability of the device is also achieved.
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http://dx.doi.org/10.1038/s41467-024-55652-6 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Microelectronic Science and Engineering, School of Physical Science and Technology, Ningbo University, Ningbo 315211, China.
Two-dimensional (2D) Ruddlesden-Popper perovskites (RPPs) have garnered significant attention due to their enhanced stability compared with their three-dimensional counterparts. However, the power conversion efficiency (PCE) of 2D perovskite solar cells (2D-PSCs) remains lower than that of 3D-PSCs. Understanding the microstructural evolution of 2D perovskite films during fabrication is essential for improving their performance.
View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Photovoltaic Science and Technology, Department of Materials Science, Institute of Optoelectronics, Fudan University, Shanghai, 200433, China.
Ferroelectric semiconductors have the advantages of switchable polarization ferroelectric field regulation and semiconductor transport characteristics, which are highly promising in ferroelectric transistors and nonvolatile memory. However, it is difficult to prepare a Sn-based perovskite film with both robust ferroelectric and semiconductor properties. Here, by doping with 2-methylbenzimidazole, Sn-based perovskite [93.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Materials, Shenzhen Campus of Sun Yat-sen University, No. 66, Gongchang Road, Guangming District, Shenzhen, Guangdong 518107, P.R. China.
Indium (In) reduction is a hot topic in transparent conductive oxide (TCO) research. So far, most strategies have been focused on reducing the layer thickness of In-based TCO films and exploring TCOs. However, no promising industrial solution has been obtained yet.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Huaqiao University College of Materials Science and Engineering, No.668 Jimei Avenue, Xiamen, Fujian, 361021, Xiamen, CHINA.
The advancement of tin-based perovskite solar cells (TPSCs) has been severely hindered by the poor controllability of perovskite crystal growth and the energy level mismatch between the perovskite and fullerene-based electron transport layer (ETL). Here, we synthesized three cis-configured pyridyl-substituted fulleropyrrolidines (PPF), specifically 2-pyridyl (PPF2), 3-pyridyl (PPF3), and 4-pyridyl (PPF4), and utilized them as precursor additives to regulate the crystallization kinetics during film formation. The spatial distance between the two pyridine groups in PPF2, PPF3, and PPF4 increases sequentially, enabling PPF4 to interact with more perovskite colloidal particles.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Chemistry, City University of Hong Kong, Kowloon, 999077, Hong Kong.
Perovskite/silicon tandem solar cells (TSCs) are promising candidates for commercialization due to their outstanding power conversion efficiencies (PCEs). However, controlling the crystallization process and alleviating the phases/composition inhomogeneity represent a considerable challenge for perovskite layers grown on rough silicon substrates, ultimately limiting the efficiency and stability of TSC. Here, this study reports a "halide locking" strategy that simultaneously modulates the nucleation and crystal growth process of wide bandgap perovskites by introducing a multifunctional ammonium salt, thioacetylacetamide hydrochloride (TAACl), to bind with all types of cations and anions in the mixed halide perovskite precursor.
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