Additives play a pivotal role in enhancing the efficiency of perovskite solar cells (PSCs), and carefully designed additives contribute to major breakthroughs in device performance. In this study, a series of novel A-π-A-type porphyrin derivatives-PPH-1, PPH-2, and PPF-1-are synthesized, each incorporating pyridyl groups, specifically engineered to function as passivation agents for PSCs. The electron-withdrawing properties of fluorine in PPF-1 increase the molecular polarity, thereby strengthening its interaction with the perovskite and enhancing the passivation efficacy. Compared to PPH-1 and PPH-2, PPF-1 not only improves crystallinity but also provides more efficient defect passivation at grain boundaries and interfaces. As a result, PSCs incorporating PPF-1 achieve a remarkable power conversion efficiency (PCE) of 24.96%, along with an open-circuit voltage (V) of 1.178 V, a short-circuit current density (J) of 24.65 mA cm, and a fill factor (FF) of 85.96%, surpassing the PCEs of 23.36%, 24.11%, and 23.93% for pristine, PPH-1-, and PPH-2-modified PSCs, respectively. In addition, the incorporation of fluorinated porphyrin in PPF-1 significantly improves the moisture resistance and thermal stability, while the device maintains high solar efficiency, opening up new alternative ways to promote solar cell innovation.
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http://dx.doi.org/10.1002/smll.202412530 | DOI Listing |
ChemSusChem
January 2025
Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P.R. China.
Inverted perovskite solar cells (IPSCs) utilizing nickel oxide (NiO) as hole transport material have made great progress, driven by improvements in materials and interface engineering. However, challenges remain due to the low intrinsic conductivity of NiO and inefficient hole transport. In this study, we introduced MoS nanoparticles at the indium tin oxide (ITO) /NiO interface to enhance the ITO surface and optimize the deposition of NiO, resulting in increased conductivity linked to a ratio of Ni:Ni.
View Article and Find Full Text PDFNanoscale
January 2025
Laboratory of New Materials for Solar Energetics, Department of Materials Science, Lomonosov Moscow State University, 1 Lenin Hills, 119991, Moscow, Russia.
Identification of crystal structures is a crucial stage in the exploration of novel functional materials. This procedure is usually time-consuming and can be false-positive or false-negative. This necessitates a significant level of expert proficiency in the field of crystallography and, especially, requires deep experience in perovskite-related structures of hybrid perovskites.
View Article and Find Full Text PDFNPG Asia Mater
May 2024
Department of Chemistry, KU Leuven, Leuven, Belgium.
All-inorganic lead halide perovskites (LHPs) and their use in optoelectronic devices have been widely explored because they are more thermally stable than their hybrid organic‒inorganic counterparts. However, the active perovskite phases of some inorganic LHPs are metastable at room temperature due to the critical structural tolerance factor. For example, black phase CsPbI is easily transformed back to the nonperovskite yellow phase at ambient temperature.
View Article and Find Full Text PDFACS Omega
January 2025
Centro de Investigación en Materiales Avanzados, S.C. (CIMAV Subsede Monterrey), Alianza Norte 202, Parque de Investigación e Innovación Tecnológica, C.P. 66628 Apodaca, Nuevo León, Mexico.
Thermal atomic layer deposition (TALD) and plasma atomic layer deposition (PALD) were used for producing thin NiO films from nickel(II) acetylacetonate Ni(acac), employing different oxidizing agents (deionized water HO, ozone O, and molecular oxygen O). The films were deposited at 300 °C (TALD) and 220 °C (PALD) over glass substrates; their physical and chemical properties were considerably influenced by the choice of oxidizing agents. In particular, ALD(HO) samples had a low growth per cycle (GPC) and a high concentration of defects.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
College of Science, Hebei University of Science and Technology, 26 Yuxiang Road, Shijiazhuang 050018, P. R. China.
The interfaces between the perovskite and charge-transporting layers typically exhibit high defect concentrations, which are the primary cause of open-circuit voltage loss. Passivating the interface between the perovskite and electron-transporting layer is particularly challenging due to the dissolution of surface treatment agents during the perovskite coating. In this study, a coherent FAPbICl buried interface was simultaneously formed during the preparation of FAPbI.
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