In this study, the effectiveness of using a perovskite/Zr-metal-organic frameworks (MOFs) heterojunction in realizing efficient and stable inverted p-i-n perovskite solar cells (PVSCs) is demonstrated. Two types of Zr-MOFs, UiO-66 and MOF-808, are investigated owing to their respectable moisture and chemical stabilities. The MOFs while serving as an interlayer in conjunction with the perovskite film are shown to possess the advantages of UV-filtering capability and enhancing perovskite crystallinity. Consequently, the UiO-66/MOF-808-modified PVSCs yield enhanced power conversion efficiencies (PCEs) of 17.01% and 16.55%, outperforming the control device (15.79%). While further utilizing a perovskite/Zr-MOF hybrid heterojunction to fabricate the devices, the hybrid MOFs are found to possibly distribute over the perovskite grain boundary providing a grain-locking effect to simultaneously passivate the defects and to reinforce the film's robustness against moisture invasion. As a result, the PCEs of the UiO-66/MOF-808-hybrid PVSCs are further enhanced to 18.01% and 17.81%, respectively. Besides, over 70% of the initial PCE is retained after being stored in air (25 °C and relative humidity of 60 ± 5%) for over 2 weeks, in contrast to the quick degradation observed for the control device. This study demonstrates the promising potential of using perovskite/MOF heterojunctions to fabricate efficient and stable PVSCs.
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http://dx.doi.org/10.1002/advs.201801715 | DOI Listing |
Nanoscale
January 2025
Centre for Nano Science and Nano Technology, S 'O' A (Deemed to be University), Bhubaneswar-751 030, Odisha, India.
Titanium (Ti)-based MOFs are promising materials known for their porosity, stability, diverse valence states, and a lower conduction band (CB) than Zr-MOFs. These features support stable ligand-to-metal charge transfer (LMCT) transitions under photoirradiation, enhancing photocatalytic performance. However, Ti-MOF structures remain a challenge owing to the highly volatile and hydrophilic nature of ionic Ti precursors.
View Article and Find Full Text PDFBraz J Microbiol
January 2025
Laboratorio de Biocatalizadores y sus Aplicaciones, Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Iguá 4225, Montevideo, Uruguay.
Proteases are hydrolases that act on peptide bonds, releasing amino acids and/or oligopeptides, and are involved in essential functions in all organisms. They represent an important segment of the global enzyme market, with applications in the food, leather, detergent, and pharmaceutical industries. Depending on their industrial use, proteases should exhibit high activity under extreme conditions, such as low temperatures, e.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan.
The visible-light-driven O evolution on oxychloride photocatalysts, such as BiNbOCl, was significantly enhanced by stirring in an aqueous solution containing IrCl in the dark. Various characterizations indicated that highly dispersed IrOHCl-like species spontaneously formed on the oxychloride surface, serving as effective and stable cocatalysts for enhancing O evolution.
View Article and Find Full Text PDFInorg Chem
January 2025
Key Laboratory of Polymer Materials of Gansu Province, Key Laboratory of Eco-functional Polymer Materials of the Ministry of Education, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, Gansu, China.
Efficient and stable nonprecious metal-based oxygen evolution reaction (OER) electrocatalysts are pivotal for water electrolysis technology. Herein, we are reporting an effective strategy for fabricating efficient Co-based OER electrocatalysts by low-level Fe doping in CoMoO to boost surface reconstruction and electronic modulation, which resulted in excellent OER electroactivity consequently. Our findings reveal that a mere 5.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, P. R. China.
Long-range ordered high-entropy intermetallics (HEIs) were synthesized a thermodynamically-driven atomic ordering strategy. The (FeCoNi)(RuPt) HEI achieves 200 mA cm at an overpotential of 56 mV and a remarkable low Tafel slope of 50.4 mV dec in alkaline seawater.
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