The past decade has witnessed tremendous progress in metal halide perovskites, particularly in lead (Pb) halide perovskites, because of their extraordinary performance in cutting-edge optoelectronic devices. However, the toxicity of Pb and the environmental stability of the perovskites are two major issues that this field is currently facing. In recent years, 2D layered perovskites have emerged as a promising alternative to the traditional 3D perovskites due to their structural flexibility and higher environmental stability, though they lack the desired level of device efficiency. Doping with target ions can drastically tune the crystal structure, optical properties, charge recombination dynamics, and electronic properties of the 2D perovskite. Although the field of doping in 2D perovskites has seen substantial growth in recent times, no comprehensive review is available on the recent advances in doping of 2D perovskites and its effect on the optoelectronic properties. In this review, we summarize the progress in doping in 2D perovskites based on different doping sites including progress in different synthesis strategies and their impact on crystal structures and various optoelectronic properties. We then highlight the recent achievements in doped 2D perovskites for photovoltaic, LED and other emerging applications. Finally, we conclude with the challenges and the future scope in the doping studies of 2D layered perovskites, which need to be addressed for further developments of next-generation 2D perovskite-based optoelectronic devices.
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http://dx.doi.org/10.1039/d1na00709b | DOI Listing |
RSC Adv
January 2025
Departamento de Física Aplicada, Facultade de Óptica e Optometríae Instituto de Materiais (iMATUS) Campus Vida, Universidade de Santiago de Compostela (USC) 15782 Galicia Spain.
The Cr and Sm doped GdAlO perovskite with formula GdSmAlCrO, was synthesized a solid-state reaction method, and its structure, morphology, and photoluminescence properties were thoroughly investigated. The compound crystallizes in the orthorhombic space group, with Cr transition-metal ions substituting Al in the octahedral symmetry site, and Sm lanthanide (rare-earth) ions occupying the tetrahedral site. The material's morphology and chemical composition homogeneity were evaluated through Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray analysis.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Henan Provincial Key Laboratory of Nanocomposites and Applications, Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou, Henan 450006, China.
Due to the high configuration entropy, unique atomic arrangement, and electronic structures, high-entropy materials are being actively pursued as bifunctional catalysts for both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in rechargeable zinc-air batteries (ZABs). However, a relevant strategy to enhance the catalytic activity of high-entropy materials is still lacking. Herein, a hole doping strategy has been employed to enable the high-entropy perovskite La(CrMnFeCoNi)O to effectively catalyze the ORR and OER.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Radiation Laboratory, University of Notre Dame, Notre Dame, Indiana 46556, United States.
Modulation of singlet and triplet energy transfer from excited semiconductor nanocrystals to attached dye molecules remains an important criterion for the design of light-harvesting assemblies. Whereas one can consider the selection of donor and acceptor with favorable energetics, spectral overlap, and kinetics of energy transfer as a means to direct the singlet and triplet energy transfer pathways, it is not obvious how to control the singlet and triplet characteristics of the donor semiconductor nanocrystal itself. By doping CsPb(ClBr) nanocrystals with Mn, we have now succeeded in increasing the triplet characteristics of semiconductor nanocrystals.
View Article and Find Full Text PDFSmall
January 2025
Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing, 100875, P. R. China.
Establishing the relationship between catalytic performance and material structure is crucial for developing design principles for highly active catalysts. Herein, a type of perovskite fluoride, NHMnF, which owns strong-field coordination including fluorine and ammonia, is in situ grown on carbon nanotubes (CNTs) and used as a model structure to study and improve the intrinsic catalytic activity through heteroatom doping strategies. This approach optimizes spin-dependent orbital interactions to alter the charge transfer between the catalyst and reactants.
View Article and Find Full Text PDFRSC Adv
January 2025
IMMM, Institut des Molécules et Matériaux du Mans Bd Charles Nicolle 72000 Le Mans France.
Samarium (Sm) modification is emerging as a powerful strategy to manipulate the electrical response of 0.8BiFeO-0.2BaTiO (BFBT) multiferroic ceramics.
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