Thermally activated delayed fluorophore and plasmonic structures integrated with perovskites for X-ray scintillation and imaging
Abstract:
The development of inexpensive and easily processable X-ray-sensitive materials is of great importance because a number of commercial scintillators, such as LaBr3(Ce), Gd3Al3Ga2O12(Ce), Cs2HfCl6, NaI:Tl, CsI:Tl, and LiI:Eu, are fabricated using highly toxic or rare-earth elements via high-temperature synthesis. This has spurred research into radioluminescence-enhancing mechanisms and solution-processable scintillating materials made from earth-abundant elements that have excellent optoelectronic properties, including high quantum yields and a low afterglow effect. In recent years, a range of metal halide perovskite (MHP) integrated with thermally activated delayed fluorescence (TADF) materials have been developed, exhibiting excellent scintillation properties and a high spatial resolution. Meanwhile, plasmonic technologies are reported to exploit light-energy confinement capabilities beyond the diffraction limit that produces local-field enhancement. This enhancement has subsequently improved the performance of small-sized optoelectronic devices such as solar cells and diagnostic optical sensors. This perspective summarizes the current development of innovative MHP, TADF, and plasmonic materials for use in scintillators and their integrated moieties while also identifying the relevant challenges. Following a thorough evaluation of the efforts made to improve the X-ray scintillation efficiency of these materials, we propose an outlook for future research in order to further enhance their scintillation properties and spatial resolution.Inhibiting the Appearance of Green Emission in Mixed Lead Halide Perovskite Nanocrystals for Pure Red Emission
Abstract:
Mixed halide perovskites exhibit promising optoelectronic properties for next-generation light-emitting diodes due to their tunable emission wavelength that covers the entire visible light spectrum. However, these materials suffer from severe phase segregation under continuous illumination, making long-term stability for pure red emission a significant challenge. In this study, we present a comprehensive analysis of the role of halide oxidation in unbalanced ion migration (I/Br) within CsPbI2Br nanocrystals and thin films. We also introduce a new approach using cyclic olefin copolymer (COC) to encapsulate CsPbI2Br perovskite nanocrystals (PNCs), effectively suppressing ion migration by increasing the corresponding activation energy. Compared with that of unencapsulated samples, we observe a substantial reduction in phase separation under intense illumination in PNCs with a COC coating. Our findings show that COC enhances phase stability by passivating uncoordinated surface defects (Pb2+ and I–), increasing the formation energy of halide vacancies, improving the charge carrier lifetime, and reducing the nonradiative recombination density.Stabilization of halide perovskites with silicon compounds for optoelectronic, catalytic, and bioimaging applications
Abstract:
Silicon belongs to group 14 elements along with carbon, germanium, tin, and lead in the periodic table. Similar to carbon, silicon is capable of forming a wide range of stable compounds, including silicon hydrides, organosilicons, silicic acids, silicon oxides, and silicone polymers. These materials have been used extensively in optoelectronic devices, sensing, catalysis, and biomedical applications. In recent years, silicon compounds have also been shown to be suitable for stabilizing delicate halide perovskite structures. These composite materials are now receiving a lot of interest for their potential use in various real‐world applications. Despite exhibiting outstanding performance in various optoelectronic devices, halide perovskites are susceptible to breakdown in the presence of moisture, oxygen, heat, and UV light. Silicon compounds are thought to be excellent materials for improving both halide perovskite stability and the performance of perovskite‐based optoelectronic devices. In this work, a wide range of silicon compounds that have been used in halide perovskite research and their applications in various fields are discussed. The interfacial stability, structure–property correlations, and various application aspects of perovskite and silicon compounds are also analyzed at the molecular level. This study also explores the developments, difficulties, and potential future directions associated with the synthesis and application of perovskite‐silicon compounds. imageReverse-cyclic performance of United States prescriptive code connectors in a novel mass timber structural composite panel
Stability of mixed lead halide perovskite films encapsulated in cyclic olefin copolymer at room and cryogenic temperatures
Abstract:
Lead Mixed Halide Perovskites (LMHPs), CsPbBrI2, have attracted significant interest as promising candidates for wide bandgap absorber layers in tandem solar cells due to their relative stability and red-light emission with a bandgap ∼1.7 eV. However, these materials segregate into Br-rich and I-rich domains upon continuous illumination, affecting their optical properties and compromising the operational stability of devices. Herein, we track the microscopic processes occurring during halide segregation by using combined spectroscopic measurements at room and cryogenic temperatures. We also evaluate a passivation strategy to mitigate the halide migration of Br/I ions in the films by overcoating with cyclic olefin copolymer (COC). Our results explain the correlation between grain size, intensity dependencies, phase segregation, activation energy barrier, and their influence on photoinduced carrier lifetimes. Importantly, COC treatment increases the lifetime charge carriers in mixed halide thin films, improving efficient charge transport in perovskite solar cell applications.