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Direct Hot-Injection Synthesis of Lead Halide Perovskite Nanocubes in Acrylic Monomers for Ultrastable and Bright Nanocrystal–Polymer Composite Films
摘要： In recent years, lead halide perovskite nanocrystals (NCs) have attracted significant attention in both fundamental research and commercial applications due to their excellent optical and optoelectrical properties. However, the protective ligands on the surface of the perovskites NCs could be easily removed after the tedious process of centrifugation, separation, and dispersion, which greatly hampers their stability against light, heat, moisture, and oxygen and limits their practical applications. Here we report a new post-processing-free strategy (i.e., without centrifugation, separation, and dispersion process) of using an UV-polymerizable acrylic monomer of lauryl methacrylate (LMA) as the solvent to synthesize CsPbBr3 NCs, and then adding polyester polyurethane acrylates oligomer, monomer (IBOA) and initiator for directly UV polymerization to fabricate NC-polymer composite films. These films exhibited an improved photoluminescence quantum yield (85-90%) than classic NC-film (40-50%), which were processed using octadecene (ODE) as the solvent for NC synthesis and post-processed for UV polymerization. Significantly, the as-fabricated films by post-processing-free strategy exhibited excellent photostability against strong Xe lamp illumination; while the other films using classic methods were quickly photo-degraded. Meanwhile, these NC-polymer composite films showed good stability against moisture and heating when aging in water at 50oC for over 200 hours. These films, along with K2SiF6:Mn4+ (KSF) phosphor emitters, were used as downconverters for blue LEDs in liquid crystal displays with a wide color gamut of 115% in the International Commission on Illumination (CIE) 1931 color space. This work provides a facile and effective strategy for the preparation of ultrastable and bright color-conversion NC films for the development of the next-generation wide color gamut displays.
关键词： display backlight,lead halide perovskite,colloidal nanocrystals,color-conversion optical films,photostability
更新于2025-11-14 17:03:37
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Engineering Charge Transfer Characteristics in Hierarchical Cu2S QDs @ ZnO Nanoneedles with p–n Heterojunctions: Towards Highly Efficient and Recyclable Photocatalysts
摘要： Equipped with staggered gap p-n heterojunctions, a new paradigm of photocatalysts based on hierarchically structured nano-match-shaped heterojunctions (NMSHs) Cu2S quantum dots (QDs)@ZnO nanoneedles (NNs) are successfully developed via engineering the successive ionic layer adsorption and reaction (SILAR). Under UV and visible light illumination, the photocatalytic characteristics of Cu2S@ZnO heterojunctions with different loading amounts of Cu2S QDs are evaluated by the corresponding photocatalytic degradation of rhodamine B (RhB) aqueous solution. The results elaborate that the optimized samples (S3 serial specimens with six cycles of SILAR reaction) by means of tailored the band diagram exhibit appreciable improvement of photocatalytic activities among all synthesized samples, attributing to the sensitization of a proper amount of Cu2S QDs. Such developed architecture not only could form p–n junctions with ZnO nanoneedles to facilitate the separation of photo-generated carries but also interact with the surface defects of ZnO NNs to reduce the electron and hole recombination probability. Moreover, the existence of Cu2S QDs could also extend the light absorption to improve the utilization rate of sunlight. Importantly, under UV light S3 samples demonstrate the remarkably enhanced RhB degradation efficiency, which is clearly testified upon the charge transfer mechanism discussions and evaluations in the present work. Further supplementary investigations illustrate that the developed nanoscale Cu2S@ZnO heterostructures also possess an excellent photo-stability during our extensive recycling photocatalytic experiments, promising for a wide range of highly efficient and sustainably recyclable photocatalysts applications.
关键词： Photocatalysis,QDs,ZnO@Cu2S hierarchical structure,Photostability,p-n heterojunctions
更新于2025-09-23 15:23:52
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Enhancement strategies of targetability, response and photostability for in vivo bioimaging
摘要： Analyses of the physiology and pathology of active biochemical species in their native contexts are critical for early diagnosis and therapy. Optical imaging has emerged as one of the promising modalities for noninvasive and real-time visualization of important biomolecules or biological events, and it has witnessed major advances in the field of imaging in vitro and in vivo. In this review, we present a survey of common approaches and tactics for enhanced targetability, response rate, and photostability in bioimaging applications. Recently developed and representative examples are illustrated on the cellular and tissue levels.
关键词： targetability,bioimaging,photostability,response rate,fluorescent probe
更新于2025-09-23 15:23:52
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Luminescence properties of a family of lanthanide metal-organic frameworks
摘要： Two isostructural series of lanthanide metal-organic frameworks denoted as SUMOF-7II (Ln) and SUMOF-7IIB (Ln) ( Ln = La, Ce, Pr, Nd, Sm, Eu, and Gd) were synthesized using4,4',4''-(pyridine-2,4,6-triyl)tris(benzoic acid) (H3L2) and a mixture of H3L2 and 4,4′,4′′-(benzene-1,3,5-triyl)tris(benzoic acid) (H3BTB) as linkers, respectively. Both series were characterized usingpowder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), thermal analysis (TGA), and photoluminescence spectroscopy. Photoluminescence measurements show that Eu-MOFs demonstrate a red emission while Pr- and Nd-MOFs display an emission in the near-infrared (NIR) range. On the other hand, La-, Ce-, Sm- and Gd-MOFs exhibit only a ligand-centered emission. The average luminescence lifetimes in the SUMOF-7IIBseries are 1.3-1.4-fold longer than the corresponding ones in the SUMOF-7II series. SUMOF-7IIs show a good photo- and thermal stability. Altogether, the properties of SUMOF-7II and SUMOF-7IIB render them promising materials for applications including sensing, biosensing, and telecommunications.
关键词： Lanthanide MOFs,Antenna Effect,Photostability,Photophysical Properties.,Metal-Organic Frameworks,Luminescence
更新于2025-09-23 15:23:52
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Light-induced effects on crystal size and photo-stability of colloidal CsPbBr<sub>3</sub> perovskite nanocrystals
摘要： CsPbBr3 perovskite nanocrystals (PNCs) have been synthesized using the hot injection method. The CsPbBr3 PNCs exhibit a high photoluminescence quantum yield (PLQY) of 73%. A comprehensive study of UV light interaction with the CsPbBr3 PNCs was performed. SEM images, photoluminescence spectra, X-Ray Diffraction and PLQY measurements were obtained for different time of UV exposure. The exposure to UV light modifies the crystal size (from 10X10 nm to 12X95 nm) and morphology (change from nanocubic to nanorods form). The XRD spectra show a change from tetragonal to cubic crystalline structure. In addition, the interaction of UV light modifies the optical properties of the PNCs by varying the photoluminescence. The material remains stable for a period of 1 hour, however, with exposure to UV light, the PNCs show a decrement in QY from 73.3% to 46.6% after 30 days. These results indicate that light-induce variation in morphological and photo-stability of CsPbBr3 PNCs.
关键词： luminescence,photostability,CsPbBr3 nanocrystals,morphological study
更新于2025-09-23 15:23:52
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Doubly N-Confused Calix[6]phyrin Bis-Organopalladium Complexes: Photostable Triplet Sensitizers for Singlet Oxygen Generation
摘要： Triplet photosensitizers that generate singlet oxygen efficiently are attractive for applications such as photodynamic therapy (PDT). Extending the absorption band to a near-infrared (NIR) region (700 nm~) with reasonable photostability is one of the major demands in the rational design of such sensitizers. We herein prepared a series of mono- and bis-palladium complexes (1-Pd-H2, 2-Pd-H2, 1-Pd-Pd, and 2-Pd-Pd) based on modified calix[6]phyrins as photosensitizers for singlet oxygen generation. These palladium complexes showed intense absorption profiles in the visible-to-NIR region (500–750 nm) depending on the number of central metals. Upon photoirradiation in the presence of 1,5-dihydroxynaphthalene (DHN) as a substrate for reactive oxygen species, the bis-palladium complexes generated singlet oxygen with high efficiency and excellent photostability. Singlet oxygen generation was confirmed from the characteristic spectral feature of the spin trapped complex in the EPR spectrum and the intact 1O2 emission at 1270 nm.
关键词： Photostability,Palladium N-confused calix[6]phyrin,Triplet Photosensitizer,Singlet oxygen
更新于2025-09-23 15:23:52
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Stable Molecular Surface Modification of Nanostructured, Mesoporous Metal Oxide Photoanodes by Silane and Click Chemistry
摘要： Binding functional molecules to nanostructured mesoporous metal oxide surfaces provides a way to derivatize metal oxide semiconductors for applications in dye-sensitized photoelectrosynthesis cells (DSPECs). The commonly used anchoring groups, phosphonates and carboxylates, are unstable as surface links to oxide surfaces at neutral and high pH, leading to rapid desorption of appended molecules. A synthetically versatile molecular attachment strategy based on initial surface-modification with a silyl azide followed by click chemistry is described here. It has been used for the stable installation of surface-bound metal complexes. The resulting surfaces are highly stabilized toward complex loss with excellent thermal, photochemical, and electrochemical stabilities. The procedure involves binding 3-azidopropyltrimethoxysilane (APTMS) to nanostructured mesoporous TiO2 or tin-doped indium oxide (ITO) electrodes by silane attachment followed by azide-terminated, Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions with an alkyne-derivatized ruthenium(II) polypyridyl complex. The chromophore-modified electrodes display enhanced photochemical and electrochemical stabilities compared to phosphonate surface binding with extended photoelectrochemical oxidation of hydroquinone for more than ~6 h with no significant decay.
关键词： DSPECs,photostability,stability,silane chemistry,electrostability,Ru(II) polypyridyl complexes,click chemistry,Dye-sensitized,photoanode
更新于2025-09-23 15:22:29
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Highly Photostable and Fluorescent Microporous Solids Prepared via Solid-state Entrapment of BODIPY Dyes in a Nascent Metal-Organic Framework
摘要： We report a strategy to synthesize highly emissive, photostable, microporous materials by solid-state entrapment of boron dipyrromethene (BODIPY) fluorophores in a metal-organic framework. Solvent-free mechanochemistry or accelerated aging enabled quantitative capture and dispersal of the PM605 dye within the ZIF-8 framework starting from inexpensive, commercial materials. While the design of emissive BODIPY solids is normally challenged by quenching in a densely-packed environment, herein reported PM605@ZIF-8 materials show excellent emissive properties and to the best of our knowledge an unprecedented ~10-fold enhancement of BODIPY photostability. Time-resolved and steady-state fluorescence studies of PM605@ZIF-8 show that interchromophore interactions are minimal at low dye loadings, but at higher ones through-pore energy transfer between chromophores and to aggregate species lead to quenching.
关键词： fluorescence,metal-organic framework,photostability,BODIPY,microporous materials
更新于2025-09-23 15:21:21
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Tenfold increase in the photostability of an azobenzene guest in vapor-deposited glass mixtures
摘要： Improvements to the photostability of organic glasses for use in electronic applications have generally relied on the modification of the chemical structure. We show here that the photostability of a guest molecule can also be significantly improved—without chemical modification—by using physical vapor deposition to pack molecules more densely. Photoisomerization of the substituted azobenzene, 4,4'-diphenyl azobenzene, was studied in a vapor-deposited glass matrix of celecoxib. We directly measure photoisomerization of trans- to cis-states via Ultraviolet-visible (UV-Vis) spectroscopy and show that the rate of photoisomerization depends upon the substrate temperature used during co-deposition of the glass. Photostability correlates reasonably with the density of the glass, where the optimum glass is about tenfold more photostable than the liquid-cooled glass. Molecular simulations, which mimic photoisomerization, also demonstrate that photoreaction of a guest molecule can be suppressed in vapor-deposited glasses. From the simulations, we estimate that the region that is disrupted by a single photoisomerization event encompasses approximately 5 molecules.
关键词： photostability,organic glasses,azobenzene,photoisomerization,physical vapor deposition,molecular simulations,UV-Vis spectroscopy
更新于2025-09-23 15:21:21
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Suppressing the Photocatalytic Activity of Zinc Oxide Electron-Transport Layer in Nonfullerene Organic Solar Cells with a Pyrene-Bodipy Interlayer
摘要： Organic solar cells based on nonfullerene acceptors have recently witnessed a significant rise in their power conversion efficiency values. However, they still suffer from severe instability issues, especially in an inverted device architecture based on the zinc oxide bottom electron transport layers. In this work, we insert a pyrene-bodipy donor?acceptor dye as a thin interlayer at the photoactive layer/zinc oxide interface to suppress the degradation reaction of the nonfullerene acceptor caused by the photocatalytic activity of zinc oxide. In particular, the pyrene-bodipy-based interlayer inhibits the direct contact between the nonfullerene acceptor and zinc oxide hence preventing the decomposition of the former by zinc oxide under illumination with UV light. As a result, the device photostability was significantly improved. The π?π interaction between the nonfullerene acceptor and the bodipy part of the interlayer facilitates charge transfer from the nonfullerene acceptor toward pyrene, which is followed by intramolecular charge transfer to bodipy part and then to zinc oxide. The bodipy-pyrene modified zinc oxide also increased the degree of crystallization of the photoactive blend and the face-on stacking of the polymer donor molecules within the blend hence contributing to both enhanced charge transport and increased absorption of the incident light. Furthermore, it decreased the surface work function as well as surface energy of the zinc oxide film all impacting in improved power conversion efficiency values of the fabricated cells with champion devices reaching values up to 9.86 and 11.80% for the fullerene and nonfullerene-based devices, respectively.
关键词： bodipy,zinc oxide,photocatalytic activity,pyrene,organic solar cells,photostability,nonfullerene acceptors
更新于2025-09-23 15:21:01