11 research outputs found

    Morphologically Controlled Synthesis of Cs<sub>2</sub>SnCl<sub>6</sub> Perovskite Crystals and Their Photoluminescence Activity

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    The Cs2SnX6 perovskites have attracted much attention due to excellent optoelectronic properties and high stability. In the present work, we have focused on the morphology control and photoluminescence characteristics of the Cs2SnCl6 perovskite crystals. The synthesis process of the Cs2SnCl6 crystals includes two stages composed of the formation of initial crystals and the growth of Cs2SnCl6; the later originated from the oxidization of CsSnCl3. This process has been confirmed by Scanning electron microscope (SEM) and X-rays diffraction (XRD). By controlling the concentration of the initial reactants and hydrochloric acid in the solution to change the supersaturation of the solution, different crystal morphologies, such as truncated octahedron, octahedron, hexapod, quasi-sphere, have been obtained. In relatively a low supersaturation solution, the amount of growth units dominates the crystal growth process to obtain the hexapod and self-assembly crystals. In contrast, in relatively high supersaturation solution, nucleation predominates to yield small size truncated octahedrons and near-spherical Cs2SnCl6 crystals. The synthesized Cs2SnCl6 crystals have shown a wide emission band peaking at 450 nm with full width at half maximum (FWHM) 63 nm due to the defects introduced by Sn2+. The photoluminescence intensities of crystals synthesized at various conditions exhibited considerable difference, which was about 60 times between the highest and the lowest

    Photoluminescence Characteristics of Sn<sup>2+</sup> and Ce<sup>3+</sup>-Doped Cs<sub>2</sub>SnCl<sub>6</sub> Double-Perovskite Crystals

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    In recent years, all-inorganic lead-halide perovskites have received extensive attention due to their many advantages, but their poor stability and high toxicity are two major problems. In this paper, a low toxicity and stable Cs2SnCl6 double perovskite crystals were prepared by aqueous phase precipitation method using SnCl2 as precursor. By the XRD, ICP-AES, XPS, photoluminescence and absorption spectra, the fluorescence decay curve, the structure and photoluminescence characteristics of Ce3+-doped and undoped samples have been investigated in detail. The results show that the photoluminescence originates from defects. [ S n S n 4 + 2 + +VCl] defect complex in the crystal is formed by Sn2+ substituting Sn4+. The number of defects formed by Sn2+ in the crystal decreases with Ce3+ content increases. Within a certain number of defects, the crystal luminescence is enhanced with the number of [ S n S n 4 + 2 + +VCl] decreased. When Ce3+ is incorporated into the crystals, the defects of [ C e 3 + S n 4 + +VCl] and [ S n S n 4 + 2 + +VCl] were formed and the crystal show the strongest emission. This provides a route to enhance the photoluminescence of Cs2SnCl6 double perovskite crystals

    Comparative Analysis of the Complete Plastomes of Apostasia wallichii and Neuwiedia singapureana (Apostasioideae) Reveals Different Evolutionary Dynamics of IR/SSC Boundary among Photosynthetic Orchids

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    Apostasioideae, consists of only two genera, Apostasia and Neuwiedia, which are mainly distributed in Southeast Asia and northern Australia. The floral structure, taxonomy, biogeography, and genome variation of Apostasioideae have been intensively studied. However, detailed analyses of plastome composition and structure and comparisons with those of other orchid subfamilies have not yet been conducted. Here, the complete plastome sequences of Apostasia wallichii and Neuwiedia singapureana were sequenced and compared with 43 previously published photosynthetic orchid plastomes to characterize the plastome structure and evolution in the orchids. Unlike many orchid plastomes (e.g., Paphiopedilum and Vanilla), the plastomes of Apostasioideae contain a full set of 11 functional NADH dehydrogenase (ndh) genes. The distribution of repeat sequences and simple sequence repeat elements enhanced the view that the mutation rate of non-coding regions was higher than that of coding regions. The 10 loci—ndhA intron, matK-5′trnK, clpP-psbB, rps8-rpl14, trnT-trnL, 3′trnK-matK, clpP intron, psbK-trnK, trnS-psbC, and ndhF-rpl32—that had the highest degrees of sequence variability were identified as mutational hotspots for the Apostasia plastome. Furthermore, our results revealed that plastid genes exhibited a variable evolution rate within and among different orchid genus. Considering the diversified evolution of both coding and non-coding regions, we suggested that the plastome-wide evolution of orchid species was disproportional. Additionally, the sequences flanking the inverted repeat/small single copy (IR/SSC) junctions of photosynthetic orchid plastomes were categorized into three types according to the presence/absence of ndh genes. Different evolutionary dynamics for each of the three IR/SSC types of photosynthetic orchid plastomes were also proposed

    Room Temperature In-Situ Synthesis of Inorganic Lead Halide Perovskite Nanocrystals Sol Using Ultraviolet Polymerized Acrylic Monomers as Solvent and Their Composites with High Stability

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    As a kind of promising optoelectrical material, all-inorganic perovskite nanocrystals CsPbX3 (X = Cl, Br, I) have attracted much attention, due to their excellent optoelectrical characteristics, in recent years. However, their synthesis approaches require rigorous conditions, including high temperature, eco-unfriendly solvent or complex post-synthesis process. Herein, to overcome these issues, we reported a novel facile room temperature in-situ strategy using ultraviolet polymerizable acrylic monomer as solvent to synthesis CsPbX3 nanocrystals without a complex post-synthesis process. In this strategy, adequate soluble precursors of Cs, Pb and Br and reaction terminating agent 3-aminopropyltriethoxysilane (APTES) were used. The obtained CsPbBr3 nanocrystals showed a high photoluminescence quantum yields (PLQY) of 87.5%. The corresponding polymer composites, by adding light initiator and oligomer under ultraviolet light radiation, performed excellent stability in light, air, moisture and high temperature. The reaction process and the effect of the reaction terminating agent have been investigated in detail. This strategy is a universal one for synthesizing CsPbX3 nanocrystals covering visible light range by introducing HCl and ZnI2

    Tuning oxidant and antioxidant activities of ceria by anchoring copper single-site for antibacterial application

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    Abstract The reaction system of hydrogen peroxide (H2O2) catalyzed by nanozyme has a broad prospect in antibacterial treatment. However, the complex catalytic activities of nanozymes lead to multiple pathways reacting in parallel, causing uncertain antibacterial results. New approach to effectively regulate the multiple catalytic activities of nanozyme is in urgent need. Herein, Cu single site is modified on nanoceria with various catalytic activities, such as peroxidase-like activity (POD) and hydroxyl radical antioxidant capacity (HORAC). Benefiting from the interaction between coordinated Cu and CeO2 substrate, POD is enhanced while HORAC is inhibited, which is further confirmed by density functional theory (DFT) calculations. Cu-CeO2 + H2O2 system shows good antibacterial properties both in vitro and in vivo. In this work, the strategy based on the interaction between coordinated metal and carrier provides a general clue for optimizing the complex activities of nanozymes

    Submersed macrophytes Vallisneria natans and Vallisneria spinulosa improve water quality and affect microbial communities in sediment and water columns

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    Healthy aquatic ecosystems are essential for human beings. However, anthropogenic activities severely worsen water quality. In this study, using assembling mesocosms, we developed an efficient and easy-to-handle method to monitor the water quality by measuring the electrical conductivity (EC) of water. Our data demonstrate that the growth of two submersed macrophytes, Vallisneria natans and Vallisneria spinulosa, improves water quality by decreasing EC. Furthermore, using high-throughput DNA sequencing, we analyzed the microbial community abundance and structure in sediment and water columns with or without plant growth. We generated 33,775 amplicon sequence variants from 69 samples of four sediment groups (BkM, CtM, VnR, and VsR) and three water column sample groups (CtW, VnW, and VsW). The results show that the relative abundance of bacteria was higher in the sediment than in the water column. Moreover, the diversity and composition of microbiomes were altered by Vallisneria spp. growth, and the ι-diversity of the microbial communities decreased due to submersed macrophytes in both the sediment and water columns. The β-diversity of the microbial communities also varied significantly with or without Vallisneria spp. growth for both the sediment and water columns

    Lianhua Qingke ameliorates lipopolysaccharide‐induced lung injury by inhibiting neutrophil extracellular traps formation and pyroptosis

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    Abstract LHQK is a patented Traditional Chinese Medicine (TCM) which is clinically used for acute tracheobronchitis, cough, and other respiratory diseases. Recent studies have proved that LHQK exhibits excellent clinical efficacy in the treatment of acute lung injury (ALI). However, the corresponding mechanisms remain largely unexplored. In this study, we investigated the effects and the underlying mechanisms of LHQK on lipopolysaccharide (LPS)‐induced ALI in mice. The pathological examination, inflammatory cytokines assessments, and mucus secretion evaluation indicated that administration of LHQK ameliorated LPS‐induced lung injury, and suppressed the secretion of Muc5AC and pro‐inflammatory cytokines (IL‐6, TNF‐α, and IL‐1β) in plasma and BALF. Furthermore, the results of cell‐free DNA level showed that LHQK significantly inhibited LPS‐induced NETs formation. Western blot revealed that LHQK effectively inhibited LPS‐triggered pyroptosis in the lung. In addition, RNA‐Seq data analysis, relatively bioinformatic analysis, and network pharmacology analysis revealed that LHQK and relative components may play multiple protective functions in LPS‐induced ALI/acute respiratory distress syndrome (ARDS) by regulating multiple targets directly or indirectly related to NETs and pyroptosis. In conclusion, LHQK can effectively attenuate lung injury and reduce lung inflammation by inhibiting LPS‐induced NETs formation and pyroptosis, which may be regulated directly or indirectly by active compounds of LHQK
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