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A new FRET-based ratiometric fluorescence probe for hypochlorous acid and its imaging in living cells
摘要： A novel ratiometric fluorescence probe for hypochlorous acid was constructed by coumarin and pyridinium fluorophore based on the Forster resonance energy transfer (FRET) and intramolecular charge transfer (ICT) platform. In this ICT/FRET system, the energy transfer efficiency is high to 94.3%. Moreover, the probe could respond to hypochlorous acid with high selectivity and sensitivity, and exhibited a large Stokes shift. It was interesting to find that the probe could recognize hypochlorous acid via a new mechanism, in which the a -position of carbonyl group was oxidized to form a diketone derivative. More importantly, the probe was successfully applied to the ratiometric imaging of both exogenous and endogenous hypochlorous acid in living RAW 264.7 cells, with low toxicity and high photo-stability.
关键词： New reaction mechanism,FRET,Hypochlorous acid,Fluorescence probe,Cell image,Ratiometric
更新于2025-11-21 11:08:12
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Rapid synthesis of AlON powders by low temperature solid-state reaction
摘要： High synthesis temperatures and long soaking times are generally required to fabricate AlON powders, which can cause coarsening and aggregation of the powder. Solid-state reaction methods form AlON powders by a direct reaction of Al2O3 and AlN, enabling rapid synthesis of AlON powder at low temperatures. In this work, single phase AlON powders were fabricated by a solid-state reaction method using Al2O3 and AlN powders as raw materials. To lower the synthesis temperature and shorten the soaking time, the raw materials particle sizes and the homogeneity of the Al2O3/AlN mixture were investigated. The effects of AlN content, synthesis temperature, and soaking time on the synthesis of AlON powders were examined. When the AlN content was 27 mol %, single phase AlON powders were synthesized by calcining Al2O3/AlN mixture at 1680 °C for 20 min. After ball-milling at 250 rpm for 24 h, the synthesized AlON powder was ground into a single phase fine AlON powder with an average particle diameter of 320 nm, a narrow size distribution, and good dispersibility. Transparent AlON ceramics with dimensions of Φ100 mm × 1 mm were fabricated by pressureless sintering the produced fine AlON powder.
关键词： B.Grain size,Aluminum oxynitride,A. Powders: solid-state reaction
更新于2025-11-19 16:56:35
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Colloidally synthesized defect-rich $$\hbox {MoSe}_{2}$$ MoSe 2 nanosheets for superior catalytic activity
摘要： Transition metal dichalcogenide (TMD) nanosheets (NSs) with defect-rich and vertically aligned edges are highly advantageous for various catalytic applications. However, colloidal synthesis of defect-rich NSs with thickness variation has been a challenging task. Here, we report a colloidal synthesis of 2H-MoSe2 NSs having a large number of defects and vertically aligned edges, where the thickness is varied by changing the amount of coordinating solvent. The Se-vacancies in these NSs have introduced defect sites which are corroborated by the presence of additional vibration modes in Raman spectra. These NSs exhibit electrocatalytic hydrogen evolution reaction performances with a low overpotential (210–225 mV) at 10 mA cm?2 current density and a small Tafel slope (54–68 mV per decade). Moreover, these MoSe2 NSs are also employed as counter electrodes (CEs) for the fabrication of dye sensitized solar cells via a cost-effective and simplified procedure. The power conversion efficiencies of 7.02 ± 0.18%, comparable with Pt CE (7.84 ± 0.10%) could be routinely achieved. These results demonstrate a novel synthetic strategy to prepare layered TMDs with superior catalytic applications.
关键词： counter electrode,Transition metal dichalcogenides,dye sensitized solar cells,MoSe2 nanosheets,hydrogen evolution reaction
更新于2025-11-19 16:56:35
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Synthesis, Crystal Structure, and Photocatalytic Properties of a Zinc(II) Coordination Polymer Based on 3-Hydroxy-2-pyridinecarboxylic Acid
摘要： The zinc(II) compound, [Zn3(HL)6]n (1) (H2L = 3-hydroxypyridine-2-carboxylic acid) was synthesized by a solvothermal reaction of Zn(NO3)2·6H2O and 3-hydroxypyridine-2-carboxylic acid as raw materials. The structure of complex 1 was determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, as well as powder X-ray diffraction. X-ray structure analysis demonstrates that the complex crystallizes in the monoclinic system, space group P21/n. There are three zinc ions in the asymmetric unit, which are either five-coordinate or six-coordinate. The asymmetric units are further bridged by the carboxylate of the organic ligands, featuring a 2D framework. The solid state diffuse-reflectance UV/Vis spectra reveals that complex 1 has semiconducting nature with the energy bandgap (Eg) estimated to be 3.11 eV. The photocatalytic properties of complex 1 in degradation of organic dyes were further investigated. Results showed that the complex could degrade 54 % of the dye methylene blue solution within 120 min under UV irradiation light and reused for five times without the decline of the photocatalytic activity.
关键词： Crystal structure,Photocatalytic properties,Zinc,3-Hydroxypyridine-2-carboxylic acid,Solvothermal reaction,Coordination polymer
更新于2025-11-19 16:56:35
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Self-generating CeVO4 as conductive channel within CeO2/CeVO4/V2O5 to induce Z-scheme-charge-transfer driven photocatalytic degradation coupled with hydrogen production
摘要： The construction of highly efficient Z-scheme photocatalytic system is regarded as a hot research topic in the fields of environmental remediation and renewable energy production. In this work, a novel Z-scheme CeO2/CeVO4/V2O5 photocatalyst is successfully prepared by using solid phase reaction method. The photocatalytic degradation of organic pollutant (Methylene Blue) with simultaneous hydrogen production is efficiently realized over the prepared Z-scheme CeO2/CeVO4/V2O5 photocatalysts under visible-light irradiation. The effects of treatment temperatures and treatment times of CeO2/V2O5 composite on the photocatalytic performance of Z-scheme CeO2/CeVO4/V2O5 photocatalyst are studied. The as-prepared Z-scheme CeO2/CeVO4/V2O5 (550-3) photocatalyst heat-treated at 550 °C for 3.0 h exhibits the highest photocatalytic performance. It can be ascribed to a moderate amount of CeVO4 nanoparticles generated between CeO2 and V2O5. The generated CeVO4 nanoparticles can be used as effective conductive channel to transfer the photo-generated carriers. At the same time, as redox reaction centers it can further accelerate the transfer of photo-generated electrons, effectively enhancing the separation efficiency of photo-generated electron and hole pairs. Furthermore, cyclic test demonstrates that the as-prepared Z-scheme CeO2/CeVO4/V2O5 (550-3) photocatalyst still maintains a high level of photocatalytic activity within five periods under the same conditions. Moreover, the related photocatalytic mechanism for degradation of organic pollutants with simultaneous hydrogen evolution over the Z-scheme CeO2/CeVO4/V2O5 (550-3) photocatalyst is proposed. Perhaps, this study affords a simple and novel method to design and develop next generation of highly efficient Z-scheme photocatalysts.
关键词： Conductive channel,Z-scheme CeO2/CeVO4/V2O5 photocatalyst,Solid phase reaction method,Simultaneous hydrogen evolution,Visible-light photocatalytic degradation
更新于2025-11-19 16:51:07
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Thiourea-assisted coating of dispersed copper electrocatalysts on Si photocathodes for solar hydrogen production
摘要： Photoelectrochemical water splitting can convert solar energy into clean hydrogen energy for storage. It is desirable to explore non-precious electrocatalysts for practical applications of a photoelectrode in a large scale. Here, we developed a facile spin-coating and in-situ photoelectrochemical reduction method to prepare a dispersed Cu electrocatalyst on a Si photocathode, which improves the performance remarkably. We find that thiourea in the precursor solution for spin-coating plays an important role in obtaining dispersed Cu particles on the surface of a Si photoelectrode. With thiourea in the precursor, the Cu/Si photocathode shows higher performance than the one without thiourea. Moreover, the Cu/Si photocathode also indicates good stability after 16 h illumination.
关键词： In-situ photoelectrochemical reduction,Cu electrocatalyst,Thiourea,Hydrogen evolution reaction
更新于2025-11-19 16:51:07
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Conjugated helical polymers: End-group control and coupling reactions
摘要： Telechelic helical poly(phenyleneethynylene)s 2 and 3 bearing end iodo and ethynyl groups were synthesized by the Sonogashira–Hagihara coupling reaction of prepolymer 1 with N-α-tert-butoxycarbonyl-3,5-diiodo-4-hydroxy-D-phenylglycine hexylamide (4) and p-diethynylbenzene (5), respectively. Polymer 2 was treated by Sonogashira–Hagihara coupling reaction with 1,6-diethynylpyrene (a) and 4,4-diethynylbiphenyl (b) to obtain the corresponding polymers 2a and 2b. Polymer 2 was also subjected to the Mizoroki–Heck coupling reaction with diphenyl(p-vinylphenyl)phosphine (e) to obtain the corresponding polymer 2e, and the incorporation of the phosphine moieties was confirmed by 31P NMR spectroscopy. In a similar fashion, polymer 3 was polymerized with 1,4-dibromonaphthalene (c) and 9,10-dibromoanthracene (d), but no concrete evidence for the formation of polymers 3c and 3d was observed. Circular dichroism (CD) spectroscopic analysis revealed that all the polymers adopted folded helical conformations with predominantly one-handed screw sense in CHCl3. The polymers exhibited photoluminescence (PL) depending on the incorporated functional groups.
关键词： helical polymer,telechelic polymer,coupling reaction,conjugated polymer
更新于2025-11-19 16:46:39
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A high-performance room temperature methanol gas sensor based on alpha-iron oxide/polyaniline/PbS quantum dots nanofilm
摘要： A high-performance room temperature methanol gas sensor based on alpha-iron oxide/polyaniline/lead sulfide quantum dots (α-Fe2O3/PANI/PbS QDs) nanofilm was demonstrated in this paper, among which the α-Fe2O3 was an urchin-shaped hollow microsphere. The sensing film was fabricated on an epoxy substrate with interdigital electrodes via successive ionic layer adsorption and reaction technique. The prepared α-Fe2O3/PANI/PbS QDs nanocomposite was examined by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, scanning election microscopy and Fourier transform infrared spectrum. The methanol sensing performances of the α-Fe2O3/PANI/PbS QDs film sensor were investigated against methanol from 10 to 100 ppm at room temperature. The experimental results indicated that the methanol sensor in this work had an excellent response, outstanding selectivity and good repeatability at room temperature. The underlying sensing mechanism of the α-Fe2O3/PANI/PbS QDs film toward methanol was ascribed to a series of interactions and changes on the surface of thin films, which make their resistance change greatly. Larger surface area and much more active adsorption sites also played an important role.
关键词： Methanol gas sensor,Room temperature,Successive ionic layer adsorption and reaction,Hydrothermal method,α-Fe2O3/PANI/PbS QDs
更新于2025-11-14 17:15:25
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Co and Fe Codoped WO <sub/>2.72</sub> as Alkaline‐Solution‐Available Oxygen Evolution Reaction Catalyst to Construct Photovoltaic Water Splitting System with Solar‐To‐Hydrogen Efficiency of 16.9%
摘要： Oxygen evolution electrode is a crucial component of efficient photovoltaic-water electrolysis systems. Previous work focuses mainly on the effect of electronic structure modulation on the oxygen evolution reaction (OER) performance of 3d-transition-metal-based electrocatalyst. However, high-atomic-number W-based compound with complex electronic structure for versatile modulation is seldom explored because of its instability in OER-favorable alkaline solution. Here, codoping induced electronic structure modulation generates a beneficial effect of transforming the alkaline-labile WO2.72 (WO) in to efficient alkaline-solution-stable Co and Fe codoped WO2.72 (Co&Fe-WO) with porous urchin-like structure. The codoping lowers the chemical valence of W to ensure the durability of W-based catalyst, improves the electron-withdrawing capability of W and O to stabilize the Co and Fe in OER-favorable high valence state, and enriches the surface hydroxyls, which act as reactive sites. The Co&Fe-WO shows ultralow overpotential (226 mV, J = 10 mA cm?2), low Tafel slope (33.7 mV dec?1), and good conductivity. This catalyst is finally applied to a photovoltaic-water splitting system to stably produce hydrogen for 50 h at a high solar-to-hydrogen efficiency of 16.9%. This work highlights the impressive effect of electronic structure modulation on W-based catalyst, and may inspire the modification of potential but unstable catalyst for solar energy conversion.
关键词： electrocatalysis,photovoltaic water splitting,oxygen evolution reaction,codoping,WO2.72
更新于2025-11-14 17:04:02
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The Preparation and Characterization of Fluorinated Graphene Oxide with Different Degrees of Oxidation
摘要： For many excellent graphene derivatives, tailoring the material properties is crucial to get a broader application. In the present work, a series of fluorinated graphene oxide (FGO) with various oxidation degree were synthesized using a modified Hummers method at different reaction temperatures. The structure and property of FGO were analyzed by X-ray diffraction (XRD), Fourier transform infra-red spectra (FT-IR), X-ray photoelectron spectra (XPS) and Zeta potential analysis. The results indicate that the oxygen contents range from 5.61 % to 21.96 % in FGO can be tuned by altering the reaction temperatures. The oxygen in FGO is presented mainly in the form of epoxide and carboxyl groups. With increasing reaction temperature from 50 °C to 90 °C, the oxygen content in FGO decreases and thicker multilayered FGO is formed with lower dispersibility.
关键词： Controllable oxidation,Fluorinated Graphene Oxide,Low temperature reaction
更新于2025-11-14 17:04:02