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Crosslink network and phenyl content on the optical, hardness, and thermal aging of PDMS LED encapsulant
摘要： This work aims to synthesize new series of polysiloxane copolymer through hydrosilylation reaction based on different level of crosslink densities and phenyl content. The results revealed that polysiloxanes resins with phenyl rings increased viscosity up to 3800 cps while displaying a relatively high refractive index of 1.531. The asymmetric phenyl substitution onto chain backbone led to formation of densely packed structure resulting in reduced water absorption and gas permeability of PDMS resins. High level of crosslinking contributed to a high shore A hardness and adhesion strength. It displayed transparency of 97% whose percentage reduction was 1.6% under thermal and 0.6% UV aging. No obvious discoloration was observed during accelerated thermal aging up to 210 min at 80 (cid:1)C. These results are key attributes that make the synthesized polysiloxane series as ideal candidate for high brightness LED encapsulant. ? 2019 Wiley Periodicals, Inc. ? 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47895.
关键词： copolymers,thermal properties,ring-opening polymerization,optical properties,synthesis and processing techniques
更新于2025-11-19 16:56:42
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One-Step Photochemical Synthesis of Transition Metal - Graphene Hybrid for Electrocatalysis
摘要： For widespread use of renewable energy such as water splitting, the development of electrocatalysts on a large-scale at a low-cost that remains safe and environmentally friendly is still a great challenge. Here, we report the use of α-aminoalkyl radicals in a one-step procedure that synthesizes transition metal nanoparticle - graphene composites via photoreduction. The organic photocatalyst 2-Methyl-1-[4-(methylthio)phenyl]-2-(morpholinyl) phenyl]-1-butanone (I-907) undergoes Norrish Type I photocleavage to generate strongly reducing α-aminoalkyl radicals, when exposed to UVA. For the first time we demonstrate its ability to reduce graphene oxide (GO) and successfully synthesize Co3O4 nanoparticles decorated on graphene (Co3O4NP-rGO). The α-aminoalkyl radicals simultaneously reduce GO and Co2+ salts which nucleates on the negatively charged GO sheets and grows to form nanoparticles. The resulting Co3O4NP-rGO showed decent catalytic activity and stability for the Oxygen Evolution Reaction (OER). Our work introduces a new and environmentally friendly synthesis procedure that can be used to produce earth abundant transition metal electrocatalysts.
关键词： photochemical synthesis,reduced graphene oxide,Graphene oxide,α-aminoalkyl radicals,water oxidation,metal nanoparticles
更新于2025-11-19 16:56:35
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Visible light-driven photoelectrocatalytic degradation of Acid Yellow 17 using Sn3O4 flower-like thin films supported on Ti substrate (Sn3O4/TiO2/Ti)
摘要： This article reports a new method for preparing mixed valence tin oxide (Sn3O4) flower-like nanostructures using a microwave-assisted route. Thin-film Sn3O4/TiO2/Ti electrodes demonstrated highly efficient visible light driven photocatalytic degradation of monoazo acid yellow 17 (AY17) dye, reaching 95% color removal after 60 min at pH 2. Moreover, under low bias potential (0.5 V), the photoelectrocatalytic efficiency increased to 97% color removal and 83% removal of total organic carbon at a kinetic rate almost 3 times higher than in photocatalysis. Liquid chromatography mass spectrometry was used to identify intermediate formation, and oxidation performance was proposed for photocatalytic and photoelectrocatalytic degradation with no organics identified after 120 min of treatment. The results indicate that Sn3O4/TiO2/Ti photoelectrodes offer a simple, green method for wastewater treatment employing visible light source.
关键词： Dye degradation,Photoelectrocatalysis,Microwave-assisted hydrothermal synthesis,Sn3O4,Visible-light photocatalysis
更新于2025-11-19 16:56:35
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Atmospheric Pressure Plasma Synthesized Gold Nanoparticle/Carbon Nanotube Hybrids for Photo-thermal Conversion
摘要： In this work, a room temperature atmospheric pressure direct-current plasma has been deployed for the one-step synthesis of gold nanoparticle/carboxyl group functionalized carbon nanotube (AuNP/CNT-COOH) nanohybrids in aqueous solution for the first time. Uniformly distributed AuNPs are formed on the surface of CNT-COOH, without the use of reducing agents or surfactants. The size of the AuNP can be tuned by changing the gold salt precursor concertation. UV-Vis, ζ-potential and X-ray photoelectron spectroscopy suggest that carboxyl surface functional groups on CNTs served as nucleation and growth sites for AuNPs and the multiple potential reaction pathways induced by the plasma-chemistry have been elucidated in detail. The nanohybrids exhibit significantly enhanced Raman scattering and photothermal conversion efficiency, properties that are essential for potential multi-modal cancer treatment applications.
关键词： Surface Enhanced Raman Scattering,Gold Nanoparticles,Photothermal Conversion,Carbon Nanotubes,Plasma Synthesis
更新于2025-11-19 16:56:35
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The Application of Green-Synthesis-Derived Carbon Quantum Dots to Bioimaging and the Analysis of Mercury(II)
摘要： Ginkgo leaves were used as precursors for the hydrothermal synthesis of carbon quantum dots (CQDs), which were subsequently characterized by transmission electron microscopy as well as Fourier-transform infrared, X-ray powder di?raction, and X-ray photoelectron spectroscopy. The prepared CQDs exhibited a ?uorescence quantum yield of 11% and superior water solubility and ?uorescence stability, as well as low cytotoxicities and excellent biocompatibilities with A549 and HeLa cells; these CQDs were also used to bioimage HeLa cells. Moreover, owing to the experimental observation that Hg2+ quenches the ?uorescence of the CQDs in a speci?c and sensitive manner, we developed a method for the detection of Hg2+ using this ?uorescence sensor. The sensor exhibited a linear range for Hg2+ of 0.50–20 μM, with an excellent coe?cient of determination (R2 ? 0.9966) and limit of detection (12.4 nM). In practice, the proposed method was shown to be highly selective and sensitive for the monitoring of Hg2+ in lake water and serum samples.
关键词： mercury(II) detection,carbon quantum dots,hydrothermal synthesis,fluorescence quenching,bioimaging
更新于2025-11-19 16:46:39
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One-step Aqueous Synthesis of Zn-based Quantum Dots as Potential Generators of Reactive Oxygen Species
摘要： The actual incorporation of dopant species into the ZnS Quantum Dots (QDs) host lattice will induce structural defects evidenced by a red shift in the corresponding exciton. The doping should create new intermediate energetic levels between the valence and conduction bands of the ZnS and affect the electron-hole recombination. These trap states would favour the energy transfer processes involved with the generation of cytotoxic radicals, so-called Reactive Oxygen Species, opening the possibility to apply these nanomaterials in cancer research. Any synthesis approach should consider the direct formation of the QDs in biocompatible medium. Accordingly, the present work addresses the microwave-assisted aqueous synthesis of pure and doped ZnS QDs. As-synthesized quantum dots were fully characterized on a structural, morphological and optical viewpoint. UV-Vis analyzes evidenced the excitonic peaks at approximately 310 nm, 314 nm and 315 nm for ZnS, Cu-ZnS and Mn-ZnS, respectively, Cu/Zn and Mn/Zn molar ratio was 0.05%. This indicates the actual incorporation of the dopant species into the host lattice. In addition, the Photoluminescence spectrum of non-doped ZnS nanoparticles showed a high emission peak that was red shifted when Mn2+ or Cu2+ were added during the synthesis process. The main emission peak of non-doped ZnS, Cu-doped ZnS and Mn-doped ZnS were observed at 438 nm, 487 nm and 521 nm, respectively. Forthcoming work will address the capacity of pure and Cu-, Mn-ZnS quantum dots to generate cytotoxic Reactive Oxygen Species for cancer treatment applications.
关键词： Cancer research,ZnS Quantum Dots,Doping,Microwave-assisted synthesis,Reactive Oxygen Species
更新于2025-11-19 16:46:39
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Ultrasonic-Assisted Synthesis of a Zn(II) Coordination Polymer in Aqueous Media and Its High-Performance Luminescent Sensing for 2,4,6-Trinitrophenol
摘要： A novel Zn(II) coordination polymer based on 5-(3-pyridyl)-1,3,4-oxadiazole-2-thiol (Hpzt), namely [Zn(pzt)2]n or (Zn-CP), was synthesized by two different synthetic methods. The bulk polycrystals and single-crystals of Zn-CP were obtained by the conventional solvothermal method at 90°C. The Zn-CP exhibits a two-dimensional (2D) coordination network that contains the uncoordinated Lewis basic sites within each layer. Interestingly, a simple environmentally friendly sonochemical synthesis of the Zn-CP in an aqueous media could be performed at room temperature. The optimal synthetic conditions were studied. The uniform microplates of Zn-CP were obtained within 30 min with the addition of pyridine, acting as a sized modulator and a deprotonating reagent. The influence of the amount of the modulator and the sonication time on their crystalline size was investigated. Moreover, the Zn-CP suspension in an ethanolic media has been used as a luminescence sensor for the detection of nitroaromatic compounds. It shows highly selective and sensitive sensing of 2,4,6-trinitrophenol (TNP) through the quenching (turn off) process under the UV light. Also, the Zn-CP microplates show the higher dispersibility and more stable suspension than those of bulk products causing an increase of the luminescent sensing performance for TNP.
关键词： 2,sonochemical synthesis,4,Zn(II),Coordination polymer,luminescence,6-trinitrophenol
更新于2025-11-19 16:46:39
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Composition-gradient ZnO/Zn(S,O) heterostructure nanorod arrays and their cathodoluminescence
摘要： Well-aligned ZnO/Zn(S,O) heterostructure nanorods have been synthesized through a well-designed chemical vapor deposition synthesis process. The as-synthesized ZnO/Zn(S,O) heterostructures exhibit a single crystal characteristic and a transitive interface with obvious composition gradient. X-ray Energy dispersive spectrometer (EDS) analysis demonstrates that ZnS-phase is rich in the nanorod bottom during the initial nucleation process and the S element content has a drastic decrease along the heterostructure nanorod from the bottom to the top, while O element is spatially detected in the whole rod. Room-temperature cathodoluminescence measurements verify two UV emissions at 330 nm and 385 nm for respective Zn(S,O) and ZnO phases with a strong defect-related emission band in visible range. Finally, the growth mechanism and optical emissions of ZnO/Zn(S,O) heterostructure nanorods are discussed.
关键词： ZnS,Heterostructures,ZnO,Synthesis,Cathodoluminescence
更新于2025-11-14 17:15:25
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Laser-induced synthesis and photocatalytic properties of hybrid organic–inorganic composite layers
摘要： A laser-based method was developed for the synthesis and simultaneous deposition of multicomponent hybrid thin layers consisting of nanoentities, graphene oxide (GO) platelets, transition metal oxide nanoparticles, urea, and graphitic carbon nitride (g-C3N4) for environmental applications. The photocatalytic properties of the layers were tested through the degradation of methyl orange organic dye probing molecule. It was further demonstrated that the synthesized hybrid compounds are suitable for the photodegradation of chloramphenicol, a widely used broad-spectrum antibiotic, active against Gram-positive and Gram-negative bacteria. However, released in aquatic media represents a serious environmental hazard, especially owing to the formation of antibiotic-resistant bacteria. The obtained results revealed that organic, urea molecules can become an alternative to noble metals co-catalysts, promoting the separation and transfer of photoinduced charge carriers in catalytic composite systems. Laser radiation induces the reduction of GO platelets and the formation of graphene-like material. During the same synthesis process, g-C3N4 was produced, by laser pyrolysis of urea molecules, without any additional heat treatment. The layers exhibit high photocatalytic activity, being a promising material for photodegradation of organic pollutants in wastewater.
关键词： transition metal oxide nanoparticles,urea,photocatalytic properties,hybrid organic–inorganic composite layers,graphene oxide,graphitic carbon nitride,methyl orange,laser-based synthesis,chloramphenicol
更新于2025-11-14 17:04:02
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In Situ Microwave-Assisted Fabrication of Hierarchically Arranged Metal Sulfide Counter Electrodes to Boost Stability and Efficiency of Quantum Dot-Sensitized Solar Cells
摘要： This study describes preparation of metal sulfide counter electrodes (CEs) through one-pot microwave-assisted route to improve power conversion efficiency (PCE) of quantum dot-sensitized solar cells at a lower cost. The CuS nanorods, Ni0.96S nanoparticles, and PbS nanocubes are synthesized and deposited in situ on fluorine-doped tin oxide substrate to serve as CEs without further post-treatment. Effects of several reaction parameters including sulfur precursor (Na2S, C2H5NS, CH4N2S), Cu concentration, reaction time, and choice of cation (Cu, Ni, Pb) on the CEs morphology, electrochemical characteristics, and PCE are studied. Furthermore, nanostructure formation and thin film growth are studied and correlated with PCE, from which morphology- and composition-performance relationships can be inferred. Hierarchically assembled nanorod CuS CEs exhibit higher electrochemical stability in the S2–/Sn2– redox reaction. Together with the efficient charge transfer and higher diffusion coefficient of polysulfide redox at the electrode/electrolyte interface, deduced from electrochemical impedance spectroscopy and Tafel analyses, a PCE of 8.32% is achieved for the CuS CE. The enhanced photovoltaic performance is ascribed to the 1D CuS nanorods forming a diffusive structure which decreases charge transfer impedance and facilitates regeneration of polysulfide redox leading to a higher short-circuit current density and fill factor.
关键词： In situ deposition,quantum dot-sensitized solar cells,counter electrode,CuS,microwave-assisted synthesis
更新于2025-11-14 17:04:02