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oe1(光电查) - 科学论文

17 条数据
?? 中文(中国)
  • La-modified TiO2/carbon nanotubes assembly nanocomposite for efficient photocatalytic hydrogen evolution from glycerol-water mixture

    摘要: Lanthanum (La) modified TiO2 embedded over carbon nanotubes (CNTs) to develop nanocomposite for enhanced photocatalytic hydrogen evolution from glycerol-water mixture has been investigated. The samples, synthesized by sol-gel assisted hydrothermal method, were characterized by XRD, FESEM, HRTEM, FTIR, BET, UVeVisible, Raman and PL spectroscopy. La/TiO2 anchored CNTs has larger surface area with uniform distribution of La3+ ions. The performance of hybrid assembly was evaluated in a continuous flow slurry photoreactor system under UVevisible light irradiations. The highest H2 evolution rate of 17265 ppm g-cat-1 h-1 was obtained over 5% La-5% CNTs/TiO2 NRs, 1.14 folds the amount produced over 5% La-5% CNTs/TiO2 NPs, 1.53 time than 5% La/TiO2 and 4.10 folds than using pure TiO2 NPs. This significant improvement in the photo-activity was obviously due to synergistic effect between La and CNTs, larger BET surface area, cleavage of glycerol by La, appropriate band structure, and hindered charges recombination rate. Among the sacrificial reagents, highest H2 evolution was obtained using glycerol due to the presence of a-hydrogen atoms attached to carbon atoms. A correlation between BET surface area and photonic flux in terms of photocatalytic H2 production rate was established to understand the performance of hybrid nanostructures. It was observed that BET surface area and photo-flux utilization for the generation of charge carriers with their efficient separation has significant contribution towards improved H2 production rate. More interestingly, catalyst persisted prolonged stability with a steady H2 production in cyclic runs. This study provides promising pathway for constructing composite of La/TiO2 coupled CNTs for efficient H2 production under visible light.

    关键词: La/TiO2,Glycerol,TiO2/CNTs hybrid,H2 production,Visible light,Photo-catalysis

    更新于2025-09-23 15:23:52

  • Biobased Aromatic-Aliphatic Polyols from Cardanol by Photochemical Thiol-ene Reaction

    摘要: Biobased aromatic-aliphatic polyols were previously synthesized from a thermal thiol-ene reaction of propoxylated cardanol with 2-mercaptoethanol (ME) in the presence of azobisisobutyronitrile (AIBN) as a radical initiator. Cardanol used for this purpose was obtained as a dark-brown liquid (Gardner Color Reference ~18). The photochemical thiol-ene reaction can also be used to prepare aromatic-aliphatic polyols by employing cardanol. Via the photochemical thiol-ene reaction, 2-mercaptoethanol was added successfully to C=C double bond of cardanol, suggesting that phenolic group may not play an inhibitory role in the radical thiol-ene reaction. However, we preferred to alkoxylate the phenolic hydroxyl group of cardanol, which is much more reactive with isocyanates than phenolic hydroxyls, to generate a new aliphatic hydroxyl group. Furthermore, the functionality of polyols was also improved by two methods: 1) using 1-thio-glycerol instead of 2-mercaptoethanol and 2) using alkoxylated cardanol with glycidol (Cardanol-GLY) instead of propoxylated cardanol (Cardanol-PO). These polyols were then used in preparation of rigid polyurethane foams that can be useful in various applications such as insulation of freezers, pipes and storage tanks in food and chemical industries.

    关键词: 1-thio-glycerol,2-mercaptoethanol,photochemical reactions,thiol-ene reaction,Cardanol

    更新于2025-09-23 15:22:29

  • Transparent and Flexible Electronics Assembled with Metallic Nanowire-Layered Non-drying Glycerogel

    摘要: There has been increasing demand for transparent and mechanically durable electrical conductors for their uses in wearable electronic devices. It is common to layer metallic nanowires on transparent but stiff polydimethylsiloxane (PDMS) or stretchable but opaque EcoflexTM-based substrates. Here, we hypothesized that layering metallic nanowires on a stretchable and hygroscopic gel would allow us to assemble a transparent, stretchable, and durable conductor. The hygroscopic property of the gel was attained by partially replacing water in the pre-formed polyacrylamide hydrogel with glycerol. The resulting gel, denoted as a glycerogel, could remain hydrated for over 6 months in air by taking up water molecules from the air. The glycerogel was tailored to be stretchable up to 8 times its original length by tuning the amount of cross-linker and acrylamide. The resulting glycerogel allowed for deposition of wavy silver nanowires using the pre-strain method up to 400 % pre-strain, without causing kinks and interfacial cracks often found with nanowires layered onto PDMS. With a pre-strain of 100%, the resulting nanowire-gel conductor exhibited optical transparency (85%) and electrical conductivity (17.1 ohm/sq) even after 5,000 cycles of deformation. The results of this study would broadly be useful to improve the performance of the next generation of flexible electronic devices.

    关键词: glycerol,toughness,hydration,stretchable hydrogel,flexible electronics

    更新于2025-09-23 15:21:01

  • Electronically-tuned 2-(2′-Hydroxyphenyl)-4-pyrenylthiazole through Bond Energy Transfer Donor-Acceptor Couples: Sensing and Biological Applications

    摘要: A novel pyrene-conjugated 2-(20-hydroxyphenyl)thiazole probe (HPTP, 1) was prepared, and its photophysical and sensing properties were investigated and compared to those of four model compounds. HPTP effectively detects CN? and glycerol in DMSO, with “turn off” at 425 nm and “turn on” at 495 nm. The sensing ability of 1 towards CN? ions in DMSO, mediated by the hydrogen bonding-induced disaggregation of aggregates, resulted in the quenching of ESIPT emission at 425 nm. By contrast, in a DMSO–glycerol mixed medium, the aggregate size increased together with the increased degree of intermolecular π–π interactions between two pyrene units located on adjacent molecules, and resulted in partial inhibition of energy/charge transfer from the pyrene unit to the thiazole unit in the excited state. Excitation energy transfer with increased photostability of the ESIPT core was effectively demonstrated in Candida albicans cell lines.

    关键词: Glycerol,Pyrene,CN?,Excited state intramolecular proton transfer,2-(2’-Hydroxyphenyl)thiazole,Aggregation-induced emission

    更新于2025-09-23 15:21:01

  • Electrocatalytic glycerol oxidation enabled by surface plasmon polariton-induced hot carriers in Kretschmann configuration

    摘要: Plasmonic hot carrier generation has attracted increasing attention due to its ability to convert light to electrical energy. The generation of plasmon-induced hot carriers can be achieved via Landau damping in the non-radiative decay process of the plasmonic excitation energy. Localized surface plasmons (LSPs) undergo both radiative and non-radiative decays, while surface plasmon polaritons (SPPs) dissipate only via the non-radiative decay. Thus, it is a challenging task to exploit the surface plasmon polaritons for the efficient generation of hot carriers and their applications. In this study, a model hot-carrier-mediated electrocatalytic conversion system was demonstrated using an Au thin film in Kretschmann configuration, which is the representative platform to excite SPPs. AgPt-decorated Au nanobipyramids (AuNBPs) were designed and introduced onto the Au film, creating hot-spots to revolutionize the thin film-based photon-to-carrier conversion efficiency. The glycerol electro-oxidation reaction enabled by such SPP-induced hot carriers was evaluated and exhibited a photon-to-hot carrier conversion efficiency of 2.4 × 10?3%, which is ~2.5 times enhanced as compared to the efficiency based on the neat Au film.

    关键词: Electrocatalytic glycerol oxidation,Surface plasmon polaritons,Au nanobipyramids,Plasmonic hot carrier generation,Kretschmann configuration

    更新于2025-09-16 10:30:52

  • Preparation and growth mechanism of CdS quantum dots in octadecene/glycerol two-phase systems

    摘要: Two-phase synthesis is an advantageous alternative to the traditional synthetic method, due to its less toxicity, controllable, mild synthetic conditions and easy large-scale synthesis. However, meeting novel synthesis, the conventional trial-and-error approach could not provide a clear understanding. We herein report synthesis and mechanism investigation of CdS quantum dots in octadecene/glycerol two-phase system. The effects of different reaction parameters and conditions including reaction temperature, reaction time, reactant concentrations, and synthesis routes (one-step and two-step approach) on both nucleation and particle growth were investigated. It was found that the synthesis course was a growth dominated process depending on both CdS(monomer) and CdS (nuclei), and controlled by the interface of ODE/glycerol. The present work provided a new and clear understanding about two-phase system synthesis on semiconductor quantum dots, noble metal nanocrystals and some alloy nanomaterials.

    关键词: Octadecene/glycerol two-phase systems,Growth mechanism,CdS quantum dots,One-step synthesis

    更新于2025-09-16 10:30:52

  • Sulfolobus acidocaldarius Microvesicles Exhibit Unusually Tight Packing Properties as Revealed by Optical Spectroscopy

    摘要: In this study, we used optical spectroscopy to characterize the physical properties of microvesicles released from the thermoacidophilic archaeon Sulfolobus acidocaldarius (Sa-MVs). The most abundant proteins in Sa-MVs are the S-layer proteins, which self-assemble on the vesicle surface forming an array of crystalline structures. Lipids in Sa-MVs are exclusively bipolar tetraethers. We found that when excited at 275 nm, intrinsic protein fluorescence of Sa-MVs at 23 °C has an emission maximum at 303 nm (or 296 nm measured at 75 °C), which is unusually low for protein samples containing multiple tryptophans and tyrosines. In the presence of 10–11 mM of the surfactant n-tetradecyl-β-d-maltoside (TDM), Sa-MVs were disintegrated, the emission maximum of intrinsic protein fluorescence was shifted to 312 nm, and the excitation maximum was changed from 288 nm to 280.5 nm, in conjunction with a significant decrease (>2 times) in excitation band sharpness. These data suggest that most of the fluorescent amino acid residues in native Sa-MVs are in a tightly packed protein matrix and that the S-layer proteins may form J-aggregates. The membranes in Sa-MVs, as well as those of unilamellar vesicles (LUVs) made of the polar lipid fraction E (PLFE) tetraether lipids isolated from S. acidocaldarius (LUVPLFE), LUVs reconstituted from the tetraether lipids extracted from Sa-MVs (LUVMV) and LUVs made of the diester lipids, were investigated using the probe 6-dodecanoyl-2-dimethylaminonaphthalene (Laurdan). The generalized polarization (GP) values of Laurdan in tightly packed Sa-MVs, LUVMV, and LUVPLFE were found to be much lower than those obtained from less tightly packed DPPC gel state, which echoes the previous finding that the GP values from tetraether lipid membranes cannot be directly compared with the GP values from diester lipid membranes, due to differences in probe disposition. Laurdan’s GP and red-edge excitation shift (REES) values in Sa-MVs and LUVMV decrease with increasing temperature monotonically with no sign for lipid phase transition. Laurdan’s REES values are high (9.3–18.9 nm) in the tetraether lipid membrane systems (i.e., Sa-MVs, LUVMV and LUVPLFE) and low (0.4–5.0 nm) in diester liposomes. The high REES and low GP values suggest that Laurdan in tetraether lipid membranes, especially in the membrane of Sa-MVs, is in a very motionally restricted environment, bound water molecules and the polar moieties in the tetraether lipid headgroups strongly interact with Laurdan’s excited state dipole moment, and “solvent” reorientation around Laurdan’s chromophore in tetraether lipid membranes occurs very slowly compared to Laurdan’s lifetime.

    关键词: glycerol dialkyl glycerol tetraether (GDGT),liposomes,intrinsic protein fluorescence,microvesicles,red edge excitation shift (REES),glycerol dialkyl calditol tetraether (GDNT),generalized polarization (GP),thermoacidophilic archaea,membrane probe,Laurdan

    更新于2025-09-11 14:15:04

  • Plasmonic Oxidation of Glycerol Using Au/TiO2 Catalysts Prepared by Sol-Immobilisation

    摘要: Au nanoparticles supported on P25 TiO2 (Au/TiO2) were prepared by a facile sol-immobilisation method and investigated for the surface plasmon-assisted glycerol oxidation under base-free conditions. The Au/TiO2 samples were characterized by UV–vis spectroscopy and transmission electron microscopy. Catalysts were prepared using polyvinyl alcohol as stabiliser as well as in the absence of polymer stabiliser. Both the conversion and the reaction selectivity are affected by the plasmon-assisted oxidation and there is an interplay between the presence of the stabiliser and the Au nanoparticle size.

    关键词: Plasmonic,Gold,Glycerol oxidation

    更新于2025-09-11 14:15:04

  • Plasmonic oxidation of glycerol using AuPd/TiO2 catalysts

    摘要: AuPd nanoparticles supported on P25 TiO2 (AuPd/TiO2) were prepared by a facile sol-immobilisation method and investigated for surface plasmon-assisted glycerol oxidation under base-free conditions. The AuPd/TiO2 samples were characterized by UV-vis spectroscopy and transmission electron microscopy. The sol-immobilisation method readily permitted the Au:Pd molar ratio to be changed over a wide range whilst keeping the mean particle size of the AuPd nanoparticles at 3nm. Visible light irradiation during the reaction has a beneficial effect on the conversion of glycerol with the most marked effect being observed with gold-rich catalysts and the increase of conversion on light irradiation increases linearly with the gold content of the nanoparticles. The reaction selectivity is also affected by the plasmon-assisted oxidation and glycolic acid, not observed during the dark reactions, was observed for all illuminated reactions due to the enhanced activity of these catalysts.

    关键词: visible light irradiation,AuPd nanoparticles,glycerol oxidation,plasmonic photocatalysis,sol-immobilisation

    更新于2025-09-11 14:15:04

  • Challenges arising from the use of TiO2/rGO/Pt photocatalysts to produce hydrogen from crude glycerol compared to synthetic glycerol

    摘要: Photoreforming has emerged as a novel technology expected to obtain chemical energy through solar energy transformation. In this way, sustainable valorization of glycerol, a biodiesel by-product, to clean fuels is a promising alternative to help meet the world's growing energy demand. In this work, TiO2/rGO(x)/Pt(y) photocatalysts have been developed for hydrogen production from synthetic and crude glycerol solutions. The effect of several key operating parameters (including vol% of glycerol, pH, catalyst loading, wt% of GO, wt% of Pt, temperature, and light source) on hydrogen production rate has been studied. The results indicated different optimal operating parameters depending on glycerol origin, achieving up to 70.8 and 12.7 mmol h?1 g?1 of hydrogen using synthetic glycerol and crude glycerol, respectively. Additionally, GO nanosheets and Pt nanoparticles strongly influenced the hydrogen production rate but not the overall reaction mechanism. Impurities contented in crude glycerol are key factors in developing realistic hydrogen production processes.

    关键词: Platinum,Graphene,Hydrogen production,Photoreforming,TiO2,Crude glycerol

    更新于2025-09-11 14:15:04